Informacja

Drogi użytkowniku, aplikacja do prawidłowego działania wymaga obsługi JavaScript. Proszę włącz obsługę JavaScript w Twojej przeglądarce.

English (EN)·Polski (PL)·Ukraiński (UK)
Przejdź do strony domowej biblioteki Uniwersytet Ekonomiczny we Wrocławiu Link otwiera się w nowym oknie Logo biblioteki Prolib Integro - strona głównaUniwersytet Ekonomiczny we Wrocławiu

Wyszukujesz frazę ""Genetic Predisposition to Disease"" wg kryterium: Temat

  Lista filtrów
Wyrównaj
Wyświetlanie 1-20 z 32150
Tytuł:
Integrative multi-omics analysis identifies genetically supported druggable targets and immune cell specificity for myasthenia gravis.
Autorzy:
Li J; Department of Neurology, Xuanwu Hospital, National Center for Neurological Disorders, Capital Medical University, Beijing, 100053, China.; Beijing Municipal Geriatric Medical Research Center, Beijing, China.; Key Laboratory for Neurodegenerative Diseases of Ministry of Education, Beijing, China.
Wang F; Department of Neurology, Xuanwu Hospital, National Center for Neurological Disorders, Capital Medical University, Beijing, 100053, China.; Key Laboratory for Neurodegenerative Diseases of Ministry of Education, Beijing, China.
Li Z; Department of Neurology, Xuanwu Hospital, National Center for Neurological Disorders, Capital Medical University, Beijing, 100053, China.
Feng J; Department of Neurology, Xuanwu Hospital, National Center for Neurological Disorders, Capital Medical University, Beijing, 100053, China.
Men Y; Department of Neurology, Xuanwu Hospital, National Center for Neurological Disorders, Capital Medical University, Beijing, 100053, China.
Han J; Department of Neurology, Xuanwu Hospital, National Center for Neurological Disorders, Capital Medical University, Beijing, 100053, China.
Xia J; Department of Neurology, Xuanwu Hospital, National Center for Neurological Disorders, Capital Medical University, Beijing, 100053, China.
Zhang C; Department of Neurology, Xuanwu Hospital, National Center for Neurological Disorders, Capital Medical University, Beijing, 100053, China.
Han Y; Department of Neurology, Xuanwu Hospital, National Center for Neurological Disorders, Capital Medical University, Beijing, 100053, China.
Chen T; Department of Neurology, Xuanwu Hospital, National Center for Neurological Disorders, Capital Medical University, Beijing, 100053, China.
Zhao Y; Department of Neurology, Xuanwu Hospital, National Center for Neurological Disorders, Capital Medical University, Beijing, 100053, China.
Zhou S; Department of Human Genetics, McGill University, Montréal, QC, Canada.
Da Y; Department of Neurology, Xuanwu Hospital, National Center for Neurological Disorders, Capital Medical University, Beijing, 100053, China.
Chai G; Department of Neurology, Xuanwu Hospital, National Center for Neurological Disorders, Capital Medical University, Beijing, 100053, China. .; Beijing Municipal Geriatric Medical Research Center, Beijing, China. .
Hao J; Department of Neurology, Xuanwu Hospital, National Center for Neurological Disorders, Capital Medical University, Beijing, 100053, China. .; Beijing Municipal Geriatric Medical Research Center, Beijing, China. .; Key Laboratory for Neurodegenerative Diseases of Ministry of Education, Beijing, China. .
Pokaż więcej
Źródło:
Journal of translational medicine [J Transl Med] 2024 Mar 24; Vol. 22 (1), pp. 302. Date of Electronic Publication: 2024 Mar 24.
Typ publikacji:
Journal Article
MeSH Terms:
Genetic Predisposition to Disease*
Myasthenia Gravis*/genetics
Humans ; Multiomics ; Genome-Wide Association Study ; Quantitative Trait Loci/genetics ; Polymorphism, Single Nucleotide/genetics
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
OPRM1 Gene Polymorphism in Women with Alcohol Use Disorder.
Autorzy:
Boroń A; Department of Clinical and Molecular Biochemistry, Pomeranian Medical University in Szczecin, Powstańców Wielkopolskich 72 St., 70-111 Szczecin, Poland.
Suchanecka A; Independent Laboratory of Health Promotion, Pomeranian Medical University in Szczecin, Powstańców Wielkopolskich 72 St., 70-111 Szczecin, Poland.
Chmielowiec K; Department of Hygiene and Epidemiology, Collegium Medicum, University of Zielona Góra, 28 Zyty St., 65-045 Zielona Góra, Poland.
Śmiarowska M; Individual Specialized Medical Practice, Swarożyca 3/6 St., 71-601 Szczecin, Poland.
Chmielowiec J; Department of Hygiene and Epidemiology, Collegium Medicum, University of Zielona Góra, 28 Zyty St., 65-045 Zielona Góra, Poland.
