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Wyszukujesz frazę ""Gene Deletion"" wg kryterium: Temat


Tytuł:
Limited threat of Plasmodium falciparum pfhrp2 and pfhrp3 gene deletion to the utility of HRP2-based malaria RDTs in Northern Uganda.
Autorzy:
Agaba BB; Faculty of Medicine, Department of Medical Laboratory Sciences, Mbarara University of Science and Technology, Mbarara, Uganda. .; National Malaria Control Division, Kampala, Uganda. .; London School of Hygiene and Tropical Medicine, London, UK. .; Infectious Diseases Research Collaboration, Kampala, Uganda. .
Smith D; QIMR Berghofer Medical Research Institute, Kelvin Grove, QLD, Australia.; Australian Defence Force Malaria and Infectious Disease Institute, Kelvin Grove, Australia.
Travis J; QIMR Berghofer Medical Research Institute, Kelvin Grove, QLD, Australia.; Australian Defence Force Malaria and Infectious Disease Institute, Kelvin Grove, Australia.
Pasay C; QIMR Berghofer Medical Research Institute, Kelvin Grove, QLD, Australia.
Nabatanzi M; National Malaria Control Division, Kampala, Uganda.
Arinaitwe E; Infectious Diseases Research Collaboration, Kampala, Uganda.
Ssewanyana I; Infectious Diseases Research Collaboration, Kampala, Uganda.; National Health Laboratory Services/Central Public Health Laboratories, Kelvin Grove, Uganda.
Nabadda S; National Health Laboratory Services/Central Public Health Laboratories, Kelvin Grove, Uganda.
Cunningham J; Global Malaria Programme, World Health Organization, Geneva, Switzerland.
Kamya MR; Faculty of Medicine, Department of Medical Laboratory Sciences, Mbarara University of Science and Technology, Mbarara, Uganda.; Infectious Diseases Research Collaboration, Kampala, Uganda.
Cheng Q; QIMR Berghofer Medical Research Institute, Kelvin Grove, QLD, Australia.; Australian Defence Force Malaria and Infectious Disease Institute, Kelvin Grove, Australia.
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Źródło:
Malaria journal [Malar J] 2024 Jan 02; Vol. 23 (1), pp. 3. Date of Electronic Publication: 2024 Jan 02.
Typ publikacji:
Journal Article
MeSH Terms:
Malaria*/diagnosis
Malaria*/genetics
Malaria, Falciparum*/diagnosis
Malaria, Falciparum*/genetics
Humans ; Antigens, Protozoan/genetics ; Cross-Sectional Studies ; Diagnostic Tests, Routine ; Gene Deletion ; L-Lactate Dehydrogenase/genetics ; Plasmodium falciparum/genetics ; Protozoan Proteins/genetics ; Rapid Diagnostic Tests ; Uganda
Czasopismo naukowe
Tytuł:
A genome-wide collection of barcoded single-gene deletion mutants in Salmonella enterica serovar Typhimurium.
Autorzy:
Porwollik S; Dept. of Microbiology and Molecular Genetics, University of California, Irvine, Irvina, CA, United States of America.
Chu W; Dept. of Microbiology and Molecular Genetics, University of California, Irvine, Irvina, CA, United States of America.
Desai PT; GSK Computational Biology, Upper Providence, PA, United States of America.
McClelland M; Dept. of Microbiology and Molecular Genetics, University of California, Irvine, Irvina, CA, United States of America.
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Źródło:
PloS one [PLoS One] 2024 Mar 07; Vol. 19 (3), pp. e0298419. Date of Electronic Publication: 2024 Mar 07 (Print Publication: 2024).
Typ publikacji:
Journal Article
MeSH Terms:
Salmonella typhimurium*/genetics
Salmonella enterica*
Animals ; Serogroup ; Gene Deletion ; Anti-Bacterial Agents ; Tetracycline ; Bacteria
Czasopismo naukowe
Tytuł:
Machine learning identifies key metabolic reactions in bacterial growth on different carbon sources.
Autorzy:
Woo H; Department of Bioscience and Biotechnology, Konkuk University, Seoul, 05029, Republic of Korea.
Kim Y; Department of Bioscience and Biotechnology, Konkuk University, Seoul, 05029, Republic of Korea.
Kim D; Department of Bioscience and Biotechnology, Konkuk University, Seoul, 05029, Republic of Korea.
Yoon SH; Department of Bioscience and Biotechnology, Konkuk University, Seoul, 05029, Republic of Korea. .
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Źródło:
Molecular systems biology [Mol Syst Biol] 2024 Mar; Vol. 20 (3), pp. 170-186. Date of Electronic Publication: 2024 Jan 30.
Typ publikacji:
Journal Article
MeSH Terms:
Carbon*/metabolism
Escherichia coli Proteins*/metabolism
Escherichia coli/metabolism ; Gene Deletion ; Machine Learning ; Metabolic Networks and Pathways ; Models, Biological
Czasopismo naukowe
Tytuł:
Targeted long-read sequencing identified a causal structural variant in X-linked nephrogenic diabetes insipidus.
Autorzy:
Strych L; Department of Medical Genetics, Faculty of Medicine in Pilsen, Charles University and University Hospital Pilsen, Pilsen, Czech Republic. .
Černá M; Department of Medical Genetics, Faculty of Medicine in Pilsen, Charles University and University Hospital Pilsen, Pilsen, Czech Republic.
Hejnalová M; Department of Medical Genetics, Faculty of Medicine in Pilsen, Charles University and University Hospital Pilsen, Pilsen, Czech Republic.
Zavoral T; Department of Medical Genetics, Faculty of Medicine in Pilsen, Charles University and University Hospital Pilsen, Pilsen, Czech Republic.
Komrsková P; Department of Medical Genetics, Faculty of Medicine in Pilsen, Charles University and University Hospital Pilsen, Pilsen, Czech Republic.
