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Volumn 41, Issue 1, 2010, Pages 193-197

Searching for new genetic risk factors for neuropsychiatric disorders in expression databases

Author keywords

Bioinformatics; Expression databases; Genetic variations; Neurogenetics; Neuropsychiatric disorders

Indexed keywords

MESSENGER RNA;

EID: 77950189472     PISSN: 08958696     EISSN: None     Source Type: Journal    
DOI: 10.1007/s12031-009-9321-5     Document Type: Article
Times cited : (10)

References (22)
  • 1
    • 48249126806 scopus 로고    scopus 로고
    • The Prion's elusive reason for being
    • 10.1146/annurev.neuro.31.060407.125620 1:CAS:528:DC%2BD1cXptleju74%3D 18558863
    • A Aguzzi F Baumann J Bremer 2008 The Prion's elusive reason for being Annu Rev Neurosci 31 439 477 10.1146/annurev.neuro.31.060407.125620 1:CAS:528:DC%2BD1cXptleju74%3D 18558863
    • (2008) Annu Rev Neurosci , vol.31 , pp. 439-477
    • Aguzzi, A.1    Baumann, F.2    Bremer, J.3
  • 4
    • 0037010289 scopus 로고    scopus 로고
    • Gene expression profiling of 12633 genes in Alzheimer hippocampal CA1: Transcription and neurotrophic factor down-regulation and up-regulation of apoptotic and pro-inflammatory signaling
    • DOI 10.1002/jnr.10351
    • V Colangelo J Schurr MJ Ball RP Pelaez NG Bazan WJ Lukiw 2002 Gene expression profiling of 12633 genes in Alzheimer hippocampal CA1: transcription and neurotrophic factor down-regulation and up-regulation of apoptotic and pro-inflammatory signaling J Neurosci Res 70 462 473 10.1002/jnr.10351 1:CAS:528:DC%2BD38XosVejsr8%3D 12391607 (Pubitemid 35222383)
    • (2002) Journal of Neuroscience Research , vol.70 , Issue.3 , pp. 462-473
    • Colangelo, V.1    Schurr, J.2    Ball, M.J.3    Pelaez, R.P.4    Bazan, N.G.5    Lukiw, W.J.6
  • 5
    • 77950461601 scopus 로고    scopus 로고
    • Origins and functional impact of copy number variation in the human genome
    • doi: 10.1038/nature08516.14August2009
    • Conrad DF, Pinto D, Redon R et al (2009) Origins and functional impact of copy number variation in the human genome. Nature doi: 10.1038/nature08516. 14 August 2009
    • (2009) Nature
    • Conrad, D.F.1    Pinto, D.2    Redon, R.3
  • 6
    • 48949093046 scopus 로고    scopus 로고
    • Gene expression study on peripheral blood identifies progranulin mutations
    • 10.1002/ana.21397 1:CAS:528:DC%2BD1cXhtVKnsrnK 18551524
    • G Coppola A Karydas R Rademakers, et al. 2008 Gene expression study on peripheral blood identifies progranulin mutations Ann Neurol 64 92 96 10.1002/ana.21397 1:CAS:528:DC%2BD1cXhtVKnsrnK 18551524
    • (2008) Ann Neurol , vol.64 , pp. 92-96
    • Coppola, G.1    Karydas, A.2    Rademakers, R.3
  • 8
    • 39849105207 scopus 로고    scopus 로고
    • EST2uni: An open, parallel tool for automated EST analysis and database creation, with a data mining web interface and microarray expression data integration
    • 10.1186/1471-2105-9-5 18179701
    • J Forment F Gilbert A Robles V Conejero F Nuez JM Blanca 2008 EST2uni: an open, parallel tool for automated EST analysis and database creation, with a data mining web interface and microarray expression data integration BMC Bioinformatics 9 5 15 10.1186/1471-2105-9-5 18179701
    • (2008) BMC Bioinformatics , vol.9 , pp. 5-15
    • Forment, J.1    Gilbert, F.2    Robles, A.3    Conejero, V.4    Nuez, F.5    Blanca, J.M.6
  • 9
    • 38649109788 scopus 로고    scopus 로고
    • Polymorphisms of two indels at the PRNP gene in three beef cattle herds
    • 10.1007/s10528-007-9113-y 1:CAS:528:DC%2BD1cXhtFKntrc%3D 18064562
    • AR Kerber D Hepp DT Passos T de Azevedo Weimer 2008 Polymorphisms of two indels at the PRNP gene in three beef cattle herds Biochem Genet 46 1 7 10.1007/s10528-007-9113-y 1:CAS:528:DC%2BD1cXhtFKntrc%3D 18064562
    • (2008) Biochem Genet , vol.46 , pp. 1-7
    • Kerber, A.R.1    Hepp, D.2    Passos, D.T.3    De Azevedo Weimer, T.4
  • 10
    • 74149085084 scopus 로고    scopus 로고
    • In silico identification of new genetic variations as potential risk factors for Alzheimeŕs Disease in a Microarray oriented simulation
    • 10.1007/s12031-009-9191-x 1:CAS:528:DC%2BD1MXhtFaksbnK 19290494
    • RR Lemos CH Castelletti JL Lima Filho ET Marques JR Oliveira 2009 In silico identification of new genetic variations as potential risk factors for Alzheimeŕs Disease in a Microarray oriented simulation J Mol Neurosci 39 242 247 10.1007/s12031-009-9191-x 1:CAS:528:DC%2BD1MXhtFaksbnK 19290494
