STRAD in Peutz-Jeghers syndrome and sporadic cancers. (Q34561256)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16189157%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

title

STRAD in Peutz-Jeghers syndrome and sporadic cancers (English)

1 reference

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7 January 2020

main subject

Peutz-Jeghers syndrome

1 reference

5

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7 January 2020

author name string

de Leng WW

1

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7 January 2020

Keller JJ

2

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7 January 2020

Luiten S

3

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7 January 2020

Musler AR

4

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7 January 2020

Baas AF

6

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7 January 2020

de Rooij FW

7

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7 January 2020

Gille JJ

8

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7 January 2020

Menko FH

9

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7 January 2020

Offerhaus GJ

10

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7 January 2020

Weterman MA

11

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7 January 2020

language of work or name

English

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publication date

1 October 2005

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Journal of Clinical Pathology

7 January 2020

published in

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7 January 2020

volume

58

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7 January 2020

issue

10

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7 January 2020

page(s)

1091-1095

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nm23-H1 expression and loss of heterozygosity in colon adenocarcinoma

7 January 2020

cites work

1 reference

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Relative frequency and morphology of cancers in STK11 mutation carriers

7 July 2018

1 reference

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Complete polarization of single intestinal epithelial cells upon activation of LKB1 by STRAD.

7 July 2018

1 reference

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The tumor suppressor LKB1 kinase directly activates AMP-activated kinase and regulates apoptosis in response to energy stress

7 July 2018

1 reference

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LKB1 (XEEK1) regulates Wnt signalling in vertebrate development

7 July 2018

1 reference

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Regulation of the Wnt signalling component PAR1A by the Peutz-Jeghers syndrome kinase LKB1

7 July 2018

1 reference

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Further observations on LKB1/STK11 status and cancer risk in Peutz-Jeghers syndrome.

7 July 2018

1 reference

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Activation of the tumour suppressor kinase LKB1 by the STE20-like pseudokinase STRAD

7 July 2018

1 reference

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Search for the second Peutz-Jeghers syndrome locus: exclusion of the STK13, PRKCG, KLK10, and PSCD2 genes on chromosome 19 and the STK11IP gene on chromosome 2

7 July 2018

1 reference

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Inactivation of LKB1/STK11 is a common event in adenocarcinomas of the lung

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1770744

LIP1, a cytoplasmic protein functionally linked to the Peutz-Jeghers syndrome kinase LKB1

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1770744

The Peutz-Jegher gene product LKB1 is a mediator of p53-dependent cell death

7 July 2018

1 reference

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Very high risk of cancer in familial Peutz-Jeghers syndrome

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1770744

Isolation and mapping of a human septin gene to a region on chromosome 17q, commonly deleted in sporadic epithelial ovarian tumors

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1770744

Growth suppression by Lkb1 is mediated by a G(1) cell cycle arrest

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1770744

Germline and somatic mutations of the STK11/LKB1 Peutz-Jeghers gene in pancreatic and biliary cancers

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1770744

Somatic mutation of the Peutz-Jeghers syndrome gene, LKB1/STK11, in malignant melanoma

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1770744

Comparison of p53 and DNA content abnormalities in adenocarcinoma of the oesophagus and gastric cardia

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1770744

Peutz-Jeghers syndrome: confirmation of linkage to chromosome 19p13.3 and identification of a potential second locus, on 19q13.4.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1770744

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

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1770744

Allele loss from large regions of chromosome 17 is common only in certain histological subtypes of ovarian carcinomas

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1770744

Rapid detection of allele loss in colorectal tumours using microsatellites and fluorescent DNA technology

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1770744

p53 gene mutations and protein accumulation in human ovarian cancer

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1770744

Ovarian sex cord tumor with annular tubules: review of 74 cases including 27 with Peutz-Jeghers syndrome and four with adenoma malignum of the cervix

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1770744

Mutation and cancer: statistical study of retinoblastoma

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1770744

Increased risk of cancer in the Peutz-Jeghers syndrome

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1770744

Loss of heterozygosity on chromosomes 3, 13, and 17 in small-cell carcinoma and on chromosome 3 in adenocarcinoma of the lung

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1770744

Genetic alterations during colorectal-tumor development

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1770744

Germline epimutation of MLH1 in individuals with multiple cancers

7 July 2018

1 reference

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Extensive but hemiallelic methylation of the hMLH1 promoter region in early-onset sporadic colon cancers with microsatellite instability

27 October 2018

1 reference

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A hereditary nonpolyposis colorectal carcinoma case associated with hypermethylation of the MLH1 gene in normal tissue and loss of heterozygosity of the unmethylated allele in the resulting microsatellite instability-high tumor

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1770744

Loss of heterozygosity (LOH) at 17q and 14q in human lung cancers.

27 October 2018

1 reference

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Generalized Intestinal Polyposis and Melanin Spots of the Oral Mucosa, Lips and Digits

27 October 2018

1 reference

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Association of Genetic Defects in Primary Resected Lung Adenocarcinoma Revealed by Targeted Allelic Imbalance Analysis

9 December 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1770744

Frequency of BRCA1 dysfunction in ovarian cancer

9 December 2018

1 reference

12 December 2020

A pericentric inversion of chromosome six in a patient with Peutz-Jeghers' syndrome and the use of FISH to localise the breakpoints on a genetic map

1 reference

12 December 2020

Frequent microsatellite instability and loss of heterozygosity in the region including BRCA1 (17q21) in young patients with gastric cancer

1 reference

12 December 2020

Loss of heterozygosity in the region including the BRCA1 gene on 17q in colon cancer

1 reference

12 December 2020

Isolation and characterization of new microsatellites at the nm23-H1 and nm23-H2 gene loci and application for loss of heterozygosity (LOH) analysis

1 reference

12 December 2020

Identifiers

DOI

10.1136/JCP.2005.026013

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16189157%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16189157%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

PubMed publication ID

16189157

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16189157%20AND%20SRC:MED&resulttype=core&format=json