Unconventional Myosins, the Basis for Deafness in Mouse and Man
Author:
Publisher
Elsevier BV
Subject
Genetics (clinical),Genetics
Reference27 articles.
1. Mutation profile of all 49 exons of the human myosin VIIA gene, and haplotype analysis, of Usher IB families from diverse origins;Adato;Am J Hum Genet,1997
2. Characterization of unconventional MYO6, the human homologue of the gene responsible for deafness in Snell's waltzer mice;Avraham;Hum Mol Genet,1997
3. The mouse Snell's waltzer deafness gene encodes an unconventional myosin required for structural integrity of inner hair cells;Avraham;Nat Genet,1995
4. Close linkage of the olfactory marker protein gene to the mouse deafness mutation shaker-1;Brown;Genomics,1992
5. Molecular cloning and domain structure of human myosin-VIIa, the gene product defective in Usher syndrome 1B;Chen;Genomics,1996
Cited by 34 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Muscle;Kelley and Firestein's Textbook of Rheumatology;2017
2. The collagen receptor DDR1 co-localizes with the non-muscle myosin IIA in mice inner ear and contributes to the cytoarchitecture and stability of motile cells;Cell and Tissue Research;2014-10-12
3. Myosin 6 Is Required for Iris Development and Normal Function of the Outer Retina;Investigative Opthalmology & Visual Science;2013-11-01
4. Muscle;Kelley's Textbook of Rheumatology;2013
5. Sensing sound: molecules that orchestrate mechanotransduction by hair cells;Trends in Neurosciences;2012-04
1.学者识别学者识别
2.学术分析学术分析
3.人才评估人才评估
"同舟云学术"是以全球学者为主线，采集、加工和组织学术论文而形成的新型学术文献查询和分析系统，可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容，当前同舟云学术共收录了国内外主流学术期刊6万余种，收集的期刊论文及会议论文总量共计约1.5亿篇，并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询！咨询电话：010-8811{复制后删除}0370
www.globalauthorid.com
TOP
Copyright © 2019-2024 北京同舟云网络信息技术有限公司 京公网安备11010802033243号 京ICP备18003416号-3