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Volumn 42, Issue 3, 2003, Pages 372-375

Genetics of childhood disorders: XLVIII. Learning and memory, Part 1: Fragile X syndrome update

Author keywords

[No Author keywords available]

Indexed keywords

FRAGILE X SYNDROME; GENETIC ASSOCIATION; HUMAN; LEARNING; MEMORY; PRIORITY JOURNAL; REVIEW; BRAIN; CHILD; DEVELOPMENTAL DISORDER; FEMALE; GENETICS; LEARNING DISORDER; MALE; MEMORY DISORDER; PATHOLOGY; SPINAL CORD;

EID: 0037362729     PISSN: 08908567     EISSN: None     Source Type: Journal    
DOI: 10.1097/00004583-200303000-00019     Document Type: Article
Times cited : (13)

References (10)
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    • Microarray identification of FMRP-associated brain mRNAs and altered mRNA translational profiles in fragile X syndrome
    • V Brown P Jin S Ceman Microarray identification of FMRP-associated brain mRNAs and altered mRNA translational profiles in fragile X syndrome Cell 107 2001 477 487
    • (2001) Cell , vol.107 , pp. 477-487
    • Brown, V1    Jin, P2    Ceman, S3
  • 2
    • 0030986183 scopus 로고    scopus 로고
    • Abnormal dendritic spines in fragile X knockout mice: maturation and pruning deficits
    • TA Comery JB Harris PJ Willems Abnormal dendritic spines in fragile X knockout mice: maturation and pruning deficits Proc Natl Acad Sci U S A 94 1997 5401 5404
    • (1997) Proc Natl Acad Sci U S A , vol.94 , pp. 5401-5404
    • Comery, TA1    Harris, JB2    Willems, PJ3
  • 3
    • 0035900649 scopus 로고    scopus 로고
    • Fragile X mental retardation protein targets G quartet mRNAs important for neuronal function
    • JC Darnell KB Jensen P Jin V Brown ST Warren RB Darnell Fragile X mental retardation protein targets G quartet mRNAs important for neuronal function Cell 107 2001 489 499
    • (2001) Cell , vol.107 , pp. 489-499
    • Darnell, JC1    Jensen, KB2    Jin, P3    Brown, V4    Warren, ST5    Darnell, RB6
  • 4
    • 0027509234 scopus 로고
    • A point mutation in the FMR-1 gene associated with fragile X mental retardation
    • K De Boulle AJ Verkerk E Reyniers A point mutation in the FMR-1 gene associated with fragile X mental retardation Nat Genet 3 1993 31 35
    • (1993) Nat Genet , vol.3 , pp. 31-35
    • De Boulle, K1    Verkerk, AJ2    Reyniers, E3
  • 6
    • 0035863624 scopus 로고    scopus 로고
    • Abnormal dendritic spine characteristics in the temporal and visual cortices of patients with fragile-X syndrome: a quantitative examination
    • SA Irwin B Patel M Idupulapati Abnormal dendritic spine characteristics in the temporal and visual cortices of patients with fragile-X syndrome: a quantitative examination Am J Med Genet 98 2001 161 167
    • (2001) Am J Med Genet , vol.98 , pp. 161-167
    • Irwin, SA1    Patel, B2    Idupulapati, M3
  • 7
    • 0029794770 scopus 로고    scopus 로고
    • A requirement for local protein synthesis in neurotrophin-induced hippocampal synaptic plasticity
    • H Kang EM Schuman A requirement for local protein synthesis in neurotrophin-induced hippocampal synaptic plasticity Science 273 1996 1402 1406
    • (1996) Science , vol.273 , pp. 1402-1406
    • Kang, H1    Schuman, EM2
  • 8
    • 0030059545 scopus 로고    scopus 로고
    • The fragile X mental retardation protein is associated with ribosomes
    • EW Khandjian F Corbin S Woerly F Rousseau The fragile X mental retardation protein is associated with ribosomes Nat Genet 12 1996 91 93
    • (1996) Nat Genet , vol.12 , pp. 91-93
    • Khandjian, EW1    Corbin, F2    Woerly, S3    Rousseau, F4
  • 9
    • 0034005882 scopus 로고    scopus 로고
    • NMDA receptor-mediated control of protein synthesis at developing synapses
    • AJ Scheetz AC Nairn M Constantine-Paton NMDA receptor-mediated control of protein synthesis at developing synapses Nat Neurosci 3 2000 211 216
    • (2000) Nat Neurosci , vol.3 , pp. 211-216
    • Scheetz, AJ1    Nairn, AC2    Constantine-Paton, M3
  • 10
    • 0025905795 scopus 로고
    • Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome
    • AJ Verkerk M Pieretti JS Sutcliffe Identification of a gene ( FMR-1 ) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome Cell 65 1991 905 914
    • (1991) Cell , vol.65 , pp. 905-914
    • Verkerk, AJ1    Pieretti, M2    Sutcliffe, JS3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.