(Q81020002)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16086322%20AND%20SRC:MED&resulttype=core&format=json

5 January 2020

title

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

1 reference

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5 January 2020

1 reference

1 reference

3

1 reference

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5 January 2020

Mef Nilbert

11

1 reference

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5 January 2020

7

Sylviane Olschwang

1 reference

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5 January 2020

author name string

Françoise Charbonnier

1

1 reference

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5 January 2020

Stephanie Baert-Desurmont

2

1 reference

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5 January 2020

Frederic Di Fiore

4

1 reference

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5 January 2020

Cosette Martin

5

1 reference

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5 January 2020

Stephanie Frerot

6

1 reference

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5 January 2020

Qing Wang

8

1 reference

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5 January 2020

Marie-Pierre Buisine

9

1 reference

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5 January 2020

Brigitte Gilbert

10

1 reference

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5 January 2020

Annika Lindblom

12

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5 January 2020

Thierry Frebourg

13

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5 January 2020

publication date

1 September 2005

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5 January 2020

1 reference

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5 January 2020

volume

26

1 reference

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5 January 2020

issue

3

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5 January 2020

page(s)

255-261

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Translocation and gross deletion breakpoints in human inherited disease and cancer I: Nucleotide composition and recombination-associated motifs

5 January 2020

cites work

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20216

7 January 2021

Alu repeats and human genomic diversity

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20216

7 January 2021

Dosage analysis of cancer predisposition genes by multiplex ligation-dependent probe amplification

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20216

7 January 2021

Alu repeats and human disease

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20216

7 January 2021

Screening for genomic rearrangements of the MMR genes must be included in the routine diagnosis of HNPCC.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20216

7 January 2021

Promoter analysis of the human mismatch repair gene hMSH2.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20216

7 January 2021

Evolutionary impact of human Alu repetitive elements

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20216

7 January 2021

A fundamental division in the Alu family of repeated sequences

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20216

7 January 2021

The role of Alu repeat clusters as mediators of recurrent chromosomal aberrations in tumors

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20216

7 January 2021

Initial sequencing and analysis of the human genome

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20216

7 January 2021

Hereditary nonpolyposis colorectal cancer and related conditions

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20216

7 January 2021

The carcinoma-associated antigen EpCAM upregulates c-myc and induces cell proliferation

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20216

7 January 2021

Identification and characterization of genomic rearrangements of MSH2 and MLH1 in Lynch syndrome (HNPCC) by novel techniques

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20216

7 January 2021

One short well conserved region of Alu-sequences is involved in human gene rearrangements and has homology with prokaryotic chi.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20216

7 January 2021

Genomic deletions in MSH2 or MLH1 are a frequent cause of hereditary non-polyposis colorectal cancer: identification of novel and recurrent deletions by MLPA.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20216

7 January 2021

New clinical criteria for hereditary nonpolyposis colorectal cancer (HNPCC, Lynch syndrome) proposed by the International Collaborative group on HNPCC.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20216

7 January 2021

Molecular analysis of hereditary nonpolyposis colorectal cancer in the United States: high mutation detection rate among clinically selected families and characterization of an American founder genomic deletion of the MSH2 gene

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20216

7 January 2021

Hereditary nonpolyposis colorectal cancer: frequent occurrence of large genomic deletions in MSH2 and MLH1 genes

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20216

7 January 2021

Identifiers

DOI

10.1002/HUMU.20216

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16086322%20AND%20SRC:MED&resulttype=core&format=json

5 January 2020

1 reference