Incomplete Segregation of MSH6 Frameshift Variants with Phenotype of Lynch Syndrome. - Wikidata - awgldk - TriplyDB

Incomplete Segregation of MSH6 Frameshift Variants with Phenotype of Lynch Syndrome.

Incomplete Segregation of MSH6 Frameshift Variants with Phenotype of Lynch Syndrome.

http://www.wikidata.org/entity/Q33755092

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Same MSH2 Gene Mutation But Variable Phenotypes in 2 Families With Lynch Syndrome: Two Case Reports and Review of Genotype-Phenotype Correlation.Novel MSH2 splice-site mutation in a young patient with Lynch syndrome.

P2860

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P2860

Incomplete Segregation of MSH6 Frameshift Variants with Phenotype of Lynch Syndrome.

http://www.wikidata.org/entity/Q33755092

description

2017 nî lūn-bûn

@nan

2017 թուականի Մայիսին հրատարակուած գիտական յօդուած

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2017 թվականի մայիսին հրատարակված գիտական հոդված

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2017年の論文

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2017年論文

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2017年論文

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2017年論文

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2017年論文

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2017年論文

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2017年论文

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name

Incomplete Segregation of MSH6 Frameshift Variants with Phenotype of Lynch Syndrome.

@ast

Incomplete Segregation of MSH6 Frameshift Variants with Phenotype of Lynch Syndrome.

@en

type

label

Incomplete Segregation of MSH6 Frameshift Variants with Phenotype of Lynch Syndrome.

@ast

Incomplete Segregation of MSH6 Frameshift Variants with Phenotype of Lynch Syndrome.

@en

prefLabel

Incomplete Segregation of MSH6 Frameshift Variants with Phenotype of Lynch Syndrome.

@ast

Incomplete Segregation of MSH6 Frameshift Variants with Phenotype of Lynch Syndrome.

@en

P1433

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P1433

International Journal of Molecular Sciences

P1476

Incomplete Segregation of MSH6 Frameshift Variants with Phenotype of Lynch Syndrome.

@en

P2093

Francesca Duraturo

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

Giovanni Battista Rossi

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

Marina De Rosa

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

Nicola Carlomagno

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

Paola Izzo

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

Raffaella Liccardo

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

P2860

Revised Bethesda Guidelines for hereditary nonpolyposis colorectal cancer (Lynch syndrome) and microsatellite instability

Lynch syndrome and Lynch syndrome mimics: The growing complex landscape of hereditary colon cancer

Germline mutation of MSH6 as the cause of hereditary nonpolyposis colorectal cancer

A National Cancer Institute Workshop on Microsatellite Instability for cancer detection and familial predisposition: development of international criteria for the determination of microsatellite instability in colorectal cancer

Isolation of an hMSH2-p160 heterodimer that restores DNA mismatch repair to tumor cells

GTBP, a 160-kilodalton protein essential for mismatch-binding activity in human cells

Somatic hypermutation in MutS homologue (MSH)3-, MSH6-, and MSH3/MSH6-deficient mice reveals a role for the MSH2-MSH6 heterodimer in modulating the base substitution pattern

The DNA mismatch repair genes Msh3 and Msh6 cooperate in intestinal tumor suppression

Dominant effects of an Msh6 missense mutation on DNA repair and cancer susceptibility

Mutation in the mismatch repair gene Msh6 causes cancer susceptibility

P31

scholarly article

P356

10.3390/IJMS18050999

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5

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2017-05-06T00:00:00Z

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28481244

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5454912

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