(Q77297258)

English

Multiple endocrine neoplasia type 2-associated RET proto-oncogene mutations do not contribute to the pathogenesis of sporadic parathyroid tumors

scientific article published on 01 September 1998

In more languages

default values for all languages

No label defined

No description defined

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9736899%20AND%20SRC:MED&resulttype=core&format=json

4 December 2019

Multiple endocrine neoplasia type 2-associated RET proto-oncogene mutations do not contribute to the pathogenesis of sporadic parathyroid tumors (English)

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9736899%20AND%20SRC:MED&resulttype=core&format=json

4 December 2019

multiple endocrine neoplasia

1 reference

based on heuristic

inferred from title

author name string

F Willeke

1

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9736899%20AND%20SRC:MED&resulttype=core&format=json

4 December 2019

M P Hauer

2

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9736899%20AND%20SRC:MED&resulttype=core&format=json

4 December 2019

R Buchcik

3

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9736899%20AND%20SRC:MED&resulttype=core&format=json

4 December 2019

J F Gebert

4

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9736899%20AND%20SRC:MED&resulttype=core&format=json

4 December 2019

M Hahn

5

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9736899%20AND%20SRC:MED&resulttype=core&format=json

4 December 2019

G Fitze

6

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9736899%20AND%20SRC:MED&resulttype=core&format=json

4 December 2019

G Mechtersheimer

7

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9736899%20AND%20SRC:MED&resulttype=core&format=json

4 December 2019

P Möller

8

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9736899%20AND%20SRC:MED&resulttype=core&format=json

4 December 2019

H D Saeger

9

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9736899%20AND%20SRC:MED&resulttype=core&format=json

4 December 2019

C Herfarth

10

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9736899%20AND%20SRC:MED&resulttype=core&format=json

4 December 2019

H K Schackert

11

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9736899%20AND%20SRC:MED&resulttype=core&format=json

4 December 2019

language of work or name

0 references

publication date

1 September 1998

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9736899%20AND%20SRC:MED&resulttype=core&format=json

4 December 2019

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9736899%20AND%20SRC:MED&resulttype=core&format=json

4 December 2019

124

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9736899%20AND%20SRC:MED&resulttype=core&format=json

4 December 2019

3

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9736899%20AND%20SRC:MED&resulttype=core&format=json

4 December 2019

484-490

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9736899%20AND%20SRC:MED&resulttype=core&format=json

4 December 2019

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

1 reference

https://api.crossref.org/works/10.1016%2FS0039-6060%2898%2970093-5

7 January 2021

based on heuristic

inferred from DOI database lookup

One gene—four syndromes

1 reference

https://api.crossref.org/works/10.1016%2FS0039-6060%2898%2970093-5

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/10.1016%2FS0039-6060%2898%2970093-5

7 January 2021

based on heuristic

inferred from DOI database lookup

Presymptomatic DNA screening in families with multiple endocrine neoplasia type 2 and familial medullary thyroid carcinoma

1 reference

https://api.crossref.org/works/10.1016%2FS0039-6060%2898%2970093-5

7 January 2021

based on heuristic

inferred from DOI database lookup

Haplotype analysis of MEN 2 mutations

1 reference

https://api.crossref.org/works/10.1016%2FS0039-6060%2898%2970093-5

7 January 2021

based on heuristic

inferred from DOI database lookup

Positional cloning of the gene for multiple endocrine neoplasia-type 1

1 reference

https://api.crossref.org/works/10.1016%2FS0039-6060%2898%2970093-5

7 January 2021

based on heuristic

inferred from DOI database lookup

Mechanism of activation of the ret proto-oncogene by multiple endocrine neoplasia 2A mutations

1 reference

https://api.crossref.org/works/10.1016%2FS0039-6060%2898%2970093-5

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/10.1016%2FS0039-6060%2898%2970093-5

7 January 2021

based on heuristic

inferred from DOI database lookup

Mechanism of ret dysfunction by Hirschsprung mutations affecting its extracellular domain

1 reference

https://api.crossref.org/works/10.1016%2FS0039-6060%2898%2970093-5

7 January 2021

based on heuristic

inferred from DOI database lookup

Direct solid phase sequencing of genomic and plasmid DNA using magnetic beads as solid support.

