Human Genome Epidemiology Literature Finder
Records 1 - 16 (of 16 Records) |
Query Trace: COL8A2[original query] |
---|
Keratoconus is not associated with mutations in COL8A1 and COL8A2. Cornea 2007 Sep 26 (8): 963-5. Aldave Anthony J, Bourla Nirit, Yellore Vivek S, Rayner Sylvia A, Khan M Ali, Salem Andrew K, Sonmez Bar |
Genetic analysis of patients with Fuchs endothelial corneal dystrophy in India. BMC ophthalmology 2010 10 (1): 3. Hemadevi Boomiraj, Srinivasan Muthiah, Arunkumar Jambulingam, Prajna Namperumalsamy V, Sundaresan Periasa |
Distribution of COL8A2 and COL8A1 gene variants in Caucasian primary open angle glaucoma patients with thin central corneal thickness. Molecular vision 2010 16 2185-91. Desronvil T, Logan-Wyatt D, Abdrabou W, Triana M, Jones R, Taheri S, Del Bono E, Pasquale L R, Olivier M, Haines J L, Fan B J, Wiggs J |
Population-based meta-analysis in Caucasians confirms association with COL5A1 and ZNF469 but not COL8A2 with central corneal thickness.
Human genetics 2012 Nov 131 (11): 1783-93. Hoehn René, Zeller Tanja, Verhoeven Virginie J M, Grus Franz, Adler Max, Wolfs Roger C, Uitterlinden André G, Castagne Raphaële, Schillert Arne, Klaver Caroline C W, Pfeiffer Norbert, Mirshahi Alire |
Differing roles for TCF4 and COL8A2 in central corneal thickness and fuchs endothelial corneal dystrophy. PloS one 2012 7 (10): e46742. Igo Robert P, Kopplin Laura J, Joseph Peronne, Truitt Barbara, Fondran Jeremy, Bardenstein David, Aldave Anthony J, Croasdale Christopher R, Price Marianne O, Rosenwasser Miriam, Lass Jonathan H, Iyengar Sudha K, |
Association of TCF4 and CLU polymorphisms with Fuchs' endothelial dystrophy and implication of CLU and TGFBI proteins in the disease process. European journal of human genetics : EJHG 2012 Jun 20 (6): 632-8. Kuot Abraham, Hewitt Alex W, Griggs Kim, Klebe Sonja, Mills Richard, Jhanji Vishal, Craig Jamie E, Sharma Shiwani, Burdon Kathryn |
Mutational spectrum of the ZEB1 gene in corneal dystrophies supports a genotype-phenotype correlation. Investigative ophthalmology & visual science 2013 May 54 (5): 3215-23. Lechner Judith, Dash Durga P, Muszynska Dorota, Hosseini Mohsen, Segev Fani, George Sonia, Frazer David G, Moore Jonathan E, Kaye Stephen B, Young Terri, Simpson David A, Churchill Amanda J, Héon Elise, Willoughby Colin |
Genetic screen of African Americans with Fuchs endothelial corneal dystrophy. Molecular vision 2013 19 2508-16. Minear Mollie A, Li Yi-Ju, Rimmler Jacqueline, Balajonda Elmer, Watson Shera, Allingham R Rand, Hauser Michael A, Klintworth Gordon K, Afshari Natalie A, Gregory Simon |
Biosynthetic and functional defects in newly identified SLC4A11 mutants and absence of COL8A2 mutations in Fuchs endothelial corneal dystrophy. Journal of human genetics 2014 Aug 59 (8): 444-53. Soumittra Nagasamy, Loganathan Sampath K, Madhavan Dharanija, Ramprasad Vedam L, Arokiasamy Tharigopala, Sumathi Sundaram, Karthiyayini Thirumalai, Rachapalli Sudhir R, Kumaramanickavel Govindasamy, Casey Joseph R, Rajagopal Ra |
[TGC Repeats in Intron 2 of the TCF4 Gene have a Good Predictive Power Regarding to Fuchs Endothelial Corneal Dystrophy]. Klinische Monatsblatter fur Augenheilkunde 2015 Aug . Luther M, Grünauer-Kloevekorn C, Weidle E, Passarge E, Rupprecht A, Hoffmann K, Foja |
Association of ZEB1 and TCF4 rs613872 changes with late onset Fuchs endothelial corneal dystrophy in patients from northern India. Molecular vision 2015 21 1252-60. Gupta Ranjan, Kumawat Babu Lal, Paliwal Preeti, Tandon Radhika, Sharma Namrata, Sen Seema, Kashyap Seema, Nag Tapas Chandra, Vajpayee Rasik B, Sharma Arundha |
TCF4 and COL8A2 Gene Polymorphism Screening in a Greek Population of Late-onset Fuchs Endothelial Corneal Dystrophy. In vivo (Athens, Greece) 0 33 (3): 963-971. Moschos Marilita M, Diamantopoulou Andriana, Gouliopoulos Nikos, Droutsas Konstantinos, Bagli Eleni, Chatzistefanou Klio, Kitsos George, Kroupis Christ |
Association of rs613872 and Trinucleotide Repeat Expansion in the TCF4 Gene of German Patients With Fuchs Endothelial Corneal Dystrophy. Cornea 2019 Apr . Okumura Naoki, Hayashi Ryousuke, Nakano Masakazu, Tashiro Kei, Yoshii Kengo, Aleff Ross, Butz Malinda, Highsmith Edward W, Wieben Eric D, Fautsch Michael P, Baratz Keith H, Komori Yuya, Ueda Emi, Nakahara Makiko, Weller Julia, Tourtas Theofilos, Schlötzer-Schrehardt Ursula, Kruse Friedrich, Koizumi Nori |
New findings in the roles of Cyclin-dependent Kinase inhibitors 2B Antisense RNA 1 (CDKN2B-AS1) rs1333049 G/C and rs4977574 A/G variants on the risk to coronary heart disease. Bioengineered 2020 10 11 (1): 1084-1098. Yuan Wei, Zhang Wei, Zhang Wei, Ruan Zhong-Bao, Zhu Li, Liu Yu, Mi Yuan-Yuan, Zhang Li-Fe |
Whole Exome-Wide Association Identifies Rare Variants in GALNT9 Associated with Middle Eastern Papillary Thyroid Carcinoma Risk. Cancers 2023 9 15 (17): . Rong Bu, Abdul K Siraj, Saud Azam, Kaleem Iqbal, Zeeshan Qadri, Maha Al-Rasheed, Saif S Al-Sobhi, Fouad Al-Dayel, Khawla S Al-Kura |
[Mutational Signatures Analysis of Micropapillary Components and Exploration of ZNF469 Gene in Early-stage Lung Adenocarcinoma with Ground-glass Opacities]. Zhongguo fei ai za zhi = Chinese journal of lung cancer 2023 12 26 (12): 889-900. Youtao Xu, Qinhong Sun, Siwei Wang, Hongyu Zhu, Guozhang Dong, Fanchen Meng, Zhijun Xia, Jing You, Xiangru Kong, Jintao Wu, Peng Chen, Fangwei Yuan, Xinyu Yu, Jinfu Ji, Zhitong Li, Pengcheng Zhu, Yuxiang Sun, Tongyan Liu, Rong Yin, Lin |
- Page last reviewed:Feb 1, 2024
- Page last updated:Apr 29, 2024
- Content source: