(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

issue

2

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13 February 2018

page(s)

84-92

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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

1 reference

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.

1 reference

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.

1 reference

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

1 reference

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

1 reference

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

1 reference

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

1 reference

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

7 January 2021

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

1 reference

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

7 January 2021

Social interaction and sensorimotor gating abnormalities in mice lacking Dvl1

1 reference

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