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http://dx.doi.org/10.1016/j.ccr.2010.08.016 | DOI Listing |
Genes Dev
February 2018
Department of Genetics, The University of Texas MD Anderson Cancer Center, Houston, Texas 77030, USA.
A delicate balance in the levels of proteins that regulate the p53 tumor suppressor pathway exists such that subtle changes alter p53 tumor suppressor activity and cancer risk. Many single-nucleotide polymorphisms (SNPs) in the p53 pathway alter p53 transcriptional activity and are associated with cancer risk. In addition, some SNPs influence the gain-of-function (GOF) activities of mutant p53 through unknown mechanisms.
View Article and Find Full Text PDFLeuk Lymphoma
August 2016
a Robert H. Lurie Comprehensive Cancer Center, Division of Hematology/Oncology , Northwestern Medicine Developmental Therapeutics Institute, Feinberg School of Medicine, Northwestern University, Chicago , IL , USA ;
Pharmacol Ther
January 2013
Department of Therapeutic Radiology, Yale School of Medicine, 15 York Street, Hunter Building, HRT-205, New Haven, CT 06510, USA.
MicroRNAs are master regulators of gene expression and control many biological pathways such as cell growth, differentiation and apoptosis. Deregulation of microRNA expression and activity results in a myriad of diseases including cancer. Recently, several reports have indicated that single nucleotide polymorphisms (SNPs) in microRNAs and microRNA-target sites impact microRNA biology and associate with cancer risk, treatment response and outcome.
View Article and Find Full Text PDFCancer Cell
September 2010
p53 Laboratory, 8A Biomedical Grove, Immunos #06-06, Singapore 138648, Republic of Singapore.
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