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Cited by 318

The DOI matches its Crossref record; 2 of the 2 references it cites were found in a registry or an index.

NeuroD-null mice are deaf due to a severe loss of the inner ear sensory neurons during development

Open access
Kim, Woo-Young, Fritzsch, Bernd, Serls, Amanda, Bakel, Leigh Anne, Huang, Eric J., Reichardt, Louis F., Barth, Daniel S., Lee, Jacqueline E.·2001·Development

Abstract

A key factor in the genetically programmed development of the nervous system is the death of massive numbers of neurons. Therefore, genetic mechanisms governing cell survival are of fundamental importance to developmental neuroscience. We report that inner ear sensory neurons are dependent on a basic helix-loop-helix transcription factor called NeuroD for survival during differentiation. Mice lacking NeuroD protein exhibit no auditory evoked potentials, reflecting a profound deafness. DiI fiber staining, immunostaining and cell death assays reveal that the deafness is due to the failure of inner ear sensory neuron survival during development. The affected inner ear sensory neurons fail to express neurotrophin receptors, TrkB and TrkC, suggesting that the ability of NeuroD to support neuronal survival may be directly mediated through regulation of responsiveness to the neurotrophins.

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Crossref · 10.1242/dev.128.3.417

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Metadata

Authors
Kim, W.-Y., Fritzsch, B., Serls, A., Bakel, L. A., Huang, E. J., Reichardt, L. F., Barth, D. S., & Lee, J. E.
Venue
Development
Published
2001-02-01
Volume
128
Issue
3
Pages
417-426
ISSN
  • 0950-1991 (ISSN-L)
  • 1477-9129
OpenAlex
W2168944480
Cited by
318
References
2
FWCI
9.74
Type
journal article
Language
en
Open access
green

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