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Academic Journal

HLA-DRB1 and HLA-DQB1 genetic diversity modulates response to lithium in bipolar affective disorders.

  • Authors : Le Clerc S; Laboratoire Génomique, Bio-Informatique et Chimie Moléculaire (EA7528), Conservatoire National des Arts et Métiers, HESAM Université, 292, rue Saint Martin, 75003, Paris, France.; Lombardi L

Subjects: Genetic Predisposition to Disease*; Bipolar Disorder/Bipolar Disorder/Bipolar Disorder/*genetics ; HLA-DQ beta-Chains/HLA-DQ beta-Chains/HLA-DQ beta-Chains/*genetics

  • Source: Scientific reports [Sci Rep] 2021 Sep 08; Vol. 11 (1), pp. 17823. Date of Electronic Publication: 2021 Sep 08.Publisher: Nature Publishing Group Country of Publication: England NLM ID: 101563288 Publication Model: Electronic Cited

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Academic Journal

Social and non-social autism symptoms and trait domains are genetically dissociable

Subjects: Autism spectrum disorders; Genetic predisposition to disease; Genome-wide association studies

  • Source: ISSN: 2399-3642 ; Communications Biology ; https://pasteur.hal.science/pasteur-03261098 ; Communications Biology, 2019, 2 (1), pp.328. ⟨10.1038/s42003-019-0558-4⟩.

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Academic Journal

Investigating the causal role of MRE11A p.E506* in breast and ovarian cancer.

  • Authors : Elkholi IE; Montreal Clinical Research Institute (IRCM), Montreal, QC, Canada.; Molecular Biology Programs, Université de Montréal, Montreal, QC, Canada.

Subjects: Genetic Predisposition to Disease* ; Mutation*; Breast Neoplasms/Breast Neoplasms/Breast Neoplasms/*genetics

  • Source: Scientific reports [Sci Rep] 2021 Jan 28; Vol. 11 (1), pp. 2409. Date of Electronic Publication: 2021 Jan 28.Publisher: Nature Publishing Group Country of Publication: England NLM ID: 101563288 Publication Model: Electronic Cited

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Academic Journal

Identifying sequence variants contributing to hereditary breast and ovarian cancer in BRCA1 and BRCA2 negative breast and ovarian cancer patients.

  • Authors : Jarhelle E; Department of Medical Genetics, Division of Child and Adolescent Health, University Hospital of North Norway, Tromsø, Norway. .; Department of Clinical Medicine, University of Tromsø, Tromsø, Norway. .

Subjects: Genetic Predisposition to Disease* ; Germ-Line Mutation*; BRCA1 Protein/BRCA1 Protein/BRCA1 Protein/*genetics

  • Source: Scientific reports [Sci Rep] 2019 Dec 27; Vol. 9 (1), pp. 19986. Date of Electronic Publication: 2019 Dec 27.Publisher: Nature Publishing Group Country of Publication: England NLM ID: 101563288 Publication Model: Electronic Cited

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Academic Journal

ISL1 is a major susceptibility gene for classic bladder exstrophy and a regulator of urinary tract development.

  • Authors : Zhang R; Institute of Human Genetics, University of Bonn, Bonn, Germany.; Department of Genomics, Life &Brain Center, University of Bonn, Bonn, Germany.

Subjects: Genetic Predisposition to Disease*; Bladder Exstrophy/Bladder Exstrophy/Bladder Exstrophy/*genetics ; LIM-Homeodomain Proteins/LIM-Homeodomain Proteins/LIM-Homeodomain Proteins/*genetics

  • Source: Scientific reports [Sci Rep] 2017 Feb 08; Vol. 7, pp. 42170. Date of Electronic Publication: 2017 Feb 08.Publisher: Nature Publishing Group Country of Publication: England NLM ID: 101563288 Publication Model: Electronic Cited

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Academic Journal

Evidence for genetic association of TBX21 and IFNG with systemic lupus erythematosus in a Chinese Han population.

  • Authors : Leng RX; Department of Epidemiology and Biostatistics, School of Public Health, Anhui Medical University, Hefei, Anhui, China.; Anhui Provincial Laboratory of Population Health and Major Disease Screening and Diagnosis, Anhui Medical University, Hefei, Anhui, China.

Subjects: Genetic Predisposition to Disease* ; Polymorphism, Single Nucleotide*; Interferon-gamma/Interferon-gamma/Interferon-gamma/*genetics

  • Source: Scientific reports [Sci Rep] 2016 Feb 26; Vol. 6, pp. 22081. Date of Electronic Publication: 2016 Feb 26.Publisher: Nature Publishing Group Country of Publication: England NLM ID: 101563288 Publication Model: Electronic Cited

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