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Volumn 1338, Issue , 2010, Pages 78-88

MicroRNAs in psychiatric and neurodevelopmental disorders

Author keywords

Autism; Chromosome 22q11.2; Mental retardation; MicroRNA; Neurodevelopment; Psychiatric disorder; Schizophrenia; Synaptic plasticity

Indexed keywords

MICRORNA;

EID: 77952583640     PISSN: 00068993     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.brainres.2010.03.109     Document Type: Review
Times cited : (91)

References (124)
  • 1
    • 26844498125 scopus 로고    scopus 로고
    • Sequence variants in SLITRK1 are associated with Tourette's syndrome
    • Abelson J.F., Kwan K.Y., O'Roak B.J., et al. Sequence variants in SLITRK1 are associated with Tourette's syndrome. Science 310 (2005) 317-320
    • (2005) Science , vol.310 , pp. 317-320
    • Abelson, J.F.1    Kwan, K.Y.2    O'Roak, B.J.3
  • 2
    • 46149103853 scopus 로고    scopus 로고
    • Heterogeneous dysregulation of microRNAs across the autism spectrum
    • Abu-Elneel K., Liu T., Gazzaniga F.S., et al. Heterogeneous dysregulation of microRNAs across the autism spectrum. Neurogenetics 9 (2008) 153-161
    • (2008) Neurogenetics , vol.9 , pp. 153-161
    • Abu-Elneel, K.1    Liu, T.2    Gazzaniga, F.S.3
  • 3
    • 0032830639 scopus 로고    scopus 로고
    • Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2
    • Amir R.E., Van den Veyver I.B., Wan M., et al. Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2. Nat. Genet. 23 (1999) 185-188
    • (1999) Nat. Genet. , vol.23 , pp. 185-188
    • Amir, R.E.1    Van den Veyver, I.B.2    Wan, M.3
  • 4
    • 0025736146 scopus 로고
    • Rett syndrome: exclusion mapping following the hypothesis of germinal mosaicism for new X-linked mutations
    • Archidiacono N., Lerone M., Rocchi M., et al. Rett syndrome: exclusion mapping following the hypothesis of germinal mosaicism for new X-linked mutations. Hum. Genet. 86 (1991) 604-606
    • (1991) Hum. Genet. , vol.86 , pp. 604-606
    • Archidiacono, N.1    Lerone, M.2    Rocchi, M.3
  • 5
    • 0028904853 scopus 로고
    • Selective dendritic alterations in the cortex of Rett syndrome
    • Armstrong D., Dunn J.K., Antalffy B., et al. Selective dendritic alterations in the cortex of Rett syndrome. J. Neuropathol. Exp. Neurol. 54 (1995) 195-201
    • (1995) J. Neuropathol. Exp. Neurol. , vol.54 , pp. 195-201
    • Armstrong, D.1    Dunn, J.K.2    Antalffy, B.3
  • 6
    • 0028906338 scopus 로고
    • Autism as a strongly genetic disorder: evidence from a British twin study
    • Bailey A., Le Couteur A., Gottesman I., et al. Autism as a strongly genetic disorder: evidence from a British twin study. Psychol. Med. 25 (1995) 63-77
    • (1995) Psychol. Med. , vol.25 , pp. 63-77
    • Bailey, A.1    Le Couteur, A.2    Gottesman, I.3
  • 7
    • 0034873653 scopus 로고    scopus 로고
    • The neurocognitive phenotype of the 22q11.2 deletion syndrome: selective deficit in visual-spatial memory
    • Bearden C.E., Woodin M.F., Wang P.P., et al. The neurocognitive phenotype of the 22q11.2 deletion syndrome: selective deficit in visual-spatial memory. J. Clin. Exp. Neuropsychol. 23 (2001) 447-464
    • (2001) J. Clin. Exp. Neuropsychol. , vol.23 , pp. 447-464
    • Bearden, C.E.1    Woodin, M.F.2    Wang, P.P.3
  • 8
    • 78650238139 scopus 로고    scopus 로고
    • Schizophrenia is associated with an increase in cortical microRNA biogenesis
    • Advance online publication 1 September 2009. doi:10.1038/mp.2009.84
    • Beveridge N.J., Gardiner E., Carroll A.P., et al. Schizophrenia is associated with an increase in cortical microRNA biogenesis. Mol. Psychiatry (2009). http://doi:10.1038/mp.2009.84 Advance online publication 1 September 2009. doi:10.1038/mp.2009.84
    • (2009) Mol. Psychiatry
    • Beveridge, N.J.1    Gardiner, E.2    Carroll, A.P.3
  • 9
    • 41849133938 scopus 로고    scopus 로고
    • Dysregulation of miRNA 181b in the temporal cortex in schizophrenia
    • Beveridge N.J., Tooney P.A., Carroll A.P., et al. Dysregulation of miRNA 181b in the temporal cortex in schizophrenia. Hum. Mol. Genet. 17 (2008) 1156-1168
    • (2008) Hum. Mol. Genet. , vol.17 , pp. 1156-1168
    • Beveridge, N.J.1    Tooney, P.A.2    Carroll, A.P.3
  • 10
    • 52949109182 scopus 로고    scopus 로고
    • Excess protein synthesis in Drosophila fragile X mutants impairs long-term memory
    • Bolduc F.V., Bell K., Cox H., et al. Excess protein synthesis in Drosophila fragile X mutants impairs long-term memory. Nat. Neurosci. 11 (2008) 1143-1145
    • (2008) Nat. Neurosci. , vol.11 , pp. 1143-1145
    • Bolduc, F.V.1    Bell, K.2    Cox, H.3
  • 11
    • 41749090491 scopus 로고    scopus 로고
    • Failure to detect the 22q11.2 duplication syndrome rearrangement among patients with schizophrenia
    • Brunet A., Armengol L., Pelaez T., et al. Failure to detect the 22q11.2 duplication syndrome rearrangement among patients with schizophrenia. Behav. Brain Funct. 4 (2008) 10
    • (2008) Behav. Brain Funct. , vol.4 , pp. 10
    • Brunet, A.1    Armengol, L.2    Pelaez, T.3
  • 12
    • 67651233780 scopus 로고    scopus 로고
    • Genome-wide analyses of exonic copy number variants in a family-based study point to novel autism susceptibility genes
    • Bucan M., Abrahams B.S., Wang K., et al. Genome-wide analyses of exonic copy number variants in a family-based study point to novel autism susceptibility genes. PLoS Genet. 5 (2009) e1000536
    • (2009) PLoS Genet. , vol.5
    • Bucan, M.1    Abrahams, B.S.2    Wang, K.3
  • 13
    • 33745602880 scopus 로고    scopus 로고
    • Noncoding RNAs in the mammalian central nervous system
    • Cao X., Yeo G., Muotri A.R., et al. Noncoding RNAs in the mammalian central nervous system. Annu. Rev. Neurosci. 29 (2006) 77-103
    • (2006) Annu. Rev. Neurosci. , vol.29 , pp. 77-103
    • Cao, X.1    Yeo, G.2    Muotri, A.R.3
  • 14
    • 0032954610 scopus 로고    scopus 로고
