Mutational Analysis of Mismatch Repair Genes, <i>hMLH1</i> and <i>hMSH2</i>, in Sporadic Endometrial Carcinomas with Microsatellite Instability
Kanji Kobayashi(Sapporo Medical University), Yusuke Nakamura(Rissho University), Satoru Sagae(Cardiovascular Center Hokkaido Ohno Hospital), S. Koi(The Cancer Institute Hospital), Mieko Matsushima(Nagoya City University), Hiroko Saito(Yokohama City University), Ryuichi Kudo(Sapporo Medical University)
Cited by 73
Related Papers
AXIN1 mutations in hepatocellular carcinomas, and growth suppression in cancer cells by virus-mediated transfer of AXIN1
|Nature Genetics|2000|950
An ancient retrotransposal insertion causes Fukuyama-type congenital muscular dystrophy
|Nature|1998|804
SNPs in KCNQ1 are associated with susceptibility to type 2 diabetes in East Asian and European populations
|Nature Genetics|2008|728
DKK1, a negative regulator of Wnt signaling, is a target of the β-catenin/TCF pathway
|Oncogene|2004|569
Genome-wide association study of hematological and biochemical traits in a Japanese population
|Nature Genetics|2010|535