Strońska-Pluta A; Independent Laboratory of Health Promotion, Pomeranian Medical University in Szczecin, Powstańców Wielkopolskich 72 St., 70-111 Szczecin, Poland.
Recław R; Foundation Strong in the Spirit, 60 Sienkiewicza St., 90-058 Łódź, Poland.
Grzywacz A; Independent Laboratory of Health Promotion, Pomeranian Medical University in Szczecin, Powstańców Wielkopolskich 72 St., 70-111 Szczecin, Poland.
Pokaż więcej
Źródło:
International journal of molecular sciences [Int J Mol Sci] 2024 Mar 06; Vol. 25 (5). Date of Electronic Publication: 2024 Mar 06.
Typ publikacji:
Journal Article
MeSH Terms:
Alcoholism*/genetics
Alcoholism*/psychology
Genetic Predisposition to Disease*
Receptors, Opioid, mu*/genetics
Personality*
Female ; Humans ; Ethanol ; Genotype ; Polymorphism, Single Nucleotide
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
An immunogenetic basis for lung cancer risk.
Autorzy:
Krishna C; Broad Institute of MIT and Harvard, Cambridge, MA 02142, USA.
Tervi A; Institute for Molecular Medicine, Finland (FIMM), HiLIFE, University of Helsinki, Helsinki 00290, Finland.
Saffern M; The Marc and Jennifer Lipschultz Precision Immunology Institute, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.; Department of Immunology and Immunotherapy, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Wilson EA; The Marc and Jennifer Lipschultz Precision Immunology Institute, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.; Department of Immunology and Immunotherapy, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.; Icahn Genomics Institute, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Yoo SK; The Marc and Jennifer Lipschultz Precision Immunology Institute, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.; Department of Immunology and Immunotherapy, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.; Icahn Genomics Institute, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Mars N; Institute for Molecular Medicine, Finland (FIMM), HiLIFE, University of Helsinki, Helsinki 00290, Finland.
Roudko V; The Marc and Jennifer Lipschultz Precision Immunology Institute, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.; Department of Immunology and Immunotherapy, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Cho BA; The Marc and Jennifer Lipschultz Precision Immunology Institute, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.; Department of Immunology and Immunotherapy, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.; Icahn Genomics Institute, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Jones SE; Institute for Molecular Medicine, Finland (FIMM), HiLIFE, University of Helsinki, Helsinki 00290, Finland.
Vaninov N; The Marc and Jennifer Lipschultz Precision Immunology Institute, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.; Department of Immunology and Immunotherapy, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Selvan ME; Department of Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Gümüş ZH; Department of Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.; Center for Thoracic Oncology, Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Lenz TL; Research Unit for Evolutionary Immunogenomics, Department of Biology, Universität Hamburg, 20146 Hamburg, Germany.
Merad M; The Marc and Jennifer Lipschultz Precision Immunology Institute, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.; Department of Immunology and Immunotherapy, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.; Department of Oncological Sciences, Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.; Division of Hematology and Medical Oncology, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.; Human Immune Monitoring Center, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Boffetta P; Department of Medical and Surgical Sciences, Alma Mater Studiorum University of Bologna, 40138 Bologna, Italy.; Stony Brook Cancer Center, Stony Brook University, New York, NY 11794, USA.
Martínez-Jiménez F; Vall d'Hebron Institute of Oncology, Barcelona 08035, Spain.; Hartwig Medical Foundation, Amsterdam 1098 XH, the Netherlands.
Ollila HM; Broad Institute of MIT and Harvard, Cambridge, MA 02142, USA.; Institute for Molecular Medicine, Finland (FIMM), HiLIFE, University of Helsinki, Helsinki 00290, Finland.; Center for Genomic Medicine, Massachusetts General Hospital and Harvard Medical School, Boston, MA 02114, USA.; Department of Anesthesia, Critical Care and Pain Medicine, Massachusetts General Hospital, Boston, MA 02114, USA.
Samstein RM; The Marc and Jennifer Lipschultz Precision Immunology Institute, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.; Department of Immunology and Immunotherapy, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.; Center for Thoracic Oncology, Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.; Department of Radiation Oncology, Mount Sinai Hospital, New York, NY 10029, USA.
Chowell D; The Marc and Jennifer Lipschultz Precision Immunology Institute, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.; Department of Immunology and Immunotherapy, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.; Icahn Genomics Institute, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.; Department of Oncological Sciences, Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Pokaż więcej
Corporate Authors:
FinnGen§
Źródło:
Science (New York, N.Y.) [Science] 2024 Feb 23; Vol. 383 (6685), pp. eadi3808. Date of Electronic Publication: 2024 Feb 23.
