Advances in genetic hearing loss: CIB2 gene
Author:
Funder
NCN
NCBiR
Publisher
Springer Science and Business Media LLC
Subject
General Medicine,Otorhinolaryngology
Link
http://link.springer.com/content/pdf/10.1007/s00405-016-4330-9.pdf
Reference43 articles.
1. World Health Organisation (2014) 2014, February; Available from: http://www.who.int/mediacentre/factsheets/fs300/en/
2. Tucci D, Merson MH, Wilson BS (2010) A summary of the literature on global hearing impairment: current status and priorities for action. Otol Neurotol 31(1):31–41
3. Mills JH, Going JA (1982) Review of environmental factors affecting hearing. Environ Health Perspect 44:119–127
4. Shearer AE et al (2011) Deafness in the genomics era. Hear Res 282(1–2):1–9
5. Riazuddin S et al (2012) Alterations of the CIB2 calcium- and integrin-binding protein cause Usher syndrome type 1 J and nonsyndromic deafness DFNB48. Nat Genet 44(11):1265–1271
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1. CIB2 mediates acquired gefitinib resistance by inducing ZEB1 expression and epithelial-mesenchymal transition;Aging;2024-09-10
2. Usher syndrome proteins ADGRV1 (USH2C) and CIB2 (USH1J) interact and share a common interactome containing TRiC/CCT-BBS chaperonins;Frontiers in Cell and Developmental Biology;2023-06-22
3. CIB2 Is a Novel Endogenous Repressor of Atrial Remodeling;Circulation;2023-06-06
4. Compound heterozygous variants in SPNS2 cause sensorineural hearing loss;European Journal of Medical Genetics;2023-01
5. Calcium- and Integrin-Binding Protein 2 (CIB2) in Physiology and Disease: Bright and Dark Sides;International Journal of Molecular Sciences;2022-03-24
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