The imprinting box of the Prader-Willi/Angelman syndrome domain

Nature Genetics

Volumn 26, Issue 4, 2000, Pages 440-443

  Shemer, Ruth ^a   Hershko, Alon Y ^a   Perk, Jonathan ^a   Mostoslavsky, Raul ^a   Tsuberi, Ben Zion ^a   Cedar, Howard ^a   Buiting, Karin ^b   Razin, Aharon ^a  

^a HEBREW UNIVERSITY   (Israel)

^b UNIVERSITY HOSPITAL ESSEN   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

ALLELE; ANIMAL TISSUE; ARTICLE; CHROMOSOME 15Q; FEMALE; GENE CLUSTER; GENE CONTROL; GENE DELETION; GENE EXPRESSION; GENE LOSS; GENE REPLICATION; GENE REPRESSION; GENETIC TRANSCRIPTION; HAPPY PUPPET SYNDROME; MALE; MOUSE; NEWBORN; NONHUMAN; PRADER WILLI SYNDROME; PRIORITY JOURNAL; PROMOTER REGION;

ALLELES; ANGELMAN SYNDROME; ANIMALS; BASE SEQUENCE; DNA METHYLATION; DNA PRIMERS; FATHERS; FEMALE; GENOMIC IMPRINTING; HUMANS; MALE; MICE; MODELS, GENETIC; MOTHERS; PEDIGREE; PRADER-WILLI SYNDROME; PROMOTER REGIONS (GENETICS);

ANIMALIA; MAMMALIA;

EID: 0033671832     PISSN: 10614036     EISSN: None     Source Type: Journal    
DOI: 10.1038/82571     Document Type: Article

References (12)

1. Imprinting in Prader-Willi and Angelman syndromes
2. Imprinting mutation mechanisms in Prader-Willi syndrome
3. A 5-kb imprinting center deletion in a family with Angelman syndrome reduces the shortest region of deletion overlap to 880 bp
4. Molecular mechanism of Angelman syndrome in two large families involves an imprinting mutation
5. Structure of the imprinted mouse Snrpn gene and establishment of its parental-specific methylation pattern
6. The imprinting box of the mouse Igf2r gene
7. Analysis of murine Snrpn and human SNRPN gene imprinting in transgenic mice
8. Asynchronous replication of imprinted genes is established in the gametes and maintained during development
9. An imprinted antisense RNA overlaps UBE3A and a second maternally expressed transcript
10. Imprinted expression of the Igf2r gene depends on an intronic CpG island
11. Developmental pattern of gene-specific DNA methylation in the mouse embryo and germline
12. Tsix, a gene antisense to Xist at the X-inactivation centre