(Q30530459)

12 August 2017

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

1 reference

12 August 2017

1 reference

Herbarth B

1

1 reference

12 August 2017

Pingault V

2

1 reference

12 August 2017

Bondurand N

3

1 reference

12 August 2017

Kuhlbrodt K

4

1 reference

12 August 2017

Hermans-Borgmeyer I

5

1 reference

12 August 2017

Puliti A

6

1 reference

12 August 2017

Lemort N

7

1 reference

12 August 2017

Goossens M

8

1 reference

12 August 2017

Wegner M

9

1 reference

12 August 2017

language of work or name

English

0 references

publication date

1 April 1998

1 reference

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

12 August 2017

1 reference

12 August 2017

95

1 reference

12 August 2017

9

1 reference

12 August 2017

5161-5165

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Sox10 mutation disrupts neural crest development in Dom Hirschsprung mouse model

12 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=20231

Sox10, a novel transcriptional modulator in glial cells

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=20231

Mutations in Hirschsprung disease: when does a mutation contribute to the phenotype

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=20231

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=20231

Cellular and molecular biology of neural crest cell lineage determination

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=20231

Sox genes find their feet

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=20231

Genes and lineages in the formation of the enteric nervous system

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=20231

Human homology and candidate genes for the Dominant megacolon locus, a mouse model of Hirschsprung disease

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=20231

SOX genes: architects of development.

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=20231

Defects in cardiac outflow tract formation and pro-B-lymphocyte expansion in mice lacking Sox-4

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=20231

Interaction of endothelin-3 with endothelin-B receptor is essential for development of epidermal melanocytes and enteric neurons

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=20231

Targeted and natural (piebald-lethal) mutations of endothelin-B receptor gene produce megacolon associated with spotted coat color in mice

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=20231

Autosomal sex reversal and campomelic dysplasia are caused by mutations in and around the SRY-related gene SOX9

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=20231

Campomelic dysplasia and autosomal sex reversal caused by mutations in an SRY-related gene

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=20231

Requirement for neuregulin receptor erbB2 in neural and cardiac development

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=20231

Multiple essential functions of neuregulin in development

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=20231

Association of megacolon with a new dominant spotting gene (Dom) in the mouse

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=20231

Development of the peripheral nervous system from the neural crest

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=20231

A gene mapping to the sex-determining region of the mouse Y chromosome is a member of a novel family of embryonically expressed genes

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=20231

A genetic study of Hirschsprung disease

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=20231

Expression of a candidate sex-determining gene during mouse testis differentiation.

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=20231

Yeast artificial chromosome libraries containing large inserts from mouse and human DNA

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=20231

Genomic analysis using a yeast artificial chromosome library with mouse DNA inserts

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=20231

Construction of a mouse yeast artificial chromosome library in a recombination-deficient strain of yeast

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=20231

A somatic cell hybrid panel for mouse gene mapping characterized by PCR and FISH

20 June 2018

1 reference

https://pubmed.ncbi.nlm.nih.gov/9560246

12 December 2020

A high-resolution genetic map of mouse chromosome 15 encompassing the Dominant megacolon (Dom) locus

1 reference

https://pubmed.ncbi.nlm.nih.gov/9560246

12 December 2020

Association of Megacolon with Two Recessive Spotting Genes in the Mouse

1 reference

https://pubmed.ncbi.nlm.nih.gov/9560246

12 December 2020

Contributions of placodal and neural crest cells to avian cranial peripheral ganglia

1 reference

https://pubmed.ncbi.nlm.nih.gov/9560246

12 December 2020

Two rhombomeres are altered in Hoxa-1 mutant mice

1 reference

https://pubmed.ncbi.nlm.nih.gov/9560246

12 December 2020

Identifiers

DOI

10.1073/PNAS.95.9.5161

1 reference

12 August 2017

0 references

1 reference

12 August 2017

PubMed publication ID

9560246

1 reference