(Q74127799)

English

A GTG to ATG novel point mutation at codon 804 in exon 14 of the RET proto-oncogene in two families affected by familial medullary thyroid carcinoma

scientific article published on 01 January 1998

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scholarly article

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Europe PubMed Central

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9 November 2019

A GTG to ATG novel point mutation at codon 804 in exon 14 of the RET proto-oncogene in two families affected by familial medullary thyroid carcinoma (English)

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9452077%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

thyroid carcinoma

1 reference

based on heuristic

inferred from title

familial medullary thyroid carcinoma

1 reference

based on heuristic

inferred from title

author name string

O Fattoruso

1

1 reference

Europe PubMed Central

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9 November 2019

L Quadro

2

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Europe PubMed Central

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9 November 2019

A Libroia

3

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Europe PubMed Central

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9 November 2019

U Verga

4

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Europe PubMed Central

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9 November 2019

G Lupoli

5

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9 November 2019

E Cascone

6

1 reference

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9 November 2019

V Colantuoni

7

1 reference

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9 November 2019

publication date

1 January 1998

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Europe PubMed Central

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9 November 2019

1 reference

Europe PubMed Central

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9 November 2019

Suppl 1

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9 November 2019

S167-71

1 reference

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PubMed publication ID

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9 November 2019

Additional RFLPs at D10S94 and the development of PCR-based variant detection systems: implications for disease genotype prediction in MEN 2A, MEN 2B, and MTC1 families

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380110156

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/10.1002%2FHUMU.1380110156

7 January 2021

based on heuristic

inferred from DOI database lookup

Multiple endocrine neoplasia type 2

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380110156

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380110156

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/10.1002%2FHUMU.1380110156

7 January 2021

based on heuristic

inferred from DOI database lookup

Antioncogenes and human cancer

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380110156

7 January 2021

based on heuristic

inferred from DOI database lookup

Genetic events in tumour initiation and progression in multiple endocrine neoplasia type 2

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380110156

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/10.1002%2FHUMU.1380110156

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/10.1002%2FHUMU.1380110156

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/10.1002%2FHUMU.1380110156

7 January 2021

based on heuristic

inferred from DOI database lookup

Multiple endocrine neoplasia type 2. Clinical features and screening.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380110156

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/10.1002%2FHUMU.1380110156

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/10.1002%2FHUMU.1380110156

7 January 2021

based on heuristic

inferred from DOI database lookup

Genetic aspects of multiple endocrine neoplasia

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380110156

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/10.1002%2FHUMU.1380110156

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1002/HUMU.1380110156

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9452077%20AND%20SRC:MED&resulttype=core&format=json

9 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:9452077%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

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