HuGE Literature Finder
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Novel cataract-causing variant c.177dupC in c-MAF regulates the expression of crystallin genes for cell apoptosis via a mitochondria-dependent pathway. Molecular genetics and genomics : MGG 2023 1 298 (2): 495-506. Li Li, Yue Jian-Fei, Kong De-Qian, Sun Miao-Miao, Li Ke, Zheng Guang-Yi |
A novel MAF missense mutation leads to congenital nuclear cataract by impacting the transactivation of crystallin and noncrystallin genes. Gene 2019 Jan 692 113-118. Si Nuo, Song Zixun, Meng Xiaolu, Li Xinru, Xiao Wei, Zhang X |
High-Throughput Genetic Screening of 51 Pediatric Cataract Genes Identifies Causative Mutations in Inherited Pediatric Cataract in South Eastern Australia. G3 (Bethesda, Md.) 2017 8 7 (10): 3257-3268. Javadiyan Shari, Craig Jamie E, Souzeau Emmanuelle, Sharma Shiwani, Lower Karen M, Mackey David A, Staffieri Sandra E, Elder James E, Taranath Deepa, Straga Tania, Black Joanna, Pater John, Casey Theresa, Hewitt Alex W, Burdon Kathryn |
Analysis of single nucleotide polymorphisms of CRYGA and CRYGB genes in control population of western Indian origin. Indian journal of ophthalmology 0 57 (3): 197-201. Kapur Suman, Mehra Shipra, Gajjar Devarshi, Vasavada Abhay, Kapoor Manav, Sharad Shashwat, Alapure Bhagwat, Rajkumar |
Polymorphisms of the gamma crystallin A and B genes among Indian patients with pediatric cataract. Journal of postgraduate medicine 0 57 (3): 201-5. Mehra S, Kapur S, Vasavada A |
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- Page last updated:Mar 31, 2023
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