Tejcová J; Department of Medical Genetics, Faculty of Medicine in Pilsen, Charles University and University Hospital Pilsen, Pilsen, Czech Republic.
Bitar I; Biomedical Center, Faculty of Medicine in Pilsen, Charles University, Pilsen, Czech Republic.; Department of Microbiology, Faculty of Medicine in Pilsen, Charles University and University Hospital Pilsen, Pilsen, Czech Republic.
Sládková E; Department of Pediatrics, Faculty of Medicine in Pilsen, Charles University and University Hospital Pilsen, Pilsen, Czech Republic.
Sýkora J; Department of Pediatrics, Faculty of Medicine in Pilsen, Charles University and University Hospital Pilsen, Pilsen, Czech Republic.
Šubrt I; Department of Medical Genetics, Faculty of Medicine in Pilsen, Charles University and University Hospital Pilsen, Pilsen, Czech Republic. .
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Źródło:
BMC medical genomics [BMC Med Genomics] 2024 Jan 22; Vol. 17 (1), pp. 29. Date of Electronic Publication: 2024 Jan 22.
Typ publikacji:
Journal Article
MeSH Terms:
Diabetes Insipidus, Nephrogenic*/genetics
Diabetes Mellitus*
Female ; Humans ; Male ; Kidney ; Gene Deletion ; Genetic Testing ; Heterozygote ; Rare Diseases
Czasopismo naukowe
Tytuł:
The clinical, myopathological, and genetic analysis of 155 Chinese mitochondrial ophthalmoplegia patients with mitochondrial DNA single large deletions.
Autorzy:
Zhao Y; Department of Neurology, Peking University First Hospital, Beijing, China.; Beijing Key Laboratory of Neurovascular Disease Discovery, Beijing, China.
Hou Y; Department of Geriatrics, Peking University First Hospital, Beijing, China.
Zhao X; Department of Neurology, Peking University First Hospital, Beijing, China.; Beijing Key Laboratory of Neurovascular Disease Discovery, Beijing, China.; Department of Neurology, Beijing Jishuitan Hospital, Beijing, China.
Liufu T; Department of Neurology, Peking University First Hospital, Beijing, China.; Beijing Key Laboratory of Neurovascular Disease Discovery, Beijing, China.
Yu M; Department of Neurology, Peking University First Hospital, Beijing, China.; Beijing Key Laboratory of Neurovascular Disease Discovery, Beijing, China.
Zhang W; Department of Neurology, Peking University First Hospital, Beijing, China.; Beijing Key Laboratory of Neurovascular Disease Discovery, Beijing, China.
Xie Z; Department of Neurology, Peking University First Hospital, Beijing, China.; Beijing Key Laboratory of Neurovascular Disease Discovery, Beijing, China.
Zhang VW; AmCare Genomics Lab, Guangzhou, China.
Yuan Y; Department of Neurology, Peking University First Hospital, Beijing, China.; Beijing Key Laboratory of Neurovascular Disease Discovery, Beijing, China.
Wang Z; Department of Neurology, Peking University First Hospital, Beijing, China.; Beijing Key Laboratory of Neurovascular Disease Discovery, Beijing, China.
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Źródło:
Molecular genetics & genomic medicine [Mol Genet Genomic Med] 2024 Jan; Vol. 12 (1), pp. e2328. Date of Electronic Publication: 2023 Nov 28.
Typ publikacji:
Journal Article
MeSH Terms:
Ophthalmoplegia*/genetics
Kearns-Sayre Syndrome*/genetics
Kearns-Sayre Syndrome*/pathology
Ophthalmoplegia, Chronic Progressive External*/genetics
Ophthalmoplegia, Chronic Progressive External*/diagnosis
Ophthalmoplegia, Chronic Progressive External*/pathology
Humans ; Retrospective Studies ; Gene Deletion ; DNA, Mitochondrial/genetics ; China
Czasopismo naukowe
Tytuł:
Screening and prenatal diagnosis of survival motor neuron gene deletion in pregnant women in Zhaoqing city, Guangdong Province.
Autorzy:
Huang Z; Clinical Laboratory, The Second People's Hospital of Zhaoqing, Zhaoqing, The People's Republic of China. .; Clinical Laboratory, The Second People's Hospital of Zhaoqing, Zhaoqing, The People's Republic of China. .; Clinical Laboratory, The Second People's Hospital of Zhaoqing, No. 2, Jiansheer Street, 526000, Zhaoqing City, Guangdong province, The People's Republic of China. .
Yang Q; Clinical Laboratory, The Second People's Hospital of Zhaoqing, Zhaoqing, The People's Republic of China.
Ye J; Clinical Laboratory, The Second People's Hospital of Zhaoqing, Zhaoqing, The People's Republic of China.
Huang J; Clinical Laboratory, The Second People's Hospital of Zhaoqing, Zhaoqing, The People's Republic of China.
Lin J; Obstetrical Department, The Second People's Hospital of Zhaoqing, Zhaoqing, The People's Republic of China.
Chen J; Prenatal Diagnosis Center, The Second People's Hospital of Zhaoqing, Zhaoqing, The People's Republic of China.
Liang Z; Clinical Laboratory, The Second People's Hospital of Zhaoqing, Zhaoqing, The People's Republic of China.
Cao Z; Clinical Laboratory, The Second People's Hospital of Zhaoqing, Zhaoqing, The People's Republic of China.
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Źródło:
BMC medical genomics [BMC Med Genomics] 2023 Mar 01; Vol. 16 (1), pp. 39. Date of Electronic Publication: 2023 Mar 01.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Gene Deletion*
Prenatal Diagnosis*
Muscular Atrophy, Spinal*/diagnosis
Survival of Motor Neuron 1 Protein*/genetics
Female ; Humans ; Pregnancy ; China ; Motor Neurons ; Pregnant Women
Czasopismo naukowe
Tytuł:
Collective production of hydrogen sulfide gas enables budding yeast lacking MET17 to overcome their metabolic defect.
