(Q35611768)

9 August 2017

title

Association of somatotrophinomas with loss of alleles on chromosome 11 and with gsp mutations (English)

1 reference

9 August 2017

Thakker RV

1

1 reference

9 August 2017

Pook MA

2

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9 August 2017

Wooding C

3

1 reference

9 August 2017

Boscaro M

4

1 reference

9 August 2017

Scanarini M

5

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9 August 2017

Clayton RN

6

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9 August 2017

language of work or name

English

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publication date

1 June 1993

1 reference

Journal of Clinical Investigation

9 August 2017

published in

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9 August 2017

volume

91

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9 August 2017

issue

6

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9 August 2017

page(s)

2815-2821

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The molecular genetics of cellular oncogenes

9 August 2017

cites work

1 reference

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12 July 2018

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A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity

12 July 2018

1 reference

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12 July 2018

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Oncogenes and tumor-suppressing genes

12 July 2018

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Isolation and characterization of the human Gs alpha gene

12 July 2018

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Retinoblastoma and the progression of tumor genetics

12 July 2018

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Chromosomal localization of genes encoding guanine nucleotide-binding protein subunits in mouse and human

12 July 2018

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

12 July 2018

1 reference

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Multi-allelic RFLP for M27 beta, an anonymous single copy genomic clone at Xp11.3-Xcen [HGM9 provisional no. DXS255].

12 July 2018

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Chromosome 5 allele loss in human colorectal carcinomas.

12 July 2018

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Genetic alterations during colorectal-tumor development

12 July 2018

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Clonality of parathyroid tumors in familial multiple endocrine neoplasia type 1

12 July 2018

1 reference

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

12 July 2018

1 reference

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Primer-directed enzymatic amplification of DNA with a thermostable DNA polymerase

12 July 2018

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Identifying tumor suppressor genes in human colorectal cancer

12 July 2018

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A genetic model for colorectal tumorigenesis

12 July 2018

1 reference

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Two G protein oncogenes in human endocrine tumors

12 July 2018

1 reference

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A new constitutively activating mutation of the Gs protein alpha subunit-gsp oncogene is found in human pituitary tumours

12 July 2018

1 reference

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Loss of heterozygosity suggests multiple genetic alterations in pheochromocytomas and medullary thyroid carcinomas

12 July 2018

1 reference

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Clonal origin of pituitary adenomas

12 July 2018

1 reference

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Mapping the gene causing X-linked recessive idiopathic hypoparathyroidism to Xq26-Xq27 by linkage studies

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=443349

Clinically nonfunctioning pituitary tumors are monoclonal in origin

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=443349

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

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=443349

Allele loss on chromosome 11 in a pituitary tumor from a patient with multiple endocrine neoplasia type 1.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=443349

Predictive testing for multiple endocrine neoplasia type 1 using DNA polymorphisms

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=443349

A donor splice site mutation in the parathyroid hormone gene is associated with autosomal recessive hypoparathyroidism

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=443349

Detection of specific sequences among DNA fragments separated by gel electrophoresis

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=443349

Quantitative Film Detection of 3H and 14C in Polyacrylamide Gels by Fluorography

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=443349

Labeling deoxyribonucleic acid to high specific activity in vitro by nick translation with DNA polymerase I

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=443349

Analysis of human Y-chromosome-specific reiterated DNA in chromosome variants

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=443349

Somatic deletion and duplication of genes on chromosome 11 in Wilms' tumours.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=443349

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

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=443349

Gene losses in human tumours

25 September 2018

1 reference

12 December 2020

1 reference

12 December 2020

Human pepsinogen A (PGA): an informative gene complex located at 11q13

1 reference

12 December 2020

FAMILIAL ACROMEGALY: STUDIES IN THREE FAMILIES

1 reference

12 December 2020

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

1 reference

12 December 2020

Identifiers

DOI

10.1172/JCI116524

1 reference

9 August 2017

1 reference

9 August 2017

1 reference