Associated Papers
Evaluation of Hybridization Capture Versus Amplicon-Based Methods for Whole-Exome Sequencing.
Samorodnitsky E et al.
Human Mutation, 2015
26110913 (PubMed )
Supplement: HUMU-36-903-s001.zip › humu22825-sup-00010-Table_S13.xlsx › Sheet1
Somatic cancer mutations in the DNMT2 tRNA methyltransferase alter its catalytic properties.
Elhardt W et al.
Biochimie, 2015
The eSNV-detect: a computational system to identify expressed single nucleotide variants from transcriptome sequencing data.
Tang X et al.
Nucleic Acids Research, 2014
25352556 (PubMed )
Supplement: supp_gku1005_nar-01266-met-n-2014-File012.xlsx › TCGA-A8-A06Q-01A.domain
[Polymorphisms of DNA methyltransferases and the risk of prostate cancer].
He BS et al.
Zhonghua Nan Ke Xue = National Journal of Andrology, 2014
Risk-association of DNA methyltransferases polymorphisms with gastric cancer in the Southern Chinese population.
Yang XX et al.
International Journal of Molecular Sciences, 2012
Lack of involvement of known DNA methyltransferases in familial hydatidiform mole implies the involvement of other factors in establishment of imprinting in the human female germline.
Hayward BE et al.
Bmc Genetics, 2003
Novel nucleotide substitutions within the coding region of DNMT2 are in strong linkage disequilibrium in Caucasians and Japanese.
Franchina M et al.
Human Heredity, 2001
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