    • International variation in reported livebirth prevalence rates of Down syndrome, adjusted for maternal age
    • Carothers A.D., Hecht C.A., and Hook E.B. International variation in reported livebirth prevalence rates of Down syndrome, adjusted for maternal age. J. Med. Genet. 36 (1999) 386-393
    • (1999) J. Med. Genet. , vol.36 , pp. 386-393
    • Carothers, A.D.1    Hecht, C.A.2    Hook, E.B.3
  • 15
    • 0036792769 scopus 로고    scopus 로고
    • Fragile X-related protein and VIG associate with the RNA interference machinery
    • Caudy A.A., Myers M., Hannon G.J., et al. Fragile X-related protein and VIG associate with the RNA interference machinery. Genes Dev. 16 (2002) 2491-2496
    • (2002) Genes Dev. , vol.16 , pp. 2491-2496
    • Caudy, A.A.1    Myers, M.2    Hannon, G.J.3
  • 17
    • 63649138643 scopus 로고    scopus 로고
    • miR-124 regulates adult neurogenesis in the subventricular zone stem cell niche
    • Cheng L.C., Pastrana E., Tavazoie M., et al. miR-124 regulates adult neurogenesis in the subventricular zone stem cell niche. Nat. Neurosci. 12 (2009) 399-408
    • (2009) Nat. Neurosci. , vol.12 , pp. 399-408
    • Cheng, L.C.1    Pastrana, E.2    Tavazoie, M.3
  • 18
    • 68949177123 scopus 로고    scopus 로고
    • Copy number variations associated with idiopathic autism identified by whole-genome microarray-based comparative genomic hybridization
    • Cho S.C., Yim S.H., Yoo H.K., et al. Copy number variations associated with idiopathic autism identified by whole-genome microarray-based comparative genomic hybridization. Psychiatr. Genet. 19 (2009) 177-185
    • (2009) Psychiatr. Genet. , vol.19 , pp. 177-185
    • Cho, S.C.1    Yim, S.H.2    Yoo, H.K.3
  • 19
    • 36048929095 scopus 로고    scopus 로고
    • Association of the Slit and Trk-like 1 gene in Taiwanese patients with Tourette syndrome
    • Chou I.C., Wan L., Liu S.C., et al. Association of the Slit and Trk-like 1 gene in Taiwanese patients with Tourette syndrome. Pediatr. Neurol. 37 (2007) 404-406
    • (2007) Pediatr. Neurol. , vol.37 , pp. 404-406
    • Chou, I.C.1    Wan, L.2    Liu, S.C.3
  • 20
    • 44349186162 scopus 로고    scopus 로고
    • Novel submicroscopic chromosomal abnormalities detected in autism spectrum disorder
    • Christian S.L., Brune C.W., Sudi J., et al. Novel submicroscopic chromosomal abnormalities detected in autism spectrum disorder. Biol. Psychiatry 63 (2008) 1111-1117
    • (2008) Biol. Psychiatry , vol.63 , pp. 1111-1117
    • Christian, S.L.1    Brune, C.W.2    Sudi, J.3
  • 21
    • 33144481470 scopus 로고    scopus 로고
    • Reciprocal actions of REST and a microRNA promote neuronal identity
    • Conaco C., Otto S., Han J.J., et al. Reciprocal actions of REST and a microRNA promote neuronal identity. Proc. Natl. Acad. Sci. U. S. A. 103 (2006) 2422-2427
    • (2006) Proc. Natl. Acad. Sci. U. S. A. , vol.103 , pp. 2422-2427
    • Conaco, C.1    Otto, S.2    Han, J.J.3
  • 22
    • 0027480909 scopus 로고
    • X chromosome linkage studies in familial Rett syndrome
    • Curtis A.R., Headland S., Lindsay S., et al. X chromosome linkage studies in familial Rett syndrome. Hum. Genet. 90 (1993) 551-555
    • (1993) Hum. Genet. , vol.90 , pp. 551-555
    • Curtis, A.R.1    Headland, S.2    Lindsay, S.3
  • 23
    • 43749120042 scopus 로고    scopus 로고
    • Conditional loss of Dicer disrupts cellular and tissue morphogenesis in the cortex and hippocampus
    • Davis T.H., Cuellar T.L., Koch S.M., et al. Conditional loss of Dicer disrupts cellular and tissue morphogenesis in the cortex and hippocampus. J. Neurosci. 28 (2008) 4322-4330
    • (2008) J. Neurosci. , vol.28 , pp. 4322-4330
    • Davis, T.H.1    Cuellar, T.L.2    Koch, S.M.3
  • 24
    • 0027874350 scopus 로고
    • Molecular mapping of twenty-four features of Down syndrome on chromosome 21
    • Delabar J.M., Theophile D., Rahmani Z., et al. Molecular mapping of twenty-four features of Down syndrome on chromosome 21. Eur. J. Hum. Genet. 1 (1993) 114-124
    • (1993) Eur. J. Hum. Genet. , vol.1 , pp. 114-124
    • Delabar, J.M.1    Theophile, D.2    Rahmani, Z.3
  • 25
    • 33750606811 scopus 로고    scopus 로고
    • Examination of the SLITRK1 gene in Caucasian patients with Tourette syndrome
    • Deng H., Le W.D., Xie W.J., et al. Examination of the SLITRK1 gene in Caucasian patients with Tourette syndrome. Acta Neurol. Scand. 114 (2006) 400-402
    • (2006) Acta Neurol. Scand. , vol.114 , pp. 400-402
    • Deng, H.1    Le, W.D.2    Xie, W.J.3
  • 26
    • 33748310866 scopus 로고    scopus 로고
    • Detection of mammalian microRNA expression by in situ hybridization with RNA oligonucleotides
    • Deo M., Yu J.Y., Chung K.H., et al. Detection of mammalian microRNA expression by in situ hybridization with RNA oligonucleotides. Dev. Dyn. 235 (2006) 2538-2548
    • (2006) Dev. Dyn. , vol.235 , pp. 2538-2548
    • Deo, M.1    Yu, J.Y.2    Chung, K.H.3
  • 27
    • 0027176361 scopus 로고
    • The FMR-1 protein is cytoplasmic, most abundant in neurons and appears normal in carriers of a fragile X premutation
    • Devys D., Lutz Y., Rouyer N., et al. The FMR-1 protein is cytoplasmic, most abundant in neurons and appears normal in carriers of a fragile X premutation. Nat. Genet. 4 (1993) 335-340
    • (1993) Nat. Genet. , vol.4 , pp. 335-340
    • Devys, D.1    Lutz, Y.2    Rouyer, N.3
  • 28
    • 44449121279 scopus 로고    scopus 로고
    • A direct role for FMRP in activity-dependent dendritic mRNA transport links filopodial-spine morphogenesis to fragile X syndrome
    • Dictenberg J.B., Swanger S.A., Antar L.N., et al. A direct role for FMRP in activity-dependent dendritic mRNA transport links filopodial-spine morphogenesis to fragile X syndrome. Dev. Cell 14 (2008) 926-939
    • (2008) Dev. Cell , vol.14 , pp. 926-939
    • Dictenberg, J.B.1    Swanger, S.A.2    Antar, L.N.3
  • 29
    • 75949101467 scopus 로고    scopus 로고
