Further observations on LKB1/STK11 status and cancer risk in Peutz-Jeghers syndrome. (Q34535544)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12865922%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

title

Further observations on LKB1/STK11 status and cancer risk in Peutz-Jeghers syndrome (English)

1 reference

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5 November 2019

7

D Eccles

2 references

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5 November 2019

2 August 2017

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5 November 2019

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I Tomlinson

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5 November 2019

author name string

W Lim

1

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5 November 2019

N Hearle

2

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5 November 2019

B Shah

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5 November 2019

V Murday

4

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5 November 2019

S V Hodgson

5

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A Lucassen

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5 November 2019

I Talbot

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K Neale

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5 November 2019

A G Lim

10

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5 November 2019

J O'Donohue

11

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5 November 2019

A Donaldson

12

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R C Macdonald

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I D Young

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5 November 2019

M H Robinson

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5 November 2019

P W R Lee

16

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5 November 2019

B J Stoodley

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5 November 2019

D Alderson

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5 November 2019

A G Holbrook

20

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S Vyas

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5 November 2019

E T Swarbrick

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5 November 2019

A A M Lewis

23

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5 November 2019

R K S Phillips

24

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5 November 2019

language of work or name

English

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publication date

1 July 2003

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British Journal of Cancer

5 November 2019

published in

1 reference

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5 November 2019

volume

89

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5 November 2019

page(s)

308-313

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5 November 2019

issue

2

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https://scigraph.springernature.com/pub.10.1038/sj.bjc.6601030

5 November 2019

exact match

0 references

cites work

Mutation screening at the RNA level of the STK11/LKB1 gene in Peutz-Jeghers syndrome reveals complex splicing abnormalities and a novel mRNA isoform (STK11 c.597(insertion mark)598insIVS4)

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

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Somatic mutations of LKB1 and beta-catenin genes in gastrointestinal polyps from patients with Peutz-Jeghers syndrome.

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Peutz-Jeghers syndrome: four novel inactivating germline mutations in the STK11 gene. Mutations in brief no. 227. Online

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7 July 2018

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7 July 2018

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7 July 2018

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7 July 2018

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7 July 2018

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7 July 2018

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7 July 2018

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7 July 2018

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7 July 2018

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Crossref

https://api.crossref.org/works/10.1038%2FSJ.BJC.6601030

Peutz-Jeghers syndrome. A clinicopathologic study of a large family with a 27-year follow-up

21 January 2018

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12 December 2020

Testicular tumors with Peutz-Jeghers syndrome

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12 December 2020

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

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12 December 2020

An aromatase-producing sex-cord tumor resulting in prepubertal gynecomastia

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12 December 2020

Feminizing Sertoli cell tumors in boys with Peutz-Jeghers syndrome

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12 December 2020

Mutation analysis in 46 German families with familial hypercholesterolemia: identification of 8 new mutations. Mutations in brief no. 226. Online

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Crossref

https://api.crossref.org/works/10.1038%2FSJ.BJC.6601030

7 January 2021

inferred from DOI database lookup

Identifiers

DOI

10.1038/SJ.BJC.6601030

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12865922%20AND%20SRC:MED&resulttype=core&format=json

Dimensions Publication ID

5 November 2019

0 references

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12865922%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

1 reference