Skocz do pozycji: 1.

Tytuł:

Estimating multiplicity of infection, allele frequencies, and prevalences accounting for incomplete data.

Autorzy:

Hashemi, Meraj (AUTHOR)
Schneider, Kristan A. (AUTHOR)

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Źródło:

PLoS ONE. 3/21/2024, Vol. 19 Issue 3, p1-35. 35p.

Czasopismo naukowe

• na półce

Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły

Skocz do pozycji: 2.

Tytuł:

Genomic Evaluation of Average Daily Gain Traits in a Mixture of Arian Line and Urmia Iranian Native Chickens.

Autorzy:

Asadollahi, H.
Mahyari, S. Ansari
Torshizi, R. Vaez
Emrani, H.
Ehsani, A.

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Alternatywny tytuł:

ارزیابی ژنومی صفت میانگین افزایش وزن روزانه در جمعیت حاصل از تلاقی لاین آرین و جوجه های بومی ارومیه ایران

Źródło:

Journal of Agricultural Science & Technology. 2024, Vol. 26 Issue 2, p299-312. 14p.

Czasopismo naukowe

• na półce

Pełny tekst  Link otwiera się w nowym oknieSzczegóły

Skocz do pozycji: 3.

Tytuł:

Investigation of HLA susceptibility alleles and genotypes with hematological disease among Chinese Han population.

Autorzy:

Li YM; Shenzhen Tissuebank Precision Medicine Co., Ltd, Shenzhen, China.
Li YX; Shanghai Tissuebank Biotechnology Co., Ltd, Shanghai, China.
Li DY; Shenzhen Tissuebank Precision Medicine Co., Ltd, Shenzhen, China.
Zhou Y; Shenzhen Tissuebank Precision Medicine Co., Ltd, Shenzhen, China.
An L; Shanghai Tissuebank Biotechnology Co., Ltd, Shanghai, China.
Yuan ZY; Shenzhen Tissuebank Precision Medicine Co., Ltd, Shenzhen, China.
Du KM; Shenzhen Tissuebank Precision Medicine Co., Ltd, Shenzhen, China.
Zheng ZZ; Shenzhen Tissuebank Precision Medicine Co., Ltd, Shenzhen, China.

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Źródło:

PloS one [PLoS One] 2024 Apr 09; Vol. 19 (4), pp. e0281698. Date of Electronic Publication: 2024 Apr 09 (Print Publication: 2024).

Typ publikacji:

Journal Article

MeSH Terms:

Histocompatibility Antigens Class I*/genetics
Hematologic Diseases*/genetics
Humans ; Gene Frequency ; Alleles ; HLA-DQ beta-Chains/genetics ; HLA-DRB1 Chains/genetics ; Genotype ; Haplotypes ; Genetic Predisposition to Disease

Czasopismo naukowe

• na półce

Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły

Skocz do pozycji: 4.

Tytuł:

Population-wide modelling reveals prospects of marker-assisted selection for parasitic mite resistance in honey bees.

Autorzy:

Lefebre R; Laboratory of Molecular Entomology and Bee Pathology (L-MEB), Department of Biochemistry and Microbiology, Faculty of Sciences, Ghent University, Ghent, Belgium. .
Broeckx BJG; Laboratory of Animal Genetics, Department of Veterinary and Biosciences, Faculty of Veterinary Medicine, Ghent University, Ghent, Belgium.
De Smet L; Laboratory of Molecular Entomology and Bee Pathology (L-MEB), Department of Biochemistry and Microbiology, Faculty of Sciences, Ghent University, Ghent, Belgium.
Peelman L; Laboratory of Animal Genetics, Department of Veterinary and Biosciences, Faculty of Veterinary Medicine, Ghent University, Ghent, Belgium.
de Graaf DC; Laboratory of Molecular Entomology and Bee Pathology (L-MEB), Department of Biochemistry and Microbiology, Faculty of Sciences, Ghent University, Ghent, Belgium.

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Źródło:

Scientific reports [Sci Rep] 2024 Apr 03; Vol. 14 (1), pp. 7866. Date of Electronic Publication: 2024 Apr 03.

Typ publikacji:

Journal Article

MeSH Terms:

Varroidae*/genetics
Bees/genetics ; Animals ; Polymorphism, Single Nucleotide ; Gene Frequency ; Belgium ; Phenotype

Czasopismo naukowe

• na półce

Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły

Skocz do pozycji: 5.

Tytuł:

Joint application of A-InDels and miniSTRs for forensic personal, full and half sibling identifications, and genetic differentiation analyses in two populations from China.

Autorzy:

Cai M; Guangzhou Key Laboratory of Forensic Multi-Omics for Precision Identification, School of Forensic Medicine, Southern Medical University, Guangzhou, Guangdong, China.
Lei F; Guangzhou Key Laboratory of Forensic Multi-Omics for Precision Identification, School of Forensic Medicine, Southern Medical University, Guangzhou, Guangdong, China.
Liu Y; Laboratory of Fundamental Nursing Research, School of Nursing, Guangdong Medical University, Dongguan, Guangdong, China.
Wang X; Guangzhou Key Laboratory of Forensic Multi-Omics for Precision Identification, School of Forensic Medicine, Southern Medical University, Guangzhou, Guangdong, China.
Wang H; Key Laboratory of Shaanxi Province for Craniofacial Precision Medicine Research, College of Stomatology, Xi'an Jiaotong University, Xi'an, Shanxi, China.
Xie W; School of Forensic Medicine, Southern Medical University, Guangzhou, Guangdong, China.
Yang Z; School of Business, Macau University of Science and Technology, Macao, China.
Yang S; The people's hospital of Hezhou, Guangxi, China. .
Zhu B; Guangzhou Key Laboratory of Forensic Multi-Omics for Precision Identification, School of Forensic Medicine, Southern Medical University, Guangzhou, Guangdong, China. .

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Źródło:

BMC genomics [BMC Genomics] 2024 Apr 02; Vol. 25 (1), pp. 329. Date of Electronic Publication: 2024 Apr 02.

Typ publikacji:

Journal Article

MeSH Terms:

Siblings*
Genetics, Population*
Humans ; Phylogeny ; China ; INDEL Mutation ; Microsatellite Repeats ; Forensic Genetics/methods ; Gene Frequency

Czasopismo naukowe

• na półce

Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły

Skocz do pozycji: 6.

Tytuł:

Forensic autosomal and gonosomal short tandem repeat marker reference database for populations in Burkina Faso.

Autorzy:

Zeye MMJ; Department of Medical Parasitology, School of Basic Medical Sciences, Central South University, No. 172, Tongzipo Road, Changsha, 410013, Hunan, People's Republic of China.; Laboratory of Molecular Biology and Genetics (LMBG) (Labiogene), University Joseph KI-ZERBO, CERBA/LABIOGENE, 01, BP 364, Ouagadougou 01, Burkina Faso.; Human Evolution, Department of Organismal Biology, Evolutionary Biology Centre, Uppsala University, Uppsala, Sweden.
Ouedraogo SY; Department of Oncology, School of Clinical Medicine, Shandong Cancer Hospital, Shandong First Medical University, Shandong Academy of Medical Sciences, 6699 Qingdao Road, Huaiyin District, Jinan, 250000, Shandong, People's Republic of China.; Laboratory of Molecular Biology and Genetics (LMBG) (Labiogene), University Joseph KI-ZERBO, CERBA/LABIOGENE, 01, BP 364, Ouagadougou 01, Burkina Faso.
Bado P; Laboratory of Molecular Biology and Genetics (LMBG) (Labiogene), University Joseph KI-ZERBO, CERBA/LABIOGENE, 01, BP 364, Ouagadougou 01, Burkina Faso.
Zoure AA; Department of Biomedical and Public Health, Research Institute of Health Sciences (IRSS/CNRST), 03 BP 7192, Ouagadougou 01, Burkina Faso.
Djigma FW; Laboratory of Molecular Biology and Genetics (LMBG) (Labiogene), University Joseph KI-ZERBO, CERBA/LABIOGENE, 01, BP 364, Ouagadougou 01, Burkina Faso.
Wu X; Department of Medical Parasitology, School of Basic Medical Sciences, Central South University, No. 172, Tongzipo Road, Changsha, 410013, Hunan, People's Republic of China. .
Simpore J; Laboratory of Molecular Biology and Genetics (LMBG) (Labiogene), University Joseph KI-ZERBO, CERBA/LABIOGENE, 01, BP 364, Ouagadougou 01, Burkina Faso. .

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Źródło:

Scientific reports [Sci Rep] 2024 Mar 28; Vol. 14 (1), pp. 7369. Date of Electronic Publication: 2024 Mar 28.

Typ publikacji:

Journal Article

MeSH Terms:

Genetics, Population*
Chromosomes, Human, X*/genetics
Male ; Humans ; Female ; Gene Frequency ; Burkina Faso ; Microsatellite Repeats/genetics ; China

Czasopismo naukowe

• na półce

Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły

Skocz do pozycji: 7.

Tytuł:

A quantitative genetic model of background selection in humans.

Autorzy:

Buffalo V; Department of Integrative Biology, University of California, Berkeley, Berkeley, California, United States of America.; Institute of Ecology and Evolution and Department of Biology, University of Oregon, Eugene, Oregon, United States of America.
Kern AD; Institute of Ecology and Evolution and Department of Biology, University of Oregon, Eugene, Oregon, United States of America.

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Źródło:

PLoS genetics [PLoS Genet] 2024 Mar 20; Vol. 20 (3), pp. e1011144. Date of Electronic Publication: 2024 Mar 20 (Print Publication: 2024).

Typ publikacji:

Journal Article

MeSH Terms:

Selection, Genetic*
Models, Genetic*
Humans ; Evolution, Molecular ; Gene Frequency/genetics ; Mutation ; Genome, Human/genetics ; Genetic Variation ; Genetic Fitness

Czasopismo naukowe

• na półce

Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły

Skocz do pozycji: 8.

Tytuł:

On the feasibility of malaria hypothesis.

Autorzy:

Habibzadeh F; Global Virus Network (GVN), Middle East Region, Shiraz, Iran. .

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Źródło:

Scientific reports [Sci Rep] 2024 Mar 09; Vol. 14 (1), pp. 5800. Date of Electronic Publication: 2024 Mar 09.

Typ publikacji:

Journal Article

MeSH Terms:

Malaria*/genetics
Anemia, Sickle Cell*/genetics
Child ; Female ; Humans ; Feasibility Studies ; Hemoglobin, Sickle/genetics ; Gene Frequency

Czasopismo naukowe

• na półce

Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły

Skocz do pozycji: 9.

Tytuł:

An elevated level of interleukin-17A in a Senegalese malaria cohort is associated with rs8193038 IL-17A genetic variant.