1 reference

https://api.crossref.org/works/10.1016%2FS0039-6060%2898%2970093-5

7 January 2021

based on heuristic

inferred from DOI database lookup

Role of proto-oncogene activation in carcinogenesis

1 reference

https://api.crossref.org/works/10.1016%2FS0039-6060%2898%2970093-5

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/10.1016%2FS0039-6060%2898%2970093-5

7 January 2021

based on heuristic

inferred from DOI database lookup

Surgical management of hyperparathyroidism in patients with multiple endocrine neoplasia type 2A

1 reference

https://api.crossref.org/works/10.1016%2FS0039-6060%2898%2970093-5

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS0039-6060%2898%2970093-5

7 January 2021

based on heuristic

inferred from DOI database lookup

Germline and somatic mutations in the tyrosine kinase domain of the MET proto-oncogene in papillary renal carcinomas

1 reference

https://api.crossref.org/works/10.1016%2FS0039-6060%2898%2970093-5

7 January 2021

based on heuristic

inferred from DOI database lookup

Obvious mRNA and protein expression but absence of mutations of the RET proto-oncogene in parathyroid tumors

1 reference

https://api.crossref.org/works/10.1016%2FS0039-6060%2898%2970093-5

7 January 2021

based on heuristic

inferred from DOI database lookup

GDNF signalling through the Ret receptor tyrosine kinase

1 reference

https://api.crossref.org/works/10.1016%2FS0039-6060%2898%2970093-5

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS0039-6060%2898%2970093-5

7 January 2021

based on heuristic

inferred from DOI database lookup

Mutation Analysis of Glial Cell Line-Derived Neurotrophic Factor, a Ligand for an RET/Coreceptor Complex, in Multiple Endocrine Neoplasia Type 2 and Sporadic Neuroendocrine Tumors

1 reference

https://api.crossref.org/works/10.1016%2FS0039-6060%2898%2970093-5

7 January 2021

based on heuristic

inferred from DOI database lookup

Association of parathyroid tumors in multiple endocrine neoplasia type 1 with loss of alleles on chromosome 11.

1 reference

https://api.crossref.org/works/10.1016%2FS0039-6060%2898%2970093-5

7 January 2021

based on heuristic

inferred from DOI database lookup

Localization of the MEN1 gene to a small region within chromosome 11q13 by deletion mapping in tumors

1 reference

https://api.crossref.org/works/10.1016%2FS0039-6060%2898%2970093-5

7 January 2021

based on heuristic

inferred from DOI database lookup

Candidate genes for multiple endocrine neoplasia type 1

1 reference

https://api.crossref.org/works/10.1016%2FS0039-6060%2898%2970093-5

7 January 2021

based on heuristic

inferred from DOI database lookup

Somatic mutation of the MEN1 gene in parathyroid tumours.

1 reference

https://api.crossref.org/works/10.1016%2FS0039-6060%2898%2970093-5

7 January 2021

based on heuristic

inferred from DOI database lookup

Genetic basis of endocrine disease 5. Molecular genetics of parathyroid gland neoplasia

1 reference

https://api.crossref.org/works/10.1016%2FS0039-6060%2898%2970093-5

7 January 2021

based on heuristic

inferred from DOI database lookup

Loss of the retinoblastoma tumor-suppressor gene in parathyroid carcinoma

1 reference

https://api.crossref.org/works/10.1016%2FS0039-6060%2898%2970093-5

7 January 2021

based on heuristic

inferred from DOI database lookup

Genetic abnormalities in sporadic parathyroid adenomas

1 reference

https://api.crossref.org/works/10.1016%2FS0039-6060%2898%2970093-5

7 January 2021

based on heuristic

inferred from DOI database lookup

Differential loss of heterozygosity in familial, sporadic, and uremic hyperparathyroidism

1 reference

https://api.crossref.org/works/10.1016%2FS0039-6060%2898%2970093-5

7 January 2021

based on heuristic

inferred from DOI database lookup

Lessons from hereditary colorectal cancer

1 reference

https://api.crossref.org/works/10.1016%2FS0039-6060%2898%2970093-5

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1016/S0039-6060(98)70093-5

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9736899%20AND%20SRC:MED&resulttype=core&format=json

4 December 2019

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9736899%20AND%20SRC:MED&resulttype=core&format=json

4 December 2019

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q77297258&oldid=2214224237"