Typ publikacji:
Journal Article
MeSH Terms:
Histocompatibility Antigens Class II*/genetics
Lung Neoplasms*/genetics
Lung Neoplasms*/immunology
Loss of Heterozygosity*
Immunologic Surveillance*/genetics
Genetic Predisposition to Disease*
Humans ; Macrophages, Alveolar/immunology ; Risk Factors ; Smoking/immunology ; Middle Aged ; Aged ; Aged, 80 and over ; Chromosome Mapping ; Polymorphism, Single Nucleotide
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Recent advances in polygenic scores: translation, equitability, methods and FAIR tools.
Autorzy:
Xiang R; Cambridge Baker Systems Genomics Initiative, Baker Heart and Diabetes Institute, Melbourne, VIC, Australia.; Cambridge Baker Systems Genomics Initiative, Department of Public Health and Primary Care, University of Cambridge, Cambridge, UK.
Kelemen M; Cambridge Baker Systems Genomics Initiative, Department of Public Health and Primary Care, University of Cambridge, Cambridge, UK.; British Heart Foundation Cardiovascular Epidemiology Unit, Department of Public Health and Primary Care, University of Cambridge, Cambridge, UK.; Victor Phillip Dahdaleh Heart and Lung Research Institute, University of Cambridge, Cambridge, UK.
Xu Y; Cambridge Baker Systems Genomics Initiative, Department of Public Health and Primary Care, University of Cambridge, Cambridge, UK.; British Heart Foundation Cardiovascular Epidemiology Unit, Department of Public Health and Primary Care, University of Cambridge, Cambridge, UK.; Victor Phillip Dahdaleh Heart and Lung Research Institute, University of Cambridge, Cambridge, UK.; Health Data Research UK Cambridge, Wellcome Genome Campus and University of Cambridge, Cambridge, UK.
Harris LW; European Molecular Biology Laboratory, European Bioinformatics Institute, Wellcome Genome Campus, Hinxton, Cambridge, UK.
Parkinson H; European Molecular Biology Laboratory, European Bioinformatics Institute, Wellcome Genome Campus, Hinxton, Cambridge, UK.
Inouye M; Cambridge Baker Systems Genomics Initiative, Baker Heart and Diabetes Institute, Melbourne, VIC, Australia. .; Cambridge Baker Systems Genomics Initiative, Department of Public Health and Primary Care, University of Cambridge, Cambridge, UK. .; British Heart Foundation Cardiovascular Epidemiology Unit, Department of Public Health and Primary Care, University of Cambridge, Cambridge, UK. .; Victor Phillip Dahdaleh Heart and Lung Research Institute, University of Cambridge, Cambridge, UK. .; Health Data Research UK Cambridge, Wellcome Genome Campus and University of Cambridge, Cambridge, UK. .; British Heart Foundation Centre of Research Excellence, University of Cambridge, Cambridge, UK. .
Lambert SA; Cambridge Baker Systems Genomics Initiative, Department of Public Health and Primary Care, University of Cambridge, Cambridge, UK.; British Heart Foundation Cardiovascular Epidemiology Unit, Department of Public Health and Primary Care, University of Cambridge, Cambridge, UK.; Victor Phillip Dahdaleh Heart and Lung Research Institute, University of Cambridge, Cambridge, UK.; Health Data Research UK Cambridge, Wellcome Genome Campus and University of Cambridge, Cambridge, UK.; European Molecular Biology Laboratory, European Bioinformatics Institute, Wellcome Genome Campus, Hinxton, Cambridge, UK.
Pokaż więcej
Źródło:
Genome medicine [Genome Med] 2024 Feb 19; Vol. 16 (1), pp. 33. Date of Electronic Publication: 2024 Feb 19.
Typ publikacji:
Journal Article; Review
MeSH Terms:
Communication*
Genetic Predisposition to Disease*
Humans ; Genomics ; Multifactorial Inheritance ; Risk Factors ; Genome-Wide Association Study
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
The frequency of pathogenic variation in the All of Us cohort reveals ancestry-driven disparities.
Autorzy:
Venner E; Human Genome Sequencing Center, Baylor College of Medicine, Houston, TX, USA. .
Patterson K; Department of Genome Sciences, University of Washington, Seattle, WA, USA.
Kalra D; Human Genome Sequencing Center, Baylor College of Medicine, Houston, TX, USA.
Wheeler MM; Department of Genome Sciences, University of Washington, Seattle, WA, USA.
Chen YJ; Human Genome Sequencing Center, Baylor College of Medicine, Houston, TX, USA.
Kalla SE; Human Genome Sequencing Center, Baylor College of Medicine, Houston, TX, USA.
Yuan B; Human Genome Sequencing Center, Baylor College of Medicine, Houston, TX, USA.
Karnes JH; University of Arizona, R Ken Coit College of Pharmacy, Department of Pharmacy Practice and Science, Tucson, AZ, USA.; Vanderbilt University Medical Center, Department of Biomedical Informatics, Boston, MA, USA.