Autorzy:

Thiam F; Groupe de Recherche Biotechnologies Appliquees & Bioprocedes Environnementaux, Ecole Superieure Polytechnique, Universite Cheikh Anta Diop de Dakar, Corniche Ouest, Dakar-Fann, BP: 5085, Senegal. .
Diop G; Departement de Biologie Animale, Faculte Des Sciences Et Techniques, Unite Postulante de Biologie GenetiqueGenomique Et Bio-Informatique (G2B), Universite Cheikh Anta DIOP, Avenue Cheikh Anta DIOP, Dakar, BP: 5005, Senegal.; Pole d'Immunophysiopathologie & Maladies Infectieuses (IMI), Institut Pasteur de Dakar, 36, Avenue Pasteur, Dakar, BP: 220, Senegal.
Coulonges C; Equipe GBA «GenomiqueBioinformatique & Applications», Conservatoire National Des Arts Et Metiers, 292, Rue Saint Martin, Paris Cedex 03, Paris, 75141, France.
Derbois C; Centre National de Recherche en Génétique Humaine (CNRGH), Institut de Biologie François Jacob, 2 Rue Gaston Crémieux, CP 5721, Evry Cedex, 91057, France.
Thiam A; Pole d'Immunophysiopathologie & Maladies Infectieuses (IMI), Institut Pasteur de Dakar, 36, Avenue Pasteur, Dakar, BP: 220, Senegal.
Diouara AAM; Groupe de Recherche Biotechnologies Appliquees & Bioprocedes Environnementaux, Ecole Superieure Polytechnique, Universite Cheikh Anta Diop de Dakar, Corniche Ouest, Dakar-Fann, BP: 5085, Senegal.
Mbaye MN; Groupe de Recherche Biotechnologies Appliquees & Bioprocedes Environnementaux, Ecole Superieure Polytechnique, Universite Cheikh Anta Diop de Dakar, Corniche Ouest, Dakar-Fann, BP: 5085, Senegal.
Diop M; Groupe de Recherche Biotechnologies Appliquees & Bioprocedes Environnementaux, Ecole Superieure Polytechnique, Universite Cheikh Anta Diop de Dakar, Corniche Ouest, Dakar-Fann, BP: 5085, Senegal.
Nguer CM; Groupe de Recherche Biotechnologies Appliquees & Bioprocedes Environnementaux, Ecole Superieure Polytechnique, Universite Cheikh Anta Diop de Dakar, Corniche Ouest, Dakar-Fann, BP: 5085, Senegal.
Dieye Y; Groupe de Recherche Biotechnologies Appliquees & Bioprocedes Environnementaux, Ecole Superieure Polytechnique, Universite Cheikh Anta Diop de Dakar, Corniche Ouest, Dakar-Fann, BP: 5085, Senegal.; Pôle de Microbiologie, Institut Pasteur de Dakar, 36 Avenue Pasteur, Dakar, BP 220, Senegal.
Mbengue B; Service d'Immunologie, Faculté de Médecine, de Pharmacie Et d'Odontostomatologie, Université Cheikh Anta DIOP, Avenue Cheikh Anta DIOP, Dakar, BP: 5005, Senegal.
Zagury JF; Equipe GBA «GenomiqueBioinformatique & Applications», Conservatoire National Des Arts Et Metiers, 292, Rue Saint Martin, Paris Cedex 03, Paris, 75141, France.
Deleuze JF; Centre National de Recherche en Génétique Humaine (CNRGH), Institut de Biologie François Jacob, 2 Rue Gaston Crémieux, CP 5721, Evry Cedex, 91057, France.
Dieye A; Service d'Immunologie, Faculté de Médecine, de Pharmacie Et d'Odontostomatologie, Université Cheikh Anta DIOP, Avenue Cheikh Anta DIOP, Dakar, BP: 5005, Senegal.

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Źródło:

BMC infectious diseases [BMC Infect Dis] 2024 Mar 04; Vol. 24 (1), pp. 275. Date of Electronic Publication: 2024 Mar 04.

Typ publikacji:

Journal Article

MeSH Terms:

Interleukin-17*/genetics
Malaria*/genetics
Humans ; Gene Frequency ; Polymorphism, Genetic ; Cytokines

Czasopismo naukowe

• na półce

Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły

Skocz do pozycji: 10.

Tytuł:

Contribution of HLA class I (A, B, C) and HLA class II (DRB1, DQA1, DQB1) alleles and haplotypes in exploring ethnic origin of central Tunisians.

Autorzy:

Ben Bnina A; Hematology Laboratory, Sahloul University Hospital, Sousse, Tunisia.; Faculty of Pharmacy, University of Monastir, Monastir, Tunisia.
Yessine A; Biochemistry Laboratory, Béchir Hamza Children's Hospital, Bab Saadoun Square, 1007, Tunis, Tunisia. .; Department of Educational Sciences, University of Jendouba, Higher Institute of Applied Studies in Humanity Le Kef, Kef, Tunisia. .
El Bahri Y; Hematology Laboratory, Sahloul University Hospital, Sousse, Tunisia.; Faculty of Medicine, University of Sousse, Sousse, Tunisia.
Chouchene S; Hematology Laboratory, Fatouma Bourguiba Teaching Hospital, Sousse, Tunisia.; Faculty of Pharmacy, University of Monastir, Monastir, Tunisia.
Ben Lazrek N; Hematology Laboratory, Sahloul University Hospital, Sousse, Tunisia.
Mimouna M; Hematology Laboratory, Sahloul University Hospital, Sousse, Tunisia.
Mlika Z; Hematology Laboratory, Sahloul University Hospital, Sousse, Tunisia.
Messoudi A; Hematology Laboratory, Sahloul University Hospital, Sousse, Tunisia.
Zellama D; Nephrology Department, Sahloul University Hospital, Sousse, Tunisia.; Faculty of Medicine, University of Sousse, Sousse, Tunisia.
Sahtout W; Nephrology Department, Sahloul University Hospital, Sousse, Tunisia.; Faculty of Medicine, University of Sousse, Sousse, Tunisia.
Bouatay A; Hematology Laboratory, Sahloul University Hospital, Sousse, Tunisia.; Faculty of Pharmacy, University of Monastir, Monastir, Tunisia.

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Źródło:

BMC medical genomics [BMC Med Genomics] 2024 Feb 29; Vol. 17 (1), pp. 65. Date of Electronic Publication: 2024 Feb 29.

Typ publikacji:

Journal Article

MeSH Terms:

Polymorphism, Genetic*
HLA-C Antigens*/genetics
North African People*
Humans ; Haplotypes ; HLA-DRB1 Chains/genetics ; Alleles ; Gene Frequency ; HLA-B Antigens/genetics ; HLA-A Antigens/genetics

Czasopismo naukowe

• na półce

Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły

Skocz do pozycji: 11.

Tytuł:

Molecular Profile of Variants Potentially Associated with Severe Forms of COVID-19 in Amazonian Indigenous Populations.

Autorzy:

Coelho RCC; Oncology Research Center, Federal University of Pará, Belém 66073-005, PA, Brazil.
Martins CLELP; Oncology Research Center, Federal University of Pará, Belém 66073-005, PA, Brazil.
Pastana LF; Oncology Research Center, Federal University of Pará, Belém 66073-005, PA, Brazil.
Rodrigues JCG; Oncology Research Center, Federal University of Pará, Belém 66073-005, PA, Brazil.
Aguiar KEC; Oncology Research Center, Federal University of Pará, Belém 66073-005, PA, Brazil.
Cohen-Paes AN; Oncology Research Center, Federal University of Pará, Belém 66073-005, PA, Brazil.
Gellen LPA; Oncology Research Center, Federal University of Pará, Belém 66073-005, PA, Brazil.
Moraes FCA; Oncology Research Center, Federal University of Pará, Belém 66073-005, PA, Brazil.
Calderaro MCL; Oncology Research Center, Federal University of Pará, Belém 66073-005, PA, Brazil.
de Assunção LA; Oncology Research Center, Federal University of Pará, Belém 66073-005, PA, Brazil.
Monte N; Oncology Research Center, Federal University of Pará, Belém 66073-005, PA, Brazil.
Pereira EEB; Oncology Research Center, Federal University of Pará, Belém 66073-005, PA, Brazil.
Ribeiro-Dos-Santos AM; Laboratory of Human and Medical Genetics, Institute of Biological Science, Federal University of Pará, Belém 66077-830, PA, Brazil.
Ribeiro-do-Santos Â; Laboratory of Human and Medical Genetics, Institute of Biological Science, Federal University of Pará, Belém 66077-830, PA, Brazil.
Rodriguez Burbano RM; Oncology Research Center, Federal University of Pará, Belém 66073-005, PA, Brazil.; Ophir Loyola Hospital, Pará State Department of Health, Belém 66063-240, PA, Brazil.
de Souza SJ; Brain Institute, Federal University of Rio Grande do Norte, Natal 59078-970, RN, Brazil.
Guerreiro JF; Laboratory of Human and Medical Genetics, Institute of Biological Science, Federal University of Pará, Belém 66077-830, PA, Brazil.
Assumpção PP; Oncology Research Center, Federal University of Pará, Belém 66073-005, PA, Brazil.
Santos SEBD; Oncology Research Center, Federal University of Pará, Belém 66073-005, PA, Brazil.; Laboratory of Human and Medical Genetics, Institute of Biological Science, Federal University of Pará, Belém 66077-830, PA, Brazil.
Fernandes MR; Oncology Research Center, Federal University of Pará, Belém 66073-005, PA, Brazil.; Ophir Loyola Hospital, Pará State Department of Health, Belém 66063-240, PA, Brazil.
Santos NPCD; Oncology Research Center, Federal University of Pará, Belém 66073-005, PA, Brazil.; Laboratory of Human and Medical Genetics, Institute of Biological Science, Federal University of Pará, Belém 66077-830, PA, Brazil.

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Źródło:

Viruses [Viruses] 2024 Feb 26; Vol. 16 (3). Date of Electronic Publication: 2024 Feb 26.

Typ publikacji:

Journal Article

MeSH Terms:

COVID-19*/epidemiology
COVID-19*/genetics
Humans ; SARS-CoV-2/genetics ; Genome-Wide Association Study ; Gene Frequency ; Indigenous Peoples/genetics ; Intracellular Signaling Peptides and Proteins ; LIM Domain Proteins

Czasopismo naukowe

• na półce

Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły

Skocz do pozycji: 12.

Tytuł:

SNVstory: inferring genetic ancestry from genome sequencing data.