Autorzy:
Sonal; Centre for Life's Origins and Evolution, Department of Genetics, Evolution and Environment, University College London, London, United Kingdom.
Yuan AE; University of Washington, Seattle, Washington, United States of America.
Yang X; School of Environmental Science and Engineering, Sun Yat-sen University, Guangzhou, China.
Shou W; Centre for Life's Origins and Evolution, Department of Genetics, Evolution and Environment, University College London, London, United Kingdom.
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Źródło:
PLoS biology [PLoS Biol] 2023 Dec 07; Vol. 21 (12), pp. e3002439. Date of Electronic Publication: 2023 Dec 07 (Print Publication: 2023).
Typ publikacji:
Journal Article
MeSH Terms:
Hydrogen Sulfide*/metabolism
Cysteine Synthase*/genetics
Cysteine Synthase*/metabolism
Saccharomyces cerevisiae Proteins*/genetics
Saccharomyces cerevisiae Proteins*/metabolism
Saccharomyces cerevisiae/genetics ; Saccharomyces cerevisiae/growth & development ; Saccharomyces cerevisiae/metabolism ; Gene Deletion ; Sulfates/metabolism ; Models, Biological
Czasopismo naukowe
Tytuł:
Paralog dispensability shapes homozygous deletion patterns in tumor genomes.
Autorzy:
De Kegel B; School of Computer Science and Systems Biology Ireland, University College Dublin, Dublin, Ireland.
Ryan CJ; School of Computer Science and Systems Biology Ireland, University College Dublin, Dublin, Ireland.; Conway Institute of Biomolecular and Biomedical Research, University College Dublin, Dublin, Ireland.
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Źródło:
Molecular systems biology [Mol Syst Biol] 2023 Dec 06; Vol. 19 (12), pp. e11987. Date of Electronic Publication: 2023 Nov 14.
Typ publikacji:
Journal Article
MeSH Terms:
DNA Copy Number Variations*/genetics
Neoplasms*/genetics
Humans ; Homozygote ; Sequence Deletion ; Cell Line ; Gene Deletion
Czasopismo naukowe
Tytuł:
Deletion of the Candida albicans TLO gene family using CRISPR-Cas9 mutagenesis allows characterisation of functional differences in α-, β- and γ- TLO gene function.
Autorzy:
Fletcher J; Division of Oral Biosciences, Dublin Dental University Hospital, & University of Dublin, Trinity College Dublin, Dublin, Ireland.
O'Connor-Moneley J; Division of Oral Biosciences, Dublin Dental University Hospital, & University of Dublin, Trinity College Dublin, Dublin, Ireland.
Frawley D; Division of Oral Biosciences, Dublin Dental University Hospital, & University of Dublin, Trinity College Dublin, Dublin, Ireland.
Flanagan PR; Division of Oral Biosciences, Dublin Dental University Hospital, & University of Dublin, Trinity College Dublin, Dublin, Ireland.
Alaalm L; Division of Oral Biosciences, Dublin Dental University Hospital, & University of Dublin, Trinity College Dublin, Dublin, Ireland.
Menendez-Manjon P; Departamento de Enfermería I, Universidad del País Vasco, Bilbao, Spain.
Estevez SV; School of Biosciences, University of Kent, Canterbury, United Kingdom.
Hendricks S; Department of Microbiology, The Ohio State University, Columbus, Ohio, United States of America.
Woodruff AL; Department of Microbiology, The Ohio State University, Columbus, Ohio, United States of America.
Buscaino A; School of Biosciences, University of Kent, Canterbury, United Kingdom.
Anderson MZ; Department of Microbiology, The Ohio State University, Columbus, Ohio, United States of America.
Sullivan DJ; Division of Oral Biosciences, Dublin Dental University Hospital, & University of Dublin, Trinity College Dublin, Dublin, Ireland.
Moran GP; Division of Oral Biosciences, Dublin Dental University Hospital, & University of Dublin, Trinity College Dublin, Dublin, Ireland.
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Źródło:
PLoS genetics [PLoS Genet] 2023 Dec 04; Vol. 19 (12), pp. e1011082. Date of Electronic Publication: 2023 Dec 04 (Print Publication: 2023).
Typ publikacji:
Journal Article
MeSH Terms:
Candida albicans*/metabolism
Fungal Proteins*/genetics
Fungal Proteins*/metabolism
Humans ; CRISPR-Cas Systems/genetics ; Mutagenesis ; Phenotype ; Gene Expression Regulation, Fungal ; Gene Deletion
Czasopismo naukowe
Tytuł:
Effect of the res2 transcription factor gene deletion on protein secretion and stress response in the hyperproducer strain Trichoderma reesei Rut-C30.
Autorzy:
Alharake J; IFP Energies Nouvelles, 1 et 4, avenue de Bois-Préau, Rueil-Malmaison Cedex, 92852, France.
Bidard F; IFP Energies Nouvelles, 1 et 4, avenue de Bois-Préau, Rueil-Malmaison Cedex, 92852, France.
Aouam T; IFP Energies Nouvelles, 1 et 4, avenue de Bois-Préau, Rueil-Malmaison Cedex, 92852, France.
Sénamaud-Beaufort C; Département de biologie, GenomiqueENS, Institut de Biologie de l'ENS (IBENS), CNRS, INSERM, Université PSL, École normale supérieure, Paris, 75005, France.
Margeot A; IFP Energies Nouvelles, 1 et 4, avenue de Bois-Préau, Rueil-Malmaison Cedex, 92852, France.
Heiss-Blanquet S; IFP Energies Nouvelles, 1 et 4, avenue de Bois-Préau, Rueil-Malmaison Cedex, 92852, France. .
