메뉴 건너뛰기




Volumn , Issue , 2013, Pages 391-399

Inducible Pluripotent Stem Cells In Autism Spectrum Disorders

Author keywords

[No Author keywords available]

Indexed keywords


EID: 84882678304     PISSN: None     EISSN: None     Source Type: Book    
DOI: 10.1016/B978-0-12-391924-3.00028-4     Document Type: Chapter
Times cited : (1)

References (62)
  • 1
    • 80053143413 scopus 로고    scopus 로고
    • Isogenic pairs of wild type and mutant induced pluripotent stem cell (iPSC) lines from Rett syndrome patients as in vitro disease model
    • Ananiev G., Williams E.C., Li H., Chang Q. Isogenic pairs of wild type and mutant induced pluripotent stem cell (iPSC) lines from Rett syndrome patients as in vitro disease model. PLoS One 2011, 6:e25255.
    • (2011) PLoS One , vol.6
    • Ananiev, G.1    Williams, E.C.2    Li, H.3    Chang, Q.4
  • 2
    • 67649506317 scopus 로고    scopus 로고
    • Down's syndrome suppression of tumor growth and the role of the calcineurin inhibitor DSCR1
    • Baek K.H., Zaslavsky A., Lynch R.C., Britt C., Okada Y., Siarey R.J., et al. Down's syndrome suppression of tumor growth and the role of the calcineurin inhibitor DSCR1. Nature 2009, 459:1126-1130.
    • (2009) Nature , vol.459 , pp. 1126-1130
    • Baek, K.H.1    Zaslavsky, A.2    Lynch, R.C.3    Britt, C.4    Okada, Y.5    Siarey, R.J.6
  • 3
    • 80054889797 scopus 로고    scopus 로고
    • Haploinsufficiency of the autism-associated Shank3 gene leads to deficits in synaptic function, social interaction, and social communication
    • Bozdagi O., Sakurai T., Papapetrou D., Wang X., Dickstein D.L., Takahashi N., et al. Haploinsufficiency of the autism-associated Shank3 gene leads to deficits in synaptic function, social interaction, and social communication. Molecular Autism 2010, 1:15.
    • (2010) Molecular Autism , vol.1 , pp. 15
    • Bozdagi, O.1    Sakurai, T.2    Papapetrou, D.3    Wang, X.4    Dickstein, D.L.5    Takahashi, N.6
  • 6
    • 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., Glessner J.T., Herman E.I., Sonnenblick L.I., et al. Genome-wide analyses of exonic copy number variants in a family-based study point to novel autism susceptibility genes. PLoS Genetics 2009, 5:e1000536.
    • (2009) PLoS Genetics , vol.5
    • Bucan, M.1    Abrahams, B.S.2    Wang, K.3    Glessner, J.T.4    Herman, E.I.5    Sonnenblick, L.I.6
  • 7
    • 79955602167 scopus 로고    scopus 로고
    • Isolation of MECP2-null Rett Syndrome patient hiPS cells and isogenic controls through X-chromosome inactivation
    • Cheung A.Y., Horvath L.M., Grafodatskaya D., Pasceri P., Weksberg R., Hotta A., et al. Isolation of MECP2-null Rett Syndrome patient hiPS cells and isogenic controls through X-chromosome inactivation. Human Molecular Genetics 2012, 20:2103-2115.
    • (2012) Human Molecular Genetics , vol.20 , pp. 2103-2115
    • Cheung, A.Y.1    Horvath, L.M.2    Grafodatskaya, D.3    Pasceri, P.4    Weksberg, R.5    Hotta, A.6
  • 8
    • 67649222358 scopus 로고    scopus 로고
    • Induced pluripotent stem cells and embryonic stem cells are distinguished by gene expression signatures
    • Chin M.H., Mason M.J., Xie W., Volinia S., Singer M., Peterson C., et al. Induced pluripotent stem cells and embryonic stem cells are distinguished by gene expression signatures. Cell Stem Cell 2009, 5:111-123.
