Human Genome Epidemiology Literature Finder
Records 1 - 12 (of 12 Records) |
Query Trace: CHST6[original query] |
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Mutations in corneal carbohydrate sulfotransferase 6 gene (CHST6) cause macular corneal dystrophy in Iceland. Molecular vision 2001 1 6 261-4. Liu N P, Dew-Knight S, Rayner M, Jonasson F, Akama T O, Fukuda M N, Bao W, Gilbert J R, Vance J M, Klintworth G |
Fine mapping and association studies of a high-density lipoprotein cholesterol linkage region on chromosome 16 in French-Canadian subjects. European journal of human genetics : EJHG 2010 Mar 18 (3): 342-7. Dastani Zari, Pajukanta Päivi, Marcil Michel, Rudzicz Nicholas, Ruel Isabelle, Bailey Swneke D, Lee Jenny C, Lemire Mathieu, Faith Janet, Platko Jill, Rioux John, Hudson Thomas J, Gaudet Daniel, Engert James C, Genest Jacqu |
Phenotype and genotype analysis in patients with macular corneal dystrophy. The British journal of ophthalmology 2014 Nov 98 (11): 1514-21. Nowinska Anna K, Wylegala Edward, Teper S?awomir, Wróblewska-Czajka Ewa, Aragona Pasquale, Roszkowska Anna M, Micali Antonio, Pisani Antonina, Puzzolo Domeni |
Molecular analysis of the CHST6 gene in Korean patients with macular corneal dystrophy: Identification of three novel mutations. Molecular vision 2015 21 1201-9. Park Shin Hae, Ahn Ye Jin, Chae Hyojin, Kim Yonggoo, Kim Man Soo, Kim Myungsh |
A Carbohydrate Sulfotransferase-6 (CHST6) gene mutation is associated with Macular Corneal Dystrophy in Labrador Retrievers. Veterinary ophthalmology 2016 Nov 19 (6): 488-492. Tetas Pont Roser, Downs Louise, Pettitt Louise, Busse Claudia, Mellersh Cathryn |
Genetic analysis of CHST6 and TGFBI in Turkish patients with corneal dystrophies: Five novel variations in CHST6. Molecular vision 2016 22 1267-1279. Yaylacioglu Tuncay Fulya, Kayman Kurekci Gülsüm, Guntekin Ergun Sezen, Pasaoglu Ozge Tugce, Akata Rustu Fikret, Dincer Pervin Ruki |
Exome-Wide Association Study of Pancreatic Cancer Risk. Gastroenterology 2017 Oct . Grant Robert C, Denroche Robert E, Borgida Ayelet, Virtanen Carl, Cook Natalie, Smith Alyssa L, Connor Ashton A, Wilson Julie M, Peterson Gloria, Roberts Nicholas J, Klein Alison P, Grimmond Sean M, Biankin Andrew, Cleary Sean, Moore Malcolm, Lemire Mathieu, Zogopoulos George, Stein Lincoln, Gallinger Stev |
Novel Mutations Associated With Various Types of Corneal Dystrophies in a Han Chinese Population. Frontiers in genetics 2019 10 881. Zhang Jing, Wu Dan, Li Yue, Fan Yidan, Chen Huiyu, Hong Jiaxu, Xu Jianjia |
Association of macular corneal dystrophy with excessive cell senescence and apoptosis induced by the novel mutant CHST6. Experimental eye research 2021 11 214 108862. Hao Xiao-Dan, Liu Ya-Ning, Hu Shao-Hua, Pan Xiao-Jing, Chen Pe |
The Role of Functional Polymorphisms in the Extracellular Matrix Modulation-Related Genes on Dupuytren's Contracture. Genes 2022 Apr 13 (5): . Samulenas Gediminas, Insodaite Ruta, Kunceviciene Edita, Poceviciute Roberta, Masionyte Lorena, Zitkeviciute Urte, Pilipaityte Loreta, Smalinskiene Ali |
Gene-Based Analysis Reveals Sex-Specific Genetic Risk Factors of COPD.
AMIA ... Annual Symposium proceedings. AMIA Symposium 2022 3 2021 601-610. Joo Jaehyun, Himes Blan |
Genetic Overlap Analysis Identifies a Shared Etiology between Migraine and Headache with Type 2 Diabetes.
Genes 2022 10 13 (10): . Islam Md Rafiqul, The International Headache Genetics Consortium Ihgc , Nyholt Dale |
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- Page last updated:Apr 22, 2024
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