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Źródło:
BMC microbiology [BMC Microbiol] 2023 Nov 30; Vol. 23 (1), pp. 374. Date of Electronic Publication: 2023 Nov 30.
Typ publikacji:
Journal Article
MeSH Terms:
Cellulase*/genetics
Trichoderma*/genetics
Lactose/metabolism ; Gene Deletion ; Transcription Factors/genetics ; Transcription Factors/metabolism
SCR Organism:
Trichoderma reesei
Czasopismo naukowe
Tytuł:
Assessing the histidine-rich protein 2/3 gene deletion in Plasmodium falciparum isolates from Burkina Faso.
Autorzy:
Tarama CW; Centre National de Recherche et de Formation sur le Paludisme, Ouagadougou, Burkina Faso.
Soré H; Centre National de Recherche et de Formation sur le Paludisme, Ouagadougou, Burkina Faso.
Siribié M; Centre National de Recherche et de Formation sur le Paludisme, Ouagadougou, Burkina Faso.
Débé S; Centre National de Recherche et de Formation sur le Paludisme, Ouagadougou, Burkina Faso.
Kinda R; Centre National de Recherche et de Formation sur le Paludisme, Ouagadougou, Burkina Faso.
Nonkani WG; Centre National de Recherche et de Formation sur le Paludisme, Ouagadougou, Burkina Faso.
Tiendrebeogo F; Centre National de Recherche et de Formation sur le Paludisme, Ouagadougou, Burkina Faso.
Bantango W; Centre National de Recherche et de Formation sur le Paludisme, Ouagadougou, Burkina Faso.
Yira K; Centre National de Recherche et de Formation sur le Paludisme, Ouagadougou, Burkina Faso.
Hien EY; Université Joseph KI-ZERBO, Ouagadougou, Burkina Faso.
Guelbéogo MW; Centre National de Recherche et de Formation sur le Paludisme, Ouagadougou, Burkina Faso.
Traoré Y; Université Joseph KI-ZERBO, Ouagadougou, Burkina Faso.
Ménard D; Institut Pasteur, Université Paris Cité, Malaria Genetic and Resistance Unit, INSERM U1201, 75015, Paris, France.; Institut Pasteur, Université Paris Cité, Malaria Parasite Biology and Vaccines, F-75015, Paris, France.; Institute of Parasitology and Tropical Diseases, Université de Strasbourg, UR7292 Dynamics of Host-Pathogen Interactions, 67000, Strasbourg, France.; Laboratory of Parasitology and Medical Mycology, CHU Strasbourg, 67000, Strasbourg, France.
Gansané A; Centre National de Recherche et de Formation sur le Paludisme, Ouagadougou, Burkina Faso. .
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Źródło:
Malaria journal [Malar J] 2023 Nov 29; Vol. 22 (1), pp. 363. Date of Electronic Publication: 2023 Nov 29.
Typ publikacji:
Journal Article
MeSH Terms:
Plasmodium falciparum*/genetics
Malaria, Falciparum*/parasitology
Child ; Humans ; Protozoan Proteins/genetics ; Antigens, Protozoan/genetics ; Antigens, Protozoan/analysis ; Histidine/genetics ; Gene Deletion ; Cross-Sectional Studies ; Burkina Faso/epidemiology ; Diagnostic Tests, Routine/methods
Czasopismo naukowe
Tytuł:
Identification of compound heterozygous deletion of the WWOX gene in WOREE syndrome.
Autorzy:
Dong XS; Prenatal Diagnosis Center, Zhongshan Boai Hospital Affiliated to Southern Medical University, Zhongshan, Guangdong, China.
Wen XJ; Reproductive Medicine Center, Zhongshan Boai Hospital Affiliated to Southern Medical University, Zhongshan, Guangdong, China.
Zhang S; Department of Pediatrics, Zhongshan Boai Hospital Affiliated to Southern Medical University, Zhongshan, Guangdong, China.
Wang DG; Prenatal Diagnosis Center, Zhongshan Boai Hospital Affiliated to Southern Medical University, Zhongshan, Guangdong, China.
Xiong Y; Prenatal Diagnosis Center, Zhongshan Boai Hospital Affiliated to Southern Medical University, Zhongshan, Guangdong, China.
Li ZM; Prenatal Diagnosis Center, Zhongshan Boai Hospital Affiliated to Southern Medical University, Zhongshan, Guangdong, China. .
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Źródło:
BMC medical genomics [BMC Med Genomics] 2023 Nov 16; Vol. 16 (1), pp. 291. Date of Electronic Publication: 2023 Nov 16.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Tumor Suppressor Proteins*/genetics
Mothers*
Female ; Humans ; Child, Preschool ; WW Domain-Containing Oxidoreductase/genetics ; Syndrome ; Real-Time Polymerase Chain Reaction ; Gene Deletion
Czasopismo naukowe
Tytuł:
Identification of a Novel 7-bp Deletion in the α-Globin Gene Cluster in One Chinese Family.
Autorzy:
Wu BD; Department of Medical Genetics the First People's Hospital of Yunnan Province, The Affiliated Hospital of Kunming University of Science and Technology, Kunming, People's Republic of China.
Zhou XY; Department of Pediatrics, Yunnan Provincial Key Laboratory for Birth Defects and Genetic Diseases, the First People's Hospital of Yunnan Province, Kunming, People's Republic of China.
Xie MJ; Department of Medical Genetics the First People's Hospital of Yunnan Province, The Affiliated Hospital of Kunming University of Science and Technology, Kunming, People's Republic of China.
Jin CC; Department of Medical Genetics the First People's Hospital of Yunnan Province, The Affiliated Hospital of Kunming University of Science and Technology, Kunming, People's Republic of China.
Yan YL; Department of Medical Genetics the First People's Hospital of Yunnan Province, The Affiliated Hospital of Kunming University of Science and Technology, Kunming, People's Republic of China.
