The RET proto-oncogene: a challenge to our understanding of disease pathogenesis (Q41350370)

29 September 2017

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title

The RET proto-oncogene: a challenge to our understanding of disease pathogenesis (English)

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29 September 2017

T Kusafuka

1

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29 September 2017

P Puri

series ordinal

2

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29 September 2017

publication date

1 January 1997

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Pediatric Surgery International

29 September 2017

published in

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29 September 2017

volume

12

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29 September 2017

issue

1

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29 September 2017

page(s)

11-18

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https://scigraph.springernature.com/pub.10.1007/bf01194794

29 September 2017

exact match

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cites work

Activation of a novel human transforming gene, ret, by DNA rearrangement

1 reference

https://api.crossref.org/works/10.1007%2FBF01194794

Exon structure and flanking intronic sequences of the human RET proto-oncogene

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF01194794

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF01194794

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF01194794

GDNF signalling through the Ret receptor tyrosine kinase

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF01194794

Characterization of a multicomponent receptor for GDNF.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF01194794

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF01194794

Protection and repair of the nigrostriatal dopaminergic system by GDNF in vivo

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF01194794

Mesencephalic dopaminergic neurons protected by GDNF from axotomy-induced degeneration in the adult brain

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF01194794

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF01194794

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF01194794

A new oncogene in human thyroid papillary carcinomas and their lymph-nodal metastases

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF01194794

PTC is a novel rearranged form of the ret proto-oncogene and is frequently detected in vivo in human thyroid papillary carcinomas

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF01194794

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF01194794

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF01194794

Germ-line mutations of the RET proto-oncogene in multiple endocrine neoplasia type 2A.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF01194794

Single missense mutation in the tyrosine kinase catalytic domain of the RET protooncogene is associated with multiple endocrine neoplasia type 2B

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF01194794

Familial Hirschsprung's disease: report of autosomal dominant and probable recessive X-linked kindreds

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF01194794

Genetic aspects of multiple endocrine neoplasia

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF01194794

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF01194794

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF01194794

Defects in enteric innervation and kidney development in mice lacking GDNF

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF01194794

Renal and neuronal abnormalities in mice lacking GDNF

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF01194794

Ret protein in the human fetal rectum.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF01194794

Postmigratory neural crest cells expressing c-RET display restricted developmental and proliferative capacities

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF01194794

Glial growth factor restricts mammalian neural crest stem cells to a glial fate

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF01194794

Isolation of a stem cell for neurons and glia from the mammalian neural crest

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF01194794

Close linkage with the RET protooncogene and boundaries of deletion mutations in autosomal dominant Hirschsprung disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF01194794

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF01194794

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF01194794

Mutations of the endothelin-B receptor and endothelin-3 genes in Hirschsprung's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF01194794

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF01194794

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF01194794

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF01194794

Exclusion of linkage between RET and neuronal intestinal dysplasia type B

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF01194794

Loss of function effect of RET mutations causing Hirschsprung disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF01194794

Characterization of an inversion on the long arm of chromosome 10 juxtaposing D10S170 and RET and creating the oncogenic sequence RET/PTC.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF01194794

Molecular characterization of a thyroid tumor-specific transforming sequence formed by the fusion of ret tyrosine kinase and the regulatory subunit RI alpha of cyclic AMP-dependent protein kinase A

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF01194794

A t(10;17) translocation creates the RET/PTC2 chimeric transforming sequence in papillary thyroid carcinoma

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF01194794

Familial medullary thyroid carcinoma and multiple endocrine neoplasia type 2B map to the same region of chromosome 10 as multiple endocrine neoplasia type 2A

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF01194794

Catalytic specificity of protein-tyrosine kinases is critical for selective signalling

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF01194794

Total colonic aganglionosis associated with interstitial deletion of the long arm of chromosome 10

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF01194794

A linked genetic marker for multiple endocrine neoplasia type 2A on chromosome 10

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF01194794

A mutation in the RET proto-oncogene associated with multiple endocrine neoplasia type 2B and sporadic medullary thyroid carcinoma

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF01194794

Assignment of multiple endocrine neoplasia type 2A to chromosome 10 by linkage

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF01194794

Specific mutations of the RET proto-oncogene are related to disease phenotype in MEN 2A and FMTC

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF01194794

Ret oncogene activation in human thyroid neoplasms is restricted to the papillary cancer subtype.

21 January 2018

1 reference

12 December 2020

Familial Hirschsprung's disease--a report of 22 affected siblings in four families

1 reference

12 December 2020

The origin of intrinsic ganglia of trunk viscera from vagal neural crest in the chick embryo

1 reference

12 December 2020

Genotype‐phenotype correlation in multiple endocrine neoplasia type 2: report of the International RET Mutation Consortium

1 reference

12 December 2020

Altered RET gene mRNA expression in Hirschsprung's disease

1 reference

12 December 2020

Mechanism of activation of the ret proto-oncogene by multiple endocrine neoplasia 2A mutations

1 reference

12 December 2020

Hirschsprung's disease associated with Ondine's curse: report of three cases and review of the literature

1 reference

12 December 2020

Common origin and developmental dependence on c-ret of subsets of enteric and sympathetic neuroblasts.