Walker K; Human Genome Sequencing Center, Baylor College of Medicine, Houston, TX, USA.
Smith JD; Department of Genome Sciences, University of Washington, Seattle, WA, USA.
McGee S; Department of Genome Sciences, University of Washington, Seattle, WA, USA.
Radhakrishnan A; Department of Genome Sciences, University of Washington, Seattle, WA, USA.
Haddad A; Department of Pharmaceutical Sciences, University of Pittsburgh School of Pharmacy, Pittsburgh, PA, USA.
Empey PE; Department of Pharmacy and Therapeutics, University of Pittsburgh School of Pharmacy, Pittsburgh, PA, USA.
Wang Q; Human Genome Sequencing Center, Baylor College of Medicine, Houston, TX, USA.
Lichtenstein L; Broad Institute of MIT and Harvard, Cambridge, MA, USA.
Toledo D; Broad Institute of MIT and Harvard, Cambridge, MA, USA.
Jarvik G; Department of Medicine (Medical Genetics), University of Washington School of Medicine, Seattle, WA, USA.; Department of Genome Sciences, University of Washington School of Medicine, Seattle, WA, USA.
Musick A; NIH All of Us Research Program, National Institutes of Health Office of the Director, Bethesda, MD, USA.
Gibbs RA; Human Genome Sequencing Center, Baylor College of Medicine, Houston, TX, USA.
Pokaż więcej
Corporate Authors:
All of Us Research Program Investigators
Źródło:
Communications biology [Commun Biol] 2024 Feb 19; Vol. 7 (1), pp. 174. Date of Electronic Publication: 2024 Feb 19.
Typ publikacji:
Journal Article
MeSH Terms:
Genetic Predisposition to Disease*
Population Health*
Humans ; Black People ; Genomics ; Hispanic or Latino/genetics ; United States/epidemiology ; European People ; African People
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Incorporating functional annotation with bilevel continuous shrinkage for polygenic risk prediction.
Autorzy:
Zhuang Y; University of Michigan, Ann Arbor, USA.
Kim NY; Seoul National University, Seoul, Republic of Korea.
Fritsche LG; University of Michigan, Ann Arbor, USA.
Mukherjee B; University of Michigan, Ann Arbor, USA. .
Lee S; Seoul National University, Seoul, Republic of Korea. .
Pokaż więcej
Źródło:
BMC bioinformatics [BMC Bioinformatics] 2024 Feb 09; Vol. 25 (1), pp. 65. Date of Electronic Publication: 2024 Feb 09.
Typ publikacji:
Journal Article
MeSH Terms:
Genetic Predisposition to Disease*
Genome-Wide Association Study*/methods
Humans ; Bayes Theorem ; Multifactorial Inheritance ; Software ; Risk Factors
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Associations of genetic variants within TYK2 with pulmonary tuberculosis among Chinese population.
Autorzy:
Zhang M; Tuberculosis Control and Prevention, Zhejiang Provincial Center for Disease Control and Prevention, Hangzhou City, China.
Liu Z; Tuberculosis Control and Prevention, Zhejiang Provincial Center for Disease Control and Prevention, Hangzhou City, China.
Zhu Y; Tuberculosis Control and Prevention, Zhejiang Provincial Center for Disease Control and Prevention, Hangzhou City, China.
Wu K; Tuberculosis Control and Prevention, Zhejiang Provincial Center for Disease Control and Prevention, Hangzhou City, China.
Zhou L; Tuberculosis Control and Prevention, Zhejiang Provincial Center for Disease Control and Prevention, Hangzhou City, China.
Peng Y; Tuberculosis Control and Prevention, Zhejiang Provincial Center for Disease Control and Prevention, Hangzhou City, China.
Pan J; Tuberculosis Control and Prevention, Zhejiang Provincial Center for Disease Control and Prevention, Hangzhou City, China.
Chen B; Tuberculosis Control and Prevention, Zhejiang Provincial Center for Disease Control and Prevention, Hangzhou City, China.
Wang X; Tuberculosis Control and Prevention, Zhejiang Provincial Center for Disease Control and Prevention, Hangzhou City, China.
Chen S; Tuberculosis Control and Prevention, Zhejiang Provincial Center for Disease Control and Prevention, Hangzhou City, China.
Pokaż więcej
Źródło:
Molecular genetics & genomic medicine [Mol Genet Genomic Med] 2024 Feb; Vol. 12 (2), pp. e2386.
Typ publikacji:
Journal Article
MeSH Terms:
Genetic Predisposition to Disease*
Tuberculosis, Pulmonary*/epidemiology
Tuberculosis, Pulmonary*/genetics
Humans ; Male ; Middle Aged ; Case-Control Studies ; Genotype ; TYK2 Kinase/genetics ; China/epidemiology
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Prevalence, associated factors, and gene polymorphisms of obesity in Tibetan adults in Qinghai, China.
