Loss of Chd7 function in gene-trapped reporter mice is embryonic lethal and associated with severe defects in multiple developing tissues. (Q38304102)

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scientific article published on 28 February 2007

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English	Loss of Chd7 function in gene-trapped reporter mice is embryonic lethal and associated with severe defects in multiple developing tissues.	scientific article published on 28 February 2007

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Europe PubMed Central

PubMed publication ID

17334657

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

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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)

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Europe PubMed Central

PubMed publication ID

17334657

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

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26 December 2019

author

Patrice L Capers

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2

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Europe PubMed Central

PubMed publication ID

17334657

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26 December 2019

author name string

Elizabeth A Hurd

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1

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PubMed publication ID

17334657

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26 December 2019

Marsha N Blauwkamp

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3

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17334657

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26 December 2019

Meredith E Adams

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4

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17334657

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26 December 2019

Yehoash Raphael

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5

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PubMed publication ID

17334657

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26 December 2019

Heather K Poucher

series ordinal

6

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PubMed publication ID

17334657

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26 December 2019

Donna M Martin

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7

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PubMed publication ID

17334657

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26 December 2019

publication date

28 February 2007

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PubMed publication ID

17334657

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26 December 2019

number of pages

11

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published in

Mammalian Genome

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Europe PubMed Central

PubMed publication ID

17334657

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26 December 2019

volume

18

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Europe PubMed Central

PubMed publication ID

17334657

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

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26 December 2019

issue

2

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Europe PubMed Central

PubMed publication ID

17334657

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26 December 2019

page(s)

94-104

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Europe PubMed Central

PubMed publication ID

17334657

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26 December 2019

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

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

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

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12 December 2020

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

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CHARGE syndrome includes hypogonadotropic hypogonadism and abnormal olfactory bulb development

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

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

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

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Gene trap mutagenesis in embryonic stem cells.

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Nestin-Cre mediated deletion of Pitx2 in the mouse

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Multiple mutations in mouse Chd7 provide models for CHARGE syndrome

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

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

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

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

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

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CHARGE syndrome: report of 47 cases and review

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Epidemiology of choanal atresia with special reference to the CHARGE association

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/17334657

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

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Death before birth: clues from gene knockouts and mutations

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Chromatin remodeling by ATP-dependent molecular machines.

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Phenotypic spectrum of CHARGE syndrome with CHD7 mutations

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12 December 2020

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Insertional mutagenesis by retroviruses and promoter traps in embryonic stem cells

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

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

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Congenital aplasia of the semicircular canals

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ATP-dependent nucleosome remodelling: factors and functions

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

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Cooperation between complexes that regulate chromatin structure and transcription

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Characterization of the CHD family of proteins

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

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PubMed

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

ATP-dependent chromatin remodeling

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17334657

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17334657

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12 December 2020

based on heuristic

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CHARGE Association in newborns: a registry-based study

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17334657

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

DOI

10.1007/S00335-006-0107-6

1 reference

stated in

Europe PubMed Central

PubMed publication ID

17334657

reference URL

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

retrieved

26 December 2019

PubMed publication ID

17334657

1 reference

stated in

Europe PubMed Central

PubMed publication ID

17334657

reference URL

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

retrieved

26 December 2019

 

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