Microphthalamia-associated transcription factor: a critical regulator of pigment cell development and survival. (Q35146535)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12789278%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

review article

1 reference

title

Microphthalamia-associated transcription factor: a critical regulator of pigment cell development and survival (English)

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4 November 2019

1

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4 November 2019

2

David E Fisher

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4 November 2019

language of work or name

English

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publication date

1 May 2003

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4 November 2019

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12789278%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

volume

22

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4 November 2019

issue

20

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4 November 2019

page(s)

3035-3041

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https://scigraph.springernature.com/pub.10.1038/sj.onc.1206443

4 November 2019

exact match

0 references

cites work

Mutation of the MITF gene in albinism-deafness syndrome (Tietz syndrome).

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206443

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206443

Melanocyte-specific expression of the human tyrosinase promoter: activation by the microphthalmia gene product and role of the initiator.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206443

Microphthalmia gene product as a signal transducer in cAMP-induced differentiation of melanocytes

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206443

Regulation of tyrosinase gene expression by cAMP in B16 melanoma cells involves two CATGTG motifs surrounding the TATA box: implication of the microphthalmia gene product

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206443

Different cis-acting elements are involved in the regulation of TRP1 and TRP2 promoter activities by cyclic AMP: pivotal role of M boxes (GTCATGTGCT) and of microphthalmia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206443

Kit/stem cell factor receptor-induced activation of phosphatidylinositol 3'-kinase is essential for male fertility

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206443

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206443

Ras mediates the cAMP-dependent activation of extracellular signal-regulated kinases (ERKs) in melanocytes

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206443

Mutations at the W locus affect survival of neural crest-derived melanocytes in the mouse.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206443

The gene encoding the T-box factor Tbx2 is a target for the microphthalmia-associated transcription factor in melanocytes

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206443

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206443

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206443

Mutation of the KIT (mast/stem cell growth factor receptor) protooncogene in human piebaldism

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206443

Curbing the nuclear activities of beta-catenin. Control over Wnt target gene expression

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206443

Mutations at the mouse microphthalmia locus are associated with defects in a gene encoding a novel basic-helix-loop-helix-zipper protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206443

Transcription factors in melanocyte development: distinct roles for Pax-3 and Mitf.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206443

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206443

Wnt signalling required for expansion of neural crest and CNS progenitors.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206443

Signalling mechanisms of endothelin-induced mitogenesis and melanogenesis in human melanocytes

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206443

Genetic and biochemical evidence that haploinsufficiency of the Nf1 tumor suppressor gene modulates melanocyte and mast cell fates in vivo

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206443

Senescence bypass screen identifies TBX2, which represses Cdkn2a (p19(ARF)) and is amplified in a subset of human breast cancers.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206443

Wnt and BMP signaling govern lineage segregation of melanocytes in the avian embryo

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206443

Microphthalmia transcription factor. A sensitive and specific melanocyte marker for MelanomaDiagnosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206443

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206443

A mouse model for vitiligo.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206443

Positive and negative elements regulate a melanocyte-specific promoter

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206443

EDNRB/EDN3 and Hirschsprung disease type II.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206443

Bcl2 regulation by the melanocyte master regulator Mitf modulates lineage survival and melanoma cell viability

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206443

Mutant laboratory mice with abnormalities in pigmentation: annotated tables

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206443

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206443

Targeted disruption of Bcl-2 alpha beta in mice: occurrence of gray hair, polycystic kidney disease, and lymphocytopenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206443

SOX10 mutations in patients with Waardenburg-Hirschsprung disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206443

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206443

Sensorineural deafness and pigmentation genes: melanocytes and the Mitf transcriptional network

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206443

Lineage-specific signaling in melanocytes. C-kit stimulation recruits p300/CBP to microphthalmia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206443

alpha-Melanocyte-stimulating hormone signaling regulates expression of microphthalmia, a gene deficient in Waardenburg syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206443

Frequent nuclear/cytoplasmic localization of beta-catenin without exon 3 mutations in malignant melanoma

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206443

Stabilization of beta-catenin by genetic defects in melanoma cell lines

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206443

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206443

The INK4a/ARF network in tumour suppression

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206443

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206443

The temporal requirement for endothelin receptor-B signalling during neural crest development

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206443

Tietz syndrome (hypopigmentation/deafness) caused by mutation of MITF

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206443

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206443

Mitf and Tfe3, two members of the Mitf-Tfe family of bHLH-Zip transcription factors, have important but functionally redundant roles in osteoclast development

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206443

MITF: a stream flowing for pigment cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206443

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206443

Ser298 of MITF, a mutation site in Waardenburg syndrome type 2, is a phosphorylation site with functional significance

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206443

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206443

The mutational spectrum in Waardenburg syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206443

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206443

TCF transcription factors, mediators of Wnt-signaling in development and cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206443

Bcl-2-deficient mice demonstrate fulminant lymphoid apoptosis, polycystic kidneys, and hypopigmented hair

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206443

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206443

Epistatic relationship between Waardenburg syndrome genes MITF and PAX3

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206443

Age-resolving osteopetrosis: a rat model implicating microphthalmia and the related transcription factor TFE3.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206443

Linkage of M-CSF signaling to Mitf, TFE3, and the osteoclast defect in Mitf(mi/mi) mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206443

Mechanisms of Wnt signaling in development

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206443

Melanocyte-stimulating hormone promotes activation of pre-existing tyrosinase molecules in Cloudman S91 melanoma cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206443

Regulation of microphthalmia-associated transcription factor MITF protein levels by association with the ubiquitin-conjugating enzyme hUBC9

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206443

A frizzled homolog functions in a vertebrate Wnt signaling pathway

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206443

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206443

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206443

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206443

MAP kinase links the transcription factor Microphthalmia to c-Kit signalling in melanocytes

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206443

microphthalmia, a critical factor in melanocyte development, defines a discrete transcription factor family

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206443