Mutations of PTEN in patients with Bannayan-Riley-Ruvalcaba phenotype (Q33681476)

28 July 2017

title

Mutations of PTEN in patients with Bannayan-Riley-Ruvalcaba phenotype (English)

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28 July 2017

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M Longy

1

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28 July 2017

V Coulon

2

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28 July 2017

B Duboué

3

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28 July 2017

A David

4

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28 July 2017

M Larrègue

5

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28 July 2017

C Eng

6

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28 July 2017

P Amati

7

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28 July 2017

J L Kraimps

8

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28 July 2017

A Bottani

9

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28 July 2017

D Lacombe

10

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28 July 2017

D Bonneau

11

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28 July 2017

publication date

1 November 1998

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Journal of Medical Genetics

28 July 2017

language of work or name

English

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published in

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28 July 2017

volume

35

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28 July 2017

issue

11

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28 July 2017

page(s)

886-889

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PTEN1 is frequently mutated in primary endometrial carcinomas

28 July 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051478

Germline mutations in the PTEN/MMAC1 gene in patients with Cowden disease.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051478

Germline mutations in PTEN are present in Bannayan-Zonana syndrome

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051478

TEP1, encoded by a candidate tumor suppressor locus, is a novel protein tyrosine phosphatase regulated by transforming growth factor beta

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051478

Germline mutations of the PTEN gene in Cowden disease, an inherited breast and thyroid cancer syndrome

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051478

Identification of a candidate tumour suppressor gene, MMAC1, at chromosome 10q23.3 that is mutated in multiple advanced cancers

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051478

PTEN, a putative protein tyrosine phosphatase gene mutated in human brain, breast, and prostate cancer

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051478

Clinicopathologic findings in the Bannayan-Riley-Ruvalcaba syndrome

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051478

Bannayan-Riley-Ruvalcaba syndrome: renaming three formerly recognized syndromes as one etiologic entity

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051478

Differential loss of heterozygosity in the region of the Cowden locus within 10q22-23 in follicular thyroid adenomas and carcinomas

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051478

Allelic loss on chromosome 10 in prostate adenocarcinoma

30 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/9832032

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Deletion ofPTEN in a patient with Bannayan-Riley-Ruvalcaba syndrome suggests allelism with Cowden disease

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/9832032

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

The Cowden syndrome: a clinical and genetic study in 21 patients

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/9832032

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1136/JMG.35.11.886

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28 July 2017

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28 July 2017

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