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Results 1 - 9 of 9 for CpG
  1. MBD5 gene 
    ... of a family of genes called the methyl-CpG-binding domain (MBD) genes. These genes provide instructions ... between individuals. More About This Health Condition methyl-CpG-binding domain protein 5 methyl-CpG-binding protein ...
    https://medlineplus.gov/genetics/gene/mbd5 - Genetics
  2. MECP2 gene 
    ... and social interaction. MeCP2 protein MECP2_HUMAN methyl CpG binding protein 2 methyl CpG binding protein 2 (Rett syndrome) MRX16 MRX79 PPMX ... of MECP2 PubMed ANGELMAN SYNDROME; AS AUTISM METHYL-CpG-BINDING PROTEIN 2; MECP2 INTELLECTUAL DEVELOPMENTAL DISORDER, X- ...
    https://medlineplus.gov/genetics/gene/mecp2 - Genetics
  3. EPG5 gene 
    The EPG5 gene provides instructions for making a protein that is involved in a cellular process called autophagy. This process recycles worn-out or unnecessary ...
    https://medlineplus.gov/genetics/gene/epg5 - Genetics
  4. F9 gene 
    ... FIXVal-10 and FIXThr-10) and an independent CpG hotspot mutation (FIXThr-10). Thromb Haemost. 2001 Mar; ...
    https://medlineplus.gov/genetics/gene/f9 - Genetics
  5. AFF2 gene 
    ... al. Trinucleotide repeat amplification and hypermethylation of a CpG island in FRAXE mental retardation. Cell. 1993 Jul ...
    https://medlineplus.gov/genetics/gene/aff2 - Genetics
  6. SMCHD1 gene 
    ... the hypermethylation of certain areas of DNA called CpG islands, although the mechanism is unclear. This hypermethylation ...
    https://medlineplus.gov/genetics/gene/smchd1 - Genetics
  7. Fragile XE syndrome 
    ... al. Trinucleotide repeat amplification and hypermethylation of a CpG island in FRAXE mental retardation. Cell. 1993 Jul ...
    https://medlineplus.gov/genetics/condition/fragile-xe-syndrome - Genetics
  8. Recurrent hydatidiform mole 
    ... lineage differentiation, binds to overexpressed YY1 and alters CpG methylation. Hum Mol Genet. 2014 Feb 1;23( ...
    https://medlineplus.gov/.../condition/recurrent-hydatidiform-mole - Genetics
  9. PAX8 gene 
    ... dysgenesis caused by PAX8 mutation: the hypermutability with CpG dinucleotides at codon 31. J Pediatr. 2001 Oct; ...
    https://medlineplus.gov/genetics/gene/pax8 - Genetics