He J; Department of Medical Genetics the First People's Hospital of Yunnan Province, The Affiliated Hospital of Kunming University of Science and Technology, Kunming, People's Republic of China.; Department of Pediatrics, Yunnan Provincial Key Laboratory for Birth Defects and Genetic Diseases, the First People's Hospital of Yunnan Province, Kunming, People's Republic of China.; Department of Hematology, the First People's Hospital of Yunnan Province, Kunming, People's Republic of China.
Zhu BS; Department of Medical Genetics the First People's Hospital of Yunnan Province, The Affiliated Hospital of Kunming University of Science and Technology, Kunming, People's Republic of China.; Department of Pediatrics, Yunnan Provincial Key Laboratory for Birth Defects and Genetic Diseases, the First People's Hospital of Yunnan Province, Kunming, People's Republic of China.; Department of Hematology, the First People's Hospital of Yunnan Province, Kunming, People's Republic of China.
Zhang J; Department of Medical Genetics the First People's Hospital of Yunnan Province, The Affiliated Hospital of Kunming University of Science and Technology, Kunming, People's Republic of China.; Department of Pediatrics, Yunnan Provincial Key Laboratory for Birth Defects and Genetic Diseases, the First People's Hospital of Yunnan Province, Kunming, People's Republic of China.; Department of Hematology, the First People's Hospital of Yunnan Province, Kunming, People's Republic of China.
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Źródło:
Hemoglobin [Hemoglobin] 2023 Nov; Vol. 47 (2), pp. 49-51. Date of Electronic Publication: 2023 May 29.
Typ publikacji:
Journal Article
MeSH Terms:
alpha-Thalassemia*/diagnosis
alpha-Thalassemia*/genetics
Humans ; alpha-Globins/genetics ; Glycated Hemoglobin ; East Asian People ; Mutation ; Multigene Family ; Gene Deletion
Czasopismo naukowe
Tytuł:
Evaluation of the Deletion of the African Swine Fever Virus Gene O174L from the Genome of the Georgia Isolate.
Autorzy:
Ramirez-Medina E; Plum Island Animal Disease Center, ARS, USDA, Greenport, NY 11944, USA.
Velazquez-Salinas L; Plum Island Animal Disease Center, ARS, USDA, Greenport, NY 11944, USA.
Rai A; Plum Island Animal Disease Center, ARS, USDA, Greenport, NY 11944, USA.; Oak Ridge Institute for Science and Education (ORISE), Oak Ridge, TN 37830, USA.
Espinoza N; Plum Island Animal Disease Center, ARS, USDA, Greenport, NY 11944, USA.
Valladares A; Plum Island Animal Disease Center, ARS, USDA, Greenport, NY 11944, USA.; Oak Ridge Institute for Science and Education (ORISE), Oak Ridge, TN 37830, USA.
Silva E; Plum Island Animal Disease Center, ARS, USDA, Greenport, NY 11944, USA.
Burton L; Plum Island Animal Disease Center, ARS, USDA, Greenport, NY 11944, USA.
Spinard E; Plum Island Animal Disease Center, ARS, USDA, Greenport, NY 11944, USA.
Meyers A; Plum Island Animal Disease Center, ARS, USDA, Greenport, NY 11944, USA.; Oak Ridge Institute for Science and Education (ORISE), Oak Ridge, TN 37830, USA.
Risatti G; Department of Pathobiology and Veterinary Science, University of Connecticut, Storrs, CT 06269, USA.
Calvelage S; Friedrich-Loeffler-Institut, Federal Research Institute for Animal Health, Südufer 10, 17493 Greifswald-Insel Riems, Germany.
Blome S; Friedrich-Loeffler-Institut, Federal Research Institute for Animal Health, Südufer 10, 17493 Greifswald-Insel Riems, Germany.
Gladue DP; Plum Island Animal Disease Center, ARS, USDA, Greenport, NY 11944, USA.
Borca MV; Plum Island Animal Disease Center, ARS, USDA, Greenport, NY 11944, USA.
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Źródło:
Viruses [Viruses] 2023 Oct 23; Vol. 15 (10). Date of Electronic Publication: 2023 Oct 23.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
African Swine Fever Virus*
African Swine Fever*
Swine ; Animals ; Georgia ; Virulence/genetics ; Gene Deletion ; Sus scrofa ; Virus Replication ; DNA-Directed DNA Polymerase/genetics
Czasopismo naukowe
Tytuł:
Whole genome sequencing resolves 10 years diagnostic odyssey in familiar myxoma.
Autorzy:
Pálla S; Department of Dermatology, Venereology and Dermatooncology, Semmelweis University, Budapest, Hungary.
Tőke J; Department of Internal Medicine and Oncology, Semmelweis University, Budapest, Hungary.; ENDO-ERN HCP Semmelweis University, Budapest, Hungary.
Bozsik A; Department of Molecular Genetics, National Institute of Oncology, Ráth György U. 7-9, 1122, Budapest, Hungary.; Hereditary Cancers Research Group, Eötvös Loránd Research Network, Semmelweis University, Budapest, Hungary.; National Tumorbiology Laboratory, Budapest, Hungary.
Butz H; Department of Molecular Genetics, National Institute of Oncology, Ráth György U. 7-9, 1122, Budapest, Hungary.; Hereditary Cancers Research Group, Eötvös Loránd Research Network, Semmelweis University, Budapest, Hungary.; National Tumorbiology Laboratory, Budapest, Hungary.
Papp J; Department of Molecular Genetics, National Institute of Oncology, Ráth György U. 7-9, 1122, Budapest, Hungary.; Hereditary Cancers Research Group, Eötvös Loránd Research Network, Semmelweis University, Budapest, Hungary.
Likó I; Hereditary Cancers Research Group, Eötvös Loránd Research Network, Semmelweis University, Budapest, Hungary.
