ILDR 1 deficiency causes degeneration of cochlear outer hair cells and disrupts the structure of the organ of Corti : a mouse model for human DFNB 42
暂无分享,去创建一个
Huawei Li | Ruizhi Feng | Qing Sang | Yao Xu | Ronggui Qu | Li Jin | Lin He | Lei Wang | Zhigang Xu | Wen Li
[1] K. Steel,et al. CRISPR/Cas9-Induced Mutagenesis Corroborates the Role of Transportin-SR2 in HIV-1 Nuclear Import , 2014, Stem Cell Research & Therapy.
[2] Y. Bae,et al. Methionine sulfoxide reductase B3 deficiency causes hearing loss due to stereocilia degeneration and apoptotic cell death in cochlear hair cells. , 2014, Human molecular genetics.
[3] G. P. Sinha,et al. Tricellulin deficiency affects tight junction architecture and cochlear hair cells. , 2013, The Journal of clinical investigation.
[4] S. Roy,et al. Inner ear supporting cells protect hair cells by secreting HSP70. , 2013, The Journal of clinical investigation.
[5] Rashmi Chandra,et al. Immunoglobulin-like domain containing receptor 1 mediates fat-stimulated cholecystokinin secretion. , 2013, The Journal of clinical investigation.
[6] M. Furuse,et al. Analysis of the ‘angulin’ proteins LSR, ILDR1 and ILDR2 – tricellulin recruitment, epithelial barrier function and implication in deafness pathogenesis , 2013, Journal of Cell Science.
[7] L. Anelli,et al. A new recurrent chromosomal translocation t(3;11)(q13;q14) in myelodysplastic syndromes associated with overexpression of the ILDR1 gene. , 2012, Leukemia research.
[8] G. Zheng,et al. Cell-cell junctions: a target of acoustic overstimulation in the sensory epithelium of the cochlea , 2012, BMC Neuroscience.
[9] M. Giacomello,et al. Hair cells, plasma membrane Ca²⁺ ATPase and deafness. , 2012, The international journal of biochemistry & cell biology.
[10] P. Olmos,et al. Mitochondrial diabetes and deafness: possible dysfunction of strial marginal cells of the inner ear. , 2011, Journal of otolaryngology - head & neck surgery = Le Journal d'oto-rhino-laryngologie et de chirurgie cervico-faciale.
[11] Todd E. Scheetz,et al. Carcinoembryonic antigen-related cell adhesion molecule 16 interacts with α-tectorin and is mutated in autosomal dominant hearing loss (DFNA4) , 2011, Proceedings of the National Academy of Sciences.
[12] S. Leal,et al. Loss-of-function mutations of ILDR1 cause autosomal-recessive hearing impairment DFNB42. , 2011, American journal of human genetics.
[13] C. V. Van Itallie,et al. Physiology and function of the tight junction. , 2009, Cold Spring Harbor perspectives in biology.
[14] W. Kimberling,et al. The Coxsackievirus and Adenovirus Receptor: A new adhesion protein in cochlear development , 2006, Hearing Research.
[15] Edwin W Rubel,et al. Mechanisms of hair cell death and protection , 2005, Current opinion in otolaryngology & head and neck surgery.
[16] J. Delabie,et al. Characterization of a novel immunoglobulin-like domain containing receptor. , 2004, Biochemical and biophysical research communications.
[17] J. Ito,et al. Compartmentalization established by claudin-11-based tight junctions in stria vascularis is required for hearing through generation of endocochlear potential , 2004, Journal of Cell Science.
[18] R. D. Lynch,et al. The tight junction: a multifunctional complex. , 2004, American journal of physiology. Cell physiology.
[19] Yehoash Raphael,et al. Claudin 14 knockout mice, a model for autosomal recessive deafness DFNB29, are deaf due to cochlear hair cell degeneration. , 2003, Human molecular genetics.
[20] K. Willecke,et al. Targeted Ablation of Connexin26 in the Inner Ear Epithelial Gap Junction Network Causes Hearing Impairment and Cell Death , 2002, Current Biology.
[21] E. Stadtman,et al. Methionine sulfoxide reductase in antioxidant defense. , 1999, Methods in enzymology.