Development and degeneration of dorsal root ganglia in the absence of the HMG-domain transcription factor Sox10 (Q57911328)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11731238%20AND%20SRC:MED&resulttype=core&format=json

4 December 2019

title

Development and degeneration of dorsal root ganglia in the absence of the HMG-domain transcription factor Sox10 (English)

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4 December 2019

5

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4 December 2019

Dieter Riethmacher

6

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4 December 2019

author name string

E Sonnenberg-Riethmacher

1

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4 December 2019

M Miehe

2

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4 December 2019

C C Stolt

3

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4 December 2019

D E Goerich

4

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4 December 2019

publication date

1 December 2001

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Mechanisms of Development

4 December 2019

published in

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4 December 2019

volume

109

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4 December 2019

issue

2

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4 December 2019

page(s)

253-265

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Glial growth factor-2 promotes the survival, migration and bromodeoxyuridine incorporation of mammalian neural crest cells in caudal neural tube explant cultures.

4 December 2019

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The ErbB2 and ErbB3 receptors and their ligand, neuregulin-1, are essential for development of the sympathetic nervous system

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

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The dominant-white spotting (W) locus of the mouse encodes the c-kit proto-oncogene

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7 January 2021

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

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7 January 2021

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

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7 January 2021

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

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A homozygous mutation in the endothelin-3 gene associated with a combined Waardenburg type 2 and Hirschsprung phenotype (Shah-Waardenburg syndrome)

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7 January 2021

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

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7 January 2021

Xsox17alpha and -beta mediate endoderm formation in Xenopus

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7 January 2021

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

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7 January 2021

Cadherin-6 expression transiently delineates specific rhombomeres, other neural tube subdivisions, and neural crest subpopulations in mouse embryos

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7 January 2021

Myelin deficiencies in both the central and the peripheral nervous systems associated with a SOX10 mutation

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7 January 2021

Early death of neural crest cells is responsible for total enteric aganglionosis in Sox10(Dom)/Sox10(Dom) mouse embryos

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7 January 2021

Sox10, a novel transcriptional modulator in glial cells

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7 January 2021

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7 January 2021

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7 January 2021

Rescue of the cardiac defect in ErbB2 mutant mice reveals essential roles of ErbB2 in peripheral nervous system development

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

Cloning of MITF, the human homolog of the mouse microphthalmia gene and assignment to chromosome 3p14.1-p12.3.

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7 January 2021

Waardenburg's syndrome patients have mutations in the human homologue of the Pax-3 paired box gene

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7 January 2021

Neurological phenotype in Waardenburg syndrome type 4 correlates with novel SOX10 truncating mutations and expression in developing brain

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7 January 2021

The SRF and MCM1 transcription factors

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7 January 2021

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

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7 January 2021

From head to toes: the multiple facets of Sox proteins

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7 January 2021

Identification of a ligand for the c-kit proto-oncogene

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7 January 2021

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7 January 2021

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Identifiers

DOI

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11731238%20AND%20SRC:MED&resulttype=core&format=json

4 December 2019

1 reference