Autorzy:
Wang Y; School of Population Medicine and Public Health, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
Pan L; Department of Epidemiology and Statistics, Institute of Basic Medical Sciences, School of Basic Medicine, Chinese Academy of Medical Sciences, Peking Union Medical College, 5 Dong Dan San Tiao, Dong Cheng District, Beijing, 100005, China.
He H; Department of Epidemiology and Statistics, Institute of Basic Medical Sciences, School of Basic Medicine, Chinese Academy of Medical Sciences, Peking Union Medical College, 5 Dong Dan San Tiao, Dong Cheng District, Beijing, 100005, China.
Li Z; Qinghai University Affiliated Hospital, Qinghai, China.
Cui S; Qinghai University Affiliated Hospital, Qinghai, China.
Yang A; Qinghai University Affiliated Hospital, Qinghai, China.
Li W; Qinghai University Affiliated Hospital, Qinghai, China.
Jia G; Qinghai University Affiliated Hospital, Qinghai, China.
Han X; Qinghai University Affiliated Hospital, Qinghai, China.
Wang X; Institute of Biomedical Engineering, Chinese Academy of Medical Sciences, Peking Union Medical College, 236 Baidi Road, Nankai District, Tianjin, 300192, China. .
Shan G; School of Population Medicine and Public Health, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China. guangliang_.; Department of Epidemiology and Statistics, Institute of Basic Medical Sciences, School of Basic Medicine, Chinese Academy of Medical Sciences, Peking Union Medical College, 5 Dong Dan San Tiao, Dong Cheng District, Beijing, 100005, China. guangliang_.
Pokaż więcej
Źródło:
BMC public health [BMC Public Health] 2024 Jan 26; Vol. 24 (1), pp. 305. Date of Electronic Publication: 2024 Jan 26.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Overweight*/epidemiology
Overweight*/genetics
Genetic Predisposition to Disease*
Adult ; Male ; Humans ; Prevalence ; Cross-Sectional Studies ; Tibet/epidemiology ; Body Mass Index ; Polymorphism, Single Nucleotide ; Obesity/epidemiology ; Obesity/genetics ; Alpha-Ketoglutarate-Dependent Dioxygenase FTO/genetics
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
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.
Pokaż więcej
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
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
HLA Polymorphisms and Clinical Manifestations in IgA Vasculitis.
Autorzy:
Held M; Department of Pediatrics, University Hospital Centre Zagreb, University of Zagreb School of Medicine, 10000 Zagreb, Croatia.
Stingl Jankovic K; Tissue Typing Centre, Clinical Department for Transfusion Medicine and Transplantation Biology, University Hospital Centre Zagreb, 10000 Zagreb, Croatia.
Sestan M; Department of Pediatrics, University Hospital Centre Zagreb, University of Zagreb School of Medicine, 10000 Zagreb, Croatia.
Sapina M; Department of Pediatrics, University Hospital Centre Osijek, Josip Juraj Strossmayer University of Osijek, Medical Faculty Osijek, 31000 Osijek, Croatia.
Kifer N; Department of Pediatrics, University Hospital Centre Zagreb, University of Zagreb School of Medicine, 10000 Zagreb, Croatia.
Srsen S; Department of Pediatrics, University of Split School of Medicine, University Hospital Centre Split, 21000 Split, Croatia.
Frkovic M; Department of Pediatrics, University Hospital Centre Zagreb, University of Zagreb School of Medicine, 10000 Zagreb, Croatia.
Gagro A; Children's Hospital Zagreb, Medical Faculty Osijek, Josip Juraj Strossmayer University of Osijek, 10000 Zagreb, Croatia.
Grubic Z; Tissue Typing Centre, Clinical Department for Transfusion Medicine and Transplantation Biology, University Hospital Centre Zagreb, 10000 Zagreb, Croatia.
Jelusic M; Department of Pediatrics, University Hospital Centre Zagreb, University of Zagreb School of Medicine, 10000 Zagreb, Croatia.
Pokaż więcej
Źródło:
International journal of molecular sciences [Int J Mol Sci] 2024 Jan 10; Vol. 25 (2). Date of Electronic Publication: 2024 Jan 10.
Typ publikacji:
Journal Article
MeSH Terms:
HLA Antigens*/genetics
IgA Vasculitis*/genetics
Genetic Predisposition to Disease*
Child ; Humans ; HLA-A Antigens ; HLA-B Antigens ; HLA-DRB1 Chains/genetics
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Associations of MMP9 polymorphism with the risk of severe pneumonia in a Southern Chinese children population.
Autorzy:
Cai L; Department of Hospital Infection Control, The Second Affiliated Hospital of Guangzhou University of Chinese Medicine, Guangzhou, Guangdong, 510120, China.
