A repetitive elements perspective in Polycomb epigenetics.
Repetitive elements comprise over two-thirds of the human genome. For a long time, these elements have received little attention since they were considered non functional. On the contrary, recent evidence indicates that they play central roles in genome integrity, gene expression and disease. Indeed...
Main Authors: | Valentina eCasa, Davide eGabellini |
---|---|
Format: | Article |
Language: | English |
Published: |
Frontiers Media S.A.
2012-10-01
|
Series: | Frontiers in Genetics |
Subjects: | |
Online Access: | http://journal.frontiersin.org/Journal/10.3389/fgene.2012.00199/full |
Similar Items
-
The French National Registry of patients with Facioscapulohumeral muscular dystrophy
by: Céline Guien, et al.
Published: (2018-12-01) -
Whole exome sequencing highlights rare variants in CTCF, DNMT1, DNMT3A, EZH2 and SUV39H1 as associated with FSHD
by: Claudia Strafella, et al.
Published: (2023-08-01) -
Ret function in muscle stem cells points to tyrosine kinase inhibitor therapy for facioscapulohumeral muscular dystrophy
by: Louise A Moyle, et al.
Published: (2016-11-01) -
Precise Epigenetic Analysis Using Targeted Bisulfite Genomic Sequencing Distinguishes FSHD1, FSHD2, and Healthy Subjects
by: Taylor Gould, et al.
Published: (2021-08-01) -
Pathomechanisms and biomarkers in facioscapulohumeral muscular dystrophy: roles of DUX4 and PAX7
by: Christopher R S Banerji, et al.
Published: (2021-06-01)