(Q83148042)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21213371%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

title

Intensity-dependent constitutional MLH1 promoter methylation leads to early onset of colorectal cancer by affecting both alleles (English)

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19 January 2020

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15

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19 January 2020

4

Christine Lasset

1 reference

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19 January 2020

author name string

Jessie Auclair

1

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19 January 2020

Thomas Vaissière

2

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19 January 2020

Françoise Desseigne

3

1 reference

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19 January 2020

Valérie Bonadona

5

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19 January 2020

Sophie Giraud

6

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19 January 2020

Jean-Christophe Saurin

7

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19 January 2020

Marie-Odile Joly

8

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19 January 2020

Dominique Leroux

9

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19 January 2020

Laurence Faivre

10

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19 January 2020

Carole Audoynaud

11

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19 January 2020

Gilles Montmain

12

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19 January 2020

Eric Ruano

13

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19 January 2020

Zdenko Herceg

14

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19 January 2020

Qing Wang

16

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19 January 2020

publication date

9 December 2010

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Genes, Chromosomes and Cancer

19 January 2020

published in

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19 January 2020

volume

50

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19 January 2020

issue

3

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19 January 2020

page(s)

178-185

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Systematic mRNA analysis for the effect of MLH1 and MSH2 missense and silent mutations on aberrant splicing.

19 January 2020

cites work

1 reference

7 January 2021

Novel biallelic mutations in MSH6 and PMS2 genes: gene conversion as a likely cause of PMS2 gene inactivation.

1 reference

7 January 2021

The 5' region of the MSH2 gene involved in hereditary non-polyposis colorectal cancer contains a high density of recombinogenic sequences

1 reference

7 January 2021

Loss of IGF2 imprinting: a potential marker of colorectal cancer risk

1 reference

7 January 2021

Incidence and functional consequences of hMLH1 promoter hypermethylation in colorectal carcinoma

1 reference

7 January 2021

MLH1 Germline Epimutations as a Factor in Hereditary Nonpolyposis Colorectal Cancer

1 reference

7 January 2021

Inheritance of a Cancer-AssociatedMLH1Germ-Line Epimutation

1 reference

7 January 2021

Lynch Syndrome (Hereditary Nonpolyposis Colorectal Cancer) Diagnostics

1 reference

7 January 2021

Heritable somatic methylation and inactivation of MSH2 in families with Lynch syndrome due to deletion of the 3' exons of TACSTD1.

1 reference

7 January 2021

Extensive but hemiallelic methylation of the hMLH1 promoter region in early-onset sporadic colon cancers with microsatellite instability

1 reference

7 January 2021

Further evidence for heritability of an epimutation in one of 12 cases with MLH1 promoter methylation in blood cells clinically displaying HNPCC

1 reference

7 January 2021

Frequent CpG island methylation in serrated adenomas of the colorectum

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7 January 2021

Germline epimutation of MLH1 in individuals with multiple cancers

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7 January 2021

MLH1 germline epimutations in selected patients with early-onset non-polyposis colorectal cancer

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7 January 2021

Epigenotyping in peripheral blood cell DNA and breast cancer risk: a proof of principle study

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7 January 2021

MLH1 promoter germline-methylation in selected probands of Chinese hereditary non-polyposis colorectal cancer families

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7 January 2021

Identifiers

DOI

10.1002/GCC.20842

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21213371%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

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