Zuo X; Department of Pediatric Surgery, Guangzhou Institute of Pediatrics, Guangzhou Women and Children's Medical Center, Guangzhou Medical University, Guangzhou, Guangdong, 510623, China.
Ma L; Department of Pediatric Surgery, Guangzhou Institute of Pediatrics, Guangzhou Women and Children's Medical Center, Guangzhou Medical University, Guangzhou, Guangdong, 510623, China.
Zhang Y; Department of Pediatric Surgery, Guangzhou Institute of Pediatrics, Guangzhou Women and Children's Medical Center, Guangzhou Medical University, Guangzhou, Guangdong, 510623, China.
Xu F; Department of Pediatrics, The Third Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan Province, 450052, China. .
Lu B; Department of Pediatric Surgery, Guangzhou Institute of Pediatrics, Guangzhou Women and Children's Medical Center, Guangzhou Medical University, Guangzhou, Guangdong, 510623, China. .; Medical Research Institute, Guangdong Provincial People's Hospital (Guangdong Academy of Medical Sciences), Southern Medical University Guangzhou, Guangzhou, Guangdong, 510080, China. .
Pokaż więcej
Źródło:
BMC infectious diseases [BMC Infect Dis] 2024 Jan 02; Vol. 24 (1), pp. 19. Date of Electronic Publication: 2024 Jan 02.
Typ publikacji:
Journal Article
MeSH Terms:
Genetic Predisposition to Disease*
Matrix Metalloproteinase 9*/genetics
Matrix Metalloproteinase 9*/metabolism
Pneumonia*/diagnosis
Pneumonia*/epidemiology
Pneumonia*/genetics
Child ; Humans ; Case-Control Studies ; China ; Genotype ; Polymorphism, Single Nucleotide
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Association of KDR (rs2071559, rs1870377), CFH (rs1061170, rs1410996) genes variants and serum levels with pituitary adenoma.
Autorzy:
Bruzaite A; Ophthalmology Laboratory, Neuroscience Institute, Lithuanian University of Health Sciences, Medical Academy, Kaunas, Lithuania.
Gedvilaite G; Ophthalmology Laboratory, Neuroscience Institute, Lithuanian University of Health Sciences, Medical Academy, Kaunas, Lithuania.
Kriauciuniene L; Ophthalmology Laboratory, Neuroscience Institute, Lithuanian University of Health Sciences, Medical Academy, Kaunas, Lithuania.
Liutkeviciene R; Ophthalmology Laboratory, Neuroscience Institute, Lithuanian University of Health Sciences, Medical Academy, Kaunas, Lithuania.
Pokaż więcej
Źródło:
Molecular genetics & genomic medicine [Mol Genet Genomic Med] 2024 Jan; Vol. 12 (1), pp. e2289. Date of Electronic Publication: 2023 Oct 06.
Typ publikacji:
Journal Article
MeSH Terms:
Genetic Predisposition to Disease*
Pituitary Neoplasms*
Humans ; DNA ; Genotype ; Polymorphism, Single Nucleotide ; Vascular Endothelial Growth Factor Receptor-2/genetics
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Association analysis of MTHFR (rs1801133 and rs1801131) and MTRR (rs1801394) gene polymorphisms towards the development of hypertension in the Bai population from Yunnan, China.
Autorzy:
Liu Y; School of Basic Medicine, Dali University, Dali, Yunnan, China.
Xu C; School of Basic Medicine, Dali University, Dali, Yunnan, China.
Wang Y; School of Basic Medicine, Dali University, Dali, Yunnan, China.
Yang C; School of Basic Medicine, Dali University, Dali, Yunnan, China.
Pu G; School of Basic Medicine, Dali University, Dali, Yunnan, China.
Zhang L; School of Basic Medicine, Dali University, Dali, Yunnan, China.
Wang Z; School of Basic Medicine, Dali University, Dali, Yunnan, China.
Tao P; School of Basic Medicine, Dali University, Dali, Yunnan, China.
Hu S; Laboratory Department, The First Affiliated Hospital of Dali University, Dali, Yunnan, China.
Lai M; School of Basic Medicine, Dali University, Dali, Yunnan, China.
Pokaż więcej
Źródło:
Clinical and experimental hypertension (New York, N.Y. : 1993) [Clin Exp Hypertens] 2023 Dec 31; Vol. 45 (1), pp. 2206066.
Typ publikacji:
Journal Article
MeSH Terms:
Genetic Predisposition to Disease*
Hypertension*/genetics
Humans ; Case-Control Studies ; China/epidemiology ; Folic Acid/metabolism ; Genotype ; Methylenetetrahydrofolate Reductase (NADPH2)/genetics ; Polymorphism, Genetic ; Polymorphism, Single Nucleotide
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknieSzczegóły
Tytuł:
Systematic analysis of Mendelian disease-associated gene variants reveals new classes of cancer-predisposing genes.