    • Regulation of synaptic structure and function by FMRP-associated microRNAs miR-125b and miR-132
    • Edbauer D., Neilson J.R., Foster K.A., et al. Regulation of synaptic structure and function by FMRP-associated microRNAs miR-125b and miR-132. Neuron 65 (2010) 373-384
    • (2010) Neuron , vol.65 , pp. 373-384
    • Edbauer, D.1    Neilson, J.R.2    Foster, K.A.3
  • 30
    • 0026567450 scopus 로고
    • Examination of X chromosome markers in Rett syndrome: exclusion mapping with a novel variation on multilocus linkage analysis
    • Ellison K.A., Fill C.P., Terwilliger J., et al. Examination of X chromosome markers in Rett syndrome: exclusion mapping with a novel variation on multilocus linkage analysis. Am. J. Hum. Genet. 50 (1992) 278-287
    • (1992) Am. J. Hum. Genet. , vol.50 , pp. 278-287
    • Ellison, K.A.1    Fill, C.P.2    Terwilliger, J.3
  • 31
    • 70350772348 scopus 로고    scopus 로고
    • MicroRNAs potentiate neural development
    • Fineberg S.K., Kosik K.S., and Davidson B.L. MicroRNAs potentiate neural development. Neuron 64 (2009) 303-309
    • (2009) Neuron , vol.64 , pp. 303-309
    • Fineberg, S.K.1    Kosik, K.S.2    Davidson, B.L.3
  • 32
    • 62649086993 scopus 로고    scopus 로고
    • Mef2-mediated transcription of the miR379-410 cluster regulates activity-dependent dendritogenesis by fine-tuning Pumilio2 protein levels
    • Fiore R., Khudayberdiev S., Christensen M., et al. Mef2-mediated transcription of the miR379-410 cluster regulates activity-dependent dendritogenesis by fine-tuning Pumilio2 protein levels. EMBO J. 28 (2009) 697-710
    • (2009) EMBO J. , vol.28 , pp. 697-710
    • Fiore, R.1    Khudayberdiev, S.2    Christensen, M.3
  • 33
    • 0017530988 scopus 로고
    • Infantile autism: a genetic study of 21 twin pairs
    • Folstein S., and Rutter M. Infantile autism: a genetic study of 21 twin pairs. J. Child Psychol. Psychiatry 18 (1977) 297-321
    • (1977) J. Child Psychol. Psychiatry , vol.18 , pp. 297-321
    • Folstein, S.1    Rutter, M.2
  • 34
    • 18244385475 scopus 로고    scopus 로고
    • MicroRNAs regulate brain morphogenesis in zebrafish
    • Giraldez A.J., Cinalli R.M., Glasner M.E., et al. MicroRNAs regulate brain morphogenesis in zebrafish. Science 308 (2005) 833-838
    • (2005) Science , vol.308 , pp. 833-838
    • Giraldez, A.J.1    Cinalli, R.M.2    Glasner, M.E.3
  • 35
    • 67349182343 scopus 로고    scopus 로고
    • Autism genome-wide copy number variation reveals ubiquitin and neuronal genes
    • Glessner J.T., Wang K., Cai G., et al. Autism genome-wide copy number variation reveals ubiquitin and neuronal genes. Nature 459 (2009) 569-573
    • (2009) Nature , vol.459 , pp. 569-573
    • Glessner, J.T.1    Wang, K.2    Cai, G.3
  • 36
    • 0034753368 scopus 로고    scopus 로고
    • Excess of twins among affected sibling pairs with autism: implications for the etiology of autism
    • Greenberg D.A., Hodge S.E., Sowinski J., et al. Excess of twins among affected sibling pairs with autism: implications for the etiology of autism. Am. J. Hum. Genet. 69 (2001) 1062-1067
    • (2001) Am. J. Hum. Genet. , vol.69 , pp. 1062-1067
    • Greenberg, D.A.1    Hodge, S.E.2    Sowinski, J.3
  • 37
    • 0021782655 scopus 로고
    • Rett syndrome: Swedish approach to analysis of prevalence and cause
    • Hagberg B. Rett syndrome: Swedish approach to analysis of prevalence and cause. Brain Dev. 7 (1985) 276-280
    • (1985) Brain Dev. , vol.7 , pp. 276-280
    • Hagberg, B.1
  • 38
    • 0020507697 scopus 로고
    • A progressive syndrome of autism, dementia, ataxia, and loss of purposeful hand use in girls: Rett's syndrome: report of 35 cases
    • Hagberg B., Aicardi J., Dias K., et al. A progressive syndrome of autism, dementia, ataxia, and loss of purposeful hand use in girls: Rett's syndrome: report of 35 cases. Ann. Neurol. 14 (1983) 471-479
    • (1983) Ann. Neurol. , vol.14 , pp. 471-479
    • Hagberg, B.1    Aicardi, J.2    Dias, K.3
  • 39
    • 58149097010 scopus 로고    scopus 로고
    • Posttranscriptional crossregulation between Drosha and DGCR8
    • Han J., Pedersen J.S., Kwon S.C., et al. Posttranscriptional crossregulation between Drosha and DGCR8. Cell 136 (2009) 75-84
    • (2009) Cell , vol.136 , pp. 75-84
    • Han, J.1    Pedersen, J.S.2    Kwon, S.C.3
  • 40
    • 40449084022 scopus 로고    scopus 로고
    • Brain expressed microRNAs implicated in schizophrenia etiology
    • Hansen T., Olsen L., Lindow M., et al. Brain expressed microRNAs implicated in schizophrenia etiology. PLoS ONE 2 (2007) e873
    • (2007) PLoS ONE , vol.2
    • Hansen, T.1    Olsen, L.2    Lindow, M.3
  • 41
    • 41349096445 scopus 로고    scopus 로고
    • Gene regulation by transcription factors and microRNAs
    • Hobert O. Gene regulation by transcription factors and microRNAs. Science 319 (2008) 1785-1786
    • (2008) Science , vol.319 , pp. 1785-1786
    • Hobert, O.1
  • 42
    • 0037188502 scopus 로고    scopus 로고
    • Altered synaptic plasticity in a mouse model of fragile X mental retardation
    • Huber K.M., Gallagher S.M., Warren S.T., et al. Altered synaptic plasticity in a mouse model of fragile X mental retardation. Proc. Natl. Acad. Sci. U. S. A. 99 (2002) 7746-7750
    • (2002) Proc. Natl. Acad. Sci. U. S. A. , vol.99 , pp. 7746-7750
    • Huber, K.M.1    Gallagher, S.M.2    Warren, S.T.3
  • 43
    • 0035800521 scopus 로고    scopus 로고
    • A cellular function for the RNA-interference enzyme Dicer in the maturation of the let-7 small temporal RNA
    • Hutvagner G., McLachlan J., Pasquinelli A.E., et al. A cellular function for the RNA-interference enzyme Dicer in the maturation of the let-7 small temporal RNA. Science 293 (2001) 834-838
    • (2001) Science , vol.293 , pp. 834-838
    • Hutvagner, G.1    McLachlan, J.2    Pasquinelli, A.E.3
  • 44
    • 78650514762 scopus 로고    scopus 로고
    • Copy number variations of chromosome 16p13.1 region associated with schizophrenia
