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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
Pełny tekst  Link otwiera się w nowym oknieSzczegóły
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
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Prevalence of ABO and Rhesus (D) Blood Group and Allelic Frequency at Blood Bank of Nigist Eleni Mohammed Hospital, Ethiopia.
Autorzy:
Lendabo F; Department of Biotechnology, College of Natural and Computational Science, Wachemo University, Hossana, Ethiopia.
Srinivasan V; M.Ct.M Chidambaram Chettyar International School, Chennai, India.
Rather RA; Department of Biotechnology, College of Natural and Computational Science, Wachemo University, Hossana, Ethiopia.
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Źródło:
BioMed research international [Biomed Res Int] 2024 Apr 08; Vol. 2024, pp. 5353528. Date of Electronic Publication: 2024 Apr 08 (Print Publication: 2024).
Typ publikacji:
Journal Article
MeSH Terms:
Blood Banks*
ABO Blood-Group System*/genetics
Humans ; Ethiopia/epidemiology ; Cross-Sectional Studies ; Prevalence ; Gene Frequency/genetics ; Rh-Hr Blood-Group System/genetics ; Hospitals, General
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
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
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
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
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Implementing a New Algorithm for Reinterpretation of Ambiguous Variants in Genetic Dilated Cardiomyopathy.
Autorzy:
Pérez-Serra A; Cardiovascular Genetics Center, Institut d'Investigació Biomèdica de Girona (IDIBGI-CERCA), Parc Hospitalari Martí i Julià, Edifici M2, 17190 Salt, Spain.; Centro de Investigación Biomédica en Red Enfermedades Cardiovasculares (CIBERCV), 28029 Madrid, Spain.
Toro R; Medicine Department, School of Medicine, Cadiz University, 11003 Cadiz, Spain.; Research Unit, Biomedical Research and Innovation Institute of Cadiz (INiBICA), Puerta del Mar University Hospital, 11009 Cadiz, Spain.
Martinez-Barrios E; European Reference Network for Rare, Low Prevalence and Complex Diseases of the Heart (ERN GUARD-Heart), 1105 AZ Amsterdam, The Netherlands.; Pediatric Arrhythmias, Inherited Cardiac Diseases and Sudden Death Unit, Cardiology Department, Sant Joan de Déu Hospital de Barcelona, 08950 Barcelona, Spain.; Arrítmies Pediàtriques, Cardiologia Genètica i Mort Sobtada, Malalties Cardiovasculars en el Desenvolupament, Institut de Recerca Sant Joan de Déu, Esplugues de Llobregat, 08950 Barcelona, Spain.
Iglesias A; Cardiovascular Genetics Center, Institut d'Investigació Biomèdica de Girona (IDIBGI-CERCA), Parc Hospitalari Martí i Julià, Edifici M2, 17190 Salt, Spain.; Centro de Investigación Biomédica en Red Enfermedades Cardiovasculares (CIBERCV), 28029 Madrid, Spain.
Fernandez-Falgueras A; Cardiovascular Genetics Center, Institut d'Investigació Biomèdica de Girona (IDIBGI-CERCA), Parc Hospitalari Martí i Julià, Edifici M2, 17190 Salt, Spain.; Centro de Investigación Biomédica en Red Enfermedades Cardiovasculares (CIBERCV), 28029 Madrid, Spain.; Cardiology Service, Hospital Josep Trueta, University of Girona, 17007 Girona, Spain.
Alcalde M; Cardiovascular Genetics Center, Institut d'Investigació Biomèdica de Girona (IDIBGI-CERCA), Parc Hospitalari Martí i Julià, Edifici M2, 17190 Salt, Spain.; Centro de Investigación Biomédica en Red Enfermedades Cardiovasculares (CIBERCV), 28029 Madrid, Spain.
Coll M; Cardiovascular Genetics Center, Institut d'Investigació Biomèdica de Girona (IDIBGI-CERCA), Parc Hospitalari Martí i Julià, Edifici M2, 17190 Salt, Spain.; Centro de Investigación Biomédica en Red Enfermedades Cardiovasculares (CIBERCV), 28029 Madrid, Spain.
Puigmulé M; Cardiovascular Genetics Center, Institut d'Investigació Biomèdica de Girona (IDIBGI-CERCA), Parc Hospitalari Martí i Julià, Edifici M2, 17190 Salt, Spain.; Centro de Investigación Biomédica en Red Enfermedades Cardiovasculares (CIBERCV), 28029 Madrid, Spain.
Del Olmo B; Cardiovascular Genetics Center, Institut d'Investigació Biomèdica de Girona (IDIBGI-CERCA), Parc Hospitalari Martí i Julià, Edifici M2, 17190 Salt, Spain.; Centro de Investigación Biomédica en Red Enfermedades Cardiovasculares (CIBERCV), 28029 Madrid, Spain.
