Melanocyte-specific microphthalmia-associated transcription factor isoform activates its own gene promoter through physical interaction with lymphoid-enhancing factor 1. (Q44016906)

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scientific article published on 4 June 2002

Language	Label	Description	Also known as
English	Melanocyte-specific microphthalmia-associated transcription factor isoform activates its own gene promoter through physical interaction with lymphoid-enhancing factor 1.	scientific article published on 4 June 2002

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

29 November 2017

Melanocyte-specific microphthalmia-associated transcription factor isoform activates its own gene promoter through physical interaction with lymphoid-enhancing factor 1. (English)

1 reference

Europe PubMed Central

PubMed publication ID

29 November 2017

Kazuhiro Takahashi

4

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29 November 2017

author name string

Hideo Saito

1

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Europe PubMed Central

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29 November 2017

Ken-Ichi Yasumoto

2

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Europe PubMed Central

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29 November 2017

Kazuhisa Takeda

3

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Europe PubMed Central

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29 November 2017

Atsushi Fukuzaki

5

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Europe PubMed Central

PubMed publication ID

29 November 2017

Seiichi Orikasa

6

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Europe PubMed Central

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29 November 2017

Shigeki Shibahara

7

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Europe PubMed Central

PubMed publication ID

29 November 2017

language of work or name

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publication date

4 June 2002

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29 November 2017

Journal of Biological Chemistry

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PubMed publication ID

29 November 2017

277

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29 November 2017

32

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29 November 2017

28787-28794

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29 November 2017

MITF: a stream flowing for pigment cells

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M203719200

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M203719200

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M203719200

21 January 2018

SOX10 mutations in patients with Waardenburg-Hirschsprung disease

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M203719200

21 January 2018

A gene for Waardenburg syndrome type 2 maps close to the human homologue of the microphthalmia gene at chromosome 3p12-p14.1.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M203719200

21 January 2018

A natural classification of the basic helix-loop-helix class of transcription factors

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M203719200

21 January 2018

Identification of a novel isoform of microphthalmia-associated transcription factor that is enriched in retinal pigment epithelium

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M203719200

21 January 2018

Role of Mitf in differentiation and transdifferentiation of chicken pigmented epithelial cell

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M203719200

21 January 2018

Molecular cloning of cDNA encoding a novel microphthalmia-associated transcription factor isoform with a distinct amino-terminus

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M203719200

21 January 2018

Structural organization of the human microphthalmia-associated transcription factor gene containing four alternative promoters.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M203719200

21 January 2018

Mitf-D, a newly identified isoform, expressed in the retinal pigment epithelium and monocyte-lineage cells affected by Mitf mutations.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M203719200

21 January 2018

Isoforms of mi transcription factor preferentially expressed in cultured mast cells of mice

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M203719200

21 January 2018

Identification of a melanocyte-type promoter of the microphthalmia-associated transcription factor gene

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M203719200

21 January 2018

Microphthalmia-associated transcription factor interacts with LEF-1, a mediator of Wnt signaling

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M203719200

21 January 2018

Wnt signaling: a common theme in animal development

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M203719200

21 January 2018

Control of neural crest cell fate by the Wnt signalling pathway.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M203719200

21 January 2018

Neural crest-directed gene transfer demonstrates Wnt1 role in melanocyte expansion and differentiation during mouse development.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M203719200

21 January 2018

Induction of melanocyte-specific microphthalmia-associated transcription factor by Wnt-3a.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M203719200

21 January 2018

Microphthalmia-associated transcription factor (MITF): multiplicity in structure, function, and regulation

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M203719200

21 January 2018

Microphthalmia-associated transcription factor as a regulator for melanocyte-specific transcription of the human tyrosinase gene

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M203719200

21 January 2018

A thymus-specific member of the HMG protein family regulates the human T cell receptor C alpha enhancer

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M203719200

21 January 2018

Functional interaction of beta-catenin with the transcription factor LEF-1

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M203719200

21 January 2018

XTcf-3 transcription factor mediates beta-catenin-induced axis formation in Xenopus embryos

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M203719200

21 January 2018

Identification of a distal enhancer for the melanocyte-specific promoter of the MITF gene.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M203719200

21 January 2018

Molecular basis of mouse microphthalmia (mi) mutations helps explain their developmental and phenotypic consequences.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M203719200

21 January 2018

Functional analysis of microphthalmia-associated transcription factor in pigment cell-specific transcription of the human tyrosinase family genes

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M203719200

21 January 2018

Rapid detection of octamer binding proteins with 'mini-extracts', prepared from a small number of cells

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M203719200

21 January 2018

Assembly and function of a TCR alpha enhancer complex is dependent on LEF-1-induced DNA bending and multiple protein-protein interactions

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M203719200

21 January 2018

Regulation of LEF-1/TCF transcription factors by Wnt and other signals

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M203719200

21 January 2018

Mutations in microphthalmia, the mouse homolog of the human deafness gene MITF, affect neuroepithelial and neural crest-derived melanocytes differently.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M203719200

21 January 2018

Inhibitory effect of the transcription factor encoded by the mutant mi microphthalmia allele on transactivation of mouse mast cell protease 7 gene

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M203719200

21 January 2018

Epistatic relationship between Waardenburg syndrome genes MITF and PAX3

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M203719200

21 January 2018

Interaction among SOX10, PAX3 and MITF, three genes altered in Waardenburg syndrome

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M203719200

21 January 2018

Direct regulation of the Microphthalmia promoter by Sox10 links Waardenburg-Shah syndrome (WS4)-associated hypopigmentation and deafness to WS2.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M203719200

21 January 2018

Transcription factor hierarchy in Waardenburg syndrome: regulation of MITF expression by SOX10 and PAX3

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M203719200

21 January 2018

Regulation of the microphthalmia-associated transcription factor gene by the Waardenburg syndrome type 4 gene, SOX10.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M203719200

21 January 2018

A mouse model for vitiligo.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M203719200

21 January 2018

An L1 element intronic insertion in the black-eyed white (Mitf[mi-bw]) gene: the loss of a single Mitf isoform responsible for the pigmentary defect and inner ear deafness

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M203719200

21 January 2018

Dysgenesis of melanocytes and cochlear dysfunction in mutant microphthalmia (mi) mice

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M203719200

21 January 2018

An HMG-box-containing T-cell factor required for thymocyte differentiation.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M203719200

21 January 2018

Identifiers

10.1074/JBC.M203719200

1 reference

Europe PubMed Central

PubMed publication ID

29 November 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

29 November 2017

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