Over-representation of a germline RET sequence variant in patients with sporadic medullary thyroid carcinoma and somatic RET codon 918 mutation (Q74450246)

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scientific article published on 01 February 1999

Language	Label	Description	Also known as
English	Over-representation of a germline RET sequence variant in patients with sporadic medullary thyroid carcinoma and somatic RET codon 918 mutation	scientific article published on 01 February 1999

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scholarly article

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10022819%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

Over-representation of a germline RET sequence variant in patients with sporadic medullary thyroid carcinoma and somatic RET codon 918 mutation (English)

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10022819%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

thyroid carcinoma

1 reference

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inferred from title

author name string

O Gimm

1

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10 November 2019

D S Neuberg

2

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10022819%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

D J Marsh

3

1 reference

Europe PubMed Central

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10 November 2019

P L Dahia

4

1 reference

Europe PubMed Central

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10 November 2019

C Hoang-Vu

5

1 reference

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10 November 2019

F Raue

6

1 reference

Europe PubMed Central

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10 November 2019

R Hinze

7

1 reference

Europe PubMed Central

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10 November 2019

H Dralle

8

1 reference

Europe PubMed Central

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10 November 2019

C Eng

9

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10 November 2019

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publication date

1 February 1999

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10 November 2019

1 reference

Europe PubMed Central

PubMed publication ID

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10 November 2019

18

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10 November 2019

6

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10 November 2019

1369-1373

1 reference

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10 November 2019

Incidence of sporadic and familial medullary thyroid carcinoma in Sweden 1959 through 1981. A nationwide study in 126 patients. Swedish MCT Study Group

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1202418

7 January 2021

based on heuristic

inferred from DOI database lookup

Somatic in frame deletions not involving juxtamembranous cysteine residues strongly activate the RET proto-oncogene

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1202418

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.1202418

7 January 2021

based on heuristic

inferred from DOI database lookup

Mutations of theRET proto-oncogene in the multiple endocrine neoplasia type 2 syndromes, related sporadic tumours, and Hirschsprung disease

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1202418

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/10.1038%2FSJ.ONC.1202418

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.1202418

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.1202418

7 January 2021

based on heuristic

inferred from DOI database lookup

Familial colorectal cancer in Ashkenazim due to a hypermutable tract in APC.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1202418

7 January 2021

based on heuristic

inferred from DOI database lookup

Two alleles of the human paraoxonase gene produce different amounts of mRNA. An explanation for differences in serum concentrations of paraoxonase associated with the (Leu-Met54) polymorphism

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1202418

7 January 2021

based on heuristic

inferred from DOI database lookup

Germline mutations of the PTEN gene in Cowden disease, an inherited breast and thyroid cancer syndrome

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1202418

7 January 2021

based on heuristic

inferred from DOI database lookup

A single nucleotide polymorphism in an exon dictates allele dependent differential splicing of episialin mRNA.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1202418

7 January 2021

based on heuristic

inferred from DOI database lookup

Somatic mutations in the RET proto-oncogene in sporadic medullary thyroid carcinoma

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1202418

7 January 2021

based on heuristic

inferred from DOI database lookup

Development of medullary thyroid carcinoma in transgenic mice expressing the RET protooncogene altered by a multiple endocrine neoplasia type 2A mutation

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1202418

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/10.1038%2FSJ.ONC.1202418

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.1202418

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.1202418

7 January 2021

based on heuristic

inferred from DOI database lookup

Prognostic factors in medullary thyroid carcinoma: evaluation of 741 patients from the German Medullary Thyroid Carcinoma Register

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1202418

7 January 2021

based on heuristic

inferred from DOI database lookup

Genetic alterations of the RET proto-oncogene in familial and sporadic pheochromocytomas

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1202418

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.1202418

7 January 2021

based on heuristic

inferred from DOI database lookup

Genetic aspects of multiple endocrine neoplasia

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1202418

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.1202418

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/10.1038%2FSJ.ONC.1202418

7 January 2021

based on heuristic

inferred from DOI database lookup

Alternative splicing of exon 3 of the human growth hormone receptor is the result of an unusual genetic polymorphism

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1202418

7 January 2021

based on heuristic

inferred from DOI database lookup

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