(Q41545196)

3 October 2017

1 reference

title

Genetic screening for RET mutations in families with multiple endocrine neoplasia 2 syndromes (English)

1 reference

multiple endocrine neoplasia

3 October 2017

main subject

1 reference

Alevizaki M

1

1 reference

3 October 2017

Sarika H

series ordinal

2

1 reference

3 October 2017

Koutras DA

series ordinal

3

1 reference

3 October 2017

Souvatzoglou A

series ordinal

4

1 reference

3 October 2017

language of work or name

English

0 references

publication date

1 June 1997

1 reference

Annals of the New York Academy of Sciences

3 October 2017

published in

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3 October 2017

volume

816

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3 October 2017

page(s)

383-388

1 reference

A 1.5-megabase yeast artificial chromosome contig from human chromosome 10q11.2 connecting three genetic loci (RET, D10S94, and D10S102) closely linked to the MEN2A locus

3 October 2017

cites work

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1997.TB52166.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1997.TB52166.X

GDNF signalling through the Ret receptor tyrosine kinase

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1997.TB52166.X

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/10.1111%2FJ.1749-6632.1997.TB52166.X

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/10.1111%2FJ.1749-6632.1997.TB52166.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1997.TB52166.X

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/10.1111%2FJ.1749-6632.1997.TB52166.X

Familial cancer syndromes

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1997.TB52166.X

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/10.1111%2FJ.1749-6632.1997.TB52166.X

10.1111/J.1749-6632.1997.TB52166.X

21 January 2018

Identifiers

DOI

1 reference

3 October 2017

1 reference