(Q78121390)

English

Biological and biochemical properties of Ret with kinase domain mutations identified in multiple endocrine neoplasia type 2B and familial medullary thyroid carcinoma

scientific article published on 01 July 1999

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10445857%20AND%20SRC:MED&resulttype=core&format=json

11 December 2019

Biological and biochemical properties of Ret with kinase domain mutations identified in multiple endocrine neoplasia type 2B and familial medullary thyroid carcinoma (English)

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10445857%20AND%20SRC:MED&resulttype=core&format=json

11 December 2019

thyroid carcinoma

1 reference

based on heuristic

inferred from title

multiple endocrine neoplasia type 2B

1 reference

based on heuristic

inferred from title

familial medullary thyroid carcinoma

1 reference

based on heuristic

inferred from title

author name string

T Iwashita

1

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10445857%20AND%20SRC:MED&resulttype=core&format=json

11 December 2019

M Kato

2

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10445857%20AND%20SRC:MED&resulttype=core&format=json

11 December 2019

H Murakami

3

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10445857%20AND%20SRC:MED&resulttype=core&format=json

11 December 2019

N Asai

4

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10445857%20AND%20SRC:MED&resulttype=core&format=json

11 December 2019

Y Ishiguro

5

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10445857%20AND%20SRC:MED&resulttype=core&format=json

11 December 2019

S Ito

6

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10445857%20AND%20SRC:MED&resulttype=core&format=json

11 December 2019

Y Iwata

7

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10445857%20AND%20SRC:MED&resulttype=core&format=json

11 December 2019

K Kawai

8

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10445857%20AND%20SRC:MED&resulttype=core&format=json

11 December 2019

M Asai

9

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10445857%20AND%20SRC:MED&resulttype=core&format=json

11 December 2019

K Kurokawa

10

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10445857%20AND%20SRC:MED&resulttype=core&format=json

11 December 2019

H Kajita

11

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10445857%20AND%20SRC:MED&resulttype=core&format=json

11 December 2019

M Takahashi

12

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10445857%20AND%20SRC:MED&resulttype=core&format=json

11 December 2019

language of work or name

0 references

publication date

1 July 1999

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10445857%20AND%20SRC:MED&resulttype=core&format=json

11 December 2019

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10445857%20AND%20SRC:MED&resulttype=core&format=json

11 December 2019

18

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10445857%20AND%20SRC:MED&resulttype=core&format=json

11 December 2019

26

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10445857%20AND%20SRC:MED&resulttype=core&format=json

11 December 2019

3919-3922

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10445857%20AND%20SRC:MED&resulttype=core&format=json

11 December 2019

https://scigraph.springernature.com/pub.10.1038/sj.onc.1202742

0 references

Identification of Shc docking site on Ret tyrosine kinase

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1202742

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/10.1038%2FSJ.ONC.1202742

7 January 2021

based on heuristic

inferred from DOI database lookup

A mutation at tyrosine 1062 in MEN2A-Ret and MEN2B-Ret impairs their transforming activity and association with shc adaptor proteins

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1202742

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1202742

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/10.1038%2FSJ.ONC.1202742

7 January 2021

based on heuristic

inferred from DOI database lookup

Shc and Enigma are both required for mitogenic signaling by Ret/ptc2.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1202742

7 January 2021

based on heuristic

inferred from DOI database lookup

Germline dinucleotide mutation in codon 883 of the RET proto-oncogene in multiple endocrine neoplasia type 2B without codon 918 mutation

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1202742

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/10.1038%2FSJ.ONC.1202742

7 January 2021

based on heuristic

inferred from DOI database lookup

A novel point mutation in the intracellular domain of the ret protooncogene in a family with medullary thyroid carcinoma

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1202742

7 January 2021

based on heuristic

inferred from DOI database lookup

Clinical screening as compared with DNA analysis in families with multiple endocrine neoplasia type 2A

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1202742

7 January 2021

based on heuristic

inferred from DOI database lookup

RET alternate splicing influences the interaction of activated RET with the SH2 and PTB domains of Shc, and the SH2 domain of Grb2

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1202742

7 January 2021

based on heuristic

inferred from DOI database lookup

A novel somatic mutation in the RET proto-oncogene in familial medullary thyroid carcinoma with a germline codon 768 mutation.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1202742

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/10.1038%2FSJ.ONC.1202742

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/10.1038%2FSJ.ONC.1202742

7 January 2021

based on heuristic

inferred from DOI database lookup

Calcium-dependent Ret activation by GDNF and neurturin

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1202742

7 January 2021

based on heuristic

inferred from DOI database lookup

Oncogenic activation of RET by two distinct FMTC mutations affecting the tyrosine kinase domain.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1202742

7 January 2021

based on heuristic

inferred from DOI database lookup

RET mutations in human disease

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1202742

7 January 2021

based on heuristic

inferred from DOI database lookup

Distinct biological properties of two RET isoforms activated by MEN 2A and MEN 2B mutations

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1202742

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/10.1038%2FSJ.ONC.1202742

7 January 2021

based on heuristic

inferred from DOI database lookup

Germline mutation of RET codon 883 in two cases of de novo MEN 2B.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1202742

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q78121390&oldid=1525809364"