Picó F; Cardiovascular Genetics Center, Institut d'Investigació Biomèdica de Girona (IDIBGI-CERCA), Parc Hospitalari Martí i Julià, Edifici M2, 17190 Salt, Spain.; Centro de Investigación Biomédica en Red Enfermedades Cardiovasculares (CIBERCV), 28029 Madrid, Spain.
Lopez L; Cardiovascular Genetics Center, Institut d'Investigació Biomèdica de Girona (IDIBGI-CERCA), Parc Hospitalari Martí i Julià, Edifici M2, 17190 Salt, Spain.; Centro de Investigación Biomédica en Red Enfermedades Cardiovasculares (CIBERCV), 28029 Madrid, Spain.
Arbelo E; Centro de Investigación Biomédica en Red Enfermedades Cardiovasculares (CIBERCV), 28029 Madrid, Spain.; European Reference Network for Rare, Low Prevalence and Complex Diseases of the Heart (ERN GUARD-Heart), 1105 AZ Amsterdam, The Netherlands.; Arrhythmias Unit, Hospital Clinic, University of Barcelona-IDIBAPS, 08036 Barcelona, Spain.
Cesar S; European Reference Network for Rare, Low Prevalence and Complex Diseases of the Heart (ERN GUARD-Heart), 1105 AZ Amsterdam, The Netherlands.; Pediatric Arrhythmias, Inherited Cardiac Diseases and Sudden Death Unit, Cardiology Department, Sant Joan de Déu Hospital de Barcelona, 08950 Barcelona, Spain.; Arrítmies Pediàtriques, Cardiologia Genètica i Mort Sobtada, Malalties Cardiovasculars en el Desenvolupament, Institut de Recerca Sant Joan de Déu, Esplugues de Llobregat, 08950 Barcelona, Spain.
Llano CT; Cardiology Service, Hospital Josep Trueta, University of Girona, 17007 Girona, Spain.
Mangas A; Medicine Department, School of Medicine, Cadiz University, 11003 Cadiz, Spain.; Research Unit, Biomedical Research and Innovation Institute of Cadiz (INiBICA), Puerta del Mar University Hospital, 11009 Cadiz, Spain.; Internal Medicine Department, Puerta del Mar University Hospital, School of Medicine, University of Cadiz, 11009 Cadiz, Spain.
Brugada J; Centro de Investigación Biomédica en Red Enfermedades Cardiovasculares (CIBERCV), 28029 Madrid, Spain.; European Reference Network for Rare, Low Prevalence and Complex Diseases of the Heart (ERN GUARD-Heart), 1105 AZ Amsterdam, The Netherlands.; Arrhythmias Unit, Hospital Clinic, University of Barcelona-IDIBAPS, 08036 Barcelona, Spain.
Sarquella-Brugada G; European Reference Network for Rare, Low Prevalence and Complex Diseases of the Heart (ERN GUARD-Heart), 1105 AZ Amsterdam, The Netherlands.; Pediatric Arrhythmias, Inherited Cardiac Diseases and Sudden Death Unit, Cardiology Department, Sant Joan de Déu Hospital de Barcelona, 08950 Barcelona, Spain.; Arrítmies Pediàtriques, Cardiologia Genètica i Mort Sobtada, Malalties Cardiovasculars en el Desenvolupament, Institut de Recerca Sant Joan de Déu, Esplugues de Llobregat, 08950 Barcelona, Spain.; Medical Science Department, School of Medicine, University of Girona, 17003 Girona, Spain.
Brugada R; Cardiovascular Genetics Center, Institut d'Investigació Biomèdica de Girona (IDIBGI-CERCA), Parc Hospitalari Martí i Julià, Edifici M2, 17190 Salt, Spain.; Centro de Investigación Biomédica en Red Enfermedades Cardiovasculares (CIBERCV), 28029 Madrid, Spain.; Cardiology Service, Hospital Josep Trueta, University of Girona, 17007 Girona, Spain.; Medical Science Department, School of Medicine, University of Girona, 17003 Girona, Spain.
Campuzano O; Cardiovascular Genetics Center, Institut d'Investigació Biomèdica de Girona (IDIBGI-CERCA), Parc Hospitalari Martí i Julià, Edifici M2, 17190 Salt, Spain.; Centro de Investigación Biomédica en Red Enfermedades Cardiovasculares (CIBERCV), 28029 Madrid, Spain.; Medical Science Department, School of Medicine, University of Girona, 17003 Girona, Spain.
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Źródło:
International journal of molecular sciences [Int J Mol Sci] 2024 Mar 29; Vol. 25 (7). Date of Electronic Publication: 2024 Mar 29.
Typ publikacji:
Journal Article
MeSH Terms:
Cardiomyopathy, Dilated*/genetics
Heart Failure*
Humans ; Algorithms ; Gene Frequency
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
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
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
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
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
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
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
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
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
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
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
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
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
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
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
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
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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
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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
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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
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Wyświetlanie 1-20 z 31648

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