(Q41487082)

English

Evidence to suggest that expression of MITF induces melanocyte differentiation and haploinsufficiency of MITF causes Waardenburg syndrome type 2A.

scientific article published on February 1997

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scholarly article

1 reference

Europe PubMed Central

1 October 2017

1 reference

Europe PubMed Central

Evidence to suggest that expression of MITF induces melanocyte differentiation and haploinsufficiency of MITF causes Waardenburg syndrome type 2A. (English)

1 reference

Europe PubMed Central

1 October 2017

haploinsufficiency

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author name string

M Tachibana

1

1 reference

Europe PubMed Central

1 October 2017

publication date

1 February 1997

1 reference

Europe PubMed Central

1 October 2017

Pigment Cell & Melanoma Research

1 reference

Europe PubMed Central

1 October 2017

10

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Europe PubMed Central

1 October 2017

1-2

1 reference

Europe PubMed Central

1 October 2017

25-33

1 reference

Europe PubMed Central

1 October 2017

An exonic mutation in the HuP2 paired domain gene causes Waardenburg's syndrome

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0749.1997.TB00462.X

21 January 2018

Induction of pigmentation in mouse fibroblasts by expression of human tyrosinase cDNA

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0749.1997.TB00462.X

21 January 2018

A helix-loop-helix protein related to the immunoglobulin E box-binding proteins

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0749.1997.TB00462.X

21 January 2018

Involvement of the 'leucine zipper' region in the oligomerization and transforming activity of human c-myc protein.

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0749.1997.TB00462.X

21 January 2018

Expression of a single transfected cDNA converts fibroblasts to myoblasts

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0749.1997.TB00462.X

21 January 2018

Mutation of the endothelin-3 gene in the Waardenburg-Hirschsprung disease (Shah-Waardenburg syndrome)

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0749.1997.TB00462.X

21 January 2018

Recognition by Max of its cognate DNA through a dimeric b/HLH/Z domain

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0749.1997.TB00462.X

21 January 2018

Mammalian achaete-scute homolog 1 is required for the early development of olfactory and autonomic neurons

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0749.1997.TB00462.X

21 January 2018

A homozygous mutation in the endothelin-3 gene associated with a combined Waardenburg type 2 and Hirschsprung phenotype (Shah-Waardenburg syndrome)

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0749.1997.TB00462.X

21 January 2018

Waardenburg syndrome type II: phenotypic findings and diagnostic criteria

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0749.1997.TB00462.X

21 January 2018

Molecular control of myogenesis: antagonism between growth and differentiation

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0749.1997.TB00462.X

21 January 2018

Rapid and sensitive detection of point mutations and DNA polymorphisms using the polymerase chain reaction

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0749.1997.TB00462.X

21 January 2018

A missense mutation of the endothelin-B receptor gene in multigenic Hirschsprung's disease

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0749.1997.TB00462.X

21 January 2018

DNA sequencing with chain-terminating inhibitors

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0749.1997.TB00462.X

21 January 2018

Ectopic expression of MITF, a gene for Waardenburg syndrome type 2, converts fibroblasts to cells with melanocyte characteristics

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0749.1997.TB00462.X

21 January 2018

Waardenburg syndrome type 2 caused by mutations in the human microphthalmia (MITF) gene.

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0749.1997.TB00462.X

21 January 2018

Waardenburg's syndrome patients have mutations in the human homologue of the Pax-3 paired box gene

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0749.1997.TB00462.X

21 January 2018

ADD1: a novel helix-loop-helix transcription factor associated with adipocyte determination and differentiation

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0749.1997.TB00462.X

21 January 2018

Expression of a mouse tyrosinase cDNA in 3T3 Swiss mouse fibroblasts

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0749.1997.TB00462.X

21 January 2018

TFEC, a basic helix-loop-helix protein, forms heterodimers with TFE3 and inhibits TFE3-dependent transcription activation

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0749.1997.TB00462.X

21 January 2018

Identifiers

10.1111/J.1600-0749.1997.TB00462.X

1 reference

Europe PubMed Central

1 October 2017

1 reference

Europe PubMed Central

1 October 2017

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