Belyantseva I A相关文献与解析，生知库 | 链接生命科学的每一步

日期影响因子

Mutations of human TMHS cause recessively inherited non-syndromic hearing loss.

人类TMHS基因突变会导致隐性遗传的非综合征性听力损失

期刊:Journal of Medical Genetics

影响因子:3.7

doi:10.1136/jmg.2005.039834

Shabbir M I, Ahmed Z M, Khan S Y, Riazuddin Saima, Waryah A M, Khan S N, Camps R D, Ghosh M, Kabra M, Belyantseva I A, Friedman T B, Riazuddin Sheikh

发表日期：2006

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ATP-Induced Ca(2+) release in cochlear outer hair cells: localization of an inositol triphosphate-gated Ca(2+) store to the base of the sensory hair bundle

ATP诱导的耳蜗外毛细胞Ca(2+)释放：肌醇三磷酸门控Ca(2+)储存库定位于感觉毛束基部

期刊:Journal of Neuroscience

doi:10.1523/JNEUROSCI.19-16-06918.1999

Mammano, F; Frolenkov, G I; Lagostena, L; Belyantseva, I A; Kurc, M; Dodane, V; Colavita, A; Kachar, B

细胞生物学

发表日期：1999

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