Human Genome Epidemiology Literature Finder
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Records 1 - 9 (of 9 Records) |
| Query Trace: Disease and CRYAB[original query] |
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| [Alpha]B-crystallin genotype has impact on the multiple sclerosis phenotype. Neurology 2003 Nov 61 (9): 1245-9. van Veen T, van Winsen L, Crusius J B A, Kalkers N F, Barkhof F, Peña A S, Polman C H, Uitdehaag B M |
| Desmin accumulation restrictive cardiomyopathy and atrioventricular block associated with desmin gene defects. European journal of heart failure 2005 12 8 (5): 477-83. Arbustini Eloisa, Pasotti Michele, Pilotto Andrea, Pellegrini Carlo, Grasso Maurizia, Previtali Stefano, Repetto Alessandra, Bellini Ornella, Azan Gaetano, Scaffino Manuela, Campana Carlo, Piccolo Giovanni, Viganò Mario, Tavazzi Lui |
| Genetic variation in healthy oldest-old. PloS one 2009 4 (8): e6641. Halaschek-Wiener Julius, Amirabbasi-Beik Mahsa, Monfared Nasim, Pieczyk Markus, Sailer Christian, Kollar Anita, Thomas Ruth, Agalaridis Georgios, Yamada So, Oliveira Lisa, Collins Jennifer A, Meneilly Graydon, Marra Marco A, Madden Kenneth M, Le Nhu D, Connors Joseph M, Brooks-Wilson Angela |
| 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 |
| High proportion of genetic cases in patients with advanced cardiomyopathy including a novel homozygous Plakophilin 2-gene mutation. PloS one 2017 12 12 (12): e0189489. Klauke Baerbel, Gaertner-Rommel Anna, Schulz Uwe, Kassner Astrid, Zu Knyphausen Edzard, Laser Thorsten, Kececioglu Deniz, Paluszkiewicz Lech, Blanz Ute, Sandica Eugen, van den Bogaerdt Antoon J, van Tintelen J Peter, Gummert Jan, Milting Hendr |
| 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 |
| 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 |
| Rare Genetic Variants Associated With Myocardial Fibrosis: Multi-Ethnic Study of Atherosclerosis. Frontiers in cardiovascular medicine 2022 3 9 804788. Shabani Mahsima, Dutta Diptavo, Ambale-Venkatesh Bharath, Post Wendy S, Taylor Kent D, Rich Stephen S, Wu Colin O, Pereira Naveen L, Shah Sanjiv J, Chatterjee Nilanjan, Rotter Jerome I, Arking Dan E, Lima Joao A |
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