Identification of somatic mutations of the MEN1 gene in sporadic endocrine tumours (Q36622047)

15 August 2017

Identification of somatic mutations of the MEN1 gene in sporadic endocrine tumours (English)

1 reference

15 August 2017

6

Teh B

1 reference

15 August 2017

Bergman L

1

1 reference

15 August 2017

Boothroyd C

2

1 reference

15 August 2017

Palmer J

3

1 reference

15 August 2017

Grimmond S

4

1 reference

15 August 2017

Walters M

5

1 reference

15 August 2017

Shepherd J

7

1 reference

15 August 2017

Hartley L

8

1 reference

15 August 2017

Hayward N

9

1 reference

15 August 2017

language of work or name

English

0 references

publication date

1 October 2000

1 reference

British Journal of Cancer

15 August 2017

1 reference

15 August 2017

83

1 reference

15 August 2017

8

1 reference

15 August 2017

1003-1008

1 reference

https://scigraph.springernature.com/pub.10.1054/bjoc.2000.1385

15 August 2017

0 references

cites work

Cutaneous tumors in patients with multiple endocrine neoplasia type 1 show allelic deletion of the MEN1 gene.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2363572

Mutations of the MEN1 tumor suppressor gene in pituitary tumors

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2363572

Identification of MEN1 gene mutations in sporadic carcinoid tumors of the lung

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2363572

The multiple endocrine neoplasia type I gene locus is involved in the pathogenesis of type II gastric carcinoids

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2363572

Identification of the multiple endocrine neoplasia type 1 (MEN1) gene. The European Consortium on MEN1

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2363572

Allelic deletions on chromosome 11q13 in multiple endocrine neoplasia type 1-associated and sporadic gastrinomas and pancreatic endocrine tumors

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2363572

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

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2363572

A simple salting out procedure for extracting DNA from human nucleated cells

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2363572

Rapid and sensitive detection of point mutations and DNA polymorphisms using the polymerase chain reaction

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2363572

Clonal loss of INT-2 alleles in sporadic and familial pancreatic endocrine tumours

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2363572

Eighteen new polymorphic markers in the multiple endocrine neoplasia type 1 (MEN1) region

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2363572

Somatic mutation of the MEN1 gene in parathyroid tumours.

28 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2363572

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

28 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2363572

GTPase inhibiting mutations activate the alpha chain of Gs and stimulate adenylyl cyclase in human pituitary tumours.

28 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2363572

Rearrangement and overexpression of D11S287E, a candidate oncogene on chromosome 11q13 in benign parathyroid tumors

28 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2363572

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

28 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2363572

Molecular characterization of the men1 tumor suppressor gene in sporadic pituitary tumors

28 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2363572

Genomic localization of novel candidate tumor suppressor gene loci in human parathyroid adenomas

20 September 2018

1 reference

12 December 2020

Frequent loss of the P16INK4a gene product in human pituitary tumors

1 reference

12 December 2020

Carcinoid tumors frequently display genetic abnormalities involving chromosome 11

1 reference

12 December 2020

Somatic mutations of the MEN1 tumor suppressor gene in sporadic gastrinomas and insulinomas

1 reference

12 December 2020

Multiple endocrine neoplasia 1 gene alterations in MEN1-associated and sporadic lipomas

1 reference

12 December 2020

Absence of germ-line mutations of the multiple endocrine neoplasia type 1 (MEN1) gene in familial pituitary adenoma in contrast to MEN1 in Japanese

1 reference

12 December 2020

Somatic mutations of multiple endocrine neoplasia type 1 gene in the sporadic endocrine tumors

1 reference

12 December 2020

Alterations of the MEN1 gene in sporadic parathyroid tumors

1 reference

12 December 2020

Parathyroid MEN1 gene mutations in relation to clinical characteristics of nonfamilial primary hyperparathyroidism

1 reference

12 December 2020

Somatic mutations of the MEN1 tumor suppressor gene detected in sporadic angiofibromas

1 reference

12 December 2020

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

1 reference

12 December 2020

Allelic deletion in pituitary adenomas reflects aggressive biological activity and has potential value as a prognostic marker

1 reference

12 December 2020

Loss of heterozygosity at 11q13: analysis of pituitary tumors, lung carcinoids, lipomas, and other uncommon tumors in subjects with familial multiple endocrine neoplasia type 1

1 reference

12 December 2020

Allelic loss on chromosome 11 is uncommon in parathyroid glands of patients with hypercalcaemic secondary hyperparathyroidism

1 reference

12 December 2020

Identifiers

DOI

10.1054/BJOC.2000.1385

1 reference

Dimensions Publication ID

15 August 2017

0 references

1 reference

15 August 2017

PubMed publication ID

10993646

1 reference