(Q34694810)

4 August 2017

Interspecies difference in the regulation of melanocyte development by SOX10 and MITF. (English)

1 reference

4 August 2017

Ling Hou

1

0 references

William J Pavan

object named as

William J Pavan

series ordinal

3

0 references

author name string

Heinz Arnheiter

series ordinal

2

1 reference

PubMed ID

16757562

4 August 2017

language of work or name

English

0 references

publication date

6 June 2006

1 reference

Proceedings of the National Academy of Sciences of the United States of America

4 August 2017

5

1 reference

based on heuristic

inferred from page(s)

published in

1 reference

4 August 2017

103

1 reference

4 August 2017

24

1 reference

4 August 2017

9081-9085

1 reference

Genetic evidence does not support direct regulation of EDNRB by SOX10 in migratory neural crest and the melanocyte lineage

4 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1482569

MITF and cell proliferation: the role of alternative splice forms

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1482569

Sumoylation modulates transcriptional activity of MITF in a promoter-specific manner

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1482569

Melanocyte stem cell maintenance and hair graying

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1482569

Secrets to a healthy Sox life: lessons for melanocytes

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1482569

Molecular mechanism for distinct neurological phenotypes conveyed by allelic truncating mutations

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1482569

The color loci of mice--a genetic century

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1482569

Transcriptional regulatory networks in Saccharomyces cerevisiae

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1482569

Artificial chromosome transgenesis in pigmentary research.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1482569

How the zebrafish gets its stripes

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1482569

The transcription factor Sox10 is a key regulator of peripheral glial development.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1482569

Signaling and transcriptional regulation in the neural crest-derived melanocyte lineage: interactions between KIT and MITF

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1482569

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

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1482569

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

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1482569

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

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1482569

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

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1482569

Mitf from neural crest to melanoma: signal transduction and transcription in the melanocyte lineage.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1482569

Development of a flexible and specific gene delivery system for production of murine tumor models

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1482569

nacre encodes a zebrafish microphthalmia-related protein that regulates neural-crest-derived pigment cell fate

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1482569

HIRA, a mammalian homologue of Saccharomyces cerevisiae transcriptional co-repressors, interacts with Pax3

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1482569

Mutation of the Sry-related Sox10 gene in Dominant megacolon, a mouse model for human Hirschsprung disease

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1482569

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

7 July 2018

2 references

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1482569

7 July 2018

https://api.crossref.org/works/10.1073%2FPNAS.0603114103

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://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1482569

SOX10 mutations in patients with Waardenburg-Hirschsprung disease

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1482569

Sox10 mutation disrupts neural crest development in Dom Hirschsprung mouse model

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1482569

Melanocyte development in vivo and in neural crest cell cultures: crucial dependence on the Mitf basic-helix-loop-helix-zipper transcription factor

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1482569

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

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1482569

TRP-2/DT, a new early melanoblast marker, shows that steel growth factor (c-kit ligand) is a survival factor

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1482569

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

7 July 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0603114103

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0603114103

Analysis of SOX10 function in neural crest-derived melanocyte development: SOX10-dependent transcriptional control of dopachrome tautomerase

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0603114103

Transcriptional regulation of mitfa accounts for the sox10 requirement in zebrafish melanophore development.

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0603114103

Molecular characterization of melanocyte stem cells in their niche.

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0603114103

Complementation of melanocyte development in SOX10 mutant neural crest using lineage-directed gene transfer.

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0603114103

Cell-autonomous and cell non-autonomous signaling through endothelin receptor B during melanocyte development

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0603114103

Tyrosinase gene expression in zebrafish embryos

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0603114103

Generation of RCAS vectors useful for functional genomic analyses.

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0603114103

Neural crest progenitors of the melanocyte lineage: coat colour patterns revisited

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1482569

Zebrafish colourless encodes sox10 and specifies non-ectomesenchymal neural crest fates.

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1482569

The ret oncogene can induce melanogenesis and melanocyte development in Wv/Wv mice

26 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/16757562

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1073/PNAS.0603114103

1 reference

release_fj7adp5it5gwxejtska5rlnoeu

4 August 2017

0 references

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/fj7adp5it5gwxejtska5rlnoeu

mapped directly with Wikidata item

24 November 2022

based on heuristic

PMCID

1482569

1 reference

4 August 2017

1 reference

PubMed ID

16757562