(Q34239731)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20864635%20AND%20SRC:MED&resulttype=core&format=json

14 February 2020

title

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

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20864635%20AND%20SRC:MED&resulttype=core&format=json

14 February 2020

1 reference

Victor-Manuel Barbera

3

1 reference

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14 February 2020

Carmen Guillen Ponce

7

1 reference

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14 February 2020

Cecilia Egoavil

10

1 reference

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14 February 2020

José Luis Soto

14

1 reference

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14 February 2020

1

Carla Guarinos

1 reference

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14 February 2020

2

Adela Castillejo

1 reference

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14 February 2020

Lucía Pérez-Carbonell

4

object named as

Lucía Pérez-Carbonell

1 reference

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Ana Beatriz Sanchez-Heras

14 February 2020

5

object named as

Ana-Beatriz Sánchez-Heras

1 reference

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14 February 2020

6

Angel Segura

1 reference

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14 February 2020

8

Ana Martínez-Cantó

1 reference

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14 February 2020

María-Isabel Castillejo

9

object named as

María-Isabel Castillejo

1 reference

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14 February 2020

11

Rodrigo Jover

1 reference

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14 February 2020

13

Cristina Alenda

1 reference

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14 February 2020

author name string

Artemio Payá

12

1 reference

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14 February 2020

publication date

23 September 2010

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20864635%20AND%20SRC:MED&resulttype=core&format=json

The Journal of Molecular Diagnostics

14 February 2020

published in

1 reference

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14 February 2020

volume

12

1 reference

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14 February 2020

issue

6

1 reference

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14 February 2020

page(s)

765-770

1 reference

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Methylation analysis of MLH1 improves the selection of patients for genetic testing in Lynch syndrome.

14 February 2020

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2963912

The MLH1 -93 G>A promoter polymorphism and genetic and epigenetic alterations in colon cancer

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2963912

Guidelines for the clinical management of Lynch syndrome (hereditary non-polyposis cancer).

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2963912

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

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2963912

Multipopulation analysis of polymorphisms in five mononucleotide repeats used to determine the microsatellite instability status of human tumors.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2963912

Accuracy of revised Bethesda guidelines, microsatellite instability, and immunohistochemistry for the identification of patients with hereditary nonpolyposis colorectal cancer.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2963912

BRAF screening as a low-cost effective strategy for simplifying HNPCC genetic testing

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2963912

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

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2963912

Frequent EpCam protein expression in human carcinomas

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2963912

Germ-line msh6 mutations in colorectal cancer families

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2963912

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

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2963912

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

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2963912

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

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2963912

MGMT germline polymorphism is associated with somatic MGMT promoter methylation and gene silencing in colorectal cancer

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2963912

Germline epimutation of MLH1 in individuals with multiple cancers.

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2963912

alpha-thalassemia resulting from a negative chromosomal position effect

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2963912

Lynch Syndrome (Hereditary Nonpolyposis Colorectal Cancer) Diagnostics

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2963912

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

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2963912

Microsatellite instability analysis and/or immunostaining for the diagnosis of hereditary nonpolyposis colorectal cancer?

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2963912

Evaluation of microsatellite instability and immunohistochemistry for the prediction of germ-line MSH2 and MLH1 mutations in hereditary nonpolyposis colon cancer families

28 October 2018

1 reference

12 December 2020

Hereditary colorectal cancer

1 reference

12 December 2020

Screening for Lynch syndrome (hereditary nonpolyposis colorectal cancer) among endometrial cancer patients

1 reference

12 December 2020

The cost-effectiveness of genetic testing strategies for Lynch syndrome among newly diagnosed patients with colorectal cancer

1 reference

12 December 2020

10.2353/JMOLDX.2010.100039

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20864635%20AND%20SRC:MED&resulttype=core&format=json

14 February 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20864635%20AND%20SRC:MED&resulttype=core&format=json

14 February 2020

1 reference