Cargando…
Global DNA Hypermethylation in Down Syndrome Placenta
Down syndrome (DS), commonly caused by an extra copy of chromosome 21 (chr21), occurs in approximately one out of 700 live births. Precisely how an extra chr21 causes over 80 clinically defined phenotypes is not yet clear. Reduced representation bisulfite sequencing (RRBS) analysis at single base re...
Autores principales: | Jin, Shengnan, Lee, Yew Kok, Lim, Yen Ching, Zheng, Zejun, Lin, Xueqin Michelle, Ng, Desmond P. Y., Holbrook, Joanna D., Law, Hai Yang, Kwek, Kenneth Y. C., Yeo, George S. H., Ding, Chunming |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2013
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3675012/ https://www.ncbi.nlm.nih.gov/pubmed/23754950 http://dx.doi.org/10.1371/journal.pgen.1003515 |
Ejemplares similares
-
Improved reduced representation bisulfite sequencing for epigenomic profiling of clinical samples
por: Lee, Yew Kok, et al.
Publicado: (2014) -
DNMT1 and AIM1 Imprinting in human placenta revealed through a genome-wide screen for allele-specific DNA methylation
por: Das, Radhika, et al.
Publicado: (2013) -
A complex association between DNA methylation and gene expression in human placenta at first and third trimesters
por: Lim, Yen Ching, et al.
Publicado: (2017) -
Developmentally linked human DNA hypermethylation is associated with down-modulation, repression, and upregulation of transcription
por: Baribault, Carl, et al.
Publicado: (2018) -
CHD5 is down-regulated through promoter hypermethylation in gastric cancer
por: Wang, Xian, et al.
Publicado: (2009)