(Q28295089)

2

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M Halushka

3

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P A Lapchak

4

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A Chakravarti

https://scigraph.springernature.com/pub.10.1038/ng1196-341

5

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language of work or name

English

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publication date

November 1996

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published in

Nature Genetics

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volume

14

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page(s)

341-4

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issue

3

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exact match

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cites work

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Defects in enteric innervation and kidney development in mice lacking GDNF

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

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

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

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

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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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Developing motor neurons rescued from programmed and axotomy-induced cell death by GDNF

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The gene coding for glial cell line derived neurotrophic factor (GDNF) maps to chromosome 5p12-p13.1

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GDNF-induced activation of the ret protein tyrosine kinase is mediated by GDNFR-alpha, a novel receptor for GDNF

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A comprehensive genetic map of the human genome based on 5,264 microsatellites

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

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

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RET mutations in human disease

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GDNF is an age-specific survival factor for sensory and autonomic neurons

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In vivo neurotrophic effects of GDNF on neonatal and adult facial motor neurons

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Embryonic expression of glial cell-line derived neurotrophic factor (GDNF) suggests multiple developmental roles in neural differentiation and epithelial-mesenchymal interactions

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GDNF signalling through the Ret receptor tyrosine kinase

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Characterization of a multicomponent receptor for GDNF.

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Functional receptor for GDNF encoded by the c-ret proto-oncogene

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Genetic analysis of autoimmune disease

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Fibroblast-growth-factor receptor mutations in human skeletal disorders

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Mutation analysis of the RET receptor tyrosine kinase in Hirschsprung disease

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Diversity of RET proto-oncogene mutations in familial and sporadic Hirschsprung disease

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Heterogeneity and low detection rate of RET mutations in Hirschsprung disease

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7 January 2021

Diverse phenotypes associated with exon 10 mutations of the RET proto-oncogene.

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Intercellular signalling. The pros and cons of c-ret

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A gene for Hirschsprung disease (megacolon) in the pericentromeric region of human chromosome 10.

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A gene for Hirschsprung disease maps to the proximal long arm of chromosome 10.

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Identity-by-descent and association mapping of a recessive gene for Hirschsprung disease on human chromosome 13q22

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GDNF: a glial cell line-derived neurotrophic factor for midbrain dopaminergic neurons

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Therapeutic potentials for glial cell line-derived neurotrophic factor (GDNF) based upon pharmacological activities in the CNS.

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GDNF: a potent survival factor for motoneurons present in peripheral nerve and muscle

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7 January 2021

Glial cell line-derived neurotrophic factor (GDNF), a new neurotrophic factor for motoneurones.

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7 January 2021

The TGF-beta superfamily: new members, new receptors, and new genetic tests of function in different organisms

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7 January 2021

Human glial cell line-derived neurotrophic factor (GDNF) maps to chromosome 5

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Structural and functional properties of the TRK family of neurotrophin receptors

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Identifiers

DOI

10.1038/NG1196-341

1 reference

Consolidated OpenCitations Corpus – April 2017

3569041

3569041

1 reference

Consolidated OpenCitations Corpus – April 2017

Consolidated OpenCitations Corpus – April 2017

1 reference