(Q57591250)

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Germline sequence variant S836S in the RET proto-oncogene is associated with low level predisposition to sporadic medullary thyroid carcinoma in the Spanish population

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11589684%20AND%20SRC:MED&resulttype=core&format=json

11 November 2019

Germline sequence variant S836S in the RET proto-oncogene is associated with low level predisposition to sporadic medullary thyroid carcinoma in the Spanish population (English)

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11589684%20AND%20SRC:MED&resulttype=core&format=json

11 November 2019

thyroid carcinoma

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based on heuristic

inferred from title

4

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11589684%20AND%20SRC:MED&resulttype=core&format=json

11 November 2019

author name string

A Ruiz

1

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Europe PubMed Central

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11 November 2019

G Antiñolo

2

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11589684%20AND%20SRC:MED&resulttype=core&format=json

11 November 2019

R M Fernández

3

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11589684%20AND%20SRC:MED&resulttype=core&format=json

11 November 2019

I Marcos

5

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11589684%20AND%20SRC:MED&resulttype=core&format=json

11 November 2019

S Borrego

6

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11 November 2019

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1 September 2001

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11 November 2019

Clinical Endocrinology

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11589684%20AND%20SRC:MED&resulttype=core&format=json

11 November 2019

55

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11 November 2019

3

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11 November 2019

399-402

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11589684%20AND%20SRC:MED&resulttype=core&format=json

11 November 2019

Molecular Analysis of the ret and GDNF Genes in a Family with Multiple Endocrine Neoplasia Type 2A and Hirschsprung Disease

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2265.2001.01328.X

21 January 2018

Specific polymorphisms in the RET proto-oncogene are over-represented in patients with Hirschsprung disease and may represent loci modifying phenotypic expression

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2265.2001.01328.X

21 January 2018

RET genotypes comprising specific haplotypes of polymorphic variants predispose to isolated Hirschsprung disease

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2265.2001.01328.X

21 January 2018

Mutation of theRET protooncogene in sporadic medullary thyroid carcinoma

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2265.2001.01328.X

21 January 2018

The relationship between specific RET proto-oncogene mutations and disease phenotype in multiple endocrine neoplasia type 2. International RET mutation consortium analysis

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2265.2001.01328.X

21 January 2018

RET proto-oncogene in the development of human cancer

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2265.2001.01328.X

21 January 2018

Association of RET protooncogene codon 45 polymorphism with Hirschsprung disease

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2265.2001.01328.X

21 January 2018

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/10.1046%2FJ.1365-2265.2001.01328.X

21 January 2018

Identifiers

10.1046/J.1365-2265.2001.01328.X

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11589684%20AND%20SRC:MED&resulttype=core&format=json

11 November 2019

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11589684%20AND%20SRC:MED&resulttype=core&format=json

11 November 2019

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