    • (2009) Cell Stem Cell , vol.5 , pp. 111-123
    • Chin, M.H.1    Mason, M.J.2    Xie, W.3    Volinia, S.4    Singer, M.5    Peterson, C.6
  • 10
    • 48749089453 scopus 로고    scopus 로고
    • The adult human brain in preclinical drug development
    • Dragunow M. The adult human brain in preclinical drug development. Nature Reviews Drug Discovery 2008, 7:659-666.
    • (2008) Nature Reviews Drug Discovery , vol.7 , pp. 659-666
    • Dragunow, M.1
  • 11
    • 58249110796 scopus 로고    scopus 로고
    • Induced pluripotent stem cells from a spinal muscular atrophy patient
    • Ebert A.D., Yu J., Rose F.F., Mattis V.B., Lorson C.L., Thomson J.A., et al. Induced pluripotent stem cells from a spinal muscular atrophy patient. Nature 2009, 457:277-280.
    • (2009) Nature , vol.457 , pp. 277-280
    • Ebert, A.D.1    Yu, J.2    Rose, F.F.3    Mattis, V.B.4    Lorson, C.L.5    Thomson, J.A.6
  • 12
    • 77049120173 scopus 로고    scopus 로고
    • The genetics of autism: Key issues, recent findings, and clinical implications
    • El-Fishawy P., State M.W. The genetics of autism: Key issues, recent findings, and clinical implications. Psychiatric Clinics of North America 2010, 33:83-105.
    • (2010) Psychiatric Clinics of North America , vol.33 , pp. 83-105
    • El-Fishawy, P.1    State, M.W.2
  • 13
    • 80051920294 scopus 로고    scopus 로고
    • Genetics of autism spectrum disorders
    • Geschwind D.H. Genetics of autism spectrum disorders. Trends in Cognitive Sciences 2011, 15:409-416.
    • (2011) Trends in Cognitive Sciences , vol.15 , pp. 409-416
    • Geschwind, D.H.1
  • 14
  • 15
    • 79958035893 scopus 로고    scopus 로고
    • Rare de novo variants associated with autism implicate a large functional network of genes involved in formation and function of synapses
    • Gilman S.R., Iossifov I., Levy D., Ronemus M., Wigler M., Vitkup D. Rare de novo variants associated with autism implicate a large functional network of genes involved in formation and function of synapses. Neuron 2011, 70:898-907.
    • (2011) Neuron , vol.70 , pp. 898-907
    • Gilman, S.R.1    Iossifov, I.2    Levy, D.3    Ronemus, M.4    Wigler, M.5    Vitkup, D.6
  • 16
    • 42649095149 scopus 로고    scopus 로고
    • Genetic modification of human embryonic stem cells for derivation of target cells
    • Giudice A., Trounson A. Genetic modification of human embryonic stem cells for derivation of target cells. Cell Stem Cell 2008, 2:422-433.
    • (2008) Cell Stem Cell , vol.2 , pp. 422-433
    • Giudice, A.1    Trounson, A.2
  • 17
    • 82455199147 scopus 로고    scopus 로고
    • Induced pluripotent stem cells - opportunities for disease modelling and drug discovery
    • Grskovic M., Javaherian A., Strulovici B., Daley G.Q. Induced pluripotent stem cells - opportunities for disease modelling and drug discovery. Nature Reviews Drug Discovery 2011, 10:915-929.
    • (2011) Nature Reviews Drug Discovery , vol.10 , pp. 915-929
    • Grskovic, M.1    Javaherian, A.2    Strulovici, B.3    Daley, G.Q.4
  • 18
    • 67349202186 scopus 로고    scopus 로고
