(Q42850964)

8 November 2017

Genetic pathways of colorectal carcinogenesis rarely involve the PTEN and LKB1 genes outside the inherited hamartoma syndromes (English)

1 reference

8 November 2017

1 reference

1 reference

Z J Wang

1

1 reference

8 November 2017

F Taylor

2

1 reference

8 November 2017

M Churchman

3

1 reference

8 November 2017

G Norbury

4

1 reference

8 November 2017

I Tomlinson

5

1 reference

8 November 2017

language of work or name

English

0 references

publication date

1 August 1998

1 reference

The American Journal of Pathology

8 November 2017

1 reference

8 November 2017

153

1 reference

8 November 2017

2

1 reference

8 November 2017

363-366

1 reference

Defects in mismatch repair occur after APC mutations in the pathogenesis of sporadic colorectal tumours

8 November 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1852980

27 May 2018

Peutz-Jeghers syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1852980

A serine/threonine kinase gene defective in Peutz-Jeghers syndrome

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1852980

PTEN/MMAC1 mutations in endometrial cancers.

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1852980

Somatic deletions and mutations in the Cowden disease gene, PTEN, in sporadic thyroid tumors.

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1852980

Disruption of the MMAC1/PTEN gene by deletion or mutation is a frequent event in malignant melanoma.

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1852980

Germline mutations in PTEN are present in Bannayan-Zonana syndrome

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1852980

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

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1852980

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

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1852980

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

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1852980

Genetic alterations and epithelial dysplasia in juvenile polyposis syndrome and sporadic juvenile polyps

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1852980

Methylation of the hMLH1 promoter correlates with lack of expression of hMLH1 in sporadic colon tumors and mismatch repair-defective human tumor cell lines

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1852980

Localization of a susceptibility locus for Peutz-Jeghers syndrome to 19p using comparative genomic hybridization and targeted linkage analysis

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1852980

APC gene: database of germline and somatic mutations in human tumors and cell lines

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1852980

Allele loss in colorectal cancer at the Cowden disease/juvenile polyposis locus on 10q.

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1852980

PTEN gene mutations are seen in high-grade but not in low-grade gliomas.

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1852980

Somatic mutations of PTEN in glioblastoma multiforme

16 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1852980

Mutation analysis of the putative tumor suppressor gene PTEN/MMAC1 in primary breast carcinomas

16 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1852980

Association between meningioma and Cowden's disease.

16 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1852980

Sensitivity of single-strand conformation polymorphism and heteroduplex method for mutation detection in the cystic fibrosis gene.

16 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1852980

Methylation of the BRCA1 gene in sporadic breast cancer

16 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1852980

The Sensitivity of Single-Strand Conformation Polymorphism Analysis for the Detection of Single Base Substitutions

3 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1852980

PTEN germ-line mutations in juvenile polyposis coli

1 December 2018

1 reference

Crossref

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2965579-4

Defects in mismatch repair occur afterAPC mutations in the pathogenesis of sporadic colorectal tumours

7 January 2021

1 reference

Crossref

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2965579-4

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

7 January 2021

1 reference

Crossref

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2965579-4

Exclusion of PTEN and 10q22-24 as the susceptibility locus for juvenile polyposis syndrome

7 January 2021

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/9708796

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Mutations in PTEN are frequent in endometrial carcinoma but rare in other common gynecological malignancies

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/9708796

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Comparative sensitivity of alternative single-strand conformation polymorphism (SSCP) methods

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/9708796

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1016/S0002-9440(10)65579-4

1 reference

8 November 2017

1 reference

8 November 2017

PubMed publication ID

9708796

1 reference