    • Ingason A., Rujescu D., Cichon S., et al. Copy number variations of chromosome 16p13.1 region associated with schizophrenia. Mol. Psychiatry (2009)
    • (2009) Mol. Psychiatry
    • Ingason, A.1    Rujescu, D.2    Cichon, S.3
  • 45
    • 51649107017 scopus 로고    scopus 로고
    • Rare chromosomal deletions and duplications increase risk of schizophrenia
    • ISC. Rare chromosomal deletions and duplications increase risk of schizophrenia. Nature 455 (2008) 237-241
    • (2008) Nature , vol.455 , pp. 237-241
    • ISC1
  • 46
    • 0036791671 scopus 로고    scopus 로고
    • A Drosophila fragile X protein interacts with components of RNAi and ribosomal proteins
    • Ishizuka A., Siomi M.C., and Siomi H. A Drosophila fragile X protein interacts with components of RNAi and ribosomal proteins. Genes Dev. 16 (2002) 2497-2508
    • (2002) Genes Dev. , vol.16 , pp. 2497-2508
    • Ishizuka, A.1    Siomi, M.C.2    Siomi, H.3
  • 47
    • 1642540373 scopus 로고    scopus 로고
    • Biochemical and genetic interaction between the fragile X mental retardation protein and the microRNA pathway
    • Jin P., Zarnescu D.C., Ceman S., et al. Biochemical and genetic interaction between the fragile X mental retardation protein and the microRNA pathway. Nat. Neurosci. 7 (2004) 113-117
    • (2004) Nat. Neurosci. , vol.7 , pp. 113-117
    • Jin, P.1    Zarnescu, D.C.2    Ceman, S.3
  • 48
    • 62549120015 scopus 로고    scopus 로고
    • Genome-wide identification of targets of the drosha-pasha/DGCR8 complex
    • Kadener S., Rodriguez J., Abruzzi K.C., et al. Genome-wide identification of targets of the drosha-pasha/DGCR8 complex. Rna 15 (2009) 537-545
    • (2009) Rna , vol.15 , pp. 537-545
    • Kadener, S.1    Rodriguez, J.2    Abruzzi, K.C.3
  • 49
    • 0029102665 scopus 로고
    • Schizophrenia susceptibility associated with interstitial deletions of chromosome 22q11
    • Karayiorgou M., Morris M.A., Morrow B., et al. Schizophrenia susceptibility associated with interstitial deletions of chromosome 22q11. Proc. Natl. Acad. Sci. U. S. A. 92 (1995) 7612-7616
    • (1995) Proc. Natl. Acad. Sci. U. S. A. , vol.92 , pp. 7612-7616
    • Karayiorgou, M.1    Morris, M.A.2    Morrow, B.3
  • 50
    • 0035043250 scopus 로고    scopus 로고
    • Developmental roles and molecular characterization of a Drosophila homologue of Arabidopsis Argonaute1, the founder of a novel gene superfamily
    • Kataoka Y., Takeichi M., and Uemura T. Developmental roles and molecular characterization of a Drosophila homologue of Arabidopsis Argonaute1, the founder of a novel gene superfamily. Genes Cells 6 (2001) 313-325
    • (2001) Genes Cells , vol.6 , pp. 313-325
    • Kataoka, Y.1    Takeichi, M.2    Uemura, T.3
  • 51
    • 34547428532 scopus 로고    scopus 로고
    • The neural correlates of non-spatial working memory in velocardiofacial syndrome (22q11.2 deletion syndrome)
    • Kates W.R., Krauss B.R., AbdulSabur N., et al. The neural correlates of non-spatial working memory in velocardiofacial syndrome (22q11.2 deletion syndrome). Neuropsychologia 45 (2007) 2863-2873
    • (2007) Neuropsychologia , vol.45 , pp. 2863-2873
    • Kates, W.R.1    Krauss, B.R.2    AbdulSabur, N.3
  • 52
    • 33750444633 scopus 로고    scopus 로고
    • Overrepresentation of rare variants in a specific ethnic group may confuse interpretation of association analyses
    • Keen-Kim D., Mathews C.A., Reus V.I., et al. Overrepresentation of rare variants in a specific ethnic group may confuse interpretation of association analyses. Hum. Mol. Genet. 15 (2006) 3324-3328
    • (2006) Hum. Mol. Genet. , vol.15 , pp. 3324-3328
    • Keen-Kim, D.1    Mathews, C.A.2    Reus, V.I.3
  • 53
    • 70449363623 scopus 로고    scopus 로고
    • Tourette syndrome and comorbid early-onset schizophrenia
    • Kerbeshian J., Peng C.Z., and Burd L. Tourette syndrome and comorbid early-onset schizophrenia. J. Psychosom. Res. 67 (2009) 515-523
    • (2009) J. Psychosom. Res. , vol.67 , pp. 515-523
    • Kerbeshian, J.1    Peng, C.Z.2    Burd, L.3
  • 54
    • 34548537573 scopus 로고    scopus 로고
    • A MicroRNA feedback circuit in midbrain dopamine neurons
    • Kim J., Inoue K., Ishii J., et al. A MicroRNA feedback circuit in midbrain dopamine neurons. Science 317 (2007) 1220-1224
    • (2007) Science , vol.317 , pp. 1220-1224
    • Kim, J.1    Inoue, K.2    Ishii, J.3
  • 55
    • 18344369543 scopus 로고    scopus 로고
    • MicroRNA biogenesis: coordinated cropping and dicing
    • Kim V.N. MicroRNA biogenesis: coordinated cropping and dicing. Nat. Rev. Mol. Cell Biol. 6 (2005) 376-385
    • (2005) Nat. Rev. Mol. Cell Biol. , vol.6 , pp. 376-385
    • Kim, V.N.1
  • 56
    • 38349106160 scopus 로고    scopus 로고
    • Comparative genome hybridization suggests a role for NRXN1 and APBA2 in schizophrenia
    • Kirov G., Gumus D., Chen W., et al. Comparative genome hybridization suggests a role for NRXN1 and APBA2 in schizophrenia. Hum. Mol. Genet. 17 (2008) 458-465
    • (2008) Hum. Mol. Genet. , vol.17 , pp. 458-465
    • Kirov, G.1    Gumus, D.2    Chen, W.3
  • 57
    • 64549147485 scopus 로고    scopus 로고
    • Support for the involvement of large copy number variants in the pathogenesis of schizophrenia
    • Kirov G., Grozeva D., Norton N., et al. Support for the involvement of large copy number variants in the pathogenesis of schizophrenia. Hum Mol Genet. 18 (2009) 1497-1503
    • (2009) Hum Mol Genet. , vol.18 , pp. 1497-1503
    • Kirov, G.1    Grozeva, D.2    Norton, N.3
  • 58
    • 36448969801 scopus 로고    scopus 로고
    • Homeostatic regulation of MeCP2 expression by a CREB-induced microRNA
    • Klein M.E., Lioy D.T., Ma L., et al. Homeostatic regulation of MeCP2 expression by a CREB-induced microRNA. Nat. Neurosci. 10 (2007) 1513-1514
    • (2007) Nat. Neurosci. , vol.10 , pp. 1513-1514
    • Klein, M.E.1    Lioy, D.T.2    Ma, L.3
  • 59
