The chromatin remodeling protein CHD7, mutated in CHARGE syndrome, is necessary for proper craniofacial and tracheal development (Q34163062)

31 July 2017

title

The chromatin remodeling protein CHD7, mutated in CHARGE syndrome, is necessary for proper craniofacial and tracheal development (English)

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31 July 2017

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Ethan D Sperry

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31 July 2017

Elizabeth A Hurd

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31 July 2017

Mark A Durham

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31 July 2017

Elyse N Reamer

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31 July 2017

Adam B Stein

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31 July 2017

Donna M Martin

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31 July 2017

language of work or name

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10 July 2014

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31 July 2017

published in

Developmental Dynamics

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31 July 2017

volume

243

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31 July 2017

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31 July 2017

page(s)

1055-1066

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describes a project that uses

31 July 2017

ImageJ

1 reference

11 June 2022

https://www.ebi.ac.uk/europepmc/webservices/rest/PMC4160830/fullTextXML

inferred from PubMed Central ID database lookup

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Delayed fusion and altered gene expression contribute to semicircular canal defects in Chd7 deficient mice

5 July 2018

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Mature middle and inner ears express Chd7 and exhibit distinctive pathologies in a mouse model of CHARGE syndrome

5 July 2018

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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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5 July 2018

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5 July 2018

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5 July 2018

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5 July 2018

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5 July 2018

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5 July 2018

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21 January 2018

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21 January 2018

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A histone lysine methyltransferase activated by non-canonical Wnt signalling suppresses PPAR-gamma transactivation

21 January 2018

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Family history and clefting as major criteria for CHARGE syndrome

28 October 2018

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21 January 2018

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28 October 2018

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12 December 2020

The Risk of Olfactory Disturbance from Conchal Plate Injury during Ethmoidectomy

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12 December 2020

The CHARGE association in a newborn infant

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12 December 2020

Defects in vestibular sensory epithelia and innervation in mice with loss ofChd7 function: Implications for human CHARGE syndrome

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12 December 2020

Clinical manifestations of airway malacia in young children

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Abnormal basiocciput development in CHARGE syndrome

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12 December 2020

Identifiers

DOI

10.1002/DVDY.24156

1 reference

31 July 2017

1 reference

31 July 2017

1 reference