Autorzy:

Bollas AE; The Steve and Cindy Rasmussen Institute for Genomic Medicine, The Abigail Wexner Research Institute, Nationwide Children's Hospital, Columbus, OH, USA.; Department of Pediatrics, The Ohio State University College of Medicine, Columbus, OH, USA.
Rajkovic A; The Steve and Cindy Rasmussen Institute for Genomic Medicine, The Abigail Wexner Research Institute, Nationwide Children's Hospital, Columbus, OH, USA.
Ceyhan D; The Steve and Cindy Rasmussen Institute for Genomic Medicine, The Abigail Wexner Research Institute, Nationwide Children's Hospital, Columbus, OH, USA.
Gaither JB; The Steve and Cindy Rasmussen Institute for Genomic Medicine, The Abigail Wexner Research Institute, Nationwide Children's Hospital, Columbus, OH, USA.
Mardis ER; The Steve and Cindy Rasmussen Institute for Genomic Medicine, The Abigail Wexner Research Institute, Nationwide Children's Hospital, Columbus, OH, USA.; Department of Pediatrics, The Ohio State University College of Medicine, Columbus, OH, USA.
White P; The Steve and Cindy Rasmussen Institute for Genomic Medicine, The Abigail Wexner Research Institute, Nationwide Children's Hospital, Columbus, OH, USA. .; Department of Pediatrics, The Ohio State University College of Medicine, Columbus, OH, USA. .

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Źródło:

BMC bioinformatics [BMC Bioinformatics] 2024 Feb 20; Vol. 25 (1), pp. 76. Date of Electronic Publication: 2024 Feb 20.

Typ publikacji:

Journal Article

MeSH Terms:

Genetics, Population*
Ethnicity*/genetics
Humans ; Reproducibility of Results ; Gene Frequency ; Genetic Testing ; Genome, Human ; Polymorphism, Single Nucleotide

Czasopismo naukowe

• na półce

Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły

Skocz do pozycji: 13.

Tytuł:

The Association of ADAMTS7 Gene Polymorphisms with the Risk of Coronary Artery Disease Occurrence and Cardiovascular Survival in the Polish Population: A Case-Control and a Prospective Cohort Study.

Autorzy:

Iwanicka J; Department of Biochemistry and Medical Genetics, School of Health Sciences in Katowice, Medical University of Silesia, Medykow Street 18, 40-752 Katowice, Poland.
Balcerzyk-Matić A; Department of Biochemistry and Medical Genetics, School of Health Sciences in Katowice, Medical University of Silesia, Medykow Street 18, 40-752 Katowice, Poland.
Iwanicki T; Department of Biochemistry and Medical Genetics, School of Health Sciences in Katowice, Medical University of Silesia, Medykow Street 18, 40-752 Katowice, Poland.
Mizia-Stec K; First Department of Cardiology, School of Medicine in Katowice, Medical University of Silesia, 47 Ziołowa St., 40-635 Katowice, Poland.
Bańka P; First Department of Cardiology, School of Medicine in Katowice, Medical University of Silesia, 47 Ziołowa St., 40-635 Katowice, Poland.
Filipecki A; First Department of Cardiology, School of Medicine in Katowice, Medical University of Silesia, 47 Ziołowa St., 40-635 Katowice, Poland.
Gawron K; Department of Molecular Biology and Genetics, Faculty of Medical Sciences in Katowice, Medical University of Silesia, Medykow 18, 40-752 Katowice, Poland.
Jarosz A; Department of Biochemistry and Medical Genetics, School of Health Sciences in Katowice, Medical University of Silesia, Medykow Street 18, 40-752 Katowice, Poland.
Nowak T; Department of Biochemistry and Medical Genetics, School of Health Sciences in Katowice, Medical University of Silesia, Medykow Street 18, 40-752 Katowice, Poland.
Krauze J; 1st Department of Cardiac Surgery/2nd Department of Cardiology, American Heart of Poland, S. A. Armii Krajowej 101, 43-316 Bielsko-Biala, Poland.
Niemiec P; Department of Biochemistry and Medical Genetics, School of Health Sciences in Katowice, Medical University of Silesia, Medykow Street 18, 40-752 Katowice, Poland.

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Źródło:

International journal of molecular sciences [Int J Mol Sci] 2024 Feb 14; Vol. 25 (4). Date of Electronic Publication: 2024 Feb 14.

Typ publikacji:

Journal Article

MeSH Terms:

ADAMTS7 Protein*/genetics
Coronary Artery Disease*/epidemiology
Coronary Artery Disease*/genetics
Humans ; Case-Control Studies ; Gene Frequency ; Genetic Predisposition to Disease ; Genotype ; Poland/epidemiology ; Polymorphism, Single Nucleotide ; Prospective Studies ; Risk Factors

Czasopismo naukowe

• na półce

Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły

Skocz do pozycji: 14.

Tytuł:

The Association of Vitamin D Receptor Gene Polymorphisms with Vitamin D, Total IgE, and Blood Eosinophils in Patients with Atopy.

Autorzy:

Bastyte D; Department of Immunology and Allergology, Lithuanian University of Health Sciences, LT-50161 Kaunas, Lithuania.; Laboratory of Immunology, Department of Immunology and Allergology, Lithuanian University of Health Sciences, LT-50161 Kaunas, Lithuania.
Tamasauskiene L; Department of Immunology and Allergology, Lithuanian University of Health Sciences, LT-50161 Kaunas, Lithuania.; Laboratory of Immunology, Department of Immunology and Allergology, Lithuanian University of Health Sciences, LT-50161 Kaunas, Lithuania.
Stakaitiene I; Department of Genetics and Molecular Medicine, Lithuanian University of Health Sciences, LT-50161 Kaunas, Lithuania.
Ugenskiene R; Department of Genetics and Molecular Medicine, Lithuanian University of Health Sciences, LT-50161 Kaunas, Lithuania.
Gradauskiene Sitkauskiene B; Department of Immunology and Allergology, Lithuanian University of Health Sciences, LT-50161 Kaunas, Lithuania.

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Źródło:

Biomolecules [Biomolecules] 2024 Feb 11; Vol. 14 (2). Date of Electronic Publication: 2024 Feb 11.

Typ publikacji:

Journal Article

MeSH Terms:

Asthma*/genetics
Dermatitis, Atopic*/genetics
Adult ; Humans ; Case-Control Studies ; Eosinophils ; Gene Frequency ; Genetic Predisposition to Disease ; Immunoglobulin E ; Polymorphism, Single Nucleotide ; Receptors, Calcitriol/genetics ; Vitamin D

Czasopismo naukowe

• na półce

Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły

Skocz do pozycji: 15.

Tytuł:

Investigating the genetic makeup of the major histocompatibility complex (MHC) in the United Arab Emirates population through next-generation sequencing.

Autorzy:

Marzouka NAD; Center for Biotechnology, Khalifa University of Science and Technology, Abu Dhabi, United Arab Emirates.
Alnaqbi H; Center for Biotechnology, Khalifa University of Science and Technology, Abu Dhabi, United Arab Emirates.
Al-Aamri A; Center for Biotechnology, Khalifa University of Science and Technology, Abu Dhabi, United Arab Emirates.
Tay G; Division of Psychiatry, Faculty of Health and Medical Sciences, Medical School, The University of Western Australia, Crawley, WA, Australia.; School of Medical and Health Sciences, Edith Cowan University, Joondalup, WA, Australia.
Alsafar H; Center for Biotechnology, Khalifa University of Science and Technology, Abu Dhabi, United Arab Emirates. .; College of Medicine and Health Sciences, Khalifa University of Science and Technology, Abu Dhabi, United Arab Emirates. .; Department of Biomedical Engineering, Khalifa University of Science and Technology, Abu Dhabi, United Arab Emirates. .

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Źródło:

Scientific reports [Sci Rep] 2024 Feb 09; Vol. 14 (1), pp. 3392. Date of Electronic Publication: 2024 Feb 09.

Typ publikacji:

Journal Article

MeSH Terms:

Histocompatibility Antigens Class I*/genetics
Histocompatibility Antigens Class II*/genetics
Humans ; United Arab Emirates ; Gene Frequency ; Major Histocompatibility Complex/genetics ; High-Throughput Nucleotide Sequencing ; Haplotypes ; Alleles ; HLA-DRB1 Chains/genetics

Czasopismo naukowe

• na półce

Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły

Skocz do pozycji: 16.

Tytuł:

Pharmacogenomics of poor drug metabolism in greyhounds: Canine P450 oxidoreductase genetic variation, breed heterogeneity, and functional characterization.

Autorzy:

Martinez SE; Pharmacogenomics Laboratory, Program in Individualized Medicine (PrIMe), Department of Veterinary Clinical Sciences, College of Veterinary Medicine, Washington State University, Pullman, Washington, United States of America.
Pandey AV; Pediatric Endocrinology, Diabetology, and Metabolism, Department of Biomedical Research, University Children's Hospital Bern, Switzerland and Translational Hormone Research Program, University of Bern, Bern, Switzerland.
Perez Jimenez TE; Pharmacogenomics Laboratory, Program in Individualized Medicine (PrIMe), Department of Veterinary Clinical Sciences, College of Veterinary Medicine, Washington State University, Pullman, Washington, United States of America.
Zhu Z; Pharmacogenomics Laboratory, Program in Individualized Medicine (PrIMe), Department of Veterinary Clinical Sciences, College of Veterinary Medicine, Washington State University, Pullman, Washington, United States of America.
Court MH; Pharmacogenomics Laboratory, Program in Individualized Medicine (PrIMe), Department of Veterinary Clinical Sciences, College of Veterinary Medicine, Washington State University, Pullman, Washington, United States of America.

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Źródło:

PloS one [PLoS One] 2024 Feb 01; Vol. 19 (2), pp. e0297191. Date of Electronic Publication: 2024 Feb 01 (Print Publication: 2024).

Typ publikacji:

Journal Article

MeSH Terms:

Pharmacogenetics*
Cytochrome P-450 Enzyme System*/genetics
Dogs ; Animals ; Gene Frequency ; Microsomes, Liver/metabolism ; Mutation ; Genetic Variation

Czasopismo naukowe

• na półce

Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły

Skocz do pozycji: 17.

Tytuł:

Carrier frequency estimation of pathogenic variants of autosomal recessive and X-linked recessive mendelian disorders using exome sequencing data in 1,642 Thais.

Autorzy:

Chetruengchai, Wanna (AUTHOR)
Phowthongkum, Prasit (AUTHOR)
Shotelersuk, Vorasuk (AUTHOR)

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Źródło:

BMC Medical Genomics. 1/2/2024, Vol. 17 Issue 1, p1-10. 10p.

Czasopismo naukowe

• na półce

Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły

Skocz do pozycji: 18.

Tytuł:

The impact of Fisher's reproductive compensation on raising equilibrium frequencies of semidominant, nonlethal mutations under mutation/selection balance.

Autorzy:

Hastings, Ian M (AUTHOR)

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Źródło:

G3: Genes | Genomes | Genetics. Jan2024, Vol. 14 Issue 1, p1-10. 10p.

Czasopismo naukowe

• na półce

Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły

Skocz do pozycji: 19.

Tytuł:

DMRT3 Allele Frequencies in Batida- and Picada-Gaited Donkeys and Mules in Brazil.

