Literature DB >> 12362032

Description and functional analysis of a novel in frame mutation linked to hereditary non-polyposis colorectal cancer.

T E Raevaara, T Timoharju, K E Lönnqvist, R Kariola, M Steinhoff, R M W Hofstra, E Mangold, Y J Vos, M Nyström-Lahti.   

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Year:  2002        PMID： 12362032      PMCID： PMC1734999          DOI： 10.1136/jmg.39.10.747

Source DB:  PubMed          Journal:  J Med Genet        ISSN： 0022-2593            Impact factor:   6.318


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  4 in total

1.  Spontaneously arising mutL mutators in evolving Escherichia coli populations are the result of changes in repeat length.

Authors:  Aaron C Shaver; Paul D Sniegowski
Journal:  J Bacteriol       Date:  2003-10       Impact factor: 3.490

2.  Disruption of an exon splicing enhancer in exon 3 of MLH1 is the cause of HNPCC in a Quebec family.

Authors:  S McVety; L Li; P H Gordon; G Chong; W D Foulkes
Journal:  J Med Genet       Date:  2005-05-27       Impact factor: 6.318

3.  Patients with an unexplained microsatellite instable tumour have a low risk of familial cancer.

Authors:  L I H Overbeek; C M Kets; K M Hebeda; D Bodmer; E van der Looij; R Willems; M Goossens; N Arts; H G Brunner; J H J M van Krieken; N Hoogerbrugge; M J L Ligtenberg
Journal:  Br J Cancer       Date:  2007-04-24       Impact factor: 7.640

4.  A Novel Germline MLH1 In-Frame Deletion in a Slovenian Lynch Syndrome Family Associated with Uncommon Isolated PMS2 Loss in Tumor Tissue.

Authors:  Gašper Klančar; Ana Blatnik; Vita Šetrajčič Dragoš; Vesna Vogrič; Vida Stegel; Olga Blatnik; Primož Drev; Barbara Gazič; Mateja Krajc; Srdjan Novaković
Journal:  Genes (Basel)       Date:  2020-03-18       Impact factor: 4.096
  4 in total

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