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Academic Journal

Analysis of Cyclin-Dependent Kinase Inhibitor-2B rs1063192 Polymorphism in Saudi Patients with Primary Open-Angle Glaucoma.

  • Authors : Abu-Amero KK; 1 Glaucoma Research Chair, Department of Ophthalmology, College of Medicine, King Saud University , Riyadh, Saudi Arabia .; 2 Department of Ophthalmology, College of Medicine, University of Florida , Jacksonville, Florida.

Subjects: Alleles* ; Gene Frequency* ; Genotype*

  • Source: Genetic testing and molecular biomarkers [Genet Test Mol Biomarkers] 2016 Oct; Vol. 20 (10), pp. 637-641. Date of Electronic Publication: 2016 Aug Publisher: Mary Ann Liebert, Inc Country of Publication: United States NLM ID: 101494210 Publication Model: Print-Electronic

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Academic Journal

Association of the Polymorphism in Nucleobindin 2 Gene and the Risk of Metabolic Syndrome.

  • Authors : Wang R; 1 Department of Blood Transfusion, Qilu Hospital, Shandong University , Qingdao, People's Republic of China .; Wang J

Subjects: Genotype* ; Polymorphism, Genetic*; Calcium-Binding Proteins/Calcium-Binding Proteins/Calcium-Binding Proteins/*genetics

  • Source: Genetic testing and molecular biomarkers [Genet Test Mol Biomarkers] 2016 Jan; Vol. 20 (1), pp. 49-52. Date of Electronic Publication: 2015 Dec 01.Publisher: Mary Ann Liebert, Inc Country of Publication: United States NLM ID: 101494210 Publication Model: Print-Electronic

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Academic Journal

Association Between Polymorphisms of DNA Repair Genes and Risk of Schizophrenia.

  • Authors : Odemis S; 1 Department of Psychiatry, Istanbul Erenkoy Psychiatric and Neurological Disorders Hospital , Istanbul, Turkey .; Tuzun E

Subjects: Genotype* ; Polymorphism, Genetic*; DNA Repair/DNA Repair/DNA Repair/*genetics

  • Source: Genetic testing and molecular biomarkers [Genet Test Mol Biomarkers] 2016 Jan; Vol. 20 (1), pp. 11-7. Date of Electronic Publication: 2015 Nov 10.Publisher: Mary Ann Liebert, Inc Country of Publication: United States NLM ID: 101494210 Publication Model: Print-Electronic

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Academic Journal

Tumor necrosis factor-alpha and polycystic ovarian syndrome: a clinical, biochemical, and molecular genetic study.

  • Authors : Thathapudi S; 1 Department of Genetics and Molecular Medicine, Vasavi Medical and Research Center , Hyderabad, India .; Kodati V

Subjects: Genotype* ; Polycystic Ovary Syndrome*/Polycystic Ovary Syndrome*/Polycystic Ovary Syndrome*/blood ; Polycystic Ovary Syndrome*/Polycystic Ovary Syndrome*/Polycystic Ovary Syndrome*/genetics

  • Source: Genetic testing and molecular biomarkers [Genet Test Mol Biomarkers] 2014 Sep; Vol. 18 (9), pp. 605-9. Date of Electronic Publication: 2014 Aug 01.Publisher: Mary Ann Liebert, Inc Country of Publication: United States NLM ID: 101494210 Publication Model: Print-Electronic

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Academic Journal

Association between interleukin-6 gene polymorphisms and bone mineral density: a meta-analysis.

  • Authors : Wang Z; 1 Department of Orthopedics, The 117th Hospital of PLA , Hangzhou, China .; Yang Y

Subjects: Genotype* ; Polymorphism, Genetic*; Bone Density/Bone Density/Bone Density/*genetics

  • Source: Genetic testing and molecular biomarkers [Genet Test Mol Biomarkers] 2013 Dec; Vol. 17 (12), pp. 898-909. Date of Electronic Publication: 2013 Sep Publisher: Mary Ann Liebert, Inc Country of Publication: United States NLM ID: 101494210 Publication Model: Print-Electronic

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Academic Journal

The interleukin-6-572G/C gene polymorphism and the risk of intracranial aneurysms in a Chinese population.

  • Authors : Liu Y; Department of Neurosurgery, West China Hospital, Sichuan University, Chengdu, China.; Sun J

Subjects: Alleles* ; Gene Frequency* ; Genotype*

  • Source: Genetic testing and molecular biomarkers [Genet Test Mol Biomarkers] 2012 Jul; Vol. 16 (7), pp. 822-6. Date of Electronic Publication: 2012 Jun 11.Publisher: Mary Ann Liebert, Inc Country of Publication: United States NLM ID: 101494210 Publication Model: Print-Electronic

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Academic Journal

The genotype distribution of the XRCC1, XRCC3, and XPD DNA repair genes and their role for the development of acute myeloblastic leukemia.

  • Authors : Sorour A; Department of Clinical Pathology, Faculty of Medicine, Alexandria University, Alexandria, Egypt.; Ayad MW

Subjects: Genotype*; DNA Repair/DNA Repair/DNA Repair/*genetics ; DNA-Binding Proteins/DNA-Binding Proteins/DNA-Binding Proteins/*genetics

  • Source: Genetic testing and molecular biomarkers [Genet Test Mol Biomarkers] 2013 Mar; Vol. 17 (3), pp. 195-201. Date of Electronic Publication: 2013 Feb 11.Publisher: Mary Ann Liebert, Inc Country of Publication: United States NLM ID: 101494210 Publication Model: Print-Electronic

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Academic Journal

Analysis of the GJB2 and GJB6 genes in Italian patients with nonsyndromic hearing loss: frequencies, novel mutations, genotypes, and degree of hearing loss.

  • Authors : Primignani P; Laboratorio di Genetica Medica, Fondazione IRCCS Ospedale Maggiore Policlinico, Mangiagalli e Regina Elena-Milano, Milan, Italy. ; Trotta L

Subjects: Genotype* ; Mutation*; Connexins/Connexins/Connexins/*genetics

  • Source: Genetic testing and molecular biomarkers [Genet Test Mol Biomarkers] 2009 Apr; Vol. 13 (2), pp. 209-17.Publisher: Mary Ann Liebert, Inc Country of Publication: United States NLM ID: 101494210 Publication Model: Print Cited

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Academic Journal

Angiotensin-converting enzyme genotype and successful ascent to extreme high altitude.

Subjects: Altitude* ; Genotype* ; Mountaineering*

  • Source: High altitude medicine & biology [High Alt Med Biol] 2007 Winter; Vol. 8 (4), pp. 278-85.Publisher: Mary Ann Liebert, Inc Country of Publication: United States NLM ID: 100901183 Publication Model: Print Cited

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  • 1-9 of  9 results for ""Polymorphism, Genetic""