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GoPubMed Proteins lists recent and important papers and reviews for proteins. Page last changed on 19 Dec 2016.

Ubiquitin specific peptidase 49

Top mentioned proteins: DPR1, CAN, SET, POLYMERASE, PRMT2
Papers on USP49
Identification of spermatozoa by tissue-specific differential DNA methylation using bisulfite modification and pyrosequencing.
McCord et al., Hattiesburg, United States. In Electrophoresis, 2014
Of the different loci tested, a panel of six markers, DACT1, USP49, DDX4, Hs_INSL6_03, Hs_ZC3H12D_05, and B_SPTB_03 were identified to contain tissue-specific differential methylation.
Body fluid identification by integrated analysis of DNA methylation and body fluid-specific microbial DNA.
Lee et al., Seoul, South Korea. In Int J Legal Med, 2014
Using the developed multiplex system, semen was distinguishable by unmethylation at the USP49, DACT1, and PFN3 tDMRs and by hypermethylation at L81528, and saliva could be identified by detection of saliva-specific bacteria, Veillonella atypica and/or Streptococcus salivarius.
USP49 deubiquitinates histone H2B and regulates cotranscriptional pre-mRNA splicing.
Wang et al., Birmingham, United States. In Genes Dev, 2013
Here we report the purification of ubiquitin-specific peptidase 49 (USP49) as a histone H2B-specific deubiquitinase and demonstrate that H2B deubiquitination by USP49 is required for efficient cotranscriptional splicing of a large set of exons.
DNA methylation-specific multiplex assays for body fluid identification.
Lee et al., Seoul, South Korea. In Int J Legal Med, 2013
After confirming the stability of the body fluid-specific DNA methylation profile over time, two different multiplex PCR systems were constructed using methylation-sensitive restriction enzyme PCR and methylation SNaPshot, in order to analyze the methylation status of specific CpG sites from the USP49, DACT1, PRMT2, and PFN3 tDMRs.
Potential forensic application of DNA methylation profiling to body fluid identification.
Shin et al., Seoul, South Korea. In Int J Legal Med, 2012
Five tDMRs for the genes DACT1, USP49, HOXA4, PFN3, and PRMT2 were selected, and DNA methylation profiles for these tDMRs were produced by bisulfite sequencing using pooled DNA from blood, saliva, semen, menstrual blood, and vaginal fluid.
A pipeline to determine RT-QPCR control genes for evolutionary studies: application to primate gene expression across multiple tissues.
Wray et al., Durham, United States. In Plos One, 2009
We identified 13 genes from the pipeline and from commonly used control genes: ACTB, USP49, ARGHGEF2, GSK3A, TBP, SDHA, EIF2B2, GPDH, YWHAZ, HPTR1, RPL13A, HMBS, and EEF2.
Effects of common germline genetic variation in cell cycle control genes on breast cancer survival: results from a population-based cohort.
Pharoah et al., Cambridge, United Kingdom. In Breast Cancer Res, 2007
This SNP is part of a large linkage disequilibrium block, which contains CCND3, BYSL, TRFP, USP49, C6ofr49, FRS3, and PGC.
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