Otitis media in a new mouse model for CHARGE syndrome with a deletion in the Chd7 gene (Q27304810)

2

0 references

Bin Yang

3

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Fengchan Han

4

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Ye Zheng

5

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Cynthia F Bartels

6

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Deborah Schelling

7

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James E Arnold

8

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Peter C Scacheri

9

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Qing Yin Zheng

Creative Commons Attribution 4.0 International

10

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language of work or name

English

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publication date

2012

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published in

PLOS One

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volume

7

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issue

4

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page(s)

e34944

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copyright license

start time

23 April 2012

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

describes a project that uses

ImageJ

1 reference

Europe PubMed Central

11 June 2022

https://www.ebi.ac.uk/europepmc/webservices/rest/PMC3335168/fullTextXML

inferred from PubMed Central ID database lookup

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Defects in neural stem cell proliferation and olfaction in Chd7 deficient mice indicate a mechanism for hyposmia in human CHARGE syndrome

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Mutations in CHD7 in patients with CHARGE syndrome cause T-B + natural killer cell + severe combined immune deficiency and may cause Omenn-like syndrome

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Spectrum of CHD7 mutations in 110 individuals with CHARGE syndrome and genotype-phenotype correlation

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CHD7 targets active gene enhancer elements to modulate ES cell-specific gene expression

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