In brief: Genomic imprinting and imprinting diseases

Journal of Pathology

Volumn 232, Issue 5, 2014, Pages 485-487

  Horsthemke, Bernhard ^a  

^a UNIVERSITY HOSPITAL ESSEN   (Germany)

Author keywords

DNA methylation; epigenetics; genomic imprinting

Indexed keywords

DNA; DNA METHYLTRANSFERASE 3A; HISTONE;

ALLELE; ARTICLE; BECKWITH WIEDEMANN SYNDROME; CHROMOSOME DELETION; DIABETES MELLITUS; DNA METHYLATION; DNA REPLICATION; EPIGENETICS; GENE; GENE DUPLICATION; GENETIC DISORDER; GENOME IMPRINTING; HAPPY PUPPET SYNDROME; HISTONE MODIFICATION; HUMAN; IMPRINTING DISEASE; LOSS OF FUNCTION MUTATION; MENTAL RETARDATION MALFORMATION SYNDROME; PRADER WILLI SYNDROME; PRIORITY JOURNAL; PSEUDOHYPOPARATHYROIDISM; SILVER RUSSELL SYNDROME; TEMPLE SYNDROME; UBE3A GENE; UNIPARENTAL DISOMY; WANG SYNDROME;

DNA METHYLATION; EPIGENETICS; GENOMIC IMPRINTING;

ANIMALS; CHROMATIN ASSEMBLY AND DISASSEMBLY; CHROMOSOME DELETION; CHROMOSOME DUPLICATION; DNA METHYLATION; FEMALE; GENE EXPRESSION REGULATION, DEVELOPMENTAL; GENE SILENCING; GENETIC DISEASES, INBORN; GENETIC PREDISPOSITION TO DISEASE; GENOMIC IMPRINTING; HUMANS; MALE; MUTATION; RISK FACTORS;

EID: 84895927433     PISSN: 00223417     EISSN: 10969896     Source Type: Journal    
DOI: 10.1002/path.4326     Document Type: Article

References (4)

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4. Uribe-Lewis S, Woodfine K, Stojic L, et al., Molecular mechanisms of genomic imprinting and clinical implications for cancer. Expert Rev Mol Med 2011; 13: e2.