    • 62549091540 scopus 로고    scopus 로고
    • MicroRNA-219 modulates NMDA receptor-mediated neurobehavioral dysfunction
    • Kocerha J., Faghihi M.A., Lopez-Toledano M.A., et al. MicroRNA-219 modulates NMDA receptor-mediated neurobehavioral dysfunction. Proc. Natl. Acad. Sci. U. S. A. 106 (2009) 3507-3512
    • (2009) Proc. Natl. Acad. Sci. U. S. A. , vol.106 , pp. 3507-3512
    • Kocerha, J.1    Faghihi, M.A.2    Lopez-Toledano, M.A.3
  • 60
    • 42749095242 scopus 로고    scopus 로고
    • Human chromosome 21-derived miRNAs are overexpressed in down syndrome brains and hearts
    • Kuhn D.E., Nuovo G.J., Martin M.M., et al. Human chromosome 21-derived miRNAs are overexpressed in down syndrome brains and hearts. Biochem. Biophys. Res. Commun. 370 (2008) 473-477
    • (2008) Biochem. Biophys. Res. Commun. , vol.370 , pp. 473-477
    • Kuhn, D.E.1    Nuovo, G.J.2    Martin, M.M.3
  • 61
    • 74049098309 scopus 로고    scopus 로고
    • Chromosome 21-derived microRNAs provide an etiological basis for aberrant protein expression in human Down syndrome brains
    • Kuhn D.E., Nuovo G.J., Terry Jr. A.V., et al. Chromosome 21-derived microRNAs provide an etiological basis for aberrant protein expression in human Down syndrome brains. J. Biol. Chem. 285 (2009) 1529-1543
    • (2009) J. Biol. Chem. , vol.285 , pp. 1529-1543
    • Kuhn, D.E.1    Nuovo, G.J.2    Terry Jr., A.V.3
  • 62
    • 38849126088 scopus 로고    scopus 로고
    • Recurrent 16p11.2 microdeletions in autism
    • Kumar R.A., KaraMohamed S., Sudi J., et al. Recurrent 16p11.2 microdeletions in autism. Hum. Mol. Genet. 17 (2008) 628-638
    • (2008) Hum. Mol. Genet. , vol.17 , pp. 628-638
    • Kumar, R.A.1    KaraMohamed, S.2    Sudi, J.3
  • 63
    • 0037197803 scopus 로고    scopus 로고
    • Identification of tissue-specific microRNAs from mouse
    • Lagos-Quintana M., Rauhut R., Yalcin A., et al. Identification of tissue-specific microRNAs from mouse. Curr. Biol. 12 (2002) 735-739
    • (2002) Curr. Biol. , vol.12 , pp. 735-739
    • Lagos-Quintana, M.1    Rauhut, R.2    Yalcin, A.3
  • 64
    • 0027751663 scopus 로고
    • The C. elegans heterochronic gene lin-4 encodes small RNAs with antisense complementarity to lin-14
    • Lee R.C., Feinbaum R.L., and Ambros V. The C. elegans heterochronic gene lin-4 encodes small RNAs with antisense complementarity to lin-14. Cell 75 (1993) 843-854
    • (1993) Cell , vol.75 , pp. 843-854
    • Lee, R.C.1    Feinbaum, R.L.2    Ambros, V.3
  • 65
    • 0031937997 scopus 로고    scopus 로고
    • Is the girl with Rett syndrome normal at birth?
    • Leonard H., and Bower C. Is the girl with Rett syndrome normal at birth?. Dev. Med. Child Neurol. 40 (1998) 115-121
    • (1998) Dev. Med. Child Neurol. , vol.40 , pp. 115-121
    • Leonard, H.1    Bower, C.2
  • 66
    • 33846340841 scopus 로고    scopus 로고
    • Schizophrenic-like neurocognitive deficits in children and adolescents with 22q11 deletion syndrome
    • Lewandowski K.E., Shashi V., Berry P.M., et al. Schizophrenic-like neurocognitive deficits in children and adolescents with 22q11 deletion syndrome. Am. J. Med. Genet. B Neuropsychiatr. Genet. 144 (2007) 27-36
    • (2007) Am. J. Med. Genet. B Neuropsychiatr. Genet. , vol.144 , pp. 27-36
    • Lewandowski, K.E.1    Shashi, V.2    Berry, P.M.3
  • 67
    • 13944282215 scopus 로고    scopus 로고
    • Microarray analysis shows that some microRNAs downregulate large numbers of target mRNAs
    • Lim L.P., Lau N.C., Garrett-Engele P., et al. Microarray analysis shows that some microRNAs downregulate large numbers of target mRNAs. Nature 433 (2005) 769-773
    • (2005) Nature , vol.433 , pp. 769-773
    • Lim, L.P.1    Lau, N.C.2    Garrett-Engele, P.3
  • 68
    • 4444368187 scopus 로고    scopus 로고
    • Argonaute2 is the catalytic engine of mammalian RNAi
    • Liu J., Carmell M.A., Rivas F.V., et al. Argonaute2 is the catalytic engine of mammalian RNAi. Science 305 (2004) 1437-1441
    • (2004) Science , vol.305 , pp. 1437-1441
    • Liu, J.1    Carmell, M.A.2    Rivas, F.V.3
  • 69
    • 51649130773 scopus 로고    scopus 로고
    • Expression of microRNAs and their precursors in synaptic fractions of adult mouse forebrain
    • Lugli G., Torvik V.I., Larson J., et al. Expression of microRNAs and their precursors in synaptic fractions of adult mouse forebrain. J. Neurochem. 106 (2008) 650-661
    • (2008) J. Neurochem. , vol.106 , pp. 650-661
    • Lugli, G.1    Torvik, V.I.2    Larson, J.3
  • 70
    • 34547212309 scopus 로고    scopus 로고
    • The MicroRNA miR-124 promotes neuronal differentiation by triggering brain-specific alternative pre-mRNA splicing
    • Makeyev E.V., Zhang J., Carrasco M.A., et al. The MicroRNA miR-124 promotes neuronal differentiation by triggering brain-specific alternative pre-mRNA splicing. Mol. Cell. 27 (2007) 435-448
    • (2007) Mol. Cell. , vol.27 , pp. 435-448
    • Makeyev, E.V.1    Zhang, J.2    Carrasco, M.A.3
  • 71
    • 40749089626 scopus 로고    scopus 로고
    • Structural variation of chromosomes in autism spectrum disorder
    • Marshall C.R., Noor A., Vincent J.B., et al. Structural variation of chromosomes in autism spectrum disorder. Am. J. Hum. Genet. 82 (2008) 477-488
    • (2008) Am. J. Hum. Genet. , vol.82 , pp. 477-488
    • Marshall, C.R.1    Noor, A.2    Vincent, J.B.3
  • 72
    • 67349117808 scopus 로고    scopus 로고
    • Molecular determinants of dysregulated GABAergic gene expression in the prefrontal cortex of subjects with schizophrenia
    • Mellios N., Huang H.S., Baker S.P., et al. Molecular determinants of dysregulated GABAergic gene expression in the prefrontal cortex of subjects with schizophrenia. Biol. Psychiatry 65 (2009) 1006-1014
    • (2009) Biol. Psychiatry , vol.65 , pp. 1006-1014
    • Mellios, N.1    Huang, H.S.2    Baker, S.P.3
  • 73
    • 0029895568 scopus 로고    scopus 로고
    • Molecular-clinical correlations in males with an expanded FMR1 mutation
