(Q55066383)

16 June 2018

title

CpG dinucleotides in the hMSH2 and hMLH1 genes are hotspots for HNPCC mutations. (English)

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16 June 2018

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Y K Maliaka

1

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16 June 2018

A P Chudina

2

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16 June 2018

N F Belev

3

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P Alday

4

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16 June 2018

N P Bochkov

5

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16 June 2018

J M Buerstedde

6

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16 June 2018

publication date

1 February 1996

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16 June 2018

published in

Human Genetics

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16 June 2018

volume

97

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16 June 2018

issue

2

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16 June 2018

page(s)

251-255

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16 June 2018

https://scigraph.springernature.com/pub.10.1007/bf02265276

exact match

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cites work

Genomic structure of human mismatch repair gene, hMLH1, and its mutation analysis in patients with hereditary non-polyposis colorectal cancer (HNPCC)

1 reference

12 December 2020

Seven new mutations in hMSH2, an HNPCC gene, identified by denaturing gradient-gel electrophoresis

1 reference

12 December 2020

Genetics, natural history, tumor spectrum, and pathology of hereditary nonpolyposis colorectal cancer: an updated review

1 reference

12 December 2020

Structure of the human MSH2 locus and analysis of two Muir-Torre kindreds for msh2 mutations

1 reference

12 December 2020

The human mutator gene homolog MSH2 and its association with hereditary nonpolyposis colon cancer

1 reference

12 December 2020

Microsatellite instability in cancer of the proximal colon

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12 December 2020

Ubiquitous somatic mutations in simple repeated sequences reveal a new mechanism for colonic carcinogenesis

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12 December 2020

Close linkage to chromosome 3p and conservation of ancestral founding haplotype in hereditary nonpolyposis colorectal cancer families

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12 December 2020

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

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12 December 2020

The mutational spectrum of single base-pair substitutions causing human genetic disease: patterns and predictions

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12 December 2020

The molecular basis of Turcot's syndrome

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12 December 2020

Mutation of a mutL homolog in hereditary colon cancer

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12 December 2020

Detection of new mutations in six out of 10 Swiss HNPCC families by genomic sequencing of the hMSH2 and hMLH1 genes

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12 December 2020

Mismatch repair gene defects in sporadic colorectal cancers with microsatellite instability

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12 December 2020

Assessing the underlying pattern of human germline mutations: lessons from the factor IX gene

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12 December 2020

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

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12 December 2020

hMSH2 mutations in hereditary nonpolyposis colorectal cancer kindreds

1 reference

12 December 2020

A novel approach to estimate the proportion of hereditary nonpolyposis colorectal cancer of total colorectal cancer burden

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12 December 2020

Identifiers

DOI

10.1007/BF02265276

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16 June 2018

Dimensions Publication ID

1016248513

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16 June 2018