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Academic Journal

Effect of L3MBTL3/PTPN9 polymorphisms on risk to alcohol-induced ONFH in Chinese Han population.

  • Authors : Xiong J; Department of Orthopedic Trauma, the Hainan Affiliated Hospital of Hainan Medical University, No. 19, Xiuhua Road, Haikou, 570311, Hainan Province, China.; Niu Y

Subjects: Asian People*/Asian People*/Asian People*/genetics ; Ethnicity*/Ethnicity*/Ethnicity*/genetics ; Femur Head Necrosis*/Femur Head Necrosis*/Femur Head Necrosis*/chemically induced

  • Source: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology [Neurol Sci] 2022 Apr; Vol. 43 (4), pp. 2823-2830. Publisher: Springer-Verlag Italia Country of Publication: Italy NLM ID: 100959175 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Academic Journal

Genetic variants in IL33 and IL1RL1 genes confer susceptibility to HBV-related liver cirrhosis in Chinese Han population.

  • Authors : Ma N; Department of Social Medicine and Health Care Management, School of Public Health, Hebei Medical University, Hebei Key Laboratory of Environment and Human Health, Shijiazhuang 050017, China.; Xu M

Subjects: Polymorphism, Single Nucleotide*; Genetic Predisposition to Disease/Genetic Predisposition to Disease/Genetic Predisposition to Disease/*genetics ; Hepatitis B/Hepatitis B/Hepatitis B/*genetics

  • Source: Infection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases [Infect Genet Evol] 2021 Oct; Vol. 94, pp. 104983. Date of Publisher: Elsevier Science Country of Publication: Netherlands NLM ID: 101084138 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Academic Journal

Analysis of STAG3 variants in Chinese non-obstructive azoospermia patients with germ cell maturation arrest.

  • Authors : Liu W; Center for Reproductive Medicine, Cheeloo College of Medicine, Shandong University, 44 Wenhua Xi Road, Jinan, 250012, Shandong, China.; Key Laboratory of Reproductive Endocrinology of Ministry of Education, Shandong University, Jinan, 250012, Shandong, China.

Subjects: Genetic Predisposition to Disease* ; Polymorphism, Single Nucleotide* ; Spermatogenesis*Azoospermia, Nonobstructive

  • Source: Scientific reports [Sci Rep] 2021 May 12; Vol. 11 (1), pp. 10077. Date of Electronic Publication: 2021 May 12.Publisher: Nature Publishing Group Country of Publication: England NLM ID: 101563288 Publication Model: Electronic Cited Medium: Internet ISSN:

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Academic Journal

HLA-DPB1 rs9277535 polymorphism is associated with rheumatoid arthritis risk in a Chinese Han population.

  • Authors : Yang Z; Department of Orthopedics, The Affiliated Changzhou No.2 People's Hospital of Nanjing Medical University, Changzhou 213003, China.; Liu W

Subjects: Genetic Predisposition to Disease*; Arthritis, Rheumatoid/Arthritis, Rheumatoid/Arthritis, Rheumatoid/*genetics ; HLA-DP beta-Chains/HLA-DP beta-Chains/HLA-DP beta-Chains/*genetics

  • Source: Aging [Aging (Albany NY)] 2021 Apr 19; Vol. 13 (8), pp. 11696-11704. Date of Electronic Publication: 2021 Apr 19.Publisher: Impact Journals, LLC Country of Publication: United States NLM ID: 101508617 Publication Model: Print-Electronic Cited Medium: Internet

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Academic Journal

Novel Risk Loci Associated With Genetic Risk for Bipolar Disorder Among Han Chinese Individuals: A Genome-Wide Association Study and Meta-analysis.

Subjects: Genome-Wide Association Study*; Asian People/Asian People/Asian People/*genetics ; Bipolar Disorder/Bipolar Disorder/Bipolar Disorder/*genetics

  • Source: JAMA psychiatry [JAMA Psychiatry] 2021 Mar 01; Vol. 78 (3), pp. 320-330.Publisher: American Medical Association Country of Publication: United States NLM ID: 101589550 Publication Model: Print Cited Medium: Internet ISSN:

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Academic Journal

The interaction of histone modification related H3F3B and NSD2 genes increases the susceptibility to schizophrenia in a Chinese population.

