Cargando…
Hypomethylation of HOXA4 promoter is common in Silver-Russell syndrome and growth restriction and associates with stature in healthy children
Silver-Russell syndrome (SRS) is a growth retardation syndrome in which loss of methylation on chromosome 11p15 (11p15 LOM) and maternal uniparental disomy for chromosome 7 [UPD(7)mat] explain 20–60% and 10% of the syndrome, respectively. To search for a molecular cause for the remaining SRS cases,...
Autores principales: | Muurinen, Mari, Hannula-Jouppi, Katariina, Reinius, Lovisa E., Söderhäll, Cilla, Merid, Simon Kebede, Bergström, Anna, Melén, Erik, Pershagen, Göran, Lipsanen-Nyman, Marita, Greco, Dario, Kere, Juha |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5691194/ https://www.ncbi.nlm.nih.gov/pubmed/29146936 http://dx.doi.org/10.1038/s41598-017-16070-5 |
Ejemplares similares
-
Differentially methylated regions in maternal and paternal uniparental disomy for chromosome 7
por: Hannula-Jouppi, Katariina, et al.
Publicado: (2014) -
Case report: A novel de novo IGF2 missense variant in a Finnish patient with Silver-Russell syndrome
por: Loid, Petra, et al.
Publicado: (2022) -
Risk of childhood asthma is associated with CpG-site polymorphisms, regional DNA methylation and mRNA levels at the GSDMB/ORMDL3 locus
por: Acevedo, Nathalie, et al.
Publicado: (2015) -
DNA Methylation in the Neuropeptide S Receptor 1 (NPSR1) Promoter in Relation to Asthma and Environmental Factors
por: Reinius, Lovisa E., et al.
Publicado: (2013) -
Differential DNA Methylation in Purified Human Blood Cells: Implications for Cell Lineage and Studies on Disease Susceptibility
por: Reinius, Lovisa E., et al.
Publicado: (2012)