(Q38304102)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17334657%20AND%20SRC:MED&resulttype=core&format=json

26 December 2019

title

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

1 reference

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26 December 2019

2

1 reference

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26 December 2019

author name string

Elizabeth A Hurd

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17334657%20AND%20SRC:MED&resulttype=core&format=json

26 December 2019

Marsha N Blauwkamp

3

1 reference

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26 December 2019

Meredith E Adams

4

1 reference

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26 December 2019

Yehoash Raphael

5

1 reference

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26 December 2019

Heather K Poucher

6

1 reference

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26 December 2019

Donna M Martin

7

1 reference

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26 December 2019

publication date

28 February 2007

1 reference

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26 December 2019

number of pages

11

1 reference

inferred from page(s)

published in

Mammalian Genome

1 reference

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26 December 2019

volume

18

1 reference

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26 December 2019

issue

2

1 reference

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26 December 2019

page(s)

94-104

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https://scigraph.springernature.com/pub.10.1007/s00335-006-0107-6

26 December 2019

exact match

0 references

cites work

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

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS00335-006-0107-6

Construction of a bifunctional mRNA in the mouse by using the internal ribosomal entry site of the encephalomyocarditis virus

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS00335-006-0107-6

Congenital malformations of the inner ear: a classification based on embryogenesis

21 January 2018

1 reference

12 December 2020

Growth failure and pituitary function in CHARGE and VATER associations

1 reference

12 December 2020

Dosage requirement of Pitx2 for development of multiple organs

1 reference

12 December 2020

Heterozygosity mapping of partially congenic lines: mapping of a semidominant neurological mutation, Wheels (Whl), on mouse chromosome 4.

1 reference

12 December 2020

The SANT domain: a unique histone-tail-binding module?

1 reference

12 December 2020

ATP-dependent nucleosome remodeling complexes: enzymes tailored to deal with chromatin

1 reference

12 December 2020

ATP-dependent nucleosome remodeling

1 reference

12 December 2020

Choanal atresia and associated multiple anomalies

1 reference

12 December 2020

Two new mouse mutants with vestibular defects that map to the highly mutable locus on chromosome 4.

1 reference

12 December 2020

Systematic identification of novel protein domain families associated with nuclear functions

1 reference

12 December 2020

Mutation of the SNF2 family member Chd2 affects mouse development and survival

1 reference

12 December 2020

Chd1 chromodomain links histone H3 methylation with SAGA- and SLIK-dependent acetylation

1 reference

12 December 2020

CHARGE syndrome includes hypogonadotropic hypogonadism and abnormal olfactory bulb development

1 reference

12 December 2020

ENU mutagenesis reveals a highly mutable locus on mouse Chromosome 4 that affects ear morphogenesis

1 reference

12 December 2020

Pitx2 distinguishes subtypes of terminally differentiated neurons in the developing mouse neuroepithelium

1 reference

12 December 2020

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

1 reference

12 December 2020

Gene trap mutagenesis in embryonic stem cells.

1 reference

12 December 2020

Nestin-Cre mediated deletion of Pitx2 in the mouse.

1 reference

12 December 2020

Multiple mutations in mouse Chd7 provide models for CHARGE syndrome

1 reference

12 December 2020

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

1 reference

12 December 2020

The Wheels mutation in the mouse causes vascular, hindbrain, and inner ear defects.

1 reference

12 December 2020

Mutagenesis and behavioral screening for altered circadian activity identifies the mouse mutant, Wheels

1 reference

12 December 2020

The Drosophila kismet gene is related to chromatin-remodeling factors and is required for both segmentation and segment identity.

1 reference

12 December 2020

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

1 reference

12 December 2020

CHARGE syndrome: report of 47 cases and review

1 reference

12 December 2020

Epidemiology of choanal atresia with special reference to the CHARGE association

1 reference

12 December 2020

Characterization and functional analysis of CReMM, a novel chromodomain helicase DNA-binding protein

1 reference

12 December 2020

Death before birth: clues from gene knockouts and mutations

1 reference

12 December 2020

Chromatin remodeling by ATP-dependent molecular machines.

1 reference

12 December 2020

Phenotypic spectrum of CHARGE syndrome with CHD7 mutations.

1 reference

12 December 2020

Insertional mutagenesis by retroviruses and promoter traps in embryonic stem cells

1 reference

12 December 2020

Identification and validation of PDGF transcriptional targets by microarray-coupled gene-trap mutagenesis.

1 reference

12 December 2020

Influence of PAX6 gene dosage on development: overexpression causes severe eye abnormalities.

1 reference

12 December 2020

Congenital aplasia of the semicircular canals

1 reference

12 December 2020

ATP-dependent nucleosome remodelling: factors and functions

1 reference

12 December 2020

Characterization of a new mouse mutant, flouncer, with a balance defect and inner ear malformation

1 reference

12 December 2020

Cooperation between complexes that regulate chromatin structure and transcription

1 reference

12 December 2020

Characterization of the CHD family of proteins

1 reference

12 December 2020

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

1 reference

12 December 2020

ATP-dependent chromatin remodeling

1 reference

12 December 2020

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

1 reference

12 December 2020

CHARGE Association in newborns: a registry-based study

1 reference

12 December 2020

10.1007/S00335-006-0107-6

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17334657%20AND%20SRC:MED&resulttype=core&format=json

26 December 2019

1 reference