Inherited variants of MYH associated with somatic G:C→T:A mutations in colorectal tumors
By Nada A. Al-Tassan, N. H. Chmiel, J. Maynard, N. Fleming, Alison L. Livingston, Geraint T. Williams, A. Hodges, D. R. Davies, S. David, J. Sampson and 1 more. Nature Genetics, 2002
1,331 citations recorded by the source corpus.
Subfields: Cancer Research, Molecular Biology, Pathology and Forensic Medicine
View Paper: https://www.semanticscholar.org/paper/a7d37685ff62c0743ec27905c0c55e469d2a0f4b
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In Cancer Research
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In Pathology and Forensic Medicine
Citations in the corpus
- Association of MUTYH and colorectal cancer (2006, background): “MUTYH has been associated with multiple colorectal adenomas (Al-Tassan et al, 2002) and with colorectal adenocarcinomas (Croitoru et al, 2004; Farrington et al, 2005).”
- Repair and genetic consequences of endogenous DNA base damage in mammalian cells. (2004, background): “The role of the Escherichia coli mug protein in the removal of uracil and 3,N(4)ethenocytosine from DNA.”
- Oxidative Stress Resistance in Deinococcus radiodurans (2011, background): “coli MutY homolog) that is involved in the repair of the mutagenic consequence of oxidative DNA damage, strongly predispose humans to a rare hereditary form of colorectal cancer called familial adenomatous polyposis (FAP) (13).”
- Milestones of Lynch syndrome: 1895–2015 (2015, background): “MYH-associated polyposis (MAP) In 2002, Al-Tassan et al.(180) reported biallelic germline mutations of the mutY homologue (MYH) base”
- Colorectal cancer and genetic alterations in the Wnt pathway (2006, background): “It was something of a surprise when a recessive ‘version’ of FAP was identified in 2002 (Al-Tassan et al., 2002).”