    • (2009) J Mol Neurosci , vol.39 , pp. 242-247
    • Lemos, R.R.1    Castelletti, C.H.2    Lima Filho, J.L.3    Marques, E.T.4    Oliveira, J.R.5
  • 12
    • 0036176676 scopus 로고    scopus 로고
    • Striatal excitatory amino acid transporter transcript expression in schizophrenia, bipolar disorder, and major depressive disorder
    • DOI 10.1016/S0893-133X(01)00370-0, PII S0893133X01003700
    • RE McCullumsmith JH Meador-Woodruff 2002 Striatal excitatory amino acid transporter transcript expression in schizophrenia, bipolar disorder, and major depressive disorder Neuropsychopharmacology 26 368 375 10.1016/S0893-133X(01) 00370-0 1:CAS:528:DC%2BD38Xht1ajtb4%3D 11850151 (Pubitemid 34159214)
    • (2002) Neuropsychopharmacology , vol.26 , Issue.3 , pp. 368-375
    • McCullumsmith, R.E.1    Meador-Woodruff, J.H.2
  • 13
    • 57249087392 scopus 로고    scopus 로고
    • Genetic risk factors for variant Creutzfeldt-Jakob disease: A genome-wide association study
    • 10.1016/S1474-4422(08)70265-5 19081515
    • S Mead M Poulter J Uphill, et al. 2009 Genetic risk factors for variant Creutzfeldt-Jakob disease: a genome-wide association study Lancet Neurol 8 57 66 10.1016/S1474-4422(08)70265-5 19081515
    • (2009) Lancet Neurol , vol.8 , pp. 57-66
    • Mead, S.1    Poulter, M.2    Uphill, J.3
  • 14
    • 38949175007 scopus 로고    scopus 로고
    • A systems level analysis of transcriptional changes in Alzheimer's disease and normal aging
    • 10.1523/JNEUROSCI.4098-07.2008 1:CAS:528:DC%2BD1cXitVSqs78%3D 18256261
    • JA Miller MC Oldham DH Geschwind 2008 A systems level analysis of transcriptional changes in Alzheimer's disease and normal aging J Neurosci 28 1410 1420 10.1523/JNEUROSCI.4098-07.2008 1:CAS:528:DC%2BD1cXitVSqs78%3D 18256261
    • (2008) J Neurosci , vol.28 , pp. 1410-1420
    • Miller, J.A.1    Oldham, M.C.2    Geschwind, D.H.3
  • 15
    • 42949123365 scopus 로고    scopus 로고
    • Targeting the glutamatergic system to develop novel, improved therapeutics for mood disorders
    • 1:CAS:528:DC%2BD1cXlt1agtbw%3D
    • G Sanacora CA Zarate JH Krystal HK Manji 2008 Targeting the glutamatergic system to develop novel, improved therapeutics for mood disorders Nature 7 426 437 1:CAS:528:DC%2BD1cXlt1agtbw%3D
    • (2008) Nature , vol.7 , pp. 426-437
    • Sanacora, G.1    Zarate, C.A.2    Krystal, J.H.3    Manji, H.K.4
  • 16
    • 49949085933 scopus 로고    scopus 로고
    • Large recurrent microdeletions associated with schizophrenia
    • 10.1038/nature07229 1:CAS:528:DC%2BD1cXhtV2qtL%2FL 18668039
    • D Stefansson D Rujescu S Cichon, et al. 2008 Large recurrent microdeletions associated with schizophrenia Nature 455 232 236 10.1038/nature07229 1:CAS:528:DC%2BD1cXhtV2qtL%2FL 18668039
    • (2008) Nature , vol.455 , pp. 232-236
    • Stefansson, D.1    Rujescu, D.2    Cichon, S.3
  • 17
    • 49949099664 scopus 로고    scopus 로고
    • Towards a cyberinfrastructure for the biological sciences: Progress, visions and challenges
    • 10.1038/nrg2414 1:CAS:528:DC%2BD1cXhtVSitrvE 18714290
    • LD Stein 2008 Towards a cyberinfrastructure for the biological sciences: progress, visions and challenges Nat Rev Genet 9 678 688 10.1038/nrg2414 1:CAS:528:DC%2BD1cXhtVSitrvE 18714290
    • (2008) Nat Rev Genet , vol.9 , pp. 678-688
    • Stein, L.D.1
  • 18
    • 0035756174 scopus 로고    scopus 로고
    • High-throughput identification, database storage and analysis of SNPs in ESTs sequences
    • 1:CAS:528:DC%2BD38XkvV2rtLw%3D 11791238
    • FJ Useche G Gao M Harafey A Rafalski 2001 High-throughput identification, database storage and analysis of SNPs in ESTs sequences Genome Informatics 12 194 203 1:CAS:528:DC%2BD38XkvV2rtLw%3D 11791238
    • (2001) Genome Informatics , vol.12 , pp. 194-203
    • Useche, F.J.1    Gao, G.2    Harafey, M.3    Rafalski, A.4
  • 19
    • 42349088634 scopus 로고    scopus 로고
    • Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophrenia
    • 10.1126/science.1155174 1:CAS:528:DC%2BD1cXkvFGkt7s%3D 18369103
    • T Walsh JM Mcclellan SE Mccarthy, et al. 2008 Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophrenia Science 320 539 543 10.1126/science.1155174 1:CAS:528:DC%2BD1cXkvFGkt7s%3D 18369103
    • (2008) Science , vol.320 , pp. 539-543
    • Walsh, T.1    McClellan, J.M.2    McCarthy, S.E.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.