Autorzy:
Song S; Cancer Research Institute, Seoul National University College of Medicine, Seoul, 03080, Republic of Korea.; Structural Biology Program, Centro Nacional de Investigaciones Oncológicas (CNIO), Calle de Melchor Fernández Almagro, 3, Madrid, 28029, Spain.
Koh Y; Cancer Research Institute, Seoul National University College of Medicine, Seoul, 03080, Republic of Korea.; Biomedical Research Institute and Departments of Internal Medicine, Seoul National University Hospital, Seoul, 03080, Republic of Korea.
Kim S; Cancer Research Institute, Seoul National University College of Medicine, Seoul, 03080, Republic of Korea.
Lee SM; Department of Chemical and Biomolecular Engineering, Korea Advanced Institute of Science and Technology (KAIST), Daejeon, 34141, Republic of Korea.
Kim HU; Department of Chemical and Biomolecular Engineering, Korea Advanced Institute of Science and Technology (KAIST), Daejeon, 34141, Republic of Korea. .
Ko JM; Department of Pediatrics, Seoul National University Children's Hospital, Seoul National University College of Medicine, Seoul, 03080, Republic of Korea. .
Lee SH; Division of Hematology-Oncology, Department of Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, 06351, Republic of Korea. .
Yoon SS; Cancer Research Institute, Seoul National University College of Medicine, Seoul, 03080, Republic of Korea. .; Biomedical Research Institute and Departments of Internal Medicine, Seoul National University Hospital, Seoul, 03080, Republic of Korea. .
Park S; Structural Biology Program, Centro Nacional de Investigaciones Oncológicas (CNIO), Calle de Melchor Fernández Almagro, 3, Madrid, 28029, Spain. .
Pokaż więcej
Źródło:
Genome medicine [Genome Med] 2023 Dec 25; Vol. 15 (1), pp. 107. Date of Electronic Publication: 2023 Dec 25.
Typ publikacji:
Journal Article
MeSH Terms:
Genetic Predisposition to Disease*
Neoplasms*/genetics
Humans ; Phenotype ; Risk
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
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. .
Pokaż więcej
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
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
[The rs7139228 polymorphism is located in the DCN gene and not in the RETN gene].
Autorzy:
Flores SV; Facultad de Ciencias de la Salud. Universidad Autónoma de Chile. Chile. Departamento de Ingeniería Industrial. Facultad de Ingeniería y Tecnología. Universidad San Sebastián.
Roco-Videla Á; Facultad de Medicina. Universidad Católica de la Santísima Concepción.
Olguín-Barraza M; Facultad de Ciencias de Salud. Programa de Magister en Ciencias Químico-Biológicas. Universidad Bernardo O'Higgins.
Maureira-Carsalade N; Departamento de Ingeniería Civil. Facultad de Ingeniería. Universidad Católica de la Santísima Concepción.
Pokaż więcej
Transliterated Title:
El polimorfismo rs7139228 se localiza en el gen DCN y no en el RETN.
Źródło:
Nutricion hospitalaria [Nutr Hosp] 2023 Dec 14; Vol. 40 (6), pp. 1305.
Typ publikacji:
English Abstract; Journal Article
MeSH Terms:
Decorin*/genetics
Genetic Predisposition to Disease*
Polymorphism, Single Nucleotide*
Humans ; Alleles ; Genotype ; Resistin/genetics
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknieSzczegóły
Tytuł:
Polymorphisms in the glucagon-like peptide-1 receptor gene and their interactions on the risk of osteoporosis in postmenopausal Chinese women.
Autorzy:
Liu C; Department of Endocrinology, Hebei Medical University Third Hospital, Shijiazhuang, China.; Key Orthopaedic Biomechanics Laboratory of Hebei Province, Orthopedic Research Institution of Hebei Province, Shijiazhuang, China.
Bao X; Department of Endocrinology, Hebei Medical University Third Hospital, Shijiazhuang, China.; Key Orthopaedic Biomechanics Laboratory of Hebei Province, Orthopedic Research Institution of Hebei Province, Shijiazhuang, China.
Tian Y; Department of Endocrinology, Hebei Medical University Third Hospital, Shijiazhuang, China.; Key Orthopaedic Biomechanics Laboratory of Hebei Province, Orthopedic Research Institution of Hebei Province, Shijiazhuang, China.
Xue P; Department of Endocrinology, Hebei Medical University Third Hospital, Shijiazhuang, China.; Key Orthopaedic Biomechanics Laboratory of Hebei Province, Orthopedic Research Institution of Hebei Province, Shijiazhuang, China.
Wang Y; Department of Endocrinology, Hebei Medical University Third Hospital, Shijiazhuang, China.; Key Orthopaedic Biomechanics Laboratory of Hebei Province, Orthopedic Research Institution of Hebei Province, Shijiazhuang, China.