    • Altered synchrony and connectivity in neuronal networks expressing an autism-related mutation of neuroligin 3
    • Gutierrez R.C., Hung J., Zhang Y., Kertesz A.C., Espina F.J., Colicos M.A. Altered synchrony and connectivity in neuronal networks expressing an autism-related mutation of neuroligin 3. Neuroscience 2009, 162:208-221.
    • (2009) Neuroscience , vol.162 , pp. 208-221
    • Gutierrez, R.C.1    Hung, J.2    Zhang, Y.3    Kertesz, A.C.4    Espina, F.J.5    Colicos, M.A.6
  • 19
    • 79251518046 scopus 로고    scopus 로고
    • Mechanistic insights into reprogramming to induced pluripotency
    • Ho R., Chronis C., Plath K. Mechanistic insights into reprogramming to induced pluripotency. Journal of Cellular Physiology 2011, 226:868-878.
    • (2011) Journal of Cellular Physiology , vol.226 , pp. 868-878
    • Ho, R.1    Chronis, C.2    Plath, K.3
  • 21
    • 42649084334 scopus 로고    scopus 로고
    • Rare independent mutations in renal salt handling genes contribute to blood pressure variation
    • Ji W., Foo J.N., O'Roak B.J., Zhao H., Larson M.G., Simon D.B., et al. Rare independent mutations in renal salt handling genes contribute to blood pressure variation. Nature Genetics 2008, 40:592-599.
    • (2008) Nature Genetics , vol.40 , pp. 592-599
    • Ji, W.1    Foo, J.N.2    O'Roak, B.J.3    Zhao, H.4    Larson, M.G.5    Simon, D.B.6
  • 24
    • 78650971216 scopus 로고    scopus 로고
    • Dynamic changes in the copy number of pluripotency and cell proliferation genes in human ESCs and iPSCs during reprogramming and time in culture
    • Laurent L.C., Ulitsky I., Slavin I., Tran H., Schork A., Morey R., et al. Dynamic changes in the copy number of pluripotency and cell proliferation genes in human ESCs and iPSCs during reprogramming and time in culture. Cell Stem Cell 2011, 8:106-118.
    • (2011) Cell Stem Cell , vol.8 , pp. 106-118
    • Laurent, L.C.1    Ulitsky, I.2    Slavin, I.3    Tran, H.4    Schork, A.5    Morey, R.6
  • 25
    • 79958032110 scopus 로고    scopus 로고
    • Rare de novo and transmitted copy-number variation in autistic spectrum disorders
    • Levy D., Ronemus M., Yamrom B., Lee Y.H., Leotta A., Kendall J., et al. Rare de novo and transmitted copy-number variation in autistic spectrum disorders. Neuron 2011, 70:886-897.
    • (2011) Neuron , vol.70 , pp. 886-897
    • Levy, D.1    Ronemus, M.2    Yamrom, B.3    Lee, Y.H.4    Leotta, A.5    Kendall, J.6
  • 26
    • 79952264847 scopus 로고    scopus 로고
    • Hotspots of aberrant epigenomic reprogramming in human induced pluripotent stem cells
    • Lister R., Pelizzola M., Kida Y.S., Hawkins R.D., Nery J.R., Hon G., et al. Hotspots of aberrant epigenomic reprogramming in human induced pluripotent stem cells. Nature 2011, 471:68-73.
    • (2011) Nature , vol.471 , pp. 68-73
    • Lister, R.1    Pelizzola, M.2    Kida, Y.S.3    Hawkins, R.D.4    Nery, J.R.5    Hon, G.6
  • 27
    • 79957866291 scopus 로고    scopus 로고
    • Targeted gene correction of laminopathy-associated LMNA mutations in patient-specific iPSCs
    • Liu G.H., Suzuki K., Qu J., Sancho-Martinez I., Yi F., Li M., et al. Targeted gene correction of laminopathy-associated LMNA mutations in patient-specific iPSCs. Cell Stem Cell 2011, 8:688-694.
    • (2011) Cell Stem Cