Functional genomics, fragile X syndrome, and RNA interference

Archives of Neurology

Volumn 60, Issue 9, 2003, Pages 1197-1200

  Kalidas, Savitha ^b   Smith, Dean P ^a  

^a UNIVERSITY OF TEXAS SOUTHWESTERN MEDICAL CENTER   (United States)

^b NONE

Author keywords

[No Author keywords available]

Indexed keywords

COMPLEMENTARY RNA; DNA DIRECTED RNA POLYMERASE III; DOUBLE STRANDED RNA; FRAGILE X MENTAL RETARDATION PROTEIN; GENE PRODUCT; MESSENGER RNA; RNA BINDING PROTEIN;

ANALYTIC METHOD; BASE PAIRING; CONFERENCE PAPER; FRAGILE X SYNDROME; GENE SEQUENCE; GENE SILENCING; GENE TARGETING; HUMAN; MOLECULAR PROBE; MOLECULAR RECOGNITION; NEUROLOGIC DISEASE; NEUROPATHOLOGY; NONHUMAN; PRIORITY JOURNAL; REGULATORY MECHANISM; RNA INTERFERENCE;

ALLELES; DNA, INTERGENIC; DOWN-REGULATION; FRAGILE X MENTAL RETARDATION PROTEIN; FRAGILE X SYNDROME; GENE TARGETING; GENE THERAPY; GENOMIC IMPRINTING; HUMANS; NERVE TISSUE PROTEINS; PHENOTYPE; RNA INTERFERENCE; RNA PRECURSORS; RNA, DOUBLE-STRANDED; RNA, MESSENGER; RNA-BINDING PROTEINS;

EID: 0042922493     PISSN: 00039942     EISSN: None     Source Type: Journal    
DOI: 10.1001/archneur.60.9.1197     Document Type: Conference Paper

References (12)

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