Li Y; Department of Endocrinology, Hebei Medical University Third Hospital, Shijiazhuang, China.; Key Orthopaedic Biomechanics Laboratory of Hebei Province, Orthopedic Research Institution of Hebei Province, Shijiazhuang, China.
Pokaż więcej
Źródło:
PloS one [PLoS One] 2023 Dec 14; Vol. 18 (12), pp. e0295451. Date of Electronic Publication: 2023 Dec 14 (Print Publication: 2023).
Typ publikacji:
Journal Article
MeSH Terms:
Genetic Predisposition to Disease*
Osteoporosis, Postmenopausal*/genetics
Female ; Humans ; Case-Control Studies ; China/epidemiology ; Glucagon-Like Peptide-1 Receptor/genetics ; Polymorphism, Single Nucleotide ; Postmenopause/genetics
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Association of lncRNA THRIL, HOTAIR genes variations and expression levels with pulmonary tuberculosis.
Autorzy:
Wang LJ; Department of Infectious Diseases, The First Affiliated Hospital of Anhui Medical University, Hefei, Anhui, China.
Li R; Department of Nosocomial Infection Management, The First Affiliated Hospital of Anhui Medical University, Hefei, China.
Zhang TP; Division of Life Sciences and Medicine, The First Affiliated Hospital of USTC, University of Science and Technology of China, Hefei, Anhui, China. .
Li HM; Department of Infectious Diseases, The First Affiliated Hospital of Anhui Medical University, Hefei, Anhui, China. .; Department of Epidemiology and Biostatistics, School of Public Health, Anhui Medical University, Hefei, China. .
Pokaż więcej
Źródło:
BMC medical genomics [BMC Med Genomics] 2023 Dec 12; Vol. 16 (1), pp. 326. Date of Electronic Publication: 2023 Dec 12.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Genetic Predisposition to Disease*
RNA, Long Noncoding*/genetics
Humans ; Alleles ; Case-Control Studies ; Genotype ; Leukocytes, Mononuclear ; Polymorphism, Single Nucleotide
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
CYP4V2 rs56413992 C > T was associated with the risk of coronary heart disease in the Chinese Han population: a case-control study.
Autorzy:
Huang K; Department of Cardiology, Central South University Xiangya School of Medicine Affiliated Haikou Hospital, No. 43, Renmin Avenue, Haikou, Hainan, China.
Ma T; Department of Cardiology, Central South University Xiangya School of Medicine Affiliated Haikou Hospital, No. 43, Renmin Avenue, Haikou, Hainan, China.
Li Q; Department of Cardiology, Central South University Xiangya School of Medicine Affiliated Haikou Hospital, No. 43, Renmin Avenue, Haikou, Hainan, China.
Zhong Z; Department of Cardiology, Central South University Xiangya School of Medicine Affiliated Haikou Hospital, No. 43, Renmin Avenue, Haikou, Hainan, China.
Zhou Y; School of Medicine, Jingchu University of Technology, Jingmen, Hubei, China.
Zhang W; Department of Cardiology, Central South University Xiangya School of Medicine Affiliated Haikou Hospital, No. 43, Renmin Avenue, Haikou, Hainan, China.
Qin T; Department of Cardiology, Central South University Xiangya School of Medicine Affiliated Haikou Hospital, No. 43, Renmin Avenue, Haikou, Hainan, China.
Tang S; Department of Cardiology, Central South University Xiangya School of Medicine Affiliated Haikou Hospital, No. 43, Renmin Avenue, Haikou, Hainan, China.
Zhong J; Department of Cardiology, Central South University Xiangya School of Medicine Affiliated Haikou Hospital, No. 43, Renmin Avenue, Haikou, Hainan, China. .
Lu S; Department of Cardiology, Central South University Xiangya School of Medicine Affiliated Haikou Hospital, No. 43, Renmin Avenue, Haikou, Hainan, China. Lu_.
Pokaż więcej
Źródło:
BMC medical genomics [BMC Med Genomics] 2023 Dec 08; Vol. 16 (1), pp. 322. Date of Electronic Publication: 2023 Dec 08.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Coronary Disease*/genetics
Cytochrome P450 Family 4*/genetics
Genetic Predisposition to Disease*
Humans ; Male ; Case-Control Studies ; China ; Genotype ; Polymorphism, Single Nucleotide ; Risk Factors
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
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. .
Pokaż więcej
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
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Wyświetlanie 1-20 z 32150

Ta witryna wykorzystuje pliki cookies do przechowywania informacji na Twoim komputerze. Pliki cookies stosujemy w celu świadczenia usług na najwyższym poziomie, w tym w sposób dostosowany do indywidualnych potrzeb. Korzystanie z witryny bez zmiany ustawień dotyczących cookies oznacza, że będą one zamieszczane w Twoim komputerze. W każdym momencie możesz dokonać zmiany ustawień dotyczących cookies