Autorzy:

Herman, Mariana (AUTHOR)
Caceres, Amanda Manara (AUTHOR)
Albuquerque, Ana Luísa H. (AUTHOR)
Leite, Raíssa O. (AUTHOR)
Araújo, César Erineudo T. (AUTHOR)
Delfiol, Diego José Z. (AUTHOR)
Curi, Rogério A. (AUTHOR)
Borges, Alexandre S. (AUTHOR)
Oliveira-Filho, José P. (AUTHOR)

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Źródło:

Animals (2076-2615). Dec2023, Vol. 13 Issue 24, p3829. 10p.

Czasopismo naukowe

• na półce

Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły

Skocz do pozycji: 20.

Tytuł:

PRNP gene polymorphism frequencies for comparing possible vulnerability to BSE in Chinese bovine population.

Autorzy:

He, Xiaoming (AUTHOR)
Memon, Sameeullah (AUTHOR)
Yue, Dan (AUTHOR)
Zhu, Junhong (AUTHOR)
Lu, Ying (AUTHOR)
Liu, Xingneng (AUTHOR)
Xiong, Heli (AUTHOR)
Li, Guozhi (AUTHOR)
Deng, Weidong (AUTHOR)
Xi, Dongmei (AUTHOR)

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Źródło:

Animal Biotechnology. Dec2023, Vol. 34 Issue 7, p2433-2440. 8p.

Czasopismo naukowe

• na półce

Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły

Skocz do pozycji: 21.

Tytuł:

Allelic frequencies of 22 short tandem repeats loci and tri-allelic patterns of Penta D and TPOX identified in Gabonese population.

Autorzy:

Lendoye, Elisabeth (AUTHOR)
Mombo, Landry Erick (AUTHOR)
N'Negue ep. Mezui-Mbeng, Marie-Andree (AUTHOR)
Komba, Opheelia Makoyo (AUTHOR)
Ngoungou, Edgard Brice (AUTHOR)
Ovono Abessolo, Felix (AUTHOR)
Djoba Siawaya, Joel Fleury (AUTHOR)
Alt-Mörbe, Juliane (AUTHOR)

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Źródło:

Scientific Reports. 11/15/2023, Vol. 13 Issue 1, p1-13. 13p.

Czasopismo naukowe

• na półce

Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły

Skocz do pozycji: 22.

Tytuł:

Leveraging a disulfidptosis/ferroptosis-based signature to predict the prognosis of lung adenocarcinoma.

Autorzy:

Ma, Xiaoqing (AUTHOR)
Deng, Zilin (AUTHOR)
Li, Zhen (AUTHOR)
Ma, Ting (AUTHOR)
Li, Guiqing (AUTHOR)
Zhang, Cuijia (AUTHOR)
Zhang, Wentao (AUTHOR)
Chang, Jin (AUTHOR)

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Źródło:

Cancer Cell International. 11/9/2023, Vol. 23 Issue 1, p1-21. 21p.

Czasopismo naukowe

• na półce

Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły

Skocz do pozycji: 23.

Tytuł:

Estimating microhaplotype allele frequencies from low-coverage or pooled sequencing data.

Autorzy:

Delomas, Thomas A. (AUTHOR)
Willis, Stuart C. (AUTHOR)

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Źródło:

BMC Bioinformatics. 11/3/2023, Vol. 24 Issue 1, p1-14. 14p.

Czasopismo naukowe

• na półce

Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły

Skocz do pozycji: 24.

Tytuł:

Annotation of structural variants with reported allele frequencies and related metrics from multiple datasets using SVAFotate.

Autorzy:

Nicholas TJ; Department of Human Genetics, Utah Center for Genetic Discovery, University of Utah, Salt Lake City, UT, 84112, USA. .
Cormier MJ; Department of Human Genetics, Utah Center for Genetic Discovery, University of Utah, Salt Lake City, UT, 84112, USA.
Quinlan AR; Department of Human Genetics, Utah Center for Genetic Discovery, University of Utah, Salt Lake City, UT, 84112, USA.; Department of Biomedical Informatics, University of Utah, Salt Lake City, UT, 84112, USA.

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Źródło:

BMC bioinformatics [BMC Bioinformatics] 2022 Nov 16; Vol. 23 (1), pp. 490. Date of Electronic Publication: 2022 Nov 16.

Typ publikacji:

Journal Article

MeSH Terms:

Gene Frequency*
High-Throughput Nucleotide Sequencing*
Software*
Humans ; Rare Diseases

Czasopismo naukowe

• na półce

Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły

Skocz do pozycji: 25.

Tytuł:

Chronic osteomyelitis risk is associated with NLRP3 gene rs10754558 polymorphism in a Chinese Han Population.

Autorzy:

Qu YD; Department of Orthopaedics, Guangdong Second Provincial General Hospital, 466 Xingang Road, Haizhu District, 510317, Guangzhou, China.
Jiang N; Division of Orthopaedics and Traumatology, Department of Orthopaedics, Nanfang Hospital, Southern Medical University, 510515, Guangzhou, China.
Li JX; Department of Orthopaedics, Guangdong Second Provincial General Hospital, 466 Xingang Road, Haizhu District, 510317, Guangzhou, China.
Zhang W; Department of Orthopaedics, Guangdong Second Provincial General Hospital, 466 Xingang Road, Haizhu District, 510317, Guangzhou, China.
Xia CL; Department of Orthopaedics, Guangdong Second Provincial General Hospital, 466 Xingang Road, Haizhu District, 510317, Guangzhou, China.
Ou SJ; Department of Orthopaedics, Guangdong Second Provincial General Hospital, 466 Xingang Road, Haizhu District, 510317, Guangzhou, China.
Yang Y; Department of Orthopaedics, Guangdong Second Provincial General Hospital, 466 Xingang Road, Haizhu District, 510317, Guangzhou, China.
Ma YF; Division of Orthopaedics and Traumatology, Department of Orthopaedics, Nanfang Hospital, Southern Medical University, 510515, Guangzhou, China.
Qi Y; Department of Orthopaedics, Guangdong Second Provincial General Hospital, 466 Xingang Road, Haizhu District, 510317, Guangzhou, China. .
Xu CP; Department of Orthopaedics, Guangdong Second Provincial General Hospital, 466 Xingang Road, Haizhu District, 510317, Guangzhou, China. .

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Źródło:

BMC medical genomics [BMC Med Genomics] 2024 Jan 29; Vol. 17 (1), pp. 38. Date of Electronic Publication: 2024 Jan 29.

Typ publikacji:

Journal Article

MeSH Terms:

NLR Family, Pyrin Domain-Containing 3 Protein*/genetics
Osteomyelitis*/genetics
Humans ; Case-Control Studies ; China ; Gene Frequency ; Genetic Predisposition to Disease ; Genotype ; Polymorphism, Single Nucleotide

Czasopismo naukowe

• na półce

Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły

Skocz do pozycji: 26.

Tytuł:

Association of IL-10-592 C > A /-1082 A > G and the TNFα -308 G > A with susceptibility to COVID-19 and clinical outcomes.

Autorzy:

Eldesouki RE; Genetics Unit, Histology Department, Faculty of Medicine, Suez Canal University, 41522, Ismailia, Egypt. .
Kishk RM; Microbiology and immunology Department, Faculty of Medicine, Suez Canal University, Ismaila, Egypt.
Abd El-Fadeal NM; Medical Biochemistry and Molecular Biology Department, Faculty of Medicine, Suez Canal University, Ismaila, Egypt.; Biochemistry Department, Ibn Sina National College for Medical Studies, Jeddah, Kingdom of Saudi Arabia.
Mahran RI; Clinical Pharmacology Department, Faculty of Medicine, Suez Canal University, Ismaila, Egypt.
Kamel N; Clinical Pathology Department, Faculty of Medicine, Suez Canal University, Ismaila, Egypt.
Riad E; Pulmonology Unit, Internal Medicine Department, Faculty of Medicine, Suez Canal University, Ismaila, Egypt.
Nemr N; Endemic and Infectious Diseases Department, Faculty of Medicine, Suez Canal University, Ismailia, Egypt.
Kishk SM; Pharmaceutical Medicinal Chemistry Department, Faculty of Pharmacy, Suez Canal University, Ismailia, Egypt.
Mohammed EA; Genetics Unit, Histology Department, Faculty of Medicine, Suez Canal University, 41522, Ismailia, Egypt.

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Źródło:

BMC medical genomics [BMC Med Genomics] 2024 Jan 29; Vol. 17 (1), pp. 40. Date of Electronic Publication: 2024 Jan 29.

Typ publikacji:

Journal Article

MeSH Terms:

COVID-19*/genetics
Interleukin-10*/genetics
Humans ; Gene Frequency ; Genetic Predisposition to Disease ; Genotype ; Polymorphism, Single Nucleotide ; RNA, Viral ; SARS-CoV-2/genetics ; Tumor Necrosis Factor-alpha/genetics

Czasopismo naukowe

• na półce

Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły

Skocz do pozycji: 27.

Tytuł:

The Influence of HLA Polymorphisms on the Severity of COVID-19 in the Romanian Population.

Autorzy:

Vică ML; Department of Cell and Molecular Biology, 'Iuliu Hațieganu' University of Medicine and Pharmacy, 400349 Cluj-Napoca, Romania.; Legal Medicine Institute, 400006 Cluj-Napoca, Romania.
Dobreanu M; Emergency Clinical County Hospital, 540136 Târgu Mureș, Romania.; Department of Laboratory Medicine, 'George Emil Palade' University of Medicine, Pharmacy, Science and Technology, 540142 Târgu Mureș, Romania.; Center for Advanced Medical and Pharmaceutical Research, 'George Emil Palade' University of Medicine, Pharmacy, Science and Technology, 540142 Târgu Mureș, Romania.
Curocichin G; Department of Family Medicine, 'Nicolae Testemițanu' State University of Medicine and Pharmacy, MD-2004 Chișinău, Moldova.
Matei HV; Department of Cell and Molecular Biology, 'Iuliu Hațieganu' University of Medicine and Pharmacy, 400349 Cluj-Napoca, Romania.; Legal Medicine Institute, 400006 Cluj-Napoca, Romania.
Bâlici Ș; Department of Cell and Molecular Biology, 'Iuliu Hațieganu' University of Medicine and Pharmacy, 400349 Cluj-Napoca, Romania.
Vușcan ME; Department of Cell and Molecular Biology, 'Iuliu Hațieganu' University of Medicine and Pharmacy, 400349 Cluj-Napoca, Romania.; Legal Medicine Institute, 400006 Cluj-Napoca, Romania.
Chiorean AD; Department of Cell and Molecular Biology, 'Iuliu Hațieganu' University of Medicine and Pharmacy, 400349 Cluj-Napoca, Romania.; Emergency Clinical Hospital for Children, 400370 Cluj-Napoca, Romania.
Nicula GZ; Department of Cell and Molecular Biology, 'Iuliu Hațieganu' University of Medicine and Pharmacy, 400349 Cluj-Napoca, Romania.
Pavel Mironescu DC; Department of Cell and Molecular Biology, 'Iuliu Hațieganu' University of Medicine and Pharmacy, 400349 Cluj-Napoca, Romania.; Legal Medicine Institute, 400006 Cluj-Napoca, Romania.
Leucuța DC; Department of Medical Informatics and Biostatistics, 'Iuliu Hațieganu' University of Medicine and Pharmacy, 400349 Cluj-Napoca, Romania.
Teodoru CA; Clinical Surgical Department, Faculty of Medicine, 'Lucian Blaga' University of Sibiu, 550169 Sibiu, Romania.
Siserman CV; Legal Medicine Institute, 400006 Cluj-Napoca, Romania.; Department of Legal Medicine, 'Iuliu Hațieganu' University of Medicine and Pharmacy, 400006 Cluj-Napoca, Romania.

