Human Genome Epidemiology Literature Finder
Records 1 - 10 (of 10 Records) |
Query Trace: Syndrome and SP1[original query] |
---|
Investigations on the genetic polymorphism in the region of CYP17 gene encoding 5'-UTR in patients with polycystic ovarian syndrome. Gynecological endocrinology : the official journal of the International Society of Gynecological Endocrinology 2001 Apr 15 (2): 123-8. Marszalek B, Laci?ski M, Babych N, Capla E, Biernacka-Lukanty J, Warenik-Szymankiewicz A, Trzeciak W |
[Relations between VDR3 and COL1A1 genes and markers of bone tissue metabolism in patients with chronic obstructive pulmonary disease]. Terapevticheski? arkhiv 2006 78 (3): 17-20. Gel'tser B I, Kochetkova E A, Grigor'eva O Iu, Al'bavichus S A, Bubnov O |
A variant of the Cockayne syndrome B gene ERCC6 confers risk of lung cancer. Human mutation 2008 Jan 29 (1): 113-22. Lin Zhongning, Zhang Xuemei, Tuo Jingsheng, Guo Yongli, Green Bridgett, Chan Chi-Chao, Tan Wen, Huang Ying, Ling Wenhua, Kadlubar Fred F, Lin Dongxin, Ning Baita |
Meta-analysis of myeloperoxidase G-463/A polymorphism in anti-neutrophil cytoplasmic autoantibody-positive vasculitis. Clinical and experimental immunology 2007 Aug 149 (2): 251-6. Rajp A, Adu D, Savage C |
[Role of resistin in insulin resistance]. Rinsho byori. The Japanese journal of clinical pathology 2008 Aug 56 (8): 698-704. Onuma Hiroshi, Osawa Haruhiko, Makino Hideic |
Functional variants of the human 5-lipoxygenase gene and their genetic diagnosis. Prostaglandins, leukotrienes, and essential fatty acids 0 80 (5-6): 255-62. Geiger Emanuel V, Doehring Alexandra, Kirchhof Anja, Lötsch Jö |
The MDM2 285G-309G haplotype is associated with an earlier age of tumour onset in patients with Li-Fraumeni syndrome. Familial cancer 2014 Mar 13 (1): 127-30. Renaux-Petel Mariette, Sesboüé Richard, Baert-Desurmont Stéphanie, Vasseur Stéphanie, Fourneaux Steeve, Bessenay Emilie, Frébourg Thierry, Bougeard Gaël |
Functional characterization of two new STAT3 mutations associated with hyper-IgE syndrome in a Mexican cohort. Clinical genetics 2015 Aug . Alcántara-Montiel Julio C, Staines-Boone Tamara, López-Herrera Gabriela, Espinosa-Rosales Francisco, Espinosa-Padilla Sara E, Hernández-Rivas Rosaura, Santos-Argumedo Leopol |
Functional Analysis of the rs774872314, rs116171003, rs200231898 and rs201107751 Polymorphisms in the Human ROR?T Gene Promoter Region. Genes 2017 Apr 8 (4): . Ratajewski Marcin, Slomka Marcin, Karas Kaja, Sobalska-Kwapis Marta, Korycka-Machala Malgorzata, Salkowska Anna, Dziadek Jaroslaw, Strapagiel Dominik, Dastych Jarosl |
Role of clusterin gene 3'-UTR polymorphisms and promoter hypomethylation in the pathogenesis of pseudoexfoliation syndrome and pseudoexfoliation glaucoma. Biochimica et biophysica acta. Gene regulatory mechanisms 2023 8 1866 (4): 194980. Ramani Shyam Kapuganti, Lipsa Sahoo, Pranjya Paramita Mohanty, Bushra Hayat, Sucheta Parija, Debasmita Pankaj Alo |
- Page last reviewed:Feb 1, 2024
- Page last updated:May 06, 2024
- Content source: