Variable maternal methylation overlapping thenc886/vtRNA2-1locus is locked between hypermethylated repeats and is frequently altered in cancer
Published 2014 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
Variable maternal methylation overlapping thenc886/vtRNA2-1locus is locked between hypermethylated repeats and is frequently altered in cancer
Authors
Keywords
-
Journal
Epigenetics
Volume 9, Issue 5, Pages 783-790
Publisher
Informa UK Limited
Online
2014-03-04
DOI
10.4161/epi.28323
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- Genome-wide parent-of-origin DNA methylation analysis reveals the intricacies of human imprinting and suggests a germline methylation-independent mechanism of establishment
- (2014) F. Court et al. GENOME RESEARCH
- Stability of Genomic Imprinting and Gestational-Age Dynamic Methylation in Complicated Pregnancies Conceived Following Assisted Reproductive Technologies1
- (2013) Cristina Camprubí et al. BIOLOGY OF REPRODUCTION
- DNA methylation contributes to natural human variation
- (2013) H. Heyn et al. GENOME RESEARCH
- Comparative Anatomy of Chromosomal Domains with Imprinted and Non-Imprinted Allele-Specific DNA Methylation
- (2013) Anupam Paliwal et al. PLoS Genetics
- Characterization of the direct physical interaction of nc886, a cellular non-coding RNA, and PKR
- (2012) Sung Ho Jeon et al. FEBS LETTERS
- A Tumor Surveillance Model: A Non-Coding RNA Senses Neoplastic Cells and Its Protein Partner Signals Cell Death
- (2012) Sung Jeon et al. INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES
- Epigenetic state and expression of imprinted genes in umbilical cord correlates with growth parameters in human pregnancy
- (2012) Ai Lin Lim et al. JOURNAL OF MEDICAL GENETICS
- A unique regulatory phase of DNA methylation in the early mammalian embryo
- (2012) Zachary D. Smith et al. NATURE
- Cell death/proliferation roles for nc886, a non-coding RNA, in the protein kinase R pathway in cholangiocarcinoma
- (2012) N Kunkeaw et al. ONCOGENE
- Differential DNA Methylation in Purified Human Blood Cells: Implications for Cell Lineage and Studies on Disease Susceptibility
- (2012) Lovisa E. Reinius et al. PLoS One
- Allelic methylation levels of the noncoding VTRNA2-1 located on chromosome 5q31.1 predict outcome in AML
- (2011) M. B. Treppendahl et al. BLOOD
- Deciphering the cancer imprintome
- (2011) D. Monk Briefings in Functional Genomics
- Dominantly Inherited Constitutional Epigenetic Silencing of MLH1 in a Cancer-Affected Family Is Linked to a Single Nucleotide Variant within the 5′UTR
- (2011) Megan P. Hitchins et al. CANCER CELL
- Dynamic CpG island methylation landscape in oocytes and preimplantation embryos
- (2011) Sébastien A Smallwood et al. NATURE GENETICS
- Equivalence of Conventionally-Derived and Parthenote-Derived Human Embryonic Stem Cells
- (2011) Julie V. Harness et al. PLoS One
- Genomic surveys by methylation-sensitive SNP analysis identify sequence-dependent allele-specific DNA methylation
- (2008) Kristi Kerkel et al. NATURE GENETICS
Find Funding. Review Successful Grants.
Explore over 25,000 new funding opportunities and over 6,000,000 successful grants.
ExploreAdd your recorded webinar
Do you already have a recorded webinar? Grow your audience and get more views by easily listing your recording on Peeref.
Upload Now