(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)

1 reference

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

4 December 2019

5

1 reference

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

4 December 2019

Dieter Riethmacher

6

1 reference

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

4 December 2019

author name string

E Sonnenberg-Riethmacher

1

1 reference

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

4 December 2019

M Miehe

2

1 reference

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

4 December 2019

C C Stolt

3

1 reference

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

4 December 2019

D E Goerich

4

1 reference

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

4 December 2019

publication date

1 December 2001

1 reference

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

Mechanisms of Development

4 December 2019

published in

1 reference

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

4 December 2019

volume

109

1 reference

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

4 December 2019

issue

2

1 reference

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

4 December 2019

page(s)

253-265

1 reference

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

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

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2801%2900547-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2801%2900547-0

7 January 2021

Expression of the SOX10 gene during human development

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2801%2900547-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2801%2900547-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2801%2900547-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2801%2900547-0

7 January 2021

Neuregulin and ErbB receptor signaling pathways in the nervous system

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2801%2900547-0

7 January 2021

GFRalpha1 is an essential receptor component for GDNF in the developing nervous system and kidney

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2801%2900547-0

7 January 2021

Neu differentiation factor is a neuron-glia signal and regulates survival, proliferation, and maturation of rat Schwann cell precursors.

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2801%2900547-0

7 January 2021

In vitro clonal analysis of progenitor cell patterns in dorsal root and sympathetic ganglia of the quail embryo

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2801%2900547-0

7 January 2021

Mutations of the RET proto-oncogene in Hirschsprung's disease

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2801%2900547-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2801%2900547-0

7 January 2021

splotch (Sp2H), a mutation affecting development of the mouse neural tube, shows a deletion within the paired homeodomain of Pax-3

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2801%2900547-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2801%2900547-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2801%2900547-0

7 January 2021

Brn-3.0: a POU-domain protein expressed in the sensory, immune, and endocrine systems that functions on elements distinct from known octamer motifs

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2801%2900547-0

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

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2801%2900547-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2801%2900547-0

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

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2801%2900547-0

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/10.1016%2FS0925-4773%2801%2900547-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2801%2900547-0

7 January 2021

Xsox17alpha and -beta mediate endoderm formation in Xenopus

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2801%2900547-0

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.

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2801%2900547-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2801%2900547-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2801%2900547-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2801%2900547-0

7 January 2021

Sox10, a novel transcriptional modulator in glial cells

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2801%2900547-0

7 January 2021

Pax3 is required for enteric ganglia formation and functions with Sox10 to modulate expression of c-ret

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2801%2900547-0

7 January 2021

Requirement for neuregulin receptor erbB2 in neural and cardiac development

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2801%2900547-0

7 January 2021

Requirement for Brn-3.0 in differentiation and survival of sensory and motor neurons

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2801%2900547-0

7 January 2021

Multiple essential functions of neuregulin in development

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2801%2900547-0

7 January 2021

SoxD: an essential mediator of induction of anterior neural tissues in Xenopus embryos

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2801%2900547-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2801%2900547-0

7 January 2021

Sox1 directly regulates the gamma-crystallin genes and is essential for lens development in mice

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2801%2900547-0

7 January 2021

Sox genes find their feet

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2801%2900547-0

7 January 2021

SOX10 mutations in patients with Waardenburg-Hirschsprung disease

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2801%2900547-0

7 January 2021

A missense mutation of the endothelin-B receptor gene in multigenic Hirschsprung's disease

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2801%2900547-0

7 January 2021

The SOX10/Sox10 gene from human and mouse: sequence, expression, and transactivation by the encoded HMG domain transcription factor

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2801%2900547-0

7 January 2021

Severe neuropathies in mice with targeted mutations in the ErbB3 receptor

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2801%2900547-0

7 January 2021

Point mutations affecting the tyrosine kinase domain of the RET proto-oncogene in Hirschsprung's disease

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2801%2900547-0

7 January 2021

Renal agenesis and the absence of enteric neurons in mice lacking GDNF

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2801%2900547-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2801%2900547-0

7 January 2021

Defects in the kidney and enteric nervous system of mice lacking the tyrosine kinase receptor Ret

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2801%2900547-0

7 January 2021

Developmental potentialities of cells derived from the truncal neural crest in clonal cultures

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2801%2900547-0

7 January 2021

A gene from the human sex-determining region encodes a protein with homology to a conserved DNA-binding motif

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2801%2900547-0

7 January 2021

Sox10 mutation disrupts neural crest development in Dom Hirschsprung mouse model

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2801%2900547-0

7 January 2021

A Schwann cell antigen recognized by monoclonal antibody 217c is the rat low-affinity nerve growth factor receptor

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2801%2900547-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2801%2900547-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2801%2900547-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2801%2900547-0

7 January 2021

The SRF and MCM1 transcription factors

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2801%2900547-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2801%2900547-0

7 January 2021

From head to toes: the multiple facets of Sox proteins

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2801%2900547-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2801%2900547-0

7 January 2021

Peripheral nervous system defects in erbB2 mutants following genetic rescue of heart development.

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2801%2900547-0

7 January 2021

10.1016/S0925-4773(01)00547-0

Identifiers

DOI

1 reference

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