Frameshift mutation of the STK11 gene in a sporadic gastrointestinal cancer with microsatellite instability.

about

Loss of imprinting of the insulin-like growth factor II gene occurs by biallelic methylation in a core region of H19-associated CTCF-binding sites in colorectal cancer Mutations in the human LKB1/STK11 gene.Molecular and prognostic heterogeneity of microsatellite-unstable colorectal cancer.

P2860

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P2860

Frameshift mutation of the STK11 gene in a sporadic gastrointestinal cancer with microsatellite instability.

Item

http://www.wikidata.org/entity/Q55092553

description

1999 nî lūn-bûn

@nan

1999年の論文

@ja

1999年学术文章

@wuu

1999年学术文章

@zh

1999年学术文章

@zh-cn

1999年学术文章

@zh-hans

1999年学术文章

@zh-my

1999年学术文章

@zh-sg

1999年學術文章

@yue

1999年學術文章

@zh-hant

name

Frameshift mutation of the STK ...... th microsatellite instability.

@en

Frameshift mutation of the STK ...... th microsatellite instability.

@nl

type

Item

label

Frameshift mutation of the STK ...... th microsatellite instability.

@en

Frameshift mutation of the STK ...... th microsatellite instability.

@nl

prefLabel

Frameshift mutation of the STK ...... th microsatellite instability.

@en

Frameshift mutation of the STK ...... th microsatellite instability.

@nl

P1476

Frameshift mutation of the STK ...... th microsatellite instability.

@en

P2093

H Nakagawa

http://www.w3.org/2001/XMLSchema#string

K Koyama

http://www.w3.org/2001/XMLSchema#string

M Kameyama

http://www.w3.org/2001/XMLSchema#string

M Monden

http://www.w3.org/2001/XMLSchema#string

S Imaoka

http://www.w3.org/2001/XMLSchema#string

S Nakamori

http://www.w3.org/2001/XMLSchema#string

Y Nakamura

http://www.w3.org/2001/XMLSchema#string

P2860

Inactivation of the type II TGF-beta receptor in colon cancer cells with microsatellite instability

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

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

Low frequency of somatic mutations in the LKB1/Peutz-Jeghers syndrome gene in sporadic breast cancer

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

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

Cancer and the Peutz-Jeghers syndrome.

Increased risk of cancer in the Peutz-Jeghers syndrome.

Somatic mutations in LKB1 are rare in sporadic colorectal and testicular tumors.

Mutations of the STK11 gene in sporadic gastric carcinoma.

P304

633-637

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.1111/J.1349-7006.1999.TB00794.X

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P433

http://www.w3.org/2001/XMLSchema#string

P478

http://www.w3.org/2001/XMLSchema#string

P577

1999-06-01T00:00:00Z

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P5875

227960390

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P698

10429655

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P921

microsatellite

P932

5926116

http://www.w3.org/2001/XMLSchema#string

Frameshift mutation of the STK11 gene in a sporadic gastrointestinal cancer with microsatellite instability.

about

P2860

P2860

Frameshift mutation of the STK11 gene in a sporadic gastrointestinal cancer with microsatellite instability.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P577

P5875

P698

P921

P932

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P577

P5875

P698

P921

P932