Human Genome Epidemiology Literature Finder
Records 1 - 9 (of 9 Records) |
Query Trace: Otosclerosis and COL1A1[original query] |
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Association of otosclerosis with Sp1 binding site polymorphism in COL1A1 gene: evidence for a shared genetic etiology with osteoporosis. Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology 2004 Jul 25 (4): 447-50. McKenna Michael J, Nguyen-Huynh Anh T, Kristiansen Arthur |
Proposed association between the COL1A1 and COL1A2 genes and otosclerosis is not supported by a case-control study in Spain. American journal of medical genetics. Part A 2004 Jul 128A (1): 19-22. Rodríguez Laura, Rodríguez Santiago, Hermida Juan, Frade Carlos, Sande Esther, Visedo Guillermo, Martín Carlos, Zapata Carl |
Single-nucleotide polymorphisms in the COL1A1 regulatory regions are associated with otosclerosis. Clinical genetics 2007 May 71 (5): 406-14. Chen W, Meyer N C, McKenna M J, Pfister M, McBride D J, Fukushima K, Thys M, Camp G V, Smith R J |
Association of COL1A1 and TGFB1 polymorphisms with otosclerosis in a Tunisian population. Annals of human genetics 2011 Sep 75 (5): 598-604. Khalfallah Ayda, Schrauwen Isabelle, Mnejja Malek, HadjKacem Hassen, Dhouib Leila, Mosrati Mohamed Ali, Hakim Bochra, Lahmar Imed, Charfeddine Ilhem, Driss Nabil, Ayadi Hammadi, Ghorbel Abdelmonem, Van Camp Guy, Masmoudi Sab |
COL1A1 association and otosclerosis: a meta-analysis. American journal of medical genetics. Part A 2012 May 158A (5): 1066-70. Schrauwen Isabelle, Khalfallah Ayda, Ealy Megan, Fransen Erik, Claes Charlotte, Huber Alex, Murillo Laura Rodriguez, Masmoudi Saber, Smith Richard J H, Van Camp G |
Association of COL1A1 polymorphism in Turkish patients with otosclerosis. American journal of otolaryngology 0 34 (5): 403-6. Ertugay Omer Cagatay, Ata Pinar, Kalaycik Ertugay Cigdem, Kaya Kerem Sami, Tatlipinar Arzu, Kulekci Sem |
Genetic association analysis in a clinically and histologically confirmed otosclerosis population confirms association with the TGFB1 gene but suggests an association of the RELN gene with a clinically indistinguishable otosclerosis-like phenotype. Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology 2014 Jul 35 (6): 1058-64. Sommen Manou, Van Camp Guy, Liktor Balázs, Csomor Péter, Fransen Erik, Sziklai István, Schrauwen Isabelle, Karosi Tam |
Evidence of distinct RELN and TGFB1 genetic associations in familial and non-familial otosclerosis in a British population. Human genetics 2018 May . Mowat Andrew J, Crompton Michael, Ziff Joanna L, Aldren Christopher P, Lavy Jeremy A, Saeed Shakeel R, Dawson Sally |
Evaluation of the Genetic Association and mRNA Expression of the COL1A1, BMP2, and BMP4 Genes in the Development of Otosclerosis. Genetic testing and molecular biomarkers 2020 5 24 (6): 343-351. Hansdah Kirtal, Singh Neha, Bouzid Amal, Priyadarshi Saurabh, Ray Chinmay Sundar, Desai Ashim, Panda Khirod Chandra, Choudhury Jyotish Chandra, Biswal Narayan Chandra, Tekari Adel, Masmoudi Saber, Ramchander Puppala Venk |
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- Page last updated:Apr 16, 2024
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