Kuroli E; Department of Dermatology, Venereology and Dermatooncology, Semmelweis University, Budapest, Hungary.; Department of Pathology and Experimental Cancer Research, Semmelweis University, Budapest, Hungary.
Bánvölgyi A; Department of Dermatology, Venereology and Dermatooncology, Semmelweis University, Budapest, Hungary.
Hamar M; Department of Surgery, Transplantation and Gastroenterology, Semmelweis University, Budapest, Hungary.
Bertherat J; Université Paris Cité, Institut Cochin, Inserm U1016, Paris, France.; Department of Endocrinology and National Reference Center for Rare Adrenal Disorders, Hôpital Cochin, Assistance Publique Hôpitaux de Paris, Paris, France.
Medvecz M; Department of Dermatology, Venereology and Dermatooncology, Semmelweis University, Budapest, Hungary.; ERN-Skin Semmelweis University, Budapest, Hungary.
Patócs A; ENDO-ERN HCP Semmelweis University, Budapest, Hungary. .; Department of Molecular Genetics, National Institute of Oncology, Ráth György U. 7-9, 1122, Budapest, Hungary. .; Hereditary Cancers Research Group, Eötvös Loránd Research Network, Semmelweis University, Budapest, Hungary. .; National Tumorbiology Laboratory, Budapest, Hungary. .; National Institute of Oncology, Oncology Biobank Center, Budapest, Hungary. .; Department of Laboratory Medicine, Semmelweis University, Budapest, Hungary. .
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Źródło:
Scientific reports [Sci Rep] 2023 Sep 05; Vol. 13 (1), pp. 14658. Date of Electronic Publication: 2023 Sep 05.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Carney Complex*/diagnosis
Carney Complex*/genetics
Cyclic AMP-Dependent Protein Kinase RIalpha Subunit*/genetics
Myxoma/genetics ; Humans ; Gene Deletion ; Pedigree ; Promoter Regions, Genetic ; Male ; Female ; Whole Genome Sequencing
Czasopismo naukowe
Tytuł:
Pharmacological Inhibition and Genetic Deletion of Cystathionine Gamma-Lyase in Mice Protects against Organ Injury in Sepsis: A Key Role of Adhesion Molecules on Endothelial Cells.
Autorzy:
Manandhar S; Department of Pathology and Biomedical Science, University of Otago, Christchurch 8140, New Zealand.
Chambers S; Department of Pathology and Biomedical Science, University of Otago, Christchurch 8140, New Zealand.
Miller A; Department of Pathology and Biomedical Science, University of Otago, Christchurch 8140, New Zealand.
Ishii I; Department of Health Chemistry, Showa Pharmaceutical University, Machida, Tokyo 194-8543, Japan.
Bhatia M; Department of Pathology and Biomedical Science, University of Otago, Christchurch 8140, New Zealand.
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Źródło:
International journal of molecular sciences [Int J Mol Sci] 2023 Sep 04; Vol. 24 (17). Date of Electronic Publication: 2023 Sep 04.
Typ publikacji:
Journal Article
MeSH Terms:
Cystathionine gamma-Lyase*/antagonists & inhibitors
Cystathionine gamma-Lyase*/genetics
Sepsis*/drug therapy
Sepsis*/genetics
Animals ; Mice ; Cell Adhesion Molecules ; Endothelial Cells ; Gene Deletion ; NF-kappa B
Czasopismo naukowe
Tytuł:
TRIM67 Implicates in Regulating the Homeostasis and Synaptic Development of Mitral Cells in the Olfactory Bulb.
Autorzy:
Cai C; Laboratory of Experimental Animal Disease Model, College of Veterinary Medicine, Sichuan Agricultural University, Chengdu 611130, China.
Luo Q; Laboratory of Experimental Animal Disease Model, College of Veterinary Medicine, Sichuan Agricultural University, Chengdu 611130, China.; Key Laboratory of Animal Disease and Human Health of Sichuan Province, College of Veterinary Medicine, Chengdu 611130, China.
Jia L; Laboratory of Experimental Animal Disease Model, College of Veterinary Medicine, Sichuan Agricultural University, Chengdu 611130, China.; Key Laboratory of Animal Disease and Human Health of Sichuan Province, College of Veterinary Medicine, Chengdu 611130, China.
Xia Y; Laboratory of Experimental Animal Disease Model, College of Veterinary Medicine, Sichuan Agricultural University, Chengdu 611130, China.
Lan X; Laboratory of Experimental Animal Disease Model, College of Veterinary Medicine, Sichuan Agricultural University, Chengdu 611130, China.
Wei X; Laboratory of Experimental Animal Disease Model, College of Veterinary Medicine, Sichuan Agricultural University, Chengdu 611130, China.
Shi S; Laboratory of Experimental Animal Disease Model, College of Veterinary Medicine, Sichuan Agricultural University, Chengdu 611130, China.
Liu Y; Laboratory of Experimental Animal Disease Model, College of Veterinary Medicine, Sichuan Agricultural University, Chengdu 611130, China.
Wang Y; Laboratory of Experimental Animal Disease Model, College of Veterinary Medicine, Sichuan Agricultural University, Chengdu 611130, China.
Xiong Z; Laboratory of Experimental Animal Disease Model, College of Veterinary Medicine, Sichuan Agricultural University, Chengdu 611130, China.
Shi R; Center for Paralysis Research, Department of Basic Medical Sciences, College of Veterinary Medicine, Purdue University, West Lafayette, IN 47907, USA.
Huang C; Laboratory of Experimental Animal Disease Model, College of Veterinary Medicine, Sichuan Agricultural University, Chengdu 611130, China.; Key Laboratory of Animal Disease and Human Health of Sichuan Province, College of Veterinary Medicine, Chengdu 611130, China.
