(Q34245273)

31 July 2017

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title

Sensorineural deafness and pigmentation genes: melanocytes and the Mitf transcriptional network (English)

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31 July 2017

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Price ER

1

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31 July 2017

Fisher DE

series ordinal

2

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31 July 2017

language of work or name

English

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publication date

1 April 2001

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31 July 2017

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31 July 2017

volume

30

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31 July 2017

issue

1

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31 July 2017

page(s)

15-18

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

31 July 2017

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2801%2900259-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2801%2900259-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2801%2900259-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2801%2900259-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2801%2900259-8

7 January 2021

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/10.1016%2FS0896-6273%2801%2900259-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2801%2900259-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2801%2900259-8

7 January 2021

https://api.crossref.org/works/10.1016%2FS0896-6273%2801%2900259-8

1 reference

7 January 2021

Inherited hearing defects in mice

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2801%2900259-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2801%2900259-8

7 January 2021

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/10.1016%2FS0896-6273%2801%2900259-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2801%2900259-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2801%2900259-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2801%2900259-8

7 January 2021

Epistatic relationship between Waardenburg syndrome genes MITF and PAX3

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2801%2900259-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2801%2900259-8

7 January 2021

10.1016/S0896-6273(01)00259-8

Identifiers

DOI

1 reference

31 July 2017

1 reference