Mutations of two PMS homologues in hereditary nonpolyposis colon cancer (Q24318484)

GOA release 2020-03-11

DNA binding

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GOA release 2020-03-11

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8

W A Haseltine

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author name string

N C Nicolaides

1

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N Papadopoulos

2

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B Liu

3

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Y F Wei

4

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K C Carter

5

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S M Ruben

6

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C A Rosen

7

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R D Fleischmann

9

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C M Fraser

10

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publication date

1 September 1994

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language of work or name

English

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number of pages

6

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

inferred from page(s)

published in

Nature

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volume

371

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issue

6492

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page(s)

75-80

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cites work

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Isolation and characterization of allelic losses and gains in colorectal tumors by arbitrarily primed polymerase chain reaction

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

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Microsatellite instability in cancer of the proximal colon

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Clues to the pathogenesis of familial colorectal cancer

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

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Hypermutability and mismatch repair deficiency in RER+ tumor cells

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Genetic mapping of a locus predisposing to human colorectal cancer

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Genetic mapping of a second locus predisposing to hereditary non–polyposis colon cancer

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

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

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Mutations of a mutS homolog in hereditary nonpolyposis colorectal cancer

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Mismatch repair and cancer

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

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Mutation of a mutL homolog in hereditary colon cancer

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Complementary DNA sequencing: expressed sequence tags and human genome project

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Rapid production of full-length cDNAs from rare transcripts: amplification using a single gene-specific oligonucleotide primer

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Point mutations define a sequence flanking the AUG initiator codon that modulates translation by eukaryotic ribosomes

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Dual requirement in yeast DNA mismatch repair for MLH1 and PMS1, two homologs of the bacterial mutL gene

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Molecular diagnosis of familial adenomatous polyposis

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Rapid detection of translation-terminating mutations at the adenomatous polyposis coli (APC) gene by direct protein truncation test

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The skipping of constitutive exons in vivo induced by nonsense mutations

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Cloning and nucleotide sequence of DNA mismatch repair gene PMS1 from Saccharomyces cerevisiae: homology of PMS1 to procaryotic MutL and HexB.

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A workbench for multiple alignment construction and analysis

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Identification of p53 gene mutations in bladder cancers and urine samples

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