KLLN epigenotype-phenotype associations in Cowden syndrome.

about

Hereditary and familial thyroid tumours.A pathogenic role for germline PTEN variants which accumulate into the nucleus.

P2860

Q48120117-C536A521-4EA9-4A6C-BD63-71D696D86FAF Q52715838-B5107616-D715-4A4D-ADF0-B609ED57D515

P2860

KLLN epigenotype-phenotype associations in Cowden syndrome.

Item

http://www.wikidata.org/entity/Q36184627

description

2015 nî lūn-bûn

@nan

2015年の論文

@ja

2015年論文

@yue

2015年論文

@zh-hant

2015年論文

@zh-hk

2015年論文

@zh-mo

2015年論文

@zh-tw

2015年论文

@wuu

2015年论文

@zh

2015年论文

@zh-cn

name

KLLN epigenotype-phenotype associations in Cowden syndrome.

@ast

KLLN epigenotype-phenotype associations in Cowden syndrome.

@en

type

Item

label

KLLN epigenotype-phenotype associations in Cowden syndrome.

@ast

KLLN epigenotype-phenotype associations in Cowden syndrome.

@en

prefLabel

KLLN epigenotype-phenotype associations in Cowden syndrome.

@ast

KLLN epigenotype-phenotype associations in Cowden syndrome.

@en

P1476

KLLN epigenotype-phenotype associations in Cowden syndrome

@en

P2093

Emily A Nizialek

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

Jessica L Mester

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

P2860

Androgen receptor-induced tumor suppressor, KLLN, inhibits breast cancer growth and transcriptionally activates p53/p73-mediated apoptosis in breast carcinomas

A clinical scoring system for selection of patients for PTEN mutation testing is proposed on the basis of a prospective study of 3042 probands

Will the real Cowden syndrome please stand up: revised diagnostic criteria

Cancer statistics, 2013

Functions of DNA methylation: islands, start sites, gene bodies and beyond

Germline PTEN mutations in Cowden syndrome-like families.

PTEN hamartoma tumor syndrome: an overview.

Germline and somatic DNA methylation and epigenetic regulation of KILLIN in renal cell carcinoma.

Incidence and clinical characteristics of thyroid cancer in prospective series of individuals with Cowden and Cowden-like syndrome characterized by germline PTEN, SDH, or KLLN alterations

Lifetime cancer risks in individuals with germline PTEN mutations.

P2888

ejhg.2015.8

P304

1538-1543

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

P31

scholarly article

P356

10.1038/EJHG.2015.8

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

P433

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

P478

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

P50

Charis Eng

Dominic J. Smiraglia

Vineet K Dhiman

P577

2015-02-11T00:00:00Z

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

P5875

272192119

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

P698

25669429

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

P932

4613489

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

KLLN epigenotype-phenotype associations in Cowden syndrome.

about

P2860

P2860

KLLN epigenotype-phenotype associations in Cowden syndrome.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P2888

P304

P31

P356

P433

P478

P50

P577

P5875

P698

P932

P356

P1433

P1476

P2093

P2860

P2888

P304

P31

P356

P433

P478

P50

P577

P5875

P698

P932