The MLH1 D132H variant is associated with susceptibility to sporadic colorectal cancer (Q46118451)

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scientific article published on 6 June 2004

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English	The MLH1 D132H variant is associated with susceptibility to sporadic colorectal cancer	scientific article published on 6 June 2004

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scholarly article

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Europe PubMed Central

PubMed publication ID

15184898

retrieved

19 December 2017

reference URL

http://europepmc.org/abstract/MED/15184898

title

The MLH1 D132H variant is associated with susceptibility to sporadic colorectal cancer (English)

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Europe PubMed Central

PubMed publication ID

15184898

retrieved

19 December 2017

reference URL

http://europepmc.org/abstract/MED/15184898

main subject

colorectal cancer

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author

Francis Collins

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14

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Francis Collins

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Europe PubMed Central

PubMed publication ID

15184898

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19 December 2017

Gad Rennert

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3

object named as

Gad Rennert

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Europe PubMed Central

PubMed publication ID

15184898

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19 December 2017

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http://europepmc.org/abstract/MED/15184898

author name string

Steven M Lipkin

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1

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PubMed publication ID

15184898

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19 December 2017

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http://europepmc.org/abstract/MED/15184898

Laura S Rozek

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2

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15184898

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19 December 2017

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http://europepmc.org/abstract/MED/15184898

Wei Yang

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4

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PubMed publication ID

15184898

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19 December 2017

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http://europepmc.org/abstract/MED/15184898

Peng-Chieh Chen

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5

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15184898

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19 December 2017

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http://europepmc.org/abstract/MED/15184898

Joseph Hacia

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6

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Europe PubMed Central

PubMed publication ID

15184898

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http://europepmc.org/abstract/MED/15184898

Nathan Hunt

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7

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15184898

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19 December 2017

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http://europepmc.org/abstract/MED/15184898

Brian Shin

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8

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PubMed publication ID

15184898

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19 December 2017

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http://europepmc.org/abstract/MED/15184898

Steve Fodor

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9

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PubMed publication ID

15184898

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19 December 2017

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http://europepmc.org/abstract/MED/15184898

Mark Kokoris

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10

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15184898

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19 December 2017

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http://europepmc.org/abstract/MED/15184898

Joel K Greenson

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11

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15184898

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19 December 2017

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http://europepmc.org/abstract/MED/15184898

Eric Fearon

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12

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Europe PubMed Central

PubMed publication ID

15184898

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19 December 2017

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http://europepmc.org/abstract/MED/15184898

Henry Lynch

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13

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PubMed publication ID

15184898

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19 December 2017

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http://europepmc.org/abstract/MED/15184898

Stephen B Gruber

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15

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Europe PubMed Central

PubMed publication ID

15184898

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19 December 2017

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http://europepmc.org/abstract/MED/15184898

language of work or name

English

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publication date

6 June 2004

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PubMed publication ID

15184898

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19 December 2017

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http://europepmc.org/abstract/MED/15184898

published in

Nature Genetics

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PubMed publication ID

15184898

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19 December 2017

reference URL

http://europepmc.org/abstract/MED/15184898

volume

36

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Europe PubMed Central

PubMed publication ID

15184898

retrieved

19 December 2017

reference URL

http://europepmc.org/abstract/MED/15184898

issue

7

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Europe PubMed Central

PubMed publication ID

15184898

retrieved

19 December 2017

reference URL

http://europepmc.org/abstract/MED/15184898

page(s)

694-699

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15184898

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19 December 2017

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http://europepmc.org/abstract/MED/15184898

cites work

Familial endometrial cancer in female carriers of MSH6 germline mutations

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FNG1374

retrieved

21 January 2018

Do MSH6 mutations contribute to double primary cancers of the colorectum and endometrium?

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FNG1374

retrieved

21 January 2018

MSH6 germline mutations are rare in colorectal cancer families.

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FNG1374

retrieved

21 January 2018

Are ATM mutations 7271T-->G and IVS10-6T-->G really high-risk breast cancer-susceptibility alleles?

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FNG1374

retrieved

21 January 2018

Familial colorectal cancer in Ashkenazim due to a hypermutable tract in APC

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FNG1374

retrieved

21 January 2018

HNPCC-like cancer predisposition in mice through simultaneous loss of Msh3 and Msh6 mismatch-repair protein functions

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FNG1374

retrieved

21 January 2018

Functional studies on the candidate ATPase domains of Saccharomyces cerevisiae MutLalpha.

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FNG1374

retrieved

21 January 2018

Identification of the ATP-binding site in the terminase subunit pUL56 of human cytomegalovirus.

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FNG1374

retrieved

21 January 2018

Structure and function of the N-terminal 40 kDa fragment of human PMS2: a monomeric GHL ATPase

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FNG1374

retrieved

21 January 2018

Systematic analysis of hMSH2 and hMLH1 in young colon cancer patients and controls

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FNG1374

retrieved

21 January 2018

The interaction of the human MutL homologues in hereditary nonpolyposis colon cancer

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FNG1374

retrieved

21 January 2018

Novel dominant mutations in Saccharomyces cerevisiae MSH6.

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FNG1374

retrieved

21 January 2018

Regulation of the Human MSH6 Gene by the Sp1 Transcription Factor and Alteration of Promoter Activity and Expression by Polymorphisms

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FNG1374

retrieved

21 January 2018

The founder mutation MSH2*1906G-->C is an important cause of hereditary nonpolyposis colorectal cancer in the Ashkenazi Jewish population

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FNG1374

retrieved

21 January 2018

Two color hybridization analysis using high density oligonucleotide arrays and energy transfer dyes.

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FNG1374

retrieved

21 January 2018

Improved methods for building protein models in electron density maps and the location of errors in these models

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FNG1374

retrieved

21 January 2018

Identification of a novel zinc finger protein binding a conserved element critical for Pit-1-dependent growth hormone gene expression

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FNG1374

retrieved

21 January 2018

The coordinated functions of the E. coli MutS and MutL proteins in mismatch repair

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FNG1374

retrieved

21 January 2018

Human mismatch-repair protein MutL homologue 1 (MLH1) interacts with Escherichia coli MutL and MutS in vivo and in vitro: a simple genetic system to assay MLH1 function

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FNG1374

retrieved

21 January 2018

The MutL ATPase is required for mismatch repair

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FNG1374

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Missense mutations in hMLH1 associated with colorectal cancer

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FNG1374

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Mutations of hMLH1 and hMSH2 in patients with suspected hereditary nonpolyposis colorectal cancer: correlation with microsatellite instability and abnormalities of mismatch repair protein expression

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FNG1374

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Missense mismatch repair gene alterations, microsatellite instability, and hereditary nonpolyposis colorectal cancer

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FNG1374

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Hereditary colorectal cancer

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FNG1374

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Mutational analyses ofBRCA1 andBRCA2 in Ashkenazi and non-Ashkenazi Jewish women with familial breast and ovarian cancer

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FNG1374

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

BLM heterozygosity and the risk of colorectal cancer

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FNG1374

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Phenotype of microsatellite unstable colorectal carcinomas: Well-differentiated and focally mucinous tumors and the absence of dirty necrosis correlate with microsatellite instability

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FNG1374

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

DOI

10.1038/NG1374

1 reference

stated in

Europe PubMed Central

PubMed publication ID

15184898

retrieved

19 December 2017

reference URL

http://europepmc.org/abstract/MED/15184898

PubMed publication ID

15184898

1 reference

stated in

Europe PubMed Central

PubMed publication ID

15184898

retrieved

19 December 2017

reference URL

http://europepmc.org/abstract/MED/15184898

ResearchGate publication ID

8521980

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