    • Merenstein S.A., Sobesky W.E., Taylor A.K., et al. Molecular-clinical correlations in males with an expanded FMR1 mutation. Am. J. Med. Genet. 64 (1996) 388-394
    • (1996) Am. J. Med. Genet. , vol.64 , pp. 388-394
    • Merenstein, S.A.1    Sobesky, W.E.2    Taylor, A.K.3
  • 74
    • 65949085347 scopus 로고    scopus 로고
    • Microdeletion/duplication at 15q13.2q13.3 among individuals with features of autism and other neuropsychiatric disorders
    • Miller D.T., Shen Y., Weiss L.A., et al. Microdeletion/duplication at 15q13.2q13.3 among individuals with features of autism and other neuropsychiatric disorders. J. Med. Genet. 46 (2009) 242-248
    • (2009) J. Med. Genet. , vol.46 , pp. 242-248
    • Miller, D.T.1    Shen, Y.2    Weiss, L.A.3
  • 77
  • 78
    • 0032882849 scopus 로고    scopus 로고
    • High rates of schizophrenia in adults with velo-cardio-facial syndrome
    • Murphy K.C., Jones L.A., and Owen M.J. High rates of schizophrenia in adults with velo-cardio-facial syndrome. Arch. Gen. Psychiatry 56 (1999) 940-945
    • (1999) Arch. Gen. Psychiatry , vol.56 , pp. 940-945
    • Murphy, K.C.1    Jones, L.A.2    Owen, M.J.3
  • 79
    • 51549108502 scopus 로고    scopus 로고
    • The fragile X syndrome protein represses activity-dependent translation through CYFIP1, a new 4E-BP
    • Napoli I., Mercaldo V., Boyl P.P., et al. The fragile X syndrome protein represses activity-dependent translation through CYFIP1, a new 4E-BP. Cell 134 (2008) 1042-1054
    • (2008) Cell , vol.134 , pp. 1042-1054
    • Napoli, I.1    Mercaldo, V.2    Boyl, P.P.3
  • 80
    • 41849119117 scopus 로고    scopus 로고
    • MeCP2-dependent repression of an imprinted miR-184 released by depolarization
    • Nomura T., Kimura M., Horii T., et al. MeCP2-dependent repression of an imprinted miR-184 released by depolarization. Hum. Mol. Genet. 17 (2008) 1192-1199
    • (2008) Hum. Mol. Genet. , vol.17 , pp. 1192-1199
    • Nomura, T.1    Kimura, M.2    Horii, T.3
  • 81
    • 70449361669 scopus 로고    scopus 로고
    • The genetics of Tourette syndrome: a review
    • O'Rourke J.A., Scharf J.M., Yu D., et al. The genetics of Tourette syndrome: a review. J. Psychosom. Res. 67 (2009) 533-545
    • (2009) J. Psychosom. Res. , vol.67 , pp. 533-545
    • O'Rourke, J.A.1    Scharf, J.M.2    Yu, D.3
  • 82
    • 33745623128 scopus 로고    scopus 로고
    • Post-transcriptional regulation of microRNA expression
    • Obernosterer G., Leuschner P.J., Alenius M., et al. Post-transcriptional regulation of microRNA expression. RNA 12 (2006) 1161-1167
    • (2006) RNA , vol.12 , pp. 1161-1167
    • Obernosterer, G.1    Leuschner, P.J.2    Alenius, M.3
  • 84
    • 34249736846 scopus 로고    scopus 로고
    • microRNA expression in the prefrontal cortex of individuals with schizophrenia and schizoaffective disorder
    • Perkins D.O., Jeffries C.D., Jarskog L.F., et al. microRNA expression in the prefrontal cortex of individuals with schizophrenia and schizoaffective disorder. Genome Biol. 8 (2007) R27
    • (2007) Genome Biol. , vol.8
    • Perkins, D.O.1    Jeffries, C.D.2    Jarskog, L.F.3
  • 85
    • 33947537457 scopus 로고    scopus 로고
    • Fragile X mental retardation protein induces synapse loss through acute postsynaptic translational regulation
    • Pfeiffer B.E., and Huber K.M. Fragile X mental retardation protein induces synapse loss through acute postsynaptic translational regulation. J. Neurosci. 27 (2007) 3120-3130
    • (2007) J. Neurosci. , vol.27 , pp. 3120-3130
    • Pfeiffer, B.E.1    Huber, K.M.2
  • 86
    • 4644310115 scopus 로고    scopus 로고
    • Tethering of human Ago proteins to mRNA mimics the miRNA-mediated repression of protein synthesis
    • Pillai R.S., Artus C.G., and Filipowicz W. Tethering of human Ago proteins to mRNA mimics the miRNA-mediated repression of protein synthesis. Rna 10 (2004) 1518-1525
    • (2004) Rna , vol.10 , pp. 1518-1525
    • Pillai, R.S.1    Artus, C.G.2    Filipowicz, W.3
  • 87
    • 60349108540 scopus 로고    scopus 로고
    • Synaptic ionotropic glutamate receptors and plasticity are developmentally altered in the CA1 field of Fmr1 knockout mice
    • Pilpel Y., Kolleker A., Berberich S., et al. Synaptic ionotropic glutamate receptors and plasticity are developmentally altered in the CA1 field of Fmr1 knockout mice. J. Physiol. 587 (2009) 787-804
    • (2009) J. Physiol. , vol.587 , pp. 787-804
    • Pilpel, Y.1    Kolleker, A.2    Berberich, S.3
  • 88
    • 0028082293 scopus 로고
    • Sequential strategy to identify a susceptibility gene for schizophrenia: report of potential linkage on chromosome 22q12-q13.1: Part 1
    • Pulver A.E., Karayiorgou M., Wolyniec P.S., et al. Sequential strategy to identify a susceptibility gene for schizophrenia: report of potential linkage on chromosome 22q12-q13.1: Part 1. Am. J. Med. Genet. 54 (1994) 36-43
    • (1994) Am. J. Med. Genet. , vol.54 , pp. 36-43
    • Pulver, A.E.1    Karayiorgou, M.2    Wolyniec, P.S.3
  • 89
    • 70349117273 scopus 로고    scopus 로고
    • Characterization of small RNAs in aplysia reveals a role for miR-124 in constraining synaptic plasticity through CREB
    • Rajasethupathy P., Fiumara F., Sheridan R., et al. Characterization of small RNAs in aplysia reveals a role for miR-124 in constraining synaptic plasticity through CREB. Neuron 63 (2009) 803-817
    • (2009) Neuron , vol.63 , pp. 803-817
    • Rajasethupathy, P.1    Fiumara, F.2    Sheridan, R.3
  • 90
    • 51749093103 scopus 로고    scopus 로고
    • Degradation of microRNAs by a family of exoribonucleases in Arabidopsis
    • Ramachandran V., and Chen X. Degradation of microRNAs by a family of exoribonucleases in Arabidopsis. Science 321 (2008) 1490-1492
    • (2008) Science , vol.321 , pp. 1490-1492
    • Ramachandran, V.1    Chen, X.2
  • 91
    • 0042090496 scopus 로고    scopus 로고
    • Diagnosing Tourette syndrome: is it a common disorder?
