Mapping the gene for hereditary hyperparathyroidism and prolactinoma (MEN1Burin) to chromosome 11q: evidence for a founder effect in patients from Newfoundland (Q35889219)

From Wikidata

Jump to navigation Jump to search

scientific article published in June 1994

Language	Label	Description	Also known as
English	Mapping the gene for hereditary hyperparathyroidism and prolactinoma (MEN1Burin) to chromosome 11q: evidence for a founder effect in patients from Newfoundland	scientific article published in June 1994

Statements

scholarly article

1 reference

Europe PubMed Central

10 August 2017

Mapping the gene for hereditary hyperparathyroidism and prolactinoma (MEN1Burin) to chromosome 11q: evidence for a founder effect in patients from Newfoundland (English)

1 reference

Europe PubMed Central

10 August 2017

hyperparathyroidism

1 reference

based on heuristic

inferred from title

1 reference

based on heuristic

inferred from title

1 reference

based on heuristic

inferred from title

author name string

E M Petty

1

1 reference

Europe PubMed Central

10 August 2017

J S Green

2

1 reference

Europe PubMed Central

10 August 2017

S J Marx

3

1 reference

Europe PubMed Central

10 August 2017

R T Taggart

4

1 reference

Europe PubMed Central

10 August 2017

N Farid

5

1 reference

Europe PubMed Central

10 August 2017

A E Bale

6

1 reference

Europe PubMed Central

10 August 2017

language of work or name

0 references

publication date

1 June 1994

1 reference

Europe PubMed Central

10 August 2017

American Journal of Human Genetics

1 reference

Europe PubMed Central

10 August 2017

54

1 reference

Europe PubMed Central

10 August 2017

1060-1066

1 reference

Europe PubMed Central

10 August 2017

6

1 reference

Europe PubMed Central

10 August 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=1918205

11 July 2018

Easy calculations of lod scores and genetic risks on small computers

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918205

11 July 2018

Genetic aspects of multiple endocrine neoplasia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918205

11 July 2018

A rapid method for the purification of DNA from blood

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918205

11 July 2018

Multiple endocrine neoplasia type 1 gene maps to chromosome 11 and is lost in insulinoma.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918205

11 July 2018

Clonality of parathyroid tumors in familial multiple endocrine neoplasia type 1

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918205

11 July 2018

Localization of the genetic defect in multiple endocrine neoplasia type 1 within a small region of chromosome 11.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918205

11 July 2018

Linkage of the multiple endocrine neoplasia type 2B gene (MEN2B) to chromosome 10 markers linked to MEN2A.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918205

11 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918205

11 July 2018

Fine-scale mapping of the gene responsible for multiple endocrine neoplasia type 1 (MEN 1)

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918205

11 July 2018

A radiation hybrid map of the proximal long arm of human chromosome 11 containing the multiple endocrine neoplasia type 1 (MEN-1) and bcl-1 disease loci.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918205

11 July 2018

Detailed physical map of human chromosomal region 11q12-13 shows high meiotic recombination rate around the MEN1 locus

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918205

11 July 2018

Isolation of 1001 new markers from human chromosome 11, excluding the region of 11p13-p15.5, and their sublocalization by a new series of radiation-reduced somatic cell hybrids

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918205

11 July 2018

Isolation and mapping of polymorphic cosmid clones used for sublocalization of the multiple endocrine neoplasia type 1 (MEN1) locus

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918205

11 July 2018

A minisatellite and a microsatellite polymorphism within 1.5 kb at the human muscle glycogen phosphorylase (PYGM) locus can be amplified by PCR and have combined informativeness of PIC 0.95

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918205

11 July 2018

Strong allelic association between the torsion dystonia gene (DYT1) andloci on chromosome 9q34 in Ashkenazi Jews

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918205

11 July 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=1918205

27 July 2018

D11S971 CATT polymorphism (RC27) located near the MEN1 locus at 11q13.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918205

24 September 2018

Mutations in the RET proto-oncogene are associated with 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=1918205

24 September 2018

D11S970 CATT polymorphism (RC29) located near the MEN1 locus at 11q13.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918205

24 September 2018

Assignment of multiple endocrine neoplasia type 2A to chromosome 10 by linkage

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918205

14 November 2018

Prolactinomas in familial multiple endocrine neoplasia syndrome type I. Relationship to HLA and carcinoid tumors

1 reference

https://pubmed.ncbi.nlm.nih.gov/7911003

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Variant multiple endocrine neoplasia I (MEN IBurin): further studies and non-linkage to HLA

1 reference

https://pubmed.ncbi.nlm.nih.gov/7911003

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Linkage analysis of multiple endocrine neoplasia type 1 with INT2 and other markers on chromosome 11

1 reference

https://pubmed.ncbi.nlm.nih.gov/7911003

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A detailed genetic map of the long arm of chromosome 11

1 reference

https://pubmed.ncbi.nlm.nih.gov/7911003

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Allelic loss on chromosome 11 in hereditary and sporadic tumors related to familial multiple endocrine neoplasia type 1

1 reference

https://pubmed.ncbi.nlm.nih.gov/7911003

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A 14-Mb physical map of the region at chromosome 11q13 harboring the MEN1 locus and the tumor amplicon region

1 reference

https://pubmed.ncbi.nlm.nih.gov/7911003

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Regional localization of the highly polymorphic locus D11S533 on the linkage map of human chromosome 11q

1 reference

https://pubmed.ncbi.nlm.nih.gov/7911003

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A pulsed-field gel electrophoresis (PFGE) map of twelve loci on chromosome 11q11-q13

1 reference

https://pubmed.ncbi.nlm.nih.gov/7911003

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prolactinomas as part of the multiple endocrine neoplastic syndrome type 1

1 reference

https://pubmed.ncbi.nlm.nih.gov/7911003

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

1 reference

Europe PubMed Central

10 August 2017

1 reference

Europe PubMed Central

10 August 2017

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=Q35889219&oldid=1965251878"