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Źródło:

International journal of molecular sciences [Int J Mol Sci] 2024 Jan 22; Vol. 25 (2). Date of Electronic Publication: 2024 Jan 22.

Typ publikacji:

Journal Article

MeSH Terms:

Genetic Predisposition to Disease*
COVID-19*/epidemiology
COVID-19*/genetics
Humans ; Romania/epidemiology ; Gene Frequency ; HLA-DRB1 Chains/genetics ; Genotype ; Haplotypes/genetics ; Alleles

Czasopismo naukowe

• na półce

Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły

Skocz do pozycji: 28.

Tytuł:

Single nucleotide polymorphism SNP19140160 A > C is a potential breeding locus for fast-growth largemouth bass (Micropterus salmoides).

Autorzy:

Hua J; Wuxi Fisheries College, Nanjing Agricultural University, Wuxi, 214081, China.; Key Laboratory of Freshwater Fisheries and Germplasm Resources Utilization, Ministry of Agriculture and Rural Affairs, Freshwater Fisheries Research Center, Chinese Academy of Fishery Sciences, Wuxi, 214081, China.
Zhong C; Wuxi Fisheries College, Nanjing Agricultural University, Wuxi, 214081, China.; Key Laboratory of Freshwater Fisheries and Germplasm Resources Utilization, Ministry of Agriculture and Rural Affairs, Freshwater Fisheries Research Center, Chinese Academy of Fishery Sciences, Wuxi, 214081, China.
Chen W; Suzhou Aquatic Technology Extension Station, Suzhou, 215004, China.
Fu J; Key Laboratory of Freshwater Fisheries and Germplasm Resources Utilization, Ministry of Agriculture and Rural Affairs, Freshwater Fisheries Research Center, Chinese Academy of Fishery Sciences, Wuxi, 214081, China.
Wang J; Guangxi Xinjian Investment Group Limited Company, Hechi, 530201, China.
Wang Q; Wuxi Fisheries College, Nanjing Agricultural University, Wuxi, 214081, China.
Zhu G; Suzhou Aquatic Technology Extension Station, Suzhou, 215004, China.
Li Y; Key Laboratory of Freshwater Fisheries and Germplasm Resources Utilization, Ministry of Agriculture and Rural Affairs, Freshwater Fisheries Research Center, Chinese Academy of Fishery Sciences, Wuxi, 214081, China.
Tao Y; Key Laboratory of Freshwater Fisheries and Germplasm Resources Utilization, Ministry of Agriculture and Rural Affairs, Freshwater Fisheries Research Center, Chinese Academy of Fishery Sciences, Wuxi, 214081, China.
Zhang M; Suzhou Aquatic Technology Extension Station, Suzhou, 215004, China.
Dong Y; Key Laboratory of Freshwater Fisheries and Germplasm Resources Utilization, Ministry of Agriculture and Rural Affairs, Freshwater Fisheries Research Center, Chinese Academy of Fishery Sciences, Wuxi, 214081, China.
Lu S; Key Laboratory of Freshwater Fisheries and Germplasm Resources Utilization, Ministry of Agriculture and Rural Affairs, Freshwater Fisheries Research Center, Chinese Academy of Fishery Sciences, Wuxi, 214081, China.
Liu W; Key Laboratory of Freshwater Fisheries and Germplasm Resources Utilization, Ministry of Agriculture and Rural Affairs, Freshwater Fisheries Research Center, Chinese Academy of Fishery Sciences, Wuxi, 214081, China.
Qiang J; Wuxi Fisheries College, Nanjing Agricultural University, Wuxi, 214081, China. .; Key Laboratory of Freshwater Fisheries and Germplasm Resources Utilization, Ministry of Agriculture and Rural Affairs, Freshwater Fisheries Research Center, Chinese Academy of Fishery Sciences, Wuxi, 214081, China. .

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Źródło:

BMC genomics [BMC Genomics] 2024 Jan 16; Vol. 25 (1), pp. 64. Date of Electronic Publication: 2024 Jan 16.

Typ publikacji:

Journal Article

MeSH Terms:

Polymorphism, Single Nucleotide*
Bass*/genetics
Animals ; Gene Frequency ; Genotype ; Body Weight/genetics

Czasopismo naukowe

• na półce

Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły

Skocz do pozycji: 29.

Tytuł:

Large scale sequence-based screen for recessive variants allows for identification and monitoring of rare deleterious variants in pigs.

Autorzy:

Boshove A; Topigs Norsvin Research Center, 's-Hertogenbosch, the Netherlands.
Derks MFL; Topigs Norsvin Research Center, 's-Hertogenbosch, the Netherlands.; Animal Breeding and Genomics, Wageningen University & Research, Wageningen, the Netherlands.
Sevillano CA; Topigs Norsvin Research Center, 's-Hertogenbosch, the Netherlands.
Lopes MS; Topigs Norsvin Research Center, 's-Hertogenbosch, the Netherlands.; Topigs Norsvin, Curitiba, Brazil.
van Son M; Norsvin SA, Hamar, Norway.
Knol EF; Topigs Norsvin Research Center, 's-Hertogenbosch, the Netherlands.
Dibbits B; Animal Breeding and Genomics, Wageningen University & Research, Wageningen, the Netherlands.
Harlizius B; Topigs Norsvin Research Center, 's-Hertogenbosch, the Netherlands.

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Źródło:

PLoS genetics [PLoS Genet] 2024 Jan 10; Vol. 20 (1), pp. e1011034. Date of Electronic Publication: 2024 Jan 10 (Print Publication: 2024).

Typ publikacji:

Journal Article

MeSH Terms:

Genome-Wide Association Study*
Polymorphism, Single Nucleotide*/genetics
Humans ; Animals ; Swine/genetics ; Quantitative Trait Loci/genetics ; Phenotype ; Gene Frequency ; Genotype ; Cytoskeletal Proteins/genetics

Czasopismo naukowe

• na półce

Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły

Skocz do pozycji: 30.

Tytuł:

How local reference panels improve imputation in French populations.

Autorzy:

Herzig AF; Univ Brest, Inserm, EFS, UMR 1078, GGB, Brest, France. .
Velo-Suárez L; Univ Brest, Inserm, EFS, UMR 1078, GGB, Brest, France.; CHRU Brest, Brest, France.
Dina C; Nantes Université, CHU Nantes, CNRS, INSERM, l'institut du thorax, Nantes, France.
Redon R; Nantes Université, CHU Nantes, CNRS, INSERM, l'institut du thorax, Nantes, France.
Deleuze JF; Centre National de Recherche en Génomique Humaine (CNRGH), Université Paris-Saclay, CEA, Evry, France.; Fondation Jean Dausset - Centre d'Etude du Polymorphisme Humain (CEPH), Paris, France.
Génin E; Univ Brest, Inserm, EFS, UMR 1078, GGB, Brest, France.; CHRU Brest, Brest, France.

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Corporate Authors:

FrEx Consortium
FranceGenRef Consortium

Źródło:

Scientific reports [Sci Rep] 2024 Jan 03; Vol. 14 (1), pp. 370. Date of Electronic Publication: 2024 Jan 03.

Typ publikacji:

Journal Article

MeSH Terms:

Genome-Wide Association Study*/methods
Genome*
Humans ; Genotype ; Gene Frequency ; Haplotypes ; Polymorphism, Single Nucleotide

Czasopismo naukowe

• na półce

Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły

Skocz do pozycji: 31.

Tytuł:

Association of MBL2 gene polymorphisms and MBL levels with dilated cardiomyopathy in a Chinese Han population.

Autorzy:

Mao Y; Institute of Dermatology and Venereology, Sichuan Provincial People's Hospital, University of Electronic Science and Technology of China, Chengdu, 610072, China.
Wei H; Department of Ophthalmology and Vision Research Laboratory, West China Hospital, Sichuan University, Chengdu, China.
Gong Y; Institute of Dermatology and Venereology, Sichuan Provincial People's Hospital, University of Electronic Science and Technology of China, Chengdu, 610072, China.
Peng L; Department of Nephrology, Sichuan Provincial People's Hospital, University of Electronic Science and Technology of China, Chengdu, 610072, China. .
Chen Y; Department of Cardiology, Sichuan Provincial People's Hospital, University of Electronic Science and Technology of China, Chengdu, 610072, China. .

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Źródło:

BMC medical genomics [BMC Med Genomics] 2024 Jan 02; Vol. 17 (1), pp. 11. Date of Electronic Publication: 2024 Jan 02.

Typ publikacji:

Journal Article; Research Support, Non-U.S. Gov't

MeSH Terms:

Cardiomyopathy, Dilated*/genetics
Mannose-Binding Lectin*/genetics
Humans ; Gene Frequency ; Genetic Predisposition to Disease ; Genotype ; Polymorphism, Single Nucleotide

Czasopismo naukowe

• na półce

Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły

Skocz do pozycji: 32.

Tytuł:

The impact of Fisher's reproductive compensation on raising equilibrium frequencies of semidominant, nonlethal mutations under mutation/selection balance.

Autorzy:

Hastings IM; Department of Tropical Disease Biology, Liverpool School of Tropical Medicine, Pembroke Place, Liverpool L3 5QA, UK.

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Źródło:

G3 (Bethesda, Md.) [G3 (Bethesda)] 2023 Dec 29; Vol. 14 (1).

Typ publikacji:

Journal Article

MeSH Terms:

Selection, Genetic*
Reproduction*/genetics
Humans ; Female ; Male ; Mutation ; Gene Frequency ; Genome ; Models, Genetic

Czasopismo naukowe

• na półce

Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły

Skocz do pozycji: 33.

Tytuł:

A rapid and reference-free imputation method for low-cost genotyping platforms.

