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  14 search results for 'mutation'

TitleAuthorsJournal
Ice-COLD-PCR enables rapid amplification and robust enrichment for low-abundance unknown DNA mutations. (2011)Milbury CA, Li J, Makrigiorgos GMNucleic Acids Res.
Two-round coamplification at lower denaturation temperature-PCR (COLD-PCR)-based sanger sequencing identifies a novel spectrum of low-level mutations in lung adenocarcinoma. (2009)Li J, Milbury CA, Li C, Makrigiorgos GMHum. Mutat.
A recent adaptive transposable element insertion near highly conserved developmental loci in Drosophila melanogaster. (2009)Gonzlez J, Macpherson JM, Petrov DAMol. Biol. Evol.
CpG island methylator phenotype-low (CIMP-low) in colorectal cancer: possible associations with male sex and KRAS mutations. (2006)Ogino S, Kawasaki T, Kirkner GJ, Loda M, Fuchs CSJ Mol Diagn
A prospective study of dietary folate and vitamin B and colon cancer according to microsatellite instability and KRAS mutational status. (2008)Schernhammer ES, Giovannuccci E, Fuchs CS, Ogino SCancer Epidemiol. Biomarkers Prev.
CpG island methylator phenotype, microsatellite instability, BRAF mutation and clinical outcome in colon cancer. (2009)Ogino S, Nosho K, Kirkner GJ, Kawasaki T, Meyerhardt JA, Loda M, Giovannucci EL, Fuchs CSGut
PIK3CA mutation in colorectal cancer: relationship with genetic and epigenetic alterations. (2008)Nosho K, Kawasaki T, Ohnishi M, Suemoto Y, Kirkner GJ, Zepf D, Yan L, Longtine JA, Fuchs CS, Ogino SNeoplasia
PIK3CA mutation is associated with poor prognosis among patients with curatively resected colon cancer. (2009)Ogino S, Nosho K, Kirkner GJ, Shima K, Irahara N, Kure S, Chan AT, Engelman JA, Kraft P, Cantley LC, Giovannucci EL, Fuchs CSJ. Clin. Oncol.
Vitamin D receptor expression is associated with PIK3CA and KRAS mutations in colorectal cancer. (2009)Kure S, Nosho K, Baba Y, Irahara N, Shima K, Ng K, Meyerhardt JA, Giovannucci EL, Fuchs CS, Ogino SCancer Epidemiol. Biomarkers Prev.
KRAS mutation in stage III colon cancer and clinical outcome following intergroup trial CALGB 89803. (2009)Ogino S, Meyerhardt JA, Irahara N, Niedzwiecki D, Hollis D, Saltz LB, Mayer RJ, Schaefer P, Whittom R, Hantel A, Benson AB, Goldberg RM, Bertagnolli MM, Fuchs CSClin. Cancer Res.
Sensitive sequencing method for KRAS mutation detection by Pyrosequencing. (2005)Ogino S, Kawasaki T, Brahmandam M, Yan L, Cantor M, Namgyal C, Mino-Kenudson M, Lauwers GY, Loda M, Fuchs CSJ Mol Diagn
The relationship between DNA methylation and telomere length in dyskeratosis congenita. (2012)Gadalla SM, Katki HA, Shebl FM, Giri N, Alter BP, Savage SAAging Cell
Folate deficiency induces genomic uracil misincorporation and hypomethylation but does not increase DNA point mutations. (2009)Linhart HG, Troen A, Bell GW, Cantu E, Chao WH, Moran E, Steine E, He T, Jaenisch RGastroenterology
Epigenetic characterization of the FMR1 gene and aberrant neurodevelopment in human induced pluripotent stem cell models of fragile X syndrome. (2011)Sheridan SD, Theriault KM, Reis SA, Zhou F, Madison JM, Daheron L, Loring JF, Haggarty SJPLoS ONE