RNA sequencing-based transcriptomic profiles of embryonic lens development for cataract gene discovery
Author:
Funder
National Eye Institute
National Institute of Dental and Craniofacial Research
Publisher
Springer Science and Business Media LLC
Subject
Genetics(clinical),Genetics
Link
http://link.springer.com/article/10.1007/s00439-018-1958-0/fulltext.html
Reference58 articles.
1. Agrawal SA, Anand D, Siddam AD et al (2015) Compound mouse mutants of bZIP transcription factors Mafg and Mafk reveal a regulatory network of non-crystallin genes associated with cataract. Hum Genet 134:717–735. https://doi.org/10.1007/s00439-015-1554-5
2. Aldahmesh MA, Khan AO, Mohamed JY et al (2012) Genomic analysis of pediatric cataract in Saudi Arabia reveals novel candidate disease genes. Genet Med 14:955–962. https://doi.org/10.1038/gim.2012.86
3. Aldahmesh MA, Alshammari MJ, Khan AO et al (2013) The syndrome of microcornea, myopic chorioretinal atrophy, and telecanthus (MMCAT) is caused by mutations in ADAMTS18. Hum Mutat 34:1195–1199. https://doi.org/10.1002/humu.22374
4. Anand D, Lachke SA (2017) Systems biology of lens development: a paradigm for disease gene discovery in the eye. Exp Eye Res 156:22–33. https://doi.org/10.1016/j.exer.2016.03.010
5. Anand D, Agrawal S, Siddam A et al (2015) An integrative approach to analyze microarray datasets for prioritization of genes relevant to lens biology and disease. Genomics Data 5:223–227. https://doi.org/10.1016/j.gdata.2015.06.017
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