Chen Z; Laboratory of Experimental Animal Disease Model, College of Veterinary Medicine, Sichuan Agricultural University, Chengdu 611130, China.; Key Laboratory of Animal Disease and Human Health of Sichuan Province, College of Veterinary Medicine, Chengdu 611130, China.
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Źródło:
International journal of molecular sciences [Int J Mol Sci] 2023 Aug 30; Vol. 24 (17). Date of Electronic Publication: 2023 Aug 30.
Typ publikacji:
Journal Article
MeSH Terms:
Olfactory Bulb*
Smell*
Animals ; Mice ; Homeostasis ; Gene Deletion ; Tripartite Motif Proteins ; Cytoskeletal Proteins
Czasopismo naukowe
Tytuł:
Recruited macrophages elicit atrial fibrillation.
Autorzy:
Hulsmans M; Center for Systems Biology, Massachusetts General Hospital and Harvard Medical School, Boston, MA, USA.; Department of Radiology, Massachusetts General Hospital and Harvard Medical School, Boston, MA, USA.
Schloss MJ; Center for Systems Biology, Massachusetts General Hospital and Harvard Medical School, Boston, MA, USA.; Department of Radiology, Massachusetts General Hospital and Harvard Medical School, Boston, MA, USA.
Lee IH; Center for Systems Biology, Massachusetts General Hospital and Harvard Medical School, Boston, MA, USA.; Department of Radiology, Massachusetts General Hospital and Harvard Medical School, Boston, MA, USA.
Bapat A; Cardiovascular Research Center, Massachusetts General Hospital and Harvard Medical School, Boston, MA, USA.
Iwamoto Y; Center for Systems Biology, Massachusetts General Hospital and Harvard Medical School, Boston, MA, USA.; Department of Radiology, Massachusetts General Hospital and Harvard Medical School, Boston, MA, USA.
Vinegoni C; Center for Systems Biology, Massachusetts General Hospital and Harvard Medical School, Boston, MA, USA.; Department of Radiology, Massachusetts General Hospital and Harvard Medical School, Boston, MA, USA.
Paccalet A; Center for Systems Biology, Massachusetts General Hospital and Harvard Medical School, Boston, MA, USA.; Department of Radiology, Massachusetts General Hospital and Harvard Medical School, Boston, MA, USA.
Yamazoe M; Center for Systems Biology, Massachusetts General Hospital and Harvard Medical School, Boston, MA, USA.; Department of Radiology, Massachusetts General Hospital and Harvard Medical School, Boston, MA, USA.
Grune J; Center for Systems Biology, Massachusetts General Hospital and Harvard Medical School, Boston, MA, USA.; Department of Radiology, Massachusetts General Hospital and Harvard Medical School, Boston, MA, USA.
Pabel S; Center for Systems Biology, Massachusetts General Hospital and Harvard Medical School, Boston, MA, USA.; Department of Radiology, Massachusetts General Hospital and Harvard Medical School, Boston, MA, USA.; Department of Internal Medicine II, University Medical Center Regensburg, Regensburg, Germany.
Momin N; Center for Systems Biology, Massachusetts General Hospital and Harvard Medical School, Boston, MA, USA.; Department of Radiology, Massachusetts General Hospital and Harvard Medical School, Boston, MA, USA.
Seung H; Center for Systems Biology, Massachusetts General Hospital and Harvard Medical School, Boston, MA, USA.; Department of Radiology, Massachusetts General Hospital and Harvard Medical School, Boston, MA, USA.
Kumowski N; Center for Systems Biology, Massachusetts General Hospital and Harvard Medical School, Boston, MA, USA.; Department of Radiology, Massachusetts General Hospital and Harvard Medical School, Boston, MA, USA.
Pulous FE; Center for Systems Biology, Massachusetts General Hospital and Harvard Medical School, Boston, MA, USA.; Department of Radiology, Massachusetts General Hospital and Harvard Medical School, Boston, MA, USA.
Keller D; Department of Thoracic and Cardiovascular Surgery, University Hospital Wuerzburg, Wuerzburg, Germany.
Bening C; Department of Thoracic and Cardiovascular Surgery, University Hospital Wuerzburg, Wuerzburg, Germany.
Green U; Department of Pathology, Center for Integrated Diagnostics, Massachusetts General Hospital and Harvard Medical School, Boston, MA, USA.
Lennerz JK; Department of Pathology, Center for Integrated Diagnostics, Massachusetts General Hospital and Harvard Medical School, Boston, MA, USA.
Mitchell RN; Department of Pathology, Brigham and Women's Hospital and Harvard Medical School, Boston, MA, USA.
Lewis A; Radcliffe Department of Medicine, NIHR Biomedical Research Centre, University of Oxford, Oxford, UK.; British Heart Foundation Centre of Research Excellence, University of Oxford, Oxford, UK.
Casadei B; Radcliffe Department of Medicine, NIHR Biomedical Research Centre, University of Oxford, Oxford, UK.; British Heart Foundation Centre of Research Excellence, University of Oxford, Oxford, UK.
Iborra-Egea O; Institut del Cor Germans Trias i Pujol, CIBERCV, Badalona, Barcelona, Spain.
Bayes-Genis A; Institut del Cor Germans Trias i Pujol, CIBERCV, Badalona, Barcelona, Spain.
Sossalla S; Department of Internal Medicine II, University Medical Center Regensburg, Regensburg, Germany.; Department of Cardiology and Angiology, University of Giessen/DZHK, Partner Site Rhein-Main, Germany.
Ong CS; Division of Cardiac Surgery, Massachusetts General Hospital and Harvard Medical School, Boston, MA, USA.; Department of Surgery, Yale School of Medicine, New Haven, CT, USA.
Pierson RN; Division of Cardiac Surgery, Massachusetts General Hospital and Harvard Medical School, Boston, MA, USA.
