(Q62937938)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17701983%20AND%20SRC:MED&resulttype=core&format=json

3 January 2020

title

Defects in vestibular sensory epithelia and innervation in mice with loss of Chd7 function: implications for human CHARGE syndrome (English)

1 reference

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3 January 2020

1 reference

Yehoash Raphael

5

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17701983%20AND%20SRC:MED&resulttype=core&format=json

3 January 2020

Meredith E Adams

1

1 reference

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3 January 2020

Elizabeth A Hurd

2

1 reference

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3 January 2020

Lisa A Beyer

3

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17701983%20AND%20SRC:MED&resulttype=core&format=json

3 January 2020

Donald L Swiderski

4

1 reference

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3 January 2020

Donna M Martin

6

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3 January 2020

language of work or name

English

0 references

publication date

1 October 2007

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17701983%20AND%20SRC:MED&resulttype=core&format=json

The Journal of Comparative Neurology

3 January 2020

published in

1 reference

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3 January 2020

volume

504

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3 January 2020

issue

5

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3 January 2020

page(s)

519-532

1 reference

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Vestibular anomalies in CHARGE syndrome: investigations on and consequences for postural development.

3 January 2020

cites work

1 reference

7 January 2021

Temporal bone anomaly proposed as a major criteria for diagnosis of CHARGE syndrome

1 reference

7 January 2021

It's a knockout! Male infertility and neuropathology.

1 reference

7 January 2021

Phenotypic spectrum of CHARGE syndrome with CHD7 mutations.

1 reference

7 January 2021

From placode to polarization: new tunes in inner ear development

1 reference

7 January 2021

Neurofilament antibodies and spiral ganglion neurons of the mammalian cochlea

1 reference

7 January 2021

Hair cells in the inner ear of the pirouette and shaker 2 mutant mice

1 reference

7 January 2021

Multiple mutations in mouse Chd7 provide models for CHARGE syndrome

1 reference

7 January 2021

Cranial nerve abnormalities in CHARGE association

1 reference

7 January 2021

The development of semicircular canals in the inner ear: role of FGFs in sensory cristae

1 reference

7 January 2021

Molecular mechanisms underlying inner ear patterning defects in kreisler mutants

1 reference

7 January 2021

Development of location-specific hair cell stereocilia in denervated embryonic ears

1 reference

7 January 2021

EphB2 guides axons at the midline and is necessary for normal vestibular function

1 reference

7 January 2021

Circling behavior in theEcl mouse is caused by lateral semicircular canal defects

1 reference

7 January 2021

Immunocytochemical localization of neurofilament subunits in the spiral ganglion of normal and neomycin-treated guinea pigs

1 reference

7 January 2021

Comparative morphology of rodent vestibular periphery. II. Cristae ampullares

1 reference

7 January 2021

Comparative morphology of rodent vestibular periphery. I. Saccular and utricular maculae

1 reference

7 January 2021

Cell fate specification in the inner ear.

1 reference

7 January 2021

Neurotrophins in the ear: their roles in sensory neuron survival and fiber guidance

1 reference

7 January 2021

Mutant mice reveal the molecular and cellular basis for specific sensory connections to inner ear epithelia and primary nuclei of the brain

1 reference

7 January 2021

Morphophysiological and ultrastructural studies in the mammalian cristae ampullares

1 reference

7 January 2021

The winged helix transcription factor Fkh10 is required for normal development of the inner ear.

1 reference

7 January 2021

Loss of Chd7 function in gene-trapped reporter mice is embryonic lethal and associated with severe defects in multiple developing tissues.

1 reference

7 January 2021

An epidemiological analysis of CHARGE syndrome: preliminary results from a Canadian study

1 reference

7 January 2021

Confirmation of CHD7 as a cause of CHARGE association identified by mapping a balanced chromosome translocation in affected monozygotic twins

1 reference

7 January 2021

CHARGE syndrome: the phenotypic spectrum of mutations in the CHD7 gene

1 reference

7 January 2021

CHARGE Association in newborns: a registry-based study

1 reference

7 January 2021

Sox2 is required for sensory organ development in the mammalian inner ear

1 reference

7 January 2021

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

1 reference

7 January 2021

Central nervous system malformations in the CHARGE association

1 reference

7 January 2021

Gbx2 is required for the morphogenesis of the mouse inner ear: a downstream candidate of hindbrain signaling

1 reference

7 January 2021

Descriptive and experimental analysis of the epithelial remodellings that control semicircular canal formation in the developing mouse inner ear

1 reference

7 January 2021

Distribution of cytokeratins in the vestibular epithelium of the guinea pig.

1 reference

7 January 2021

Mutation of the novel gene Tmie results in sensory cell defects in the inner ear of spinner, a mouse model of human hearing loss DFNB6

1 reference

7 January 2021

Development of the mouse inner ear and origin of its sensory organs.

1 reference

7 January 2021

Association of cadherin 23 with polygenic inheritance and genetic modification of sensorineural hearing loss

1 reference

7 January 2021

Expression and function of FGF10 in mammalian inner ear development

1 reference

7 January 2021

Foxg1 is required for morphogenesis and histogenesis of the mammalian inner ear

1 reference

7 January 2021

The nuclear receptor Nor-1 is essential for proliferation of the semicircular canals of the mouse inner ear

1 reference

7 January 2021

Abnormal vestibular control of gaze and posture in a strain of a waltzing rat

1 reference

7 January 2021

F-actin, tubulin and spectrin in the organ of Corti: comparative distribution in different cell types and mammalian species.

1 reference

7 January 2021

Phenotypic spectrum of CHARGE syndrome in fetuses with CHD7 truncating mutations correlates with expression during human development.

1 reference

7 January 2021

CHARGE syndrome: report of 47 cases and review

1 reference

7 January 2021

Retinoic acid repression of bone morphogenetic protein 4 in inner ear development

1 reference

7 January 2021

The mouse slalom mutant demonstrates a role for Jagged1 in neuroepithelial patterning in the organ of Corti

1 reference

7 January 2021

Updated diagnostic criteria for CHARGE syndrome: a proposal

1 reference

7 January 2021

Mutations in a new member of the chromodomain gene family cause CHARGE syndrome

1 reference

7 January 2021

Hmx2 and Hmx3 homeobox genes direct development of the murine inner ear and hypothalamus and can be functionally replaced by Drosophila Hmx

1 reference

7 January 2021

Characterization of the CHD family of proteins

1 reference

7 January 2021

Identifiers

DOI

10.1002/CNE.21460

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17701983%20AND%20SRC:MED&resulttype=core&format=json

3 January 2020

1 reference