Cargando…
Is ZFP57 binding to H19/IGF2:IG-DMR affected in Silver-Russell syndrome?
BACKGROUND: Loss of paternal methylation (LOM) of the H19/IGF2 intergenic differentially methylated region (H19/IGF2:IG-DMR) causes alteration of H19/IGF2 imprinting and Silver-Russell syndrome (SRS). Recently, internal deletions of the H19/IGF2:IG-DMR have been associated with LOM and SRS when pres...
Autores principales: | Sparago, Angela, Cerrato, Flavia, Riccio, Andrea |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5822596/ https://www.ncbi.nlm.nih.gov/pubmed/29484033 http://dx.doi.org/10.1186/s13148-018-0454-7 |
Ejemplares similares
-
The number of the CTCF binding sites of the H19/IGF2:IG-DMR correlates with DNA methylation and expression imprinting in a humanized mouse model
por: Freschi, Andrea, et al.
Publicado: (2021) -
Mosaic Segmental and Whole-Chromosome Upd(11)mat in Silver-Russell Syndrome
por: Pignata, Laura, et al.
Publicado: (2021) -
Disruption of genomic neighbourhood at the imprinted IGF2-H19 locus in Beckwith–Wiedemann syndrome and Silver–Russell syndrome
por: Nativio, Raffaella, et al.
Publicado: (2011) -
Epimutations of the IG-DMR and the MEG3-DMR at the 14q32.2 imprinted region in two patients with Silver–Russell Syndrome-compatible phenotype
por: Kagami, Masayo, et al.
Publicado: (2015) -
Genetic and epigenetic mutations affect the DNA binding capability of human ZFP57 in transient neonatal diabetes type 1
por: Baglivo, Ilaria, et al.
Publicado: (2013)