  • Authors : Liu W; Shanghai Key Laboratory of Psychotic Disorders, Shanghai Mental Health Center, Shanghai Jiao Tong University School of Medicine, Shanghai, China; College of Life Sciences, Shanghai Normal University, Shanghai, China.

Subjects: Population Surveillance*; Epistasis, Genetic/Epistasis, Genetic/Epistasis, Genetic/*physiology ; Genetic Predisposition to Disease/Genetic Predisposition to Disease/Genetic Predisposition to Disease/*genetics

  • Source: Progress in neuro-psychopharmacology & biological psychiatry [Prog Neuropsychopharmacol Biol Psychiatry] 2020 Jul 13; Vol. 101, pp. 109918. Date of Electronic Publication: 2020 MarPublisher: Pergamon Press Country of Publication: England NLM ID: 8211617 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Academic Journal

Genetic Study in a Large Cohort Supported Different Pathogenesis of Graves' Disease and Hashimoto's Hypothyroidism.

  • Authors : Zhang QY; The Core Laboratory in Medical Center of Clinical Research, Department of Molecular Diagnostic and Endocrinology, Shanghai Ninth People's Hospital, State Key Laboratory of Medical Genomics, Shanghai Jiao Tong University School of Medicine, Shanghai, China.; Liu W

Subjects: Genetic Loci* ; Genetic Predisposition to Disease* ; Polymorphism, Single Nucleotide*

  • Source: The Journal of clinical endocrinology and metabolism [J Clin Endocrinol Metab] 2020 Jul 01; Vol. 105 (7).Publisher: Oxford University Press Country of Publication: United States NLM ID: 0375362 Publication Model: Print Cited Medium: Internet ISSN:

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Academic Journal

The role of SLITRK6 in the pathogenesis of Tourette syndrome: From the conclusion of a family-based study in the Chinese Han population.

  • Authors : Liu W; Medical Genetics Department, The Affiliated Hospital of Qingdao University, Qingdao, Shandong, China.; The Prenatal diagnosis center, The Affiliated Hospital of Qingdao University, Qingdao, Shandong, China.

Subjects: Genetic Predisposition to Disease* ; Polymorphism, Single Nucleotide*; Membrane Proteins/Membrane Proteins/Membrane Proteins/*genetics

  • Source: The journal of gene medicine [J Gene Med] 2020 Jun; Vol. 22 (6), pp. e3173. Date of Electronic Publication: 2020 Mar 02.Publisher: John Wiley & Sons Country of Publication: England NLM ID: 9815764 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Academic Journal

DUOX2 and DUOXA2 Variants Confer Susceptibility to Thyroid Dysgenesis and Gland- in-situ With Congenital Hypothyroidism.

  • Authors : Wang F; Medical Genetic Department, The Affiliated Hospital of Qingdao University, Qingdao, China.; Prenatal Diagnosis Center, The Affiliated Hospital of Qingdao University, Qingdao, China.

Subjects: Genetic Predisposition to Disease* ; Mutation*; Congenital Hypothyroidism/Congenital Hypothyroidism/Congenital Hypothyroidism/*pathology

  • Source: Frontiers in endocrinology [Front Endocrinol (Lausanne)] 2020 Apr 21; Vol. 11, pp. 237. Date of Electronic Publication: 2020 Apr 21 (Print Publication: 2020).Publisher: Frontiers Research Foundation] Country of Publication: Switzerland NLM ID: 101555782 Publication Model: eCollection Cited Medium: Print

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Academic Journal

Associations of the IL-1B level, IL-1A and IL-1B gene polymorphisms and ankylosing spondylitis risk in a Chinese Han population.

  • Authors : Liu W; Xuzhou Medical University, Xuzhou 221004, China.; Yang Z

Subjects: Genetic Predisposition to Disease/Genetic Predisposition to Disease/Genetic Predisposition to Disease/*genetics ; Interleukin-1alpha/Interleukin-1alpha/Interleukin-1alpha/*genetics ; Interleukin-1beta/Interleukin-1beta/Interleukin-1beta/*genetics

  • Source: Cytokine [Cytokine] 2020 Feb; Vol. 126, pp. 154918. Date of Electronic Publication: 2019 Nov 11.Publisher: Elsevier Science Ltd Country of Publication: England NLM ID: 9005353 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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