    • Robertson M.M. Diagnosing Tourette syndrome: is it a common disorder?. J. Psychosom. Res. 55 (2003) 3-6
    • (2003) J. Psychosom. Res. , vol.55 , pp. 3-6
    • Robertson, M.M.1
  • 92
    • 34447261382 scopus 로고    scopus 로고
    • Cerebellar neurodegeneration in the absence of microRNAs
    • Schaefer A., O'Carroll D., Tan C.L., et al. Cerebellar neurodegeneration in the absence of microRNAs. J. Exp. Med. 204 (2007) 1553-1558
    • (2007) J. Exp. Med. , vol.204 , pp. 1553-1558
    • Schaefer, A.1    O'Carroll, D.2    Tan, C.L.3
  • 93
    • 42049101407 scopus 로고    scopus 로고
    • Lack of association between SLITRK1var321 and Tourette syndrome in a large family-based sample
    • Scharf J.M., Moorjani P., Fagerness J., et al. Lack of association between SLITRK1var321 and Tourette syndrome in a large family-based sample. Neurology 70 (2008) 1495-1496
    • (2008) Neurology , vol.70 , pp. 1495-1496
    • Scharf, J.M.1    Moorjani, P.2    Fagerness, J.3
  • 94
    • 70450248489 scopus 로고    scopus 로고
    • microRNAs at the synapse
    • Schratt G. microRNAs at the synapse. Nat. Rev. Neurosci. 10 (2009) 842-849
    • (2009) Nat. Rev. Neurosci. , vol.10 , pp. 842-849
    • Schratt, G.1
  • 95
    • 31144479591 scopus 로고    scopus 로고
    • A brain-specific microRNA regulates dendritic spine development
    • Schratt G.M., Tuebing F., Nigh E.A., et al. A brain-specific microRNA regulates dendritic spine development. Nature 439 (2006) 283-289
    • (2006) Nature , vol.439 , pp. 283-289
    • Schratt, G.M.1    Tuebing, F.2    Nigh, E.A.3
  • 96
    • 34247481814 scopus 로고    scopus 로고
    • Strong association of de novo copy number mutations with autism
    • Sebat J., Lakshmi B., Malhotra D., et al. Strong association of de novo copy number mutations with autism. Science 316 (2007) 445-449
    • (2007) Science , vol.316 , pp. 445-449
    • Sebat, J.1    Lakshmi, B.2    Malhotra, D.3
  • 97
    • 0032231652 scopus 로고    scopus 로고
    • Rett syndrome: confirmation of X-linked dominant inheritance, and localization of the gene to Xq28
    • Sirianni N., Naidu S., Pereira J., et al. Rett syndrome: confirmation of X-linked dominant inheritance, and localization of the gene to Xq28. Am. J. Hum. Genet. 63 (1998) 1552-1558
    • (1998) Am. J. Hum. Genet. , vol.63 , pp. 1552-1558
    • Sirianni, N.1    Naidu, S.2    Pereira, J.3
  • 98
    • 17144423635 scopus 로고    scopus 로고
    • Neuropsychological characteristics of children with the 22q11 Deletion Syndrome: a descriptive analysis
    • Sobin C., Kiley-Brabeck K., Daniels S., et al. Neuropsychological characteristics of children with the 22q11 Deletion Syndrome: a descriptive analysis. Child Neuropsychol. 11 (2005) 39-53
    • (2005) Child Neuropsychol. , vol.11 , pp. 39-53
    • Sobin, C.1    Kiley-Brabeck, K.2    Daniels, S.3
  • 99
    • 0031020846 scopus 로고    scopus 로고
    • Tourette disorder: a cross-cultural review
    • Staley D., Wand R., and Shady G. Tourette disorder: a cross-cultural review. Compr. Psychiatry 38 (1997) 6-16
    • (1997) Compr. Psychiatry , vol.38 , pp. 6-16
    • Staley, D.1    Wand, R.2    Shady, G.3
  • 100
    • 43949124669 scopus 로고    scopus 로고
    • Altered brain microRNA biogenesis contributes to phenotypic deficits in a 22q11-deletion mouse model
    • Stark K.L., Xu B., Bagchi A., et al. Altered brain microRNA biogenesis contributes to phenotypic deficits in a 22q11-deletion mouse model. Nat. Genet. 40 (2008) 751-760
    • (2008) Nat. Genet. , vol.40 , pp. 751-760
    • Stark, K.L.1    Xu, B.2    Bagchi, A.3
  • 101
    • 49949085933 scopus 로고    scopus 로고
    • Large recurrent microdeletions associated with schizophrenia
    • Stefansson H., Rujescu D., Cichon S., et al. Large recurrent microdeletions associated with schizophrenia. Nature 455 (2008) 232-236
    • (2008) Nature , vol.455 , pp. 232-236
    • Stefansson, H.1    Rujescu, D.2    Cichon, S.3
  • 102
    • 0024523493 scopus 로고
    • A twin study of autism in Denmark, Finland, Iceland, Norway and Sweden
    • Steffenburg S., Gillberg C., Hellgren L., et al. A twin study of autism in Denmark, Finland, Iceland, Norway and Sweden. J. Child Psychol. Psychiatry 30 (1989) 405-416
    • (1989) J. Child Psychol. Psychiatry , vol.30 , pp. 405-416
    • Steffenburg, S.1    Gillberg, C.2    Hellgren, L.3
  • 103
    • 33847327313 scopus 로고    scopus 로고
    • Mapping autism risk loci using genetic linkage and chromosomal rearrangements
    • Szatmari P., Paterson A.D., Zwaigenbaum L., et al. Mapping autism risk loci using genetic linkage and chromosomal rearrangements. Nat. Genet. 39 (2007) 319-328
    • (2007) Nat. Genet. , vol.39 , pp. 319-328
    • Szatmari, P.1    Paterson, A.D.2    Zwaigenbaum, L.3
  • 104
    • 66349107637 scopus 로고    scopus 로고
    • Feasibility and relevance of examining lymphoblastoid cell lines to study role of microRNAs in autism
    • Talebizadeh Z., Butler M.G., and Theodoro M.F. Feasibility and relevance of examining lymphoblastoid cell lines to study role of microRNAs in autism. Autism Res. 1 (2008) 307
    • (2008) Autism Res. , vol.1 , pp. 307
    • Talebizadeh, Z.1    Butler, M.G.2    Theodoro, M.F.3
  • 105
    • 33747334621 scopus 로고    scopus 로고
    • Extensive post-transcriptional regulation of microRNAs and its implications for cancer
    • Thomson J.M., Newman M., Parker J.S., et al. Extensive post-transcriptional regulation of microRNAs and its implications for cancer. Genes Dev. 20 (2006) 2202-2207
    • (2006) Genes Dev. , vol.20 , pp. 2202-2207
    • Thomson, J.M.1    Newman, M.2    Parker, J.S.3
  • 106
    • 66449118741 scopus 로고    scopus 로고
    • Post-transcriptional control of DGCR8 expression by the Microprocessor
    • Triboulet R., Chang H.M., Lapierre R.J., et al. Post-transcriptional control of DGCR8 expression by the Microprocessor. Rna 15 (2009) 1005-1011
    • (2009) Rna , vol.15 , pp. 1005-1011
    • Triboulet, R.1    Chang, H.M.2    Lapierre, R.J.3
  • 107
    • 4544306641 scopus 로고    scopus 로고
    • Neuropsychiatric symptoms of fragile X syndrome: pathophysiology and pharmacotherapy
    • Tsiouris J.A., and Brown W.T. Neuropsychiatric symptoms of fragile X syndrome: pathophysiology and pharmacotherapy. CNS Drugs. 18 (2004) 687-703
    • (2004) CNS Drugs. , vol.18 , pp. 687-703
    • Tsiouris, J.A.1    Brown, W.T.2
  • 108
    • 0029924873 scopus 로고    scopus 로고
    • Prevalence of fragile X syndrome
    • Turner G., Webb T., Wake S., et al. Prevalence of fragile X syndrome. Am. J. Med. Genet. 64 (1996) 196-197
    • (1996) Am. J. Med. Genet. , vol.64 , pp. 196-197