Autorzy:

Chi Duong V; Center for Biomedical Informatics, Vingroup Big Data Institute, Hanoi, Vietnam.; GeneStory Joint Stock Company, Hanoi, Vietnam.
Minh Vu G; Center for Biomedical Informatics, Vingroup Big Data Institute, Hanoi, Vietnam.; GeneStory Joint Stock Company, Hanoi, Vietnam.
Khac Nguyen T; GeneStory Joint Stock Company, Hanoi, Vietnam.
Tran The Nguyen H; Center for Biomedical Informatics, Vingroup Big Data Institute, Hanoi, Vietnam.; Nanyang Technological University, Singapore, Singapore.
Luong Pham T; GeneStory Joint Stock Company, Hanoi, Vietnam.
S Vo N; Center for Biomedical Informatics, Vingroup Big Data Institute, Hanoi, Vietnam. .; GeneStory Joint Stock Company, Hanoi, Vietnam. .
Hong Hoang T; Center for Biomedical Informatics, Vingroup Big Data Institute, Hanoi, Vietnam. .; GeneStory Joint Stock Company, Hanoi, Vietnam. .

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Źródło:

Scientific reports [Sci Rep] 2023 Dec 27; Vol. 13 (1), pp. 23083. Date of Electronic Publication: 2023 Dec 27.

Typ publikacji:

Journal Article

MeSH Terms:

Polymorphism, Single Nucleotide*
Genome*
Humans ; Genotype ; Gene Frequency ; Genome-Wide Association Study/methods ; Genotyping Techniques/methods

Czasopismo naukowe

• na półce

Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły

Skocz do pozycji: 34.

Tytuł:

Significance of LHCGR polymorphisms in polycystic ovary syndrome: an association study.

Autorzy:

Singh S; Department of Human Genetics, Guru Nanak Dev University, Amritsar, Punjab, 143005, India.
Kaur M; Department of Human Genetics, Guru Nanak Dev University, Amritsar, Punjab, 143005, India.
Beri A; Beri Maternity Hospital, Southend Beri Fertility and IVF, Amritsar, Punjab, 143001, India.
Kaur A; Department of Human Genetics, Guru Nanak Dev University, Amritsar, Punjab, 143005, India. .

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Źródło:

Scientific reports [Sci Rep] 2023 Dec 21; Vol. 13 (1), pp. 22841. Date of Electronic Publication: 2023 Dec 21.

Typ publikacji:

Journal Article

MeSH Terms:

Genetic Predisposition to Disease*
Polycystic Ovary Syndrome*/genetics
Polycystic Ovary Syndrome*/complications
Female ; Humans ; Case-Control Studies ; Gene Frequency ; Genotype ; Luteinizing Hormone/genetics ; Polymorphism, Single Nucleotide ; Receptors, G-Protein-Coupled/genetics

Czasopismo naukowe

• na półce

Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły

Skocz do pozycji: 35.

Tytuł:

The diagnostic yield of exome sequencing in liver diseases from a curated gene panel.

Autorzy:

Kong XF; Division of Digestive and Liver Diseases, Department of Medicine, Columbia University Irving Medical Center, Hammer Health Sciences Building Rm 402, 701 W 168th St, New York, NY, 10032, USA. .; Center for Precision Medicine and Genomics, Department of Medicine, Columbia University Irving Medical Center, New York, NY, 10032, USA. .; Institute for Genomic Medicine, Columbia University Irving Medical Center, New York, NY, 10032, USA. .; Department of Medicine, McDermott Center for Human Growth and Development, UT Southwestern Medical Center, Dallas, TX, 75390-9151, USA. .
Bogyo K; Center for Precision Medicine and Genomics, Department of Medicine, Columbia University Irving Medical Center, New York, NY, 10032, USA.
Kapoor S; Center for Precision Medicine and Genomics, Department of Medicine, Columbia University Irving Medical Center, New York, NY, 10032, USA.
Shea PR; Center for Precision Medicine and Genomics, Department of Medicine, Columbia University Irving Medical Center, New York, NY, 10032, USA.; Institute for Genomic Medicine, Columbia University Irving Medical Center, New York, NY, 10032, USA.
Groopman EE; Center for Precision Medicine and Genomics, Department of Medicine, Columbia University Irving Medical Center, New York, NY, 10032, USA.
Thomas-Wilson A; Department of Pathology and Cell Biology, Columbia University Irving Medical Center, New York, NY, 10032, USA.; Molecular Diagnostics, New York Genome Center, New York, NY, USA.
Cocchi E; Center for Precision Medicine and Genomics, Department of Medicine, Columbia University Irving Medical Center, New York, NY, 10032, USA.
Milo Rasouly H; Center for Precision Medicine and Genomics, Department of Medicine, Columbia University Irving Medical Center, New York, NY, 10032, USA.
Zheng B; Division of Digestive and Liver Diseases, Department of Medicine, Columbia University Irving Medical Center, Hammer Health Sciences Building Rm 402, 701 W 168th St, New York, NY, 10032, USA.
Sun S; Division of Digestive and Liver Diseases, Department of Medicine, Columbia University Irving Medical Center, Hammer Health Sciences Building Rm 402, 701 W 168th St, New York, NY, 10032, USA.
Zhang J; Center for Precision Medicine and Genomics, Department of Medicine, Columbia University Irving Medical Center, New York, NY, 10032, USA.
Martinez M; Center for Liver Disease and Transplantation, Columbia University Irving Medical Center, 622 West 168th Street, PH 14-105D, New York, NY, 10032, USA.
Vittorio JM; Center for Liver Disease and Transplantation, Columbia University Irving Medical Center, 622 West 168th Street, PH 14-105D, New York, NY, 10032, USA.; NYU Transplant Institute, NYU Langone Health, New York, NY, USA.
Dove LM; Division of Digestive and Liver Diseases, Department of Medicine, Columbia University Irving Medical Center, Hammer Health Sciences Building Rm 402, 701 W 168th St, New York, NY, 10032, USA.; Center for Liver Disease and Transplantation, Columbia University Irving Medical Center, 622 West 168th Street, PH 14-105D, New York, NY, 10032, USA.
Marasa M; Center for Precision Medicine and Genomics, Department of Medicine, Columbia University Irving Medical Center, New York, NY, 10032, USA.
Wang TC; Division of Digestive and Liver Diseases, Department of Medicine, Columbia University Irving Medical Center, Hammer Health Sciences Building Rm 402, 701 W 168th St, New York, NY, 10032, USA.
Verna EC; Division of Digestive and Liver Diseases, Department of Medicine, Columbia University Irving Medical Center, Hammer Health Sciences Building Rm 402, 701 W 168th St, New York, NY, 10032, USA.; Center for Liver Disease and Transplantation, Columbia University Irving Medical Center, 622 West 168th Street, PH 14-105D, New York, NY, 10032, USA.
Worman HJ; Division of Digestive and Liver Diseases, Department of Medicine, Columbia University Irving Medical Center, Hammer Health Sciences Building Rm 402, 701 W 168th St, New York, NY, 10032, USA.; Department of Pathology and Cell Biology, Columbia University Irving Medical Center, New York, NY, 10032, USA.
Gharavi AG; Center for Precision Medicine and Genomics, Department of Medicine, Columbia University Irving Medical Center, New York, NY, 10032, USA.; Institute for Genomic Medicine, Columbia University Irving Medical Center, New York, NY, 10032, USA.
Goldstein DB; Institute for Genomic Medicine, Columbia University Irving Medical Center, New York, NY, 10032, USA.
Wattacheril J; Division of Digestive and Liver Diseases, Department of Medicine, Columbia University Irving Medical Center, Hammer Health Sciences Building Rm 402, 701 W 168th St, New York, NY, 10032, USA. .; Center for Liver Disease and Transplantation, Columbia University Irving Medical Center, 622 West 168th Street, PH 14-105D, New York, NY, 10032, USA. .

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Źródło:

Scientific reports [Sci Rep] 2023 Dec 06; Vol. 13 (1), pp. 21540. Date of Electronic Publication: 2023 Dec 06.

Typ publikacji:

Journal Article

MeSH Terms:

Liver Diseases*/diagnosis
Liver Diseases*/genetics
Kidney Diseases*
Humans ; Exome Sequencing ; Gene Frequency ; Phenotype

Czasopismo naukowe

• na półce

Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły

Skocz do pozycji: 36.

Tytuł:

Effective fitness under fluctuating selection with genetic drift.

Autorzy:

Song S; Department of Ecology and Evolutionary Biology, University of Michigan, Ann Arbor, MI 48109, USA.
Zhang J; Department of Ecology and Evolutionary Biology, University of Michigan, Ann Arbor, MI 48109, USA.

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Źródło:

G3 (Bethesda, Md.) [G3 (Bethesda)] 2023 Dec 06; Vol. 13 (12).

Typ publikacji:

Journal Article

MeSH Terms:

Selection, Genetic*
Models, Genetic*
Computer Simulation ; Genetic Drift ; Gene Frequency ; Genetic Fitness

Czasopismo naukowe

• na półce

Pełny tekst  Link otwiera się w nowym oknieSzczegóły

Skocz do pozycji: 37.

Tytuł:

Highlighting allelic variations at the interleukin-19 locus in term of preeclampsia predisposing factors and access to an accurate diagnostic/screening option.

Autorzy:

Parhoudeh S; Department of Genetics, College of Science, Kazerun Branch, Islamic Azad University, Kazerun, Iran.
Saadaty A; Department of Genetics, College of Science, Kazerun Branch, Islamic Azad University, Kazerun, Iran.
Khashei Varnamkhasti K; Department of Medical Laboratory Sciences, Faculty of Medicine, Kazerun Branch, Islamic Azad University, Kazerun, Iran.
Khashei Varnamkhasti S; Department of Medical Laboratory Sciences, Faculty of Medicine, Kazerun Branch, Islamic Azad University, Kazerun, Iran.
Naeimi L; Department of Genetics, College of Science, Kazerun Branch, Islamic Azad University, Kazerun, Iran.
Naeimi S; Department of Genetics, College of Science, Kazerun Branch, Islamic Azad University, Kazerun, Iran. .

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Źródło:

BMC pregnancy and childbirth [BMC Pregnancy Childbirth] 2023 Dec 06; Vol. 23 (1), pp. 839. Date of Electronic Publication: 2023 Dec 06.

Typ publikacji:

Journal Article

MeSH Terms:

Genetic Predisposition to Disease*
Pre-Eclampsia*/diagnosis
Pre-Eclampsia*/genetics
Pre-Eclampsia*/pathology
Female ; Humans ; Infant, Newborn ; Pregnancy ; Alleles ; Case-Control Studies ; Causality ; Cytokines ; Gene Frequency ; Genotype ; Interleukin-13/genetics ; Interleukins/genetics ; Polymorphism, Single Nucleotide

Czasopismo naukowe

• na półce

Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły

Skocz do pozycji: 38.

Tytuł:

Genetic adaptations in the population history of Arabidopsis thaliana.

