A computational screen for C/D box snoRNAs in the human genomic region associated with Prader-Willi and Angelman syndromes

Journal of Biomedical Science

Volumn 15, Issue 6, 2008, Pages 697-705

  Sridhar, Padmavati ^a   Gan, Hin Hark ^a   Schlick, Tamar ^a,b  

^a NEW YORK UNIVERSITY   (United States)

^b NEW YORK UNIVERSITY   (United States)

Author keywords

Angelman syndrome; C D box snoRNA; Prader Willi syndrome; RNA motif scanning; RNA RNA hybridization; Serotonin receptor 2C mRNA

Indexed keywords

COMPLEMENTARY RNA; MESSENGER RNA; RIBOSOME RNA; RNA 18S; RNA 28S; SEROTONIN RECEPTOR; SEROTONIN RECEPTOR 2C; SMALL NUCLEOLAR RNA; UNCLASSIFIED DRUG;

ALGORITHM; ARTICLE; CHROMOSOME 15Q; FALSE NEGATIVE RESULT; FALSE POSITIVE RESULT; GENETIC SCREENING; HAPPY PUPPET SYNDROME; HUMAN GENOME; INTERMETHOD COMPARISON; NUCLEOTIDE SEQUENCE; PRADER WILLI SYNDROME; PRIORITY JOURNAL; PROTEIN MOTIF; PROTEIN SECONDARY STRUCTURE; QUANTITATIVE ANALYSIS; RNA HYBRIDIZATION; RNA METHYLATION; RNA SEQUENCE; RNA SPLICING;

ALGORITHMS; ANGELMAN SYNDROME; BASE SEQUENCE; COMPUTATIONAL BIOLOGY; GENE ORDER; GENOME, HUMAN; HUMANS; MOLECULAR SEQUENCE DATA; NUCLEIC ACID CONFORMATION; NUCLEIC ACID HYBRIDIZATION; PRADER-WILLI SYNDROME; RNA, SMALL NUCLEOLAR; SEQUENCE ALIGNMENT;

EID: 56349156916     PISSN: 10217770     EISSN: 14230127     Source Type: Journal    
DOI: 10.1007/s11373-008-9271-x     Document Type: Article

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