Human Genome Epidemiology Literature Finder
Records 1 - 20 (of 20 Records) |
Query Trace: CRYAA[original query] |
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A novel mutation (F71L) in alphaA-crystallin with defective chaperone-like function associated with age-related cataract. Biochimica et biophysica acta 2009 Jul . Bhagyalaxmi SG, Srinivas PN, Barton KA, Kumar KR, Vidyavathi M, Petrash JM, Reddy GB, Padma T |
Association of G>A transition in exon-1 of alpha crystallin gene in age-related cataracts. Oman journal of ophthalmology 2010 Jan 3 (1): 7-12. Bhagyalaxmi S G, Padma T, Reddy G B, Reddy K R |
Meta-analysis of genome-wide association studies in multiethnic Asians identifies two loci for age-related nuclear cataract.
Human molecular genetics 2014 Nov 23 (22): 6119-28. Liao Jiemin, Su Xinyi, Chen Peng, Wang Xu, Xu Liang, Li Xiang, Thean Lennard, Tan Clement, Tan Ava G, Tay Wan-Ting, Jun Gyungah, Zheng Yingfeng, Chew Merwyn, Wang Ya Xing, Tan Queenie S, Barathi Veluchamy A, Klein Barbara E, Saw Seang-Mei, Vithana Eranga N, Tai E-Shyong, Iyengar Sudha K, Mitchell Paul, Khor Chiea-Chuen, Aung Tin, Wang Jie Jin, Jonas Jost B, Teo Yik-Ying, Wong Tien Yin, Cheng Ching- |
Mutation analysis of the genes associated with anterior segment dysgenesis, microcornea and microphthalmia in 257 patients with glaucoma. International journal of molecular medicine 2015 Oct 36 (4): 1111-7. Huang Xiaobo, Xiao Xueshan, Jia Xiaoyun, Li Shiqiang, Li Miaoling, Guo Xiangming, Liu Xing, Zhang Qingjio |
Polymorphism rs7278468 is associated with Age-related cataract through decreasing transcriptional activity of the CRYAA promoter. Scientific reports 2016 6 23206. Ma Xiaoyin, Jiao Xiaodong, Ma Zhiwei, Hejtmancik J Fieldi |
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 |
Association of alpha A-crystallin polymorphisms with susceptibility to nuclear age-related cataract in a Han Chinese population. BMC ophthalmology 2017 Jul 17 (1): 133. Zhao Zhennan, Fan Qi, Zhou Peng, Ye HongFei, Cai Lei, Lu |
Novel Mutations in the Crystallin Gene in Age-Related Cataract Patients from a North Indian Population. Molecular syndromology 2017 Jun 8 (4): 179-186. Patel Rashmi, Zenith Ravish K, Chandra Abhishek, Ali Akht |
A silent mutation in human alpha-A crystallin gene in patients with age-related nuclear or cortical cataract. Bosnian journal of basic medical sciences 2017 Feb . Mynampati Bharani K, Muthukumarappa Thungapathra, Ghosh Sujata, Ram Jag |
Clinical and genetic characteristics of Chinese patients with familial or sporadic pediatric cataract. Orphanet journal of rare diseases 2018 6 13 (1): 94. Li Jingyan, Leng Yunji, Han Shirui, Yan Lulu, Lu Chaoxia, Luo Yang, Zhang Xue, Cao Lih |
Mutation screening of crystallin genes in Chinese families with congenital cataracts. Molecular vision 2019 9 25 427-437. Zhuang Jianfu, Cao Zongfu, Zhu Yihua, Liu Lijuan, Tong Yi, Chen Xiaole, Wang Yaduan, Lu Cailing, Ma Xu, Yang Juh |
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 |
Common variants in SOX-2 and congenital cataract genes contribute to age-related nuclear cataract.
Communications biology 2020 Dec 3 (1): 755. Yonova-Doing Ekaterina, Zhao Wanting, Igo Robert P, Wang Chaolong, Sundaresan Periasamy, Lee Kristine E, Jun Gyungah R, Alves Alexessander Couto, Chai Xiaoran, Chan Anita S Y, Lee Mei Chin, Fong Allan, Tan Ava G, Khor Chiea Chuen, Chew Emily Y, Hysi Pirro G, Fan Qiao, Chua Jacqueline, Chung Jaeyoon, Liao Jiemin, Colijn Johanna M, Burdon Kathryn P, Fritsche Lars G, Swift Maria K, Hilmy Maryam H, Chee Miao Ling, Tedja Milly, Bonnemaijer Pieter W M, Gupta Preeti, Tan Queenie S, Li Zheng, Vithana Eranga N, Ravindran Ravilla D, Chee Soon-Phaik, Shi Yuan, Liu Wenting, Su Xinyi, Sim Xueling, Shen Yang, Wang Ya Xing, Li Hengtong, Tham Yih-Chung, Teo Yik Ying, Aung Tin, Small Kerrin S, Mitchell Paul, Jonas Jost B, Wong Tien Yin, Fletcher Astrid E, Klaver Caroline C W, Klein Barbara E K, Wang Jie Jin, Iyengar Sudha K, Hammond Christopher J, Cheng Ching- |
A functional polymorphism in the promoter of ?A-crystallin increases the risk of nAMD. International journal of clinical and experimental pathology 2019 12 (5): 1782-1787. Xu Hui, Piao Zhenyu, Ma Xiaoyun, Huang Lvzhen, Zhou Peng, Yu Wenzhen, Xu Qiong, Zhao Mingw |
Deciphering the association of intronic single nucleotide polymorphisms of crystallin gene family with congenital cataract. Indian journal of ophthalmology 2021 Aug 69 (8): 2064-2070. Nair Vidya, Sankaranarayanan Rajkumar, Vasavada Abhay Raghuka |
Polymorphisms in CRYAA Promoter with Susceptibility to Cataract: A Meta-Analysis. Seminars in ophthalmology 2021 5 36 (5-6): 429-436. Yu Hongtao, Liu Kaifeng, Lu Peiro |
Crystalline gene mutations in Turkish children with congenital cataracts. International ophthalmology 2021 4 41 (8): 2847-2852. Karahan Mine, Demirta? At?l?m Arma?an, Erdem Seyfettin, Ava Sedat, Teke? Selahattin, Keklikçi U? |
Association of single nucleotide polymorphism variations in CRYAA and CRYAB genes with congenital cataract in Pakistani population. Saudi journal of biological sciences 2022 5 29 (4): 2727-2732. Jarwar Priya, Waryah Yar Muhammad, Rafiq Muhammad, Waryah Ali Muhamm |
Association between single nucleotide polymorphisms in exon 3 of the alpha-A-crystallin gene and susceptibility to age-related cataract. Ophthalmic genetics 2022 11 1-6. Zhao Zhennan, Chen Jiahui, Yuan Wenyi, Jiang Yongxiang, Lu |
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 |
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- Page last updated:Apr 22, 2024
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