Autorzy:

Kishino H; Graduate School of Agricultural and Life Sciences, The University of Tokyo, 1-1-1 Yayoi, Bunkyo-ku, Tokyo 113-8657, Japan.; Research and Development Initiative, Chuo University, 1-13-27 Kasuga, Bunkyo-ku, Tokyo 112-8551, Japan.
Nakamichi R; Fisheries Resources Institute, Japan Fisheries Research and Education Agency, 2-12-4 Fukuura, Kanazawa-ku, Yokohama, Kanagawa 236-8648, Japan.
Kitada S; Graduate School of Marine Science and Technology, Tokyo University of Marine Science and Technology, 4-5-7 Konan, Minato-ku, Tokyo 108-8477, Japan.

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Źródło:

G3 (Bethesda, Md.) [G3 (Bethesda)] 2023 Dec 06; Vol. 13 (12).

Typ publikacji:

Journal Article

MeSH Terms:

Arabidopsis*/metabolism
Arabidopsis Proteins*/genetics
Gene Frequency ; Soil ; Phenotype

Czasopismo naukowe

• na półce

Pełny tekst  Link otwiera się w nowym oknieSzczegóły

Skocz do pozycji: 39.

Tytuł:

Prediction of asthma using a four-locus gene model including IL13, IL4, FCER1B, and ADRB2 in children of Kazak nationality.

Autorzy:

Bai S; Department of Pediatric Pulmonology, Xinhua Hospital Affiliated to Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Lu J; Children's Respiratory Diagnosis and Treatment Center, Urumqi First People's Hospital, Xinjiang, China.
Hua L; Department of Pediatric Pulmonology, Xinhua Hospital Affiliated to Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Liu Q; Department of Pediatric Pulmonology, Xinhua Hospital Affiliated to Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Chen M; Department of Pediatric Pulmonology, Xinhua Hospital Affiliated to Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Gu Y; Department of Pediatric Pulmonology, Xinhua Hospital Affiliated to Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Zhang J; Department of Pediatric Pulmonology, Xinhua Hospital Affiliated to Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Ma D; Children's Respiratory Diagnosis and Treatment Center, Urumqi First People's Hospital, Xinjiang, China.
Bao Y; Department of Pediatric Pulmonology, Xinhua Hospital Affiliated to Shanghai Jiao Tong University School of Medicine, Shanghai, China. asthma_group_.

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Źródło:

Italian journal of pediatrics [Ital J Pediatr] 2023 Dec 04; Vol. 49 (1), pp. 162. Date of Electronic Publication: 2023 Dec 04.

Typ publikacji:

Journal Article

MeSH Terms:

Ethnicity*
Asthma*/genetics
Humans ; Child ; Interleukin-4/genetics ; Interleukin-13/genetics ; Genotype ; Polymorphism, Single Nucleotide ; China/epidemiology ; Gene Frequency ; Genetic Predisposition to Disease ; Receptors, Adrenergic, beta-2/genetics

Czasopismo naukowe

• na półce

Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły

Skocz do pozycji: 40.

Tytuł:

Genetic variants of TORC1 gene promoter and their association with carcass quality and body measurement traits in Qinchuan beef cattle.

Autorzy:

Zhao X; College of Pharmacy, Heze University, Heze, China.
Khan R; Department of Livestock Management, Breeding and Genetic, The University of Agriculture Peshawar, Peshawar, Pakistan.
Hongfang G; Medical College, Xuchang University, Xuchang, China.
Abbas Raza SH; College of Animal Science and Technology, Northwest A&F University, Yangling, China.
Ayari-Akkari A; Biology Department, College of Science, King Khalid University, Abha, Saudi Arabia.; Laboratory of Diversity, Management and Conservation of Biological Systems, Faculty of Sciences of Tunis, University of Tunis El Manar, Tunis, Tunisia.
Othman G; Biology Department, College of Science, King Khalid University, Abha, Saudi Arabia.
Alshammari AM; Department of Biology, College of Science, University of Hail, Ha'il, Saudi Arabia.
Aloufi BH; Department of Biology, College of Science, University of Hail, Ha'il, Saudi Arabia.
Alabbosh KF; Department of Biology, College of Science, University of Hail, Ha'il, Saudi Arabia.
Alshammari WB; Department of Biology, College of Science, University of Hail, Ha'il, Saudi Arabia.
Linsen Z; College of Animal Science and Technology, Northwest A&F University, Yangling, China.

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Źródło:

Animal biotechnology [Anim Biotechnol] 2023 Dec; Vol. 34 (7), pp. 2537-2545. Date of Electronic Publication: 2022 Aug 02.

Typ publikacji:

Journal Article

MeSH Terms:

Polymorphism, Single Nucleotide*/genetics
Body Weights and Measures*
Cattle/genetics ; Animals ; Phenotype ; Genotype ; Genetic Markers ; Gene Frequency ; Meat

Czasopismo naukowe

• na półce

Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły

Skocz do pozycji: 41.

Tytuł:

Investigation of the association between goat DNMT3B gene polymorphism and growth traits.

Autorzy:

Yang Y; College of Animal Science and Technology, Northwest A&F University, Yangling, China.
Hui Y; College of Animal Science and Technology, Northwest A&F University, Yangling, China.
Guo Z; Bijie Animal Husbandry and Veterinary Science Research Institute, Bijie, Guizhou, China.
Song X; College of Life Sciences, Yulin University, Yulin, China.
Zhu H; College of Life Sciences, Yulin University, Yulin, China.
Pan C; College of Animal Science and Technology, Northwest A&F University, Yangling, China.
Lan X; College of Animal Science and Technology, Northwest A&F University, Yangling, China.

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Źródło:

Animal biotechnology [Anim Biotechnol] 2023 Dec; Vol. 34 (7), pp. 2492-2498. Date of Electronic Publication: 2022 Jul 27.

Typ publikacji:

Journal Article

MeSH Terms:

Goats*/genetics
Polymorphism, Genetic*/genetics
Animals ; Phenotype ; Gene Frequency ; Genotype

Czasopismo naukowe

• na półce

Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły

Skocz do pozycji: 42.

Tytuł:

Association of single nucleotide polymorphisms in heat stress protein 70 ( HSP70 ) and 90 ( HSP90 ) with the susceptibility of Pakistani sheep breeds to hemoparasitic infections.

Autorzy:

Sheraz M; Institute of Zoology, Bahauddin Zakariya University, Multan, Pakistan.
Ud Din F; Department of Zoology, Ghazi University, Dera Ghazi Khan, Pakistan.
Saad Un Nabi M; Institute of Zoology, Bahauddin Zakariya University, Multan, Pakistan.
Rao S; Institute of Zoology, Bahauddin Zakariya University, Multan, Pakistan.
Shafiq B; Institute of Zoology, Bahauddin Zakariya University, Multan, Pakistan.
Murtaza G; Institute of Zoology, Bahauddin Zakariya University, Multan, Pakistan.
Farooq M; Department of Zoology, Ghazi University, Dera Ghazi Khan, Pakistan.
Iqbal F; Institute of Zoology, Bahauddin Zakariya University, Multan, Pakistan.

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Źródło:

Animal biotechnology [Anim Biotechnol] 2023 Dec; Vol. 34 (9), pp. 4608-4615. Date of Electronic Publication: 2023 Feb 09.

Typ publikacji:

Journal Article

MeSH Terms:

Parasitic Diseases*
Sheep Diseases*/genetics
Sheep/genetics ; Animals ; Polymorphism, Single Nucleotide/genetics ; Pakistan ; Gene Frequency ; Genotype ; Heat-Shock Proteins/genetics

Czasopismo naukowe

• na półce

Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły

Skocz do pozycji: 43.

Tytuł:

Potential status of A1 and A2 variants of bovine beta-casein gene in milk samples of Indian cattle breeds.

Autorzy:

Khan R; Parul Institute of Applied Sciences, Parul University, Vadodara, India.
De S; Animal Biotechnology Center, National Dairy Research Institute, Karnal, India.
Dewangan R; Genetics, A2 Milk Research Corporation, Raipur, India.
Tamboli R; Genetics, A2 Milk Research Corporation, Raipur, India.
Gupta R; Parul Institute of Applied Sciences, Parul University, Vadodara, India.

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Źródło:

Animal biotechnology [Anim Biotechnol] 2023 Dec; Vol. 34 (9), pp. 4878-4884. Date of Electronic Publication: 2023 Apr 18.

Typ publikacji:

Journal Article

MeSH Terms:

Caseins*/genetics
Milk*
Cattle/genetics ; Animals ; Polymorphism, Genetic ; Gene Frequency ; Genotype

Czasopismo naukowe

• na półce

Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły

Skocz do pozycji: 44.

Tytuł:

Determination of declined genetic diversity of Holstein stud bulls based on microsatellite markers.

Autorzy:

Unlusoy I; Department of Animal Breeding and Genetics, International Center for Livestock Research and Training, Ankara, Turkiye.

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Źródło:

Animal biotechnology [Anim Biotechnol] 2023 Dec; Vol. 34 (9), pp. 4627-4633. Date of Electronic Publication: 2023 Feb 27.

Typ publikacji:

Journal Article

MeSH Terms:

Genetic Variation*/genetics
Microsatellite Repeats*/genetics
Cattle/genetics ; Animals ; Male ; Gene Frequency/genetics ; Heterozygote ; Phenotype

Czasopismo naukowe

• na półce

Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły

Skocz do pozycji: 45.

Tytuł:

Effect of NLR family pyrin domain containing 9 gene polymorphism on litter size in large white pigs.

Autorzy:

Zhang Y; College of Animal Science and Technology, Hainan University, Haikou, Hainan, China.; College of Animal Science, Fujian Agriculture and Forestry University, Fuzhou, Fujian, China.
Song Y; Ruzhou Vocational and Technical College, Ruzhou, Henan, China.
Zhang W; College of Animal Science, Fujian Agriculture and Forestry University, Fuzhou, Fujian, China.
Xiao T; College of Animal Science, Fujian Agriculture and Forestry University, Fuzhou, Fujian, China.
Peng H; College of Animal Science and Technology, Hainan University, Haikou, Hainan, China.

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Źródło:

Animal biotechnology [Anim Biotechnol] 2023 Dec; Vol. 34 (9), pp. 4547-4552. Date of Electronic Publication: 2023 Jan 18.

Typ publikacji:

Journal Article

MeSH Terms:

Pyrin Domain*
Polymorphism, Single Nucleotide*/genetics
Pregnancy ; Swine/genetics ; Animals ; Female ; Litter Size/genetics ; Gene Frequency ; Genotype ; Mammals

Czasopismo naukowe

• na półce

Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły

Skocz do pozycji: 46.

Tytuł:

Rare functional variants in the CRP and G6PC genes modify the relationship between obesity and serum C-reactive protein in white British population.

