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

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Language	Label	Description	Also known as
English	Mutations of PTEN in patients with Bannayan-Riley-Ruvalcaba phenotype	scientific article

Statements

instance of

scholarly article

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9832032

retrieved

28 July 2017

title

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

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stated in

Europe PubMed Central

PubMed publication ID

9832032

retrieved

28 July 2017

main subject

phenotype

1 reference

based on heuristic

inferred from title

author name string

M Longy

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1

1 reference

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Europe PubMed Central

PubMed publication ID

9832032

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28 July 2017

V Coulon

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2

1 reference

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Europe PubMed Central

PubMed publication ID

9832032

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28 July 2017

B Duboué

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3

1 reference

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Europe PubMed Central

PubMed publication ID

9832032

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28 July 2017

A David

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4

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9832032

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28 July 2017

M Larrègue

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5

1 reference

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Europe PubMed Central

PubMed publication ID

9832032

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28 July 2017

C Eng

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6

1 reference

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Europe PubMed Central

PubMed publication ID

9832032

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28 July 2017

P Amati

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7

1 reference

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Europe PubMed Central

PubMed publication ID

9832032

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28 July 2017

J L Kraimps

series ordinal

8

1 reference

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Europe PubMed Central

PubMed publication ID

9832032

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28 July 2017

A Bottani

series ordinal

9

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9832032

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28 July 2017

D Lacombe

series ordinal

10

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9832032

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28 July 2017

D Bonneau

series ordinal

11

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9832032

retrieved

28 July 2017

language of work or name

English

0 references

publication date

1 November 1998

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9832032

retrieved

28 July 2017

published in

Journal of Medical Genetics

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stated in

Europe PubMed Central

PubMed publication ID

9832032

retrieved

28 July 2017

volume

35

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9832032

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28 July 2017

issue

11

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9832032

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28 July 2017

page(s)

886-889

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Europe PubMed Central

PubMed publication ID

9832032

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28 July 2017

cites work

PTEN1 is frequently mutated in primary endometrial carcinomas

1 reference

stated in

PubMed Central

reference URL

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

retrieved

21 June 2018

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

1 reference

stated in

PubMed Central

reference URL

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

retrieved

21 June 2018

Germline mutations in PTEN are present in Bannayan-Zonana syndrome

1 reference

stated in

PubMed Central

reference URL

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

retrieved

21 June 2018

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

1 reference

stated in

PubMed Central

reference URL

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

retrieved

21 June 2018

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

1 reference

stated in

PubMed Central

reference URL

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

retrieved

21 June 2018

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

1 reference

stated in

PubMed Central

reference URL

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

retrieved

21 June 2018

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

1 reference

stated in

PubMed Central

reference URL

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

retrieved

21 June 2018

Clinicopathologic findings in the Bannayan-Riley-Ruvalcaba syndrome

1 reference

stated in

PubMed Central

reference URL

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

retrieved

21 June 2018

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

1 reference

stated in

PubMed Central

reference URL

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

retrieved

21 June 2018

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

1 reference

stated in

PubMed Central

reference URL

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

retrieved

30 October 2018

Allelic loss on chromosome 10 in prostate adenocarcinoma

1 reference

stated in

PubMed

reference URL

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

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

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

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

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

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

DOI

10.1136/JMG.35.11.886

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9832032

retrieved

28 July 2017

PMC publication ID

1051478

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9832032

retrieved

28 July 2017

PubMed publication ID

9832032

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9832032

retrieved

28 July 2017

ResearchGate publication ID

13454805

0 references

 

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