(Q45002058)

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Mapping of a translocation breakpoint in a Peutz-Jeghers hamartoma to the putative PJS locus at 19q13.4 and mutation analysis of candidate genes in polyp and STK11-negative PJS cases

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Europe PubMed Central

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8 December 2017

Mapping of a translocation breakpoint in a Peutz-Jeghers hamartoma to the putative PJS locus at 19q13.4 and mutation analysis of candidate genes in polyp and STK11-negative PJS cases (English)

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Europe PubMed Central

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8 December 2017

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Richard Houlston

9

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8 December 2017

object named as

Janet Shipley

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Nicholas Hearle

1

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8 December 2017

Anneke Lucassen

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8 December 2017

Rubin Wang

3

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8 December 2017

Wendy Lim

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8 December 2017

Fiona Ross

5

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8 December 2017

Robert Wheeler

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8 December 2017

Isabella Moore

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8 December 2017

language of work or name

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publication date

1 October 2004

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8 December 2017

Genes, Chromosomes and Cancer

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8 December 2017

41

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8 December 2017

2

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8 December 2017

163-169

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8 December 2017

Third report of t(19q)(13.4) in mesenchymal hamartoma of liver with comments on link to embryonal sarcoma.

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20067

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20067

7 January 2021

based on heuristic

inferred from DOI database lookup

Molecular definition of chromosome translocations involving 10q24 and 19q13 in human malignant glioma cells

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https://api.crossref.org/works/10.1002%2FGCC.20067

7 January 2021

based on heuristic

inferred from DOI database lookup

Mutations in SOX2 cause anophthalmia

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20067

7 January 2021

based on heuristic

inferred from DOI database lookup

Campomelic dysplasia and autosomal sex reversal caused by mutations in an SRY-related gene

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20067

7 January 2021

based on heuristic

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Conformation-sensitive gel electrophoresis for rapid detection of single-base differences in double-stranded PCR products and DNA fragments: evidence for solvent-induced bends in DNA heteroduplexes

1 reference

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7 January 2021

based on heuristic

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Increased risk of cancer in the Peutz-Jeghers syndrome

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

Very high risk of cancer in familial Peutz-Jeghers syndrome

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

Complexes between the LKB1 tumor suppressor, STRAD alpha/beta and MO25 alpha/beta are upstream kinases in the AMP-activated protein kinase cascade

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20067

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20067

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20067

7 January 2021

based on heuristic

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Peutz-Jeghers syndrome is caused by mutations in a novel serine threonine kinase

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20067

7 January 2021

based on heuristic

inferred from DOI database lookup

STK11/LKB1 germline mutations are not identified in most Peutz-Jeghers syndrome patients

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20067

7 January 2021

based on heuristic

inferred from DOI database lookup

Position effect in human genetic disease

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20067

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20067

7 January 2021

based on heuristic

inferred from DOI database lookup

Gene for the human transmembrane-type protein tyrosine phosphatase H (PTPRH): genomic structure, fine-mapping and its exclusion as a candidate for Peutz-Jeghers syndrome

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20067

7 January 2021

based on heuristic

inferred from DOI database lookup

Second report of a translocation involving 19q13.4 in a mesenchymal hamartoma of the liver

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20067

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20067

7 January 2021

based on heuristic

inferred from DOI database lookup

Loss of LKB1 kinase activity in Peutz-Jeghers syndrome, and evidence for allelic and locus heterogeneity

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20067

7 January 2021

based on heuristic

inferred from DOI database lookup

Nine novel germline mutations of STK11 in ten families with Peutz-Jeghers syndrome

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20067

7 January 2021

based on heuristic

inferred from DOI database lookup

Peutz-Jeghers families unlinked to STK11/LKB1 gene mutations are highly predisposed to primitive biliary adenocarcinoma

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20067

7 January 2021

based on heuristic

inferred from DOI database lookup

Chromosome-wide distribution of haplotype blocks and the role of recombination hot spots

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20067

7 January 2021

based on heuristic

inferred from DOI database lookup

Two novel mutations and a new STK11/LKB1 gene isoform in Peutz-Jeghers patients.

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20067

7 January 2021

based on heuristic

inferred from DOI database lookup

Peutz-Jeghers syndrome and ureteral polyposis

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20067

7 January 2021

based on heuristic

inferred from DOI database lookup

Cytogenetic analysis of a mesenchymal hamartoma of the liver

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20067

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20067

7 January 2021

based on heuristic

inferred from DOI database lookup

Cancer and the Peutz-Jeghers syndrome

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20067

7 January 2021

based on heuristic

inferred from DOI database lookup

Peutz-Jeghers syndrome

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20067

7 January 2021

based on heuristic

inferred from DOI database lookup

Carcinoma and polyps of the gallbladder associated with Peutz-Jeghers syndrome

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20067

7 January 2021

based on heuristic

inferred from DOI database lookup

Autosomal sex reversal and campomelic dysplasia are caused by mutations in and around the SRY-related gene SOX9

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20067

7 January 2021

based on heuristic

inferred from DOI database lookup

Peutz-Jeghers syndrome: risks of a hereditary condition.

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20067

7 January 2021

based on heuristic

inferred from DOI database lookup

LKB1 is the upstream kinase in the AMP-activated protein kinase cascade

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20067

7 January 2021

based on heuristic

inferred from DOI database lookup

Mutations and impaired function of LKB1 in familial and non-familial Peutz-Jeghers syndrome and a sporadic testicular cancer.

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20067

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1002/GCC.20067

1 reference

Europe PubMed Central

PubMed publication ID

8 December 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

8 December 2017

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