A new mutation of the Atoh1 gene in mice with normal life span allows analysis of inner ear and cerebellar phenotype in aging.
about
Neurog1 can partially substitute for Atoh1 function in hair cell differentiation and maintenance during organ of Corti developmentThe quest for restoring hearing: Understanding ear development more completely.Opportunities and limits of the one gene approach: the ability of Atoh1 to differentiate and maintain hair cells depends on the molecular contextIncomplete and delayed Sox2 deletion defines residual ear neurosensory development and maintenanceMolecular cloning and functional characterisation of chicken Atonal homologue 1: a comparison with human Atoh1.
P2860
A new mutation of the Atoh1 gene in mice with normal life span allows analysis of inner ear and cerebellar phenotype in aging.
description
2013 nî lūn-bûn
@nan
2013 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
2013 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
2013年の論文
@ja
2013年論文
@yue
2013年論文
@zh-hant
2013年論文
@zh-hk
2013年論文
@zh-mo
2013年論文
@zh-tw
2013年论文
@wuu
name
A new mutation of the Atoh1 ge ...... cerebellar phenotype in aging.
@ast
A new mutation of the Atoh1 ge ...... cerebellar phenotype in aging.
@en
type
label
A new mutation of the Atoh1 ge ...... cerebellar phenotype in aging.
@ast
A new mutation of the Atoh1 ge ...... cerebellar phenotype in aging.
@en
prefLabel
A new mutation of the Atoh1 ge ...... cerebellar phenotype in aging.
@ast
A new mutation of the Atoh1 ge ...... cerebellar phenotype in aging.
@en
P2093
P2860
P1433
P1476
A new mutation of the Atoh1 ge ...... cerebellar phenotype in aging.
@en
P2093
Casey Nava
Kianoush Sheykholeslami
Qing Yin Zheng
Sheng Li Li
Shuqing Liu
Tihua Zheng
Vikrum Thimmappa
Zhaoqiang Zhang
P2860
P304
P356
10.1371/JOURNAL.PONE.0079791
P407
P50
P577
2013-11-12T00:00:00Z