1 reference

12 December 2020

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

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12 December 2020

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

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12 December 2020

A genetic study of Hirschsprung disease

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12 December 2020

Involvement of RET oncogene in human tumours: specificity of RET activation to thyroid tumours

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12 December 2020

Congenital central hypoventilation syndrome: mutation analysis of the receptor tyrosine kinase RET

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12 December 2020

In vitro irradiation is able to cause RET oncogene rearrangement

1 reference

12 December 2020

Mutation of theRET protooncogene in sporadic medullary thyroid carcinoma

1 reference

12 December 2020

Activation of RET as a dominant transforming gene by germline mutations of MEN2A and MEN2B

1 reference

12 December 2020

Expression of the c-ret proto-oncogene during mouse embryogenesis

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12 December 2020

RET proto-oncogene mutations in French MEN 2A and FMTC families

1 reference

12 December 2020

Cloning and expression of the ret proto-oncogene encoding a tyrosine kinase with two potential transmembrane domains

1 reference

12 December 2020

Familial medullary thyroid carcinoma without associated endocrinopathies: a distinct clinical entity

1 reference

12 December 2020

Localisation of the gene for multiple endocrine neoplasia type 2A to a 480 kb region in chromosome band 10q11.2.

1 reference

12 December 2020

Frequent activation of ret protooncogene by fusion with a new activating gene in papillary thyroid carcinomas.

1 reference

12 December 2020

Genetic linkage studies map the multiple endocrine neoplasia type 2 loci to a small interval on chromosome 10q11.2

1 reference

12 December 2020

The protein kinase family: conserved features and deduced phylogeny of the catalytic domains

1 reference

12 December 2020

Hirschsprung's disease associated with a deletion of chromosome 10 (q11.2q21.2): a further link with the neurocristopathies?

1 reference

12 December 2020

The migration of neural crest cells to the wall of the digestive tract in avian embryo

1 reference

12 December 2020

Spatial and temporal expression of the ret proto-oncogene product in embryonic, infant and adult rat tissues.

1 reference

12 December 2020

Point mutation within the tyrosine kinase domain of the RET proto-oncogene in multiple endocrine neoplasia type 2B and related sporadic tumours

1 reference

12 December 2020

Characterization of ret proto-oncogene mRNAs encoding two isoforms of the protein product in a human neuroblastoma cell line

1 reference

12 December 2020

Immunohistochemical localization of RET protein in Hirschsprung's disease

1 reference

12 December 2020

Mutation analysis of the RET, the endothelin-B receptor, and the endothelin-3 genes in sporadic cases of Hirschsprung's disease

1 reference

12 December 2020

Molecular characterization of RET/PTC3; a novel rearranged version of the RETproto-oncogene in a human thyroid papillary carcinoma

1 reference

12 December 2020

RET activation by germline MEN2A and MEN2B mutations

1 reference

12 December 2020

The human protooncogene ret: a communicative cadherin?

1 reference

12 December 2020

Activated RET oncogene in thyroid cancers of children from areas contaminated by Chernobyl accident

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12 December 2020

Endothelin receptor-mediated signaling in hirschsprung disease.

1 reference

12 December 2020

Characterization of the promoter region and oligomerization domain of H4 (D10S170), a gene frequently rearranged with the ret proto-oncogene

1 reference

12 December 2020

RET mutations in exons 13 and 14 of FMTC patients

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12 December 2020

The two genes generating RET/PTC3 are localized in chromosomal band 10q11.2.

1 reference

12 December 2020

Hirschsprung's disease in a family with multiple endocrine neoplasia type 2.

1 reference

12 December 2020

Mutations in the RET proto-oncogene are associated with MEN 2A and FMTC.

1 reference

12 December 2020

Developmental expression of the RET protooncogene.

1 reference

12 December 2020

Isolation of ret proto-oncogene cDNA with an amino-terminal signal sequence

1 reference

12 December 2020

Structural analysis of the human ret proto-oncogene using exon trapping.

1 reference

12 December 2020

Syndrome of bilateral pheochromocytoma, medullary thyroid carcinoma and multiple neuromas. A possible regulatory defect in the differentiation of chromaffin tissue

1 reference

12 December 2020

Human ret proto-oncogene mapped to chromosome 10q11.2.

1 reference

12 December 2020

Medullary carcinoma of the thyroid gland

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12 December 2020

A novel point mutation in the tyrosine kinase domain of the RET proto-oncogene in sporadic medullary thyroid carcinoma and in a family with FMTC

1 reference

12 December 2020

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

1 reference

12 December 2020

Mutation analysis of the RET receptor tyrosine kinase in Hirschsprung disease

1 reference

12 December 2020

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

1 reference

12 December 2020

The mutation for medullary thyroid carcinoma with parathyroid tumors (MTC with PTs) is closely linked to the centromeric region of chromosome 10

1 reference

12 December 2020

Mutational analysis of multiple endocrine neoplasia type 2A associated with Hirschsprung's disease

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12 December 2020

Identifiers

DOI

10.1007/BF01194794

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Dimensions Publication ID

29 September 2017

1023005319

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