(Q47713981)

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Functional analysis of human MLH1 mutations in Saccharomyces cerevisiae

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Europe PubMed Central

PubMed publication ID

5 February 2018

http://europepmc.org/abstract/MED/9697702

Functional analysis of human MLH1 mutations in Saccharomyces cerevisiae (English)

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Europe PubMed Central

PubMed publication ID

5 February 2018

http://europepmc.org/abstract/MED/9697702

Saccharomyces cerevisiae

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5

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Europe PubMed Central

PubMed publication ID

5 February 2018

http://europepmc.org/abstract/MED/9697702

author name string

H Shimodaira

1

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Europe PubMed Central

PubMed publication ID

5 February 2018

http://europepmc.org/abstract/MED/9697702

N Filosi

2

1 reference

Europe PubMed Central

PubMed publication ID

5 February 2018

http://europepmc.org/abstract/MED/9697702

H Shibata

3

1 reference

Europe PubMed Central

PubMed publication ID

5 February 2018

http://europepmc.org/abstract/MED/9697702

T Suzuki

4

1 reference

Europe PubMed Central

PubMed publication ID

5 February 2018

http://europepmc.org/abstract/MED/9697702

R Kanamaru

6

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Europe PubMed Central

PubMed publication ID

5 February 2018

http://europepmc.org/abstract/MED/9697702

S H Friend

7

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Europe PubMed Central

PubMed publication ID

5 February 2018

http://europepmc.org/abstract/MED/9697702

R D Kolodner

8

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Europe PubMed Central

PubMed publication ID

5 February 2018

http://europepmc.org/abstract/MED/9697702

C Ishioka

9

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Europe PubMed Central

PubMed publication ID

5 February 2018

http://europepmc.org/abstract/MED/9697702

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1 August 1998

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Europe PubMed Central

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5 February 2018

http://europepmc.org/abstract/MED/9697702

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6

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Nature Genetics

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Europe PubMed Central

PubMed publication ID

5 February 2018

http://europepmc.org/abstract/MED/9697702

19

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Europe PubMed Central

PubMed publication ID

5 February 2018

http://europepmc.org/abstract/MED/9697702

4

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Europe PubMed Central

PubMed publication ID

5 February 2018

http://europepmc.org/abstract/MED/9697702

384-389

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Europe PubMed Central

PubMed publication ID

5 February 2018

http://europepmc.org/abstract/MED/9697702

Overview of natural history, pathology, molecular genetics and management of HNPCC (Lynch Syndrome).

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Detection of heterozygous truncating mutations in the BRCA1 and APC genes by using a rapid screening assay in yeast

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Biochemistry and genetics of eukaryotic mismatch repair

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Destabilization of tracts of simple repetitive DNA in yeast by mutations affecting DNA mismatch repair

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Microsatellite instability in yeast: dependence on repeat unit size and DNA mismatch repair genes

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Screening patients for heterozygous p53 mutations using a functional assay in yeast

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Mean age of tumor onset in hereditary nonpolyposis colorectal cancer (HNPCC) families correlates with the presence of mutations in DNA mismatch repair genes

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Redundancy of Saccharomyces cerevisiae MSH3 and MSH6 in MSH2-dependent mismatch repair

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The distribution of the numbers of mutants in bacterial populations

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inferred from DOI database lookup

Multifunctional yeast high-copy-number shuttle vectors

1 reference

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7 January 2021

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Mutation in the DNA mismatch repair gene homologue hMLH1 is associated with hereditary non-polyposis colon cancer

1 reference

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The International Collaborative Group on Hereditary Non-Polyposis Colorectal Cancer (ICG-HNPCC)

1 reference

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Characterization of MSH2 and MLH1 mutations in Italian families with hereditary nonpolyposis colorectal cancer

1 reference

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Europe PubMed Central

PubMed publication ID

5 February 2018

http://europepmc.org/abstract/MED/9697702

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

5 February 2018

http://europepmc.org/abstract/MED/9697702

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