Mouse Dach2 mutants do not exhibit gross defects in eye development or brain function. (Q48654275)

13 February 2018

title

Mouse Dach2 mutants do not exhibit gross defects in eye development or brain function. (English)

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13 February 2018

author name string

Richard J Davis

1

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13 February 2018

Yakov I Pesah

2

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13 February 2018

Mark Harding

3

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13 February 2018

Richard Paylor

4

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13 February 2018

Graeme Mardon

5

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13 February 2018

publication date

1 February 2006

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13 February 2018

published in

Genesis

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13 February 2018

volume

44

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13 February 2018

page(s)

84-92

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13 February 2018

issue

2

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13 February 2018

DACH: genomic characterization, evaluation as a candidate for postaxial polydactyly type A2, and developmental expression pattern of the mouse homologue

cites work

1 reference

https://api.crossref.org/works/10.1002%2FGENE.20188

7 January 2021

Targeted disruption of mouse Dach1 results in postnatal lethality

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https://api.crossref.org/works/10.1002%2FGENE.20188

7 January 2021

Mutation analysis of two candidate genes for premature ovarian failure, DACH2 and POF1B.

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https://api.crossref.org/works/10.1002%2FGENE.20188

7 January 2021

The T-box transcription factor gene TBX22 is mutated in X-linked cleft palate and ankyloglossia.

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https://api.crossref.org/works/10.1002%2FGENE.20188

7 January 2021

Craniofacial expression of human and murine TBX22 correlates with the cleft palate and ankyloglossia phenotype observed in CPX patients.

1 reference

https://api.crossref.org/works/10.1002%2FGENE.20188

7 January 2021

Dachshund and eyes absent proteins form a complex and function synergistically to induce ectopic eye development in Drosophila

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https://api.crossref.org/works/10.1002%2FGENE.20188

7 January 2021

A proposed test battery and constellations of specific behavioral paradigms to investigate the behavioral phenotypes of transgenic and knockout mice

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https://api.crossref.org/works/10.1002%2FGENE.20188

7 January 2021

Physical fine mapping of the choroideremia locus using Xq21 deletions associated with complex syndromes.

1 reference

https://api.crossref.org/works/10.1002%2FGENE.20188

7 January 2021

Mouse Dach, a homologue of Drosophila dachshund, is expressed in the developing retina, brain and limbs.

1 reference

https://api.crossref.org/works/10.1002%2FGENE.20188

7 January 2021

Dach1 mutant mice bear no gross abnormalities in eye, limb, and brain development and exhibit postnatal lethality

1 reference

https://api.crossref.org/works/10.1002%2FGENE.20188

7 January 2021

Characterization of mouse Dach2, a homologue of Drosophila dachshund

1 reference

https://api.crossref.org/works/10.1002%2FGENE.20188

7 January 2021

Association between X-linked mixed deafness and mutations in the POU domain gene POU3F4

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https://api.crossref.org/works/10.1002%2FGENE.20188

7 January 2021

Impaired conditioned fear and enhanced long-term potentiation in Fmr2 knock-out mice

1 reference

https://api.crossref.org/works/10.1002%2FGENE.20188

7 January 2021

Mammalian and Drosophila dachshund genes are related to the Ski proto-oncogene and are expressed in eye and limb

1 reference

https://api.crossref.org/works/10.1002%2FGENE.20188

7 January 2021

Synergistic regulation of vertebrate muscle development by Dach2, Eya2, and Six1, homologs of genes required for Drosophila eye formation

1 reference

https://api.crossref.org/works/10.1002%2FGENE.20188

7 January 2021

Dach1, a vertebrate homologue of Drosophila dachshund, is expressed in the developing eye and ear of both chick and mouse and is regulated independently of Pax and Eya genes

1 reference

https://api.crossref.org/works/10.1002%2FGENE.20188

7 January 2021

X-linked mixed deafness (DFN3): cloning and characterization of the critical region allows the identification of novel microdeletions.

1 reference

https://api.crossref.org/works/10.1002%2FGENE.20188

7 January 2021

Localization of the human homologue of the Drosophila dachshund gene (DACH) to chromosome 13q21

1 reference

https://api.crossref.org/works/10.1002%2FGENE.20188

7 January 2021

Molecular cloning and expression of the human and mouse homologues of the Drosophila dachshund gene

1 reference

https://api.crossref.org/works/10.1002%2FGENE.20188

7 January 2021

Six3 repression of Wnt signaling in the anterior neuroectoderm is essential for vertebrate forebrain development

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https://api.crossref.org/works/10.1002%2FGENE.20188

7 January 2021

Efficient in vivo manipulation of mouse genomic sequences at the zygote stage

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7 January 2021

Social interaction and sensorimotor gating abnormalities in mice lacking Dvl1

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https://api.crossref.org/works/10.1002%2FGENE.20188

7 January 2021

Choroideremia gene testing

1 reference

https://api.crossref.org/works/10.1002%2FGENE.20188

7 January 2021

TBX22 mutations are a frequent cause of cleft palate

1 reference

https://api.crossref.org/works/10.1002%2FGENE.20188

7 January 2021

Molecular analysis of four males with mental retardation and deletions of Xq21 places the putative MR region in Xq21.1 between DXS233 and CHM.

1 reference

https://api.crossref.org/works/10.1002%2FGENE.20188

7 January 2021

The use of behavioral test batteries: effects of training history.

1 reference

https://api.crossref.org/works/10.1002%2FGENE.20188

7 January 2021

An Fgf8 mutant allelic series generated by Cre- and Flp-mediated recombination

1 reference

https://api.crossref.org/works/10.1002%2FGENE.20188

7 January 2021

Independent roles of the dachshund and eyes absent genes in BMP signaling, axon pathfinding and neuronal specification.

1 reference

https://api.crossref.org/works/10.1002%2FGENE.20188

7 January 2021

Learning impairments and motor dysfunctions in adult Lhx5-deficient mice displaying hippocampal disorganization

1 reference

https://api.crossref.org/works/10.1002%2FGENE.20188

7 January 2021

The eye-specification proteins So and Eya form a complex and regulate multiple steps in Drosophila eye development

1 reference

https://api.crossref.org/works/10.1002%2FGENE.20188

7 January 2021

Most X;autosome translocations associated with premature ovarian failure do not interrupt X-linked genes.

1 reference

https://api.crossref.org/works/10.1002%2FGENE.20188

7 January 2021

Eleven X chromosome breakpoints associated with premature ovarian failure (POF) map to a 15-Mb YAC contig spanning Xq21.

1 reference

https://api.crossref.org/works/10.1002%2FGENE.20188

7 January 2021

Genes and translocations involved in POF.

1 reference

https://api.crossref.org/works/10.1002%2FGENE.20188

7 January 2021

Structure-function analysis of the Drosophila retinal determination protein Dachshund

1 reference

https://api.crossref.org/works/10.1002%2FGENE.20188

7 January 2021

Mutation spectrum in the CHM gene of Danish and Swedish choroideremia patients

1 reference

https://api.crossref.org/works/10.1002%2FGENE.20188

7 January 2021

Identifiers

DOI

10.1002/GENE.20188

1 reference

13 February 2018

PubMed ID

16470613

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13 February 2018