Prevalence and parental origin of de novo RET mutations in multiple endocrine neoplasia type 2A and familial medullary thyroid carcinoma. Le Groupe d'Etude des Tumeurs a Calcitonine (Q24680144)

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English	Prevalence and parental origin of de novo RET mutations in multiple endocrine neoplasia type 2A and familial medullary thyroid carcinoma. Le Groupe d'Etude des Tumeurs a Calcitonine	scientific article

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scholarly article

1 reference

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22 October 2019

Prevalence and parental origin of de novo RET mutations in multiple endocrine neoplasia type 2A and familial medullary thyroid carcinoma. Le Groupe d'Etude des Tumeurs a Calcitonine (English)

1 reference

Europe PubMed Central

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22 October 2019

multiple endocrine neoplasia type 2A

1 reference

based on heuristic

inferred from title

author name string

I Schuffenecker

1

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22 October 2019

N Ginet

2

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22 October 2019

D Goldgar

3

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22 October 2019

C Eng

4

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22 October 2019

B Chambe

5

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22 October 2019

A Boneu

6

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22 October 2019

C Houdent

7

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22 October 2019

D Pallo

8

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22 October 2019

M Schlumberger

9

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22 October 2019

C Thivolet

10

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22 October 2019

G M Lenoir

11

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22 October 2019

language of work or name

0 references

publication date

1 January 1997

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22 October 2019

American Journal of Human Genetics

1 reference

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22 October 2019

60

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22 October 2019

1

1 reference

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22 October 2019

233-237

1 reference

Europe PubMed Central

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22 October 2019

GDNF-induced activation of the ret protein tyrosine kinase is mediated by GDNFR-alpha, a novel receptor for GDNF

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712555

7 April 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712555

7 April 2017

Parent-of-origin effects in multiple endocrine neoplasia type 2B

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712555

7 April 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712555

7 April 2017

Mutations of the RET proto-oncogene in multiple endocrine neoplasia type 2.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712555

28 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712555

28 September 2017

Low frequency of germline mutations in the RET proto-oncogene in patients with apparently sporadic medullary thyroid carcinoma

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712555

28 September 2017

Isolation and mapping of a polymorphic DNA sequence pYNH24 on chromosome 2 (D2S44).

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712555

28 September 2017

Functional receptor for GDNF encoded by the c-ret proto-oncogene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712555

28 September 2017

Parental origin effects, genome imprinting, and sex-ratio distortion: double or nothing?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712555

30 May 2018

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://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712555

30 May 2018

A mutation in the RET proto-oncogene associated with multiple endocrine neoplasia type 2B and sporadic medullary thyroid carcinoma

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712555

28 July 2018

A polymorphic dinucleotide repeat at the ZNF22 locus.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712555

28 November 2018

Specific mutations of the RET proto-oncogene are related to disease phenotype in MEN 2A and FMTC

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712555

28 November 2018

The physical map of the human RET proto-oncogene.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712555

28 November 2018

Relevance of RET proto-oncogene mutations in sporadic medullary thyroid carcinoma

1 reference

https://pubmed.ncbi.nlm.nih.gov/8981969

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A de novo mutation of the RET proto-oncogene in a patient with MEN 2A

1 reference

https://pubmed.ncbi.nlm.nih.gov/8981969

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

RET proto-oncogene mutations in French MEN 2A and FMTC families

1 reference

https://pubmed.ncbi.nlm.nih.gov/8981969

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A novel point mutation in the tyrosine kinase domain of the RET proto-oncogene in sporadic medullary thyroid carcinoma and in a family with FMTC

1 reference

https://pubmed.ncbi.nlm.nih.gov/8981969

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Detection of a germline mutation at codon 918 of the RET proto-oncogene in French MEN 2B families

1 reference

https://pubmed.ncbi.nlm.nih.gov/8981969

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

RET mutations in exons 13 and 14 of FMTC patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/8981969

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Pheochromocytoma in multiple endocrine neoplasia type 2: European study

1 reference

https://pubmed.ncbi.nlm.nih.gov/8981969

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Two maternally derived missense mutations in the tyrosine kinase domain of the RET protooncogene in a patient with de novo MEN 2B

1 reference

https://pubmed.ncbi.nlm.nih.gov/8981969

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8981969%20AND%20SRC:MED&resulttype=core&format=json

22 October 2019

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8981969%20AND%20SRC:MED&resulttype=core&format=json

22 October 2019

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