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Academic Journal

Association between PDCD1 Gene Polymorphisms and Risk of Systemic Lupus Erythematosus in Three Main Ethnic Groups of the Malaysian Population.

  • Authors : Chua KH; Department of Biomedical Science, Faculty of Medicine, University of Malaya, 50603 Kuala Lumpur, Malaysia. .; Lian LH

Subjects: Genetic Association Studies* ; Genetic Predisposition to Disease*; Ethnicity/Ethnicity/Ethnicity/*genetics

  • Source: International journal of molecular sciences [Int J Mol Sci] 2015 Apr 29; Vol. 16 (5), pp. 9794-803. Date of Electronic Publication: 2015 Apr 29.Publisher: MDPI Country of Publication: Switzerland NLM ID: 101092791 Publication Model: Electronic Cited Medium: Internet ISSN: 1422-0067

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Academic Journal

Single nucleotide polymorphism of SREBF-1 gene associated with an increased risk of endometrial cancer in Chinese women.

  • Authors : Qiu CP; Department of Obstetrics and Gynecology, Qilu Hospital, Shandong University, Jinan, P R China.; Lv QT

Subjects: Genetic Association Studies* ; Genetic Predisposition to Disease*; Asian People/Asian People/Asian People/*genetics

  • Source: PloS one [PLoS One] 2014 Mar 10; Vol. 9 (3), pp. e90491. Date of Electronic Publication: 2014 Mar 10 (Print Publication: 2014).Publisher: Public Library of Science Country of Publication: United States NLM ID: 101285081 Publication Model: eCollection Cited Medium: Internet

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Academic Journal

Association of autoimmune Addison's disease with alleles of STAT4 and GATA3 in European cohorts.

  • Authors : Mitchell AL; Institute of Genetic Medicine, Newcastle University, Newcastle, United Kingdom.; Macarthur KD

Subjects: Alleles* ; Genetic Association Studies* ; Genetic Predisposition to Disease*

  • Source: PloS one [PLoS One] 2014 Mar 10; Vol. 9 (3), pp. e88991. Date of Electronic Publication: 2014 Mar 10 (Print Publication: 2014).Publisher: Public Library of Science Country of Publication: United States NLM ID: 101285081 Publication Model: eCollection Cited Medium: Internet

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Academic Journal

Stratified whole genome linkage analysis of Chiari type I malformation implicates known Klippel-Feil syndrome genes as putative disease candidates.

  • Authors : Markunas CA; Department of Medicine, Duke University Medical Center, Durham, North Carolina, USA.; Soldano K

Subjects: Genetic Association Studies* ; Genetic Linkage* ; Genetic Predisposition to Disease*

  • Source: PloS one [PLoS One] 2013 Apr 19; Vol. 8 (4), pp. e61521. Date of Electronic Publication: 2013 Apr 19 (Print Publication: 2013).Publisher: Public Library of Science Country of Publication: United States NLM ID: 101285081 Publication Model: Electronic-Print Cited Medium: Internet

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Academic Journal

Association between FGFR1OP2/wit3.0 polymorphisms and residual ridge resorption of mandible in Korean population.

  • Authors : Kim JH; Department of Prosthodontics, College of Dentistry, Yonsei University, Seoul, Korea.; Oh MY

Subjects: Genetic Association Studies* ; Genetic Predisposition to Disease*; Alveolar Bone Loss/Alveolar Bone Loss/Alveolar Bone Loss/*genetics

  • Source: PloS one [PLoS One] 2012; Vol. 7 (8), pp. e42734. Date of Electronic Publication: 2012 Aug 06.Publisher: Public Library of Science Country of Publication: United States NLM ID: 101285081 Publication Model: Print-Electronic Cited Medium: Internet

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Academic Journal

Genetic studies of multiple consanguineous Pakistani families segregating oculocutaneous albinism identified novel and reported mutations.

  • Authors : Gul H; Department of Biological Sciences, Faculty of Sciences, Gomal University, D.I. Khan, Pakistan.; Shah AH

Subjects: Consanguinity* ; Genetic Association Studies* ; Genetic Predisposition to Disease*

  • Source: Annals of human genetics [Ann Hum Genet] 2019 Jul; Vol. 83 (4), pp. 278-284. Date of Electronic Publication: 2019 Mar 13.Publisher: Wiley-Blackwell Country of Publication: England NLM ID: 0416661 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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