(Q44080353)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21309036%20AND%20SRC:MED&resulttype=core&format=json

22 January 2020

title

Recurrence and variability of germline EPCAM deletions in Lynch syndrome (English)

1 reference

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22 January 2020

2

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22 January 2020

Iris Nagtegaal

30

1 reference

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22 January 2020

Han van Krieken

31

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22 January 2020

Nicoline Hoogerbrugge

33

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22 January 2020

Marjolijn J L Ligtenberg

35

object named as

Marjolijn J L Ligtenberg

1 reference

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22 January 2020

19

Elke Holinski-Feder

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22 January 2020

author name string

Roland P Kuiper

1

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22 January 2020

Ramprasath Venkatachalam

3

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22 January 2020

Danielle Bodmer

4

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22 January 2020

Eveline Hoenselaar

5

1 reference

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22 January 2020

Monique Goossens

6

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22 January 2020

Aline Haufe

7

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22 January 2020

Eveline Kamping

8

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22 January 2020

Renée C Niessen

9

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22 January 2020

Frans B L Hogervorst

10

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22 January 2020

Johan J P Gille

11

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22 January 2020

Bert Redeker

12

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22 January 2020

Carli M J Tops

13

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22 January 2020

Marielle E van Gijn

14

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22 January 2020

Ans M W van den Ouweland

15

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22 January 2020

Nils Rahner

16

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22 January 2020

Verena Steinke

17

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22 January 2020

Philip Kahl

18

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22 January 2020

Monika Morak

20

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22 January 2020

Matthias Kloor

21

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22 January 2020

Susanne Stemmler

22

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22 January 2020

Beate Betz

23

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22 January 2020

Pierre Hutter

24

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22 January 2020

David J Bunyan

25

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22 January 2020

Sapna Syngal

26

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22 January 2020

Julie O Culver

27

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22 January 2020

Tracy Graham

28

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22 January 2020

Tsun L Chan

29

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22 January 2020

Hans K Schackert

32

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22 January 2020

Ad Geurts van Kessel

34

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22 January 2020

language of work or name

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1 March 2011

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22 January 2020

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22 January 2020

volume

32

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22 January 2020

issue

4

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22 January 2020

page(s)

407-414

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Identification and survival of carriers of mutations in DNA mismatch-repair genes in colon cancer

22 January 2020

cites work

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21446

Alu repeats and human genomic diversity

21 January 2018

1 reference

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Heritable germline epimutation of MSH2 in a family with hereditary nonpolyposis colorectal cancer

21 January 2018

1 reference

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Transcription is required for establishment of germline methylation marks at imprinted genes

21 January 2018

1 reference

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Alu-Alu recombination underlies the vast majority of large VHL germline deletions: Molecular characterization and genotype-phenotype correlations in VHL patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21446

EPCAM germ line deletions as causes of Lynch syndrome in Spanish patients

21 January 2018

1 reference

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Screening for the Lynch syndrome (hereditary nonpolyposis colorectal cancer).

21 January 2018

1 reference

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Promoter targeted small RNAs induce long-term transcriptional gene silencing in human cells

21 January 2018

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Epimutations and cancer predisposition: importance and mechanisms

21 January 2018

1 reference

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Inheritance of a Cancer-AssociatedMLH1Germ-Line Epimutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21446

Risk of colorectal and endometrial cancers in EPCAM deletion-positive Lynch syndrome: a cohort study

21 January 2018

1 reference

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Deletions removing the last exon of TACSTD1 constitute a distinct class of mutations predisposing to Lynch syndrome.

21 January 2018

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https://api.crossref.org/works/10.1002%2FHUMU.21446

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

21 January 2018

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Somatic hypermethylation of MSH2 is a frequent event in Lynch Syndrome colorectal cancers

21 January 2018

1 reference

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Germline hypermethylation of MLH1 and EPCAM deletions are a frequent cause of Lynch syndrome.

21 January 2018

1 reference

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Ptprj is a candidate for the mouse colon-cancer susceptibility locus Scc1 and is frequently deleted in human cancers

21 January 2018

1 reference

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Structural variation in the human genome and its role in disease

21 January 2018

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Germline epimutation of MLH1 in individuals with multiple cancers.

21 January 2018

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Transcription of antisense RNA leading to gene silencing and methylation as a novel cause of human genetic disease

21 January 2018

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Molecular characterization of the spectrum of genomic deletions in the mismatch repair genesMSH2,MLH1,MSH6, andPMS2 responsible for hereditary nonpolyposis colorectal cancer (HNPCC)

21 January 2018

1 reference

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Germline epigenetic silencing of the tumor suppressor gene PTPRJ in early-onset familial colorectal cancer

21 January 2018

1 reference

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Rare pathogenic microdeletions and tandem duplications are microhomology-mediated and stimulated by local genomic architecture

21 January 2018

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The risk of extra-colonic, extra-endometrial cancer in the Lynch syndrome.

21 January 2018

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The epithelial cell adhesion molecule (Ep-CAM) as a morphoregulatory molecule is a tool in surgical pathology

21 January 2018

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Epigenetic silencing of tumour suppressor gene p15 by its antisense RNA

21 January 2018

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Incidence of Hereditary Nonpolyposis Colorectal Cancer and the Feasibility of Molecular Screening for the Disease

21 January 2018

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Distinct patterns of germ-line deletions inMLH1 andMSH2: the implication of Alu repetitive element in the genetic etiology of Lynch syndrome (HNPCC)

21 January 2018

1 reference

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Novel genomic insertion-deletion in MLH1: possible mechanistic role for non-homologous end-joining DNA repair

21 January 2018

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Deletion of the NESP55 differentially methylated region causes loss of maternal GNAS imprints and pseudohypoparathyroidism type Ib

21 January 2018

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7 January 2021

Hereditary colorectal cancer

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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

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7 January 2021

MSH2 genomic deletions are a frequent cause of HNPCC

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7 January 2021