Aster JC; Department of Pathology, Brigham and Women's Hospital and Harvard Medical School, Boston, MA, USA.
Rohde D; Center for Systems Biology, Massachusetts General Hospital and Harvard Medical School, Boston, MA, USA.; Department of Radiology, Massachusetts General Hospital and Harvard Medical School, Boston, MA, USA.
Wojtkiewicz GR; Center for Systems Biology, Massachusetts General Hospital and Harvard Medical School, Boston, MA, USA.; Department of Radiology, Massachusetts General Hospital and Harvard Medical School, Boston, MA, USA.
Weissleder R; Center for Systems Biology, Massachusetts General Hospital and Harvard Medical School, Boston, MA, USA.; Department of Radiology, Massachusetts General Hospital and Harvard Medical School, Boston, MA, USA.
Swirski FK; Cardiovascular Research Institute, Icahn School of Medicine at Mount Sinai, New York, NY, USA.; Department of Medicine, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Tellides G; Department of Surgery, Yale School of Medicine, New Haven, CT, USA.
Tolis G Jr; Department of Cardiac Surgery, Brigham and Women's Hospital and Harvard Medical School, Boston, MA, USA.
Melnitchouk S; Division of Cardiac Surgery, Massachusetts General Hospital and Harvard Medical School, Boston, MA, USA.
Milan DJ; Leducq Foundation, Boston, MA, USA.
Ellinor PT; Cardiovascular Research Center, Massachusetts General Hospital and Harvard Medical School, Boston, MA, USA.; Cardiovascular Disease Initiative, The Broad Institute of MIT and Harvard University, Cambridge, MA, USA.
Naxerova K; Center for Systems Biology, Massachusetts General Hospital and Harvard Medical School, Boston, MA, USA.; Department of Radiology, Massachusetts General Hospital and Harvard Medical School, Boston, MA, USA.
Nahrendorf M; Center for Systems Biology, Massachusetts General Hospital and Harvard Medical School, Boston, MA, USA.; Department of Radiology, Massachusetts General Hospital and Harvard Medical School, Boston, MA, USA.; Cardiovascular Research Center, Massachusetts General Hospital and Harvard Medical School, Boston, MA, USA.; Department of Internal Medicine I, University Hospital Wuerzburg, Wuerzburg, Germany.
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Źródło:
Science (New York, N.Y.) [Science] 2023 Jul 14; Vol. 381 (6654), pp. 231-239. Date of Electronic Publication: 2023 Jul 13.
Typ publikacji:
Journal Article
MeSH Terms:
Atrial Fibrillation*/genetics
Atrial Fibrillation*/immunology
Macrophages*/immunology
Osteopontin*/genetics
Animals ; Humans ; Mice ; Heart Atria ; Mitral Valve Insufficiency/genetics ; Gene Deletion ; Cell Movement ; Single-Cell Gene Expression Analysis
Czasopismo naukowe
Tytuł:
High prevalence of CFHR deletions in Indian women with pregnancy-associated hemolytic uremic syndrome.
Autorzy:
Kandari S; Renal Unit, KEM Hospital, Pune, India.
Chakurkar V; Renal Unit, KEM Hospital, Pune, India.
Gaikwad S; Renal Unit, KEM Hospital, Pune, India.
Agarwal M; GenePath Laboratories, Pune, India.
Phadke N; GenePath Laboratories, Pune, India.
Lobo V; Renal Unit, KEM Hospital, Pune, India.
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Źródło:
Nephrology (Carlton, Vic.) [Nephrology (Carlton)] 2022 Mar; Vol. 27 (3), pp. 231-237. Date of Electronic Publication: 2021 Dec 07.
Typ publikacji:
Journal Article; Observational Study
MeSH Terms:
Gene Deletion*
Blood Proteins/*genetics
Complement C3b Inactivator Proteins/*genetics
Hemolytic-Uremic Syndrome/*genetics
Pregnancy Complications/*genetics
Adult ; Female ; Humans ; India ; Pregnancy ; Prospective Studies ; Young Adult
Czasopismo naukowe
Tytuł:
Approaches for Detection of Hepatitis B Virus Pre-S Gene Deletions and Pre-S Deleted Proteins and Their Application in Prediction of Higher Risk of Hepatocellular Carcinoma Development and Recurrence.
Autorzy:
Lin YT; Cancer Genome Research Center, Chang Gung Memorial Hospital, Taoyuan 333, Taiwan.
Jeng LB; Organ Transplantation Center, China Medical University Hospital, Taichung 404, Taiwan.
Su IJ; Department of Biotechnology, Southern Taiwan University of Science and Technology, Tainan 710, Taiwan.
Teng CF; Organ Transplantation Center, China Medical University Hospital, Taichung 404, Taiwan.; Graduate Institute of Biomedical Sciences, China Medical University, Taichung 404, Taiwan.; Research Center for Cancer Biology, China Medical University, Taichung 404, Taiwan.
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Źródło:
Viruses [Viruses] 2022 Feb 18; Vol. 14 (2). Date of Electronic Publication: 2022 Feb 18.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't; Review
MeSH Terms:
Gene Deletion*
Hepatitis B Surface Antigens/*genetics
Hepatitis B virus/*genetics
Hepatitis B, Chronic/*virology
Animals ; Base Sequence ; Biomarkers ; Carcinoma, Hepatocellular/etiology ; Carcinoma, Hepatocellular/pathology ; Disease Models, Animal ; Gene Expression Regulation, Viral ; Hepatitis B virus/physiology ; Hepatitis B, Chronic/complications ; High-Throughput Nucleotide Sequencing ; Humans ; Immunohistochemistry ; Liver Neoplasms/etiology ; Liver Neoplasms/pathology ; Neoplasm Recurrence, Local/etiology ; Neoplasm Recurrence, Local/pathology ; Prognosis ; Signal Transduction ; Virus Replication
Czasopismo naukowe

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