Autorzy:

Li X; School of Public Health and Emergency Management, Southern University of Science and Technology, Shenzhen, China.; Shenzhen Key Laboratory of Cardiovascular Health and Precision Medicine, Southern University of Science and Technology, Shenzhen, China.; Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Stockholm, Sweden.
Ploner A; Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Stockholm, Sweden.
Wang Y; Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Stockholm, Sweden.
Mak JKL; Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Stockholm, Sweden.
Lu Y; Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Stockholm, Sweden.
Magnusson PKE; Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Stockholm, Sweden.
Jylhävä J; Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Stockholm, Sweden.; Social Sciences (Health Sciences) and Gerontology Research Center (GEREC), University of Tampere, Tampere, Finland.
Hägg S; Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Stockholm, Sweden.

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Źródło:

Molecular genetics & genomic medicine [Mol Genet Genomic Med] 2023 Dec; Vol. 11 (12), pp. e2255. Date of Electronic Publication: 2023 Jul 26.

Typ publikacji:

Journal Article

MeSH Terms:

C-Reactive Protein*/genetics
C-Reactive Protein*/analysis
Obesity*/genetics
Polymorphism, Single Nucleotide*
Glucose-6-Phosphatase*/genetics
Humans ; Gene Frequency ; White People/genetics

Czasopismo naukowe

• na półce

Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły

Skocz do pozycji: 47.

Tytuł:

Evaluating the association of biallelic OGDHL variants with significant phenotypic heterogeneity.

Autorzy:

Lin SJ; Genes & Human Disease Research Program, Oklahoma Medical Research Foundation, Oklahoma City, OK, 73104, USA.
Vona B; Institute of Human Genetics, Julius Maximilians University Würzburg, Würzburg, Germany.; Institute of Human Genetics, University Medical Center Göttingen, Göttingen, Germany.; Institute for Auditory Neuroscience and InnerEarLab, University Medical Center Göttingen, Göttingen, Germany.; Department of Otolaryngology-Head and Neck Surgery, Tübingen Hearing Research Center, Eberhard Karls University, Tübingen, 72076, Germany.
Lau T; Department of Neuromuscular Disorders, Queen Square Institute of Neurology, University College London, London, UK.
Huang K; Genes & Human Disease Research Program, Oklahoma Medical Research Foundation, Oklahoma City, OK, 73104, USA.
Zaki MS; Clinical Genetics Department, Human Genetics and Genome Research Institute, National Research Centre, Cairo, Egypt.
Aldeen HS; Department of Neuromuscular Disorders, Queen Square Institute of Neurology, University College London, London, UK.
Karimiani EG; Molecular and Clinical Sciences Institute, St. George's, University of London, Cranmer Terrace London, London, UK.
Rocca C; Department of Neuromuscular Disorders, Queen Square Institute of Neurology, University College London, London, UK.
Noureldeen MM; Department of Pediatrics, Faculty of Medicine, Beni-Suef University, Beni-Suef, Egypt.
Saad AK; Medical Molecular Genetics Department, Human Genetics and Genome Research Institute, National Research Centre, Cairo, Egypt.
Petree C; Genes & Human Disease Research Program, Oklahoma Medical Research Foundation, Oklahoma City, OK, 73104, USA.
Bartolomaeus T; Institute of Human Genetics, University of Leipzig Medical Center, Leipzig, Germany.
Abou Jamra R; Institute of Human Genetics, University of Leipzig Medical Center, Leipzig, Germany.
Zifarelli G; Centogene GmbH, Rostock, Germany.
Gotkhindikar A; Bioinformatics Centre, S. P. Pune University, Pune, India.
Wentzensen IM; GeneDx, Gaithersburg, MD, 20877, USA.
Liao M; GeneDx, Gaithersburg, MD, 20877, USA.
Cork EE; Department of Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai, New York, NY, USA.; Department of Pediatrics, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Varshney P; Genes & Human Disease Research Program, Oklahoma Medical Research Foundation, Oklahoma City, OK, 73104, USA.
Hashemi N; Department of Pediatrics, School of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran.
Mohammadi MH; Department of Pediatrics, Zabol University of Medical Sciences, Zabol, Iran.
Rad A; Department of Otolaryngology-Head and Neck Surgery, Tübingen Hearing Research Center, Eberhard Karls University, Tübingen, 72076, Germany.
Neira J; Department of Human Genetics, Emory University, Atlanta, GA, 30322, USA.
Toosi MB; Department of Pediatrics, School of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran.
Knopp C; Institute for Human Genetics and Genomic Medicine, RWTH Aachen University, Pauwelsstr. 30, Aachen, 52074, Germany.
Kurth I; Institute for Human Genetics and Genomic Medicine, RWTH Aachen University, Pauwelsstr. 30, Aachen, 52074, Germany.
Challman TD; Autism & Developmental Medicine Institute, Geisinger, Lewisburg, PA, USA.
Smith R; Autism & Developmental Medicine Institute, Geisinger, Lewisburg, PA, USA.
Abdalla A; Department of Pediatric Endocrinology, Gaafar Ibn Auf Children's Tertiary Hospital, Khartoum, Sudan.
Haaf T; Institute of Human Genetics, Julius Maximilians University Würzburg, Würzburg, Germany.
Suri M; Nottingham Clinical Genetics Service, Nottingham University Hospitals NHS Trust, Nottingham, UK.
Joshi M; Bioinformatics Centre, S. P. Pune University, Pune, India.
Chung WK; Department of Pediatrics, Boston Children's Hospitaland, Harvard Medical School , Boston, MA, USA.
Moreno-De-Luca A; Department of Diagnostic Radiology, Kingston Health Sciences Centre, Queen's University, Kingston, ON, Canada.
Houlden H; Department of Neuromuscular Disorders, Queen Square Institute of Neurology, University College London, London, UK.
Maroofian R; Department of Neuromuscular Disorders, Queen Square Institute of Neurology, University College London, London, UK. .
Varshney GK; Genes & Human Disease Research Program, Oklahoma Medical Research Foundation, Oklahoma City, OK, 73104, USA. .

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Źródło:

Genome medicine [Genome Med] 2023 Nov 29; Vol. 15 (1), pp. 102. Date of Electronic Publication: 2023 Nov 29.

Typ publikacji:

Journal Article

MeSH Terms:

Proteins*/genetics
Zebrafish*/genetics
Animals ; Humans ; Gene Frequency ; Ketoglutarate Dehydrogenase Complex/genetics ; Ketoglutarate Dehydrogenase Complex/metabolism ; Phenotype

Czasopismo naukowe

• na półce

Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły

Skocz do pozycji: 48.

Tytuł:

A phenome-wide scan reveals convergence of common and rare variant associations.

Autorzy:

Zhou D; School of Public Health and the Second Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China. .; Division of Genetic Medicine, Department of Medicine, Vanderbilt University Medical Center, Nashville, TN, USA. .; Vanderbilt Genetics Institute, Vanderbilt University Medical Center, Nashville, TN, USA. .; The Key Laboratory of Intelligent Preventive Medicine of Zhejiang Province, Hangzhou, China. .
Zhou Y; Department of Biostatistics and Center for Quantitative Sciences, Vanderbilt University Medical Center, Nashville, TN, USA.
Xu Y; School of Public Health and the Second Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.; The Key Laboratory of Intelligent Preventive Medicine of Zhejiang Province, Hangzhou, China.
Meng R; School of Public Health and the Second Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Gamazon ER; Division of Genetic Medicine, Department of Medicine, Vanderbilt University Medical Center, Nashville, TN, USA. .; Vanderbilt Genetics Institute, Vanderbilt University Medical Center, Nashville, TN, USA. .; Data Science Institute, Vanderbilt University Medical Center, Nashville, TN, USA. .

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Źródło:

Genome medicine [Genome Med] 2023 Nov 28; Vol. 15 (1), pp. 101. Date of Electronic Publication: 2023 Nov 28.

Typ publikacji:

Journal Article

MeSH Terms:

Genome-Wide Association Study*
Genomics*
Humans ; Gene Frequency ; Phenotype ; Phenomics

Czasopismo naukowe

• na półce

Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły

Skocz do pozycji: 49.

Tytuł:

An X-STRs analysis of the Iraqi Sorani Kurds.

Autorzy:

M Albarzinji B; Kurdistan Institution for Strategic Studies and Scientific Research (KISSR), Sulaymaniyah, Iraq.
Hadi S; University of Central Lancashire Medical School, Preston, United Kingdom.
Ismael B; Kurdistan Institution for Strategic Studies and Scientific Research (KISSR), Sulaymaniyah, Iraq.
Barqee A; Kurdistan Institution for Strategic Studies and Scientific Research (KISSR), Sulaymaniyah, Iraq.
Hadi A; University of Central Lancashire Medical School, Preston, United Kingdom.
Lazim H; Faculty of Health, Social Care and Medicine (FHSCM), School of Medicine, Edge Hill University, Ormskirk, United Kingdom.

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Źródło:

PloS one [PLoS One] 2023 Nov 27; Vol. 18 (11), pp. e0294973. Date of Electronic Publication: 2023 Nov 27 (Print Publication: 2023).

Typ publikacji:

Journal Article

MeSH Terms:

Chromosomes, Human, X*
Genetics, Population*
Humans ; Iraq ; Polymorphism, Genetic ; Microsatellite Repeats/genetics ; DNA Fingerprinting ; Gene Frequency

Czasopismo naukowe

• na półce

Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły

Skocz do pozycji: 50.

Tytuł:

Evaluating the performance of low-frequency variant calling tools for the detection of variants from short-read deep sequencing data.

Autorzy:

Xiang X; Chongqing Key Laboratory of Big Data for Bio Intelligence, Chongqing University of Posts and Telecommunications, Chongqing, 400065, China.
Lu B; Chongqing Key Laboratory of Big Data for Bio Intelligence, Chongqing University of Posts and Telecommunications, Chongqing, 400065, China.
Song D; Chongqing Key Laboratory of Big Data for Bio Intelligence, Chongqing University of Posts and Telecommunications, Chongqing, 400065, China.
Li J; Chongqing Key Laboratory of Big Data for Bio Intelligence, Chongqing University of Posts and Telecommunications, Chongqing, 400065, China.
Shu K; Chongqing Key Laboratory of Big Data for Bio Intelligence, Chongqing University of Posts and Telecommunications, Chongqing, 400065, China. .
Pu D; Chongqing Key Laboratory of Big Data for Bio Intelligence, Chongqing University of Posts and Telecommunications, Chongqing, 400065, China. .

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Źródło:

Scientific reports [Sci Rep] 2023 Nov 22; Vol. 13 (1), pp. 20444. Date of Electronic Publication: 2023 Nov 22.

Typ publikacji:

Journal Article

MeSH Terms:

Polymorphism, Single Nucleotide*
Biomedical Research*
Algorithms ; Gene Frequency ; High-Throughput Nucleotide Sequencing/methods

Czasopismo naukowe

• na półce

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