(Q24291495)

positive regulation of transcription by RNA polymerase II

GOA release 2020-03-11

1 reference

GOA release 2020-03-11

author name string

P Jacquemin

1

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V J Lannoy

2

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J O'Sullivan

3

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A Read

4

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F P Lemaigre

5

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G G Rousseau

Biochemical and Biophysical Research Communications

6

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language of work or name

English

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publication date

3 August 2001

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published in

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volume

285

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issue

5

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page(s)

1200-5

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cites work

Waardenburg syndrome type II: phenotypic findings and diagnostic criteria

1 reference

https://api.crossref.org/works/10.1006%2FBBRC.2001.5294

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1006%2FBBRC.2001.5294

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1006%2FBBRC.2001.5294

7 January 2021

Insight into the microphthalmia gene

1 reference

https://api.crossref.org/works/10.1006%2FBBRC.2001.5294

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1006%2FBBRC.2001.5294

7 January 2021

Mutations in the PAX3 gene causing Waardenburg syndrome type 1 and type 2

1 reference

https://api.crossref.org/works/10.1006%2FBBRC.2001.5294

7 January 2021

SOX10 mutations in patients with Waardenburg-Hirschsprung disease

1 reference

https://api.crossref.org/works/10.1006%2FBBRC.2001.5294

7 January 2021

Epistatic relationship between Waardenburg syndrome genes MITF and PAX3

1 reference

https://api.crossref.org/works/10.1006%2FBBRC.2001.5294

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1006%2FBBRC.2001.5294

7 January 2021

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/10.1006%2FBBRC.2001.5294

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/10.1006%2FBBRC.2001.5294

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1006%2FBBRC.2001.5294

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1006%2FBBRC.2001.5294

7 January 2021

A novel family of developmentally regulated mammalian transcription factors containing the TEA/ATTS DNA binding domain

1 reference

https://api.crossref.org/works/10.1006%2FBBRC.2001.5294

7 January 2021

Human TEF-5 is preferentially expressed in placenta and binds to multiple functional elements of the human chorionic somatomammotropin-B gene enhancer

1 reference

https://api.crossref.org/works/10.1006%2FBBRC.2001.5294

7 January 2021

Isoforms of hepatocyte nuclear factor-6 differ in DNA-binding properties, contain a bifunctional homeodomain, and define the new ONECUT class of homeodomain proteins

1 reference

https://api.crossref.org/works/10.1006%2FBBRC.2001.5294

7 January 2021

OC-2, a novel mammalian member of the ONECUT class of homeodomain transcription factors whose function in liver partially overlaps with that of hepatocyte nuclear factor-6

1 reference

https://api.crossref.org/works/10.1006%2FBBRC.2001.5294

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1006%2FBBRC.2001.5294

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/10.1006%2FBBRC.2001.5294

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/10.1006%2FBBRC.2001.5294

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1006%2FBBRC.2001.5294

7 January 2021

The mutational spectrum in Waardenburg syndrome.

1 reference

https://api.crossref.org/works/10.1006%2FBBRC.2001.5294

7 January 2021

Mutation of the endothelin-receptor B gene in Waardenburg-Hirschsprung disease

1 reference

https://api.crossref.org/works/10.1006%2FBBRC.2001.5294

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1006%2FBBRC.2001.5294

7 January 2021

https://api.crossref.org/works/10.1006%2FBBRC.2001.5294

1 reference

7 January 2021