    • Turner, G.1    Webb, T.2    Wake, S.3
  • 109
    • 33749143420 scopus 로고    scopus 로고
    • Genetic and clinical analysis of a large Dutch Gilles de la Tourette family
    • Verkerk A.J., Cath D.C., van der Linde H.C., et al. Genetic and clinical analysis of a large Dutch Gilles de la Tourette family. Mol. Psychiatry 11 (2006) 954-964
    • (2006) Mol. Psychiatry , vol.11 , pp. 954-964
    • Verkerk, A.J.1    Cath, D.C.2    van der Linde, H.C.3
  • 110
    • 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
    • Verkerk A.J., Pieretti M., Sutcliffe J.S., et al. 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, A.J.1    Pieretti, M.2    Sutcliffe, J.S.3
  • 111
    • 28044439909 scopus 로고    scopus 로고
    • A cAMP-response element binding protein-induced microRNA regulates neuronal morphogenesis
    • Vo N., Klein M.E., Varlamova O., et al. A cAMP-response element binding protein-induced microRNA regulates neuronal morphogenesis. Proc. Natl. Acad. Sci. U. S. A. 102 (2005) 16426-16431
    • (2005) Proc. Natl. Acad. Sci. U. S. A. , vol.102 , pp. 16426-16431
    • Vo, N.1    Klein, M.E.2    Varlamova, O.3
  • 112
    • 33847323881 scopus 로고    scopus 로고
    • DGCR8 is essential for microRNA biogenesis and silencing of embryonic stem cell self-renewal
    • Wang Y., Medvid R., Melton C., et al. DGCR8 is essential for microRNA biogenesis and silencing of embryonic stem cell self-renewal. Nat. Genet. 39 (2007) 380-385
    • (2007) Nat. Genet. , vol.39 , pp. 380-385
    • Wang, Y.1    Medvid, R.2    Melton, C.3
  • 113
    • 48249095979 scopus 로고    scopus 로고
    • An activity-regulated microRNA controls dendritic plasticity by down-regulating p250GAP
    • Wayman G.A., Davare M., Ando H., et al. An activity-regulated microRNA controls dendritic plasticity by down-regulating p250GAP. Proc. Natl. Acad. Sci. U. S. A. 105 (2008) 9093-9098
    • (2008) Proc. Natl. Acad. Sci. U. S. A. , vol.105 , pp. 9093-9098
    • Wayman, G.A.1    Davare, M.2    Ando, H.3
  • 114
    • 39049163023 scopus 로고    scopus 로고
    • Association between microdeletion and microduplication at 16p11.2 and autism
    • Weiss L.A., Shen Y., Korn J.M., et al. Association between microdeletion and microduplication at 16p11.2 and autism. N. Engl. J. Med. 358 (2008) 667-675
    • (2008) N. Engl. J. Med. , vol.358 , pp. 667-675
    • Weiss, L.A.1    Shen, Y.2    Korn, J.M.3
  • 115
    • 33748092355 scopus 로고    scopus 로고
    • Functional SLITRK1 var321, varCDfs and SLC6A4 G56A variants and susceptibility to obsessive-compulsive disorder
    • Wendland J.R., Kruse M.R., and Murphy D.L. Functional SLITRK1 var321, varCDfs and SLC6A4 G56A variants and susceptibility to obsessive-compulsive disorder. Mol. Psychiatry 11 (2006) 802-804
    • (2006) Mol. Psychiatry , vol.11 , pp. 802-804
    • Wendland, J.R.1    Kruse, M.R.2    Murphy, D.L.3
  • 116
    • 0021956826 scopus 로고
    • Occurrence of neuropathological changes and dementia of Alzheimer's disease in Down's syndrome
    • Wisniewski K.E., Wisniewski H.M., and Wen G.Y. Occurrence of neuropathological changes and dementia of Alzheimer's disease in Down's syndrome. Ann. Neurol. 17 (1985) 278-282
    • (1985) Ann. Neurol. , vol.17 , pp. 278-282
    • Wisniewski, K.E.1    Wisniewski, H.M.2    Wen, G.Y.3
  • 117
    • 0026765446 scopus 로고
    • Age-related occurrence of signs and symptoms in the Rett syndrome
    • Witt Engerstrom I. Age-related occurrence of signs and symptoms in the Rett syndrome. Brain Dev. 14 Suppl (1992) S11-S20
    • (1992) Brain Dev. , vol.14 SUPPL
    • Witt Engerstrom, I.1
  • 118
    • 33750432857 scopus 로고    scopus 로고
    • Comparative sequence analysis reveals an intricate network among REST, CREB and miRNA in mediating neuronal gene expression
    • Wu J., and Xie X. Comparative sequence analysis reveals an intricate network among REST, CREB and miRNA in mediating neuronal gene expression. Genome Biol. 7 (2006) R85
    • (2006) Genome Biol. , vol.7
    • Wu, J.1    Xie, X.2
  • 119
    • 46249093584 scopus 로고    scopus 로고
    • Strong association of de novo copy number mutations with sporadic schizophrenia
    • Xu B., Roos J.L., Levy S., et al. Strong association of de novo copy number mutations with sporadic schizophrenia. Nat. Genet. 40 (2008) 880-885
    • (2008) Nat. Genet. , vol.40 , pp. 880-885
    • Xu, B.1    Roos, J.L.2    Levy, S.3
  • 120
    • 58149357047 scopus 로고    scopus 로고
    • The steady-state level of the nervous-system-specific microRNA-124a is regulated by dFMR1 in Drosophila
    • Xu X.L., Li Y., Wang F., et al. The steady-state level of the nervous-system-specific microRNA-124a is regulated by dFMR1 in Drosophila. J. Neurosci. 28 (2008) 11883-11889
    • (2008) J. Neurosci. , vol.28 , pp. 11883-11889
    • Xu, X.L.1    Li, Y.2    Wang, F.3
  • 121
    • 48849103603 scopus 로고    scopus 로고
    • MicroRNA miR-124 regulates neurite outgrowth during neuronal differentiation
    • Yu J.Y., Chung K.H., Deo M., et al. MicroRNA miR-124 regulates neurite outgrowth during neuronal differentiation. Exp. Cell Res. 314 (2008) 2618-2633
    • (2008) Exp. Cell Res. , vol.314 , pp. 2618-2633
    • Yu, J.Y.1    Chung, K.H.2    Deo, M.3
  • 122
    • 0035977134 scopus 로고    scopus 로고
    • Drosophila fragile X-related gene regulates the MAP1B homolog Futsch to control synaptic structure and function
    • Zhang Y.Q., Bailey A.M., Matthies H.J., et al. Drosophila fragile X-related gene regulates the MAP1B homolog Futsch to control synaptic structure and function. Cell 107 (2001) 591-603
    • (2001) Cell , vol.107 , pp. 591-603
    • Zhang, Y.Q.1    Bailey, A.M.2    Matthies, H.J.3
  • 123
    • 64949159019 scopus 로고    scopus 로고
    • Evidence for selective microRNAs and their effectors as common long-term targets for the actions of mood stabilizers
    • Zhou R., Yuan P., Wang Y., et al. Evidence for selective microRNAs and their effectors as common long-term targets for the actions of mood stabilizers. Neuropsychopharmacology 34 (2009) 1395-1405
    • (2009) Neuropsychopharmacology , vol.34 , pp. 1395-1405
    • Zhou, R.1    Yuan, P.2    Wang, Y.3
  • 124
    • 57149124492 scopus 로고    scopus 로고
    • Sequence analysis of the complete SLITRK1 gene in Austrian patients with Tourette's disorder
    • Zimprich A., Hatala K., Riederer F., et al. Sequence analysis of the complete SLITRK1 gene in Austrian patients with Tourette's disorder. Psychiatr. Genet. 18 (2008) 308-309
    • (2008) Psychiatr. Genet. , vol.18 , pp. 308-309
    • Zimprich, A.1    Hatala, K.2    Riederer, F.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.