(Q41099821)

English

RET oncogene

scientific article published on February 1996

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Statements

scholarly article

1 reference

Europe PubMed Central

26 September 2017

1 reference

Europe PubMed Central

RET oncogene (English)

1 reference

Europe PubMed Central

26 September 2017

author name string

Mak YF

1

1 reference

Europe PubMed Central

26 September 2017

Ponder BA

2

1 reference

Europe PubMed Central

26 September 2017

publication date

1 February 1996

1 reference

Europe PubMed Central

26 September 2017

Current Opinion in Genetics & Development

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Europe PubMed Central

26 September 2017

6

1 reference

Europe PubMed Central

26 September 2017

1

1 reference

Europe PubMed Central

26 September 2017

82-86

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Europe PubMed Central

26 September 2017

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

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2896%2990015-5

7 January 2021

based on heuristic

inferred from DOI database lookup

ret transforming gene encodes a fusion protein homologous to tyrosine kinases

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2896%2990015-5

7 January 2021

based on heuristic

inferred from DOI database lookup

SH2 and SH3 domains

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2896%2990015-5

7 January 2021

based on heuristic

inferred from DOI database lookup

Dimerization of cell surface receptors in signal transduction

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2896%2990015-5

7 January 2021

based on heuristic

inferred from DOI database lookup

The human protooncogene ret: a communicative cadherin?

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2896%2990015-5

7 January 2021

based on heuristic

inferred from DOI database lookup

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%2FS0959-437X%2896%2990015-5

7 January 2021

based on heuristic

inferred from DOI database lookup

An epidermal growth factor receptor/ret chimera generates mitogenic and transforming signals: evidence for a ret-specific signaling pathway

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2896%2990015-5

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2896%2990015-5

7 January 2021

based on heuristic

inferred from DOI database lookup

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%2FS0959-437X%2896%2990015-5

7 January 2021

based on heuristic

inferred from DOI database lookup

A 7 bp deletion of the RET proto-oncogene in familial Hirschsprung‘s disease

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2896%2990015-5

7 January 2021

based on heuristic

inferred from DOI database lookup

Mutation analysis of the RET receptor tyrosine kinase in Hirschsprung disease

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2896%2990015-5

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2896%2990015-5

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2896%2990015-5

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2896%2990015-5

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2896%2990015-5

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2896%2990015-5

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2896%2990015-5

7 January 2021

based on heuristic

inferred from DOI database lookup

Haplotype analysis of MEN 2 mutations

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2896%2990015-5

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2896%2990015-5

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2896%2990015-5

7 January 2021

based on heuristic

inferred from DOI database lookup

Mutation of theRET protooncogene in sporadic medullary thyroid carcinoma

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2896%2990015-5

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2896%2990015-5

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2896%2990015-5

7 January 2021

based on heuristic

inferred from DOI database lookup

Loss of function effect of RET mutations causing Hirschsprung disease.

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2896%2990015-5

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2896%2990015-5

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2896%2990015-5

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2896%2990015-5

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1016/S0959-437X(96)90015-5

1 reference

Europe PubMed Central

26 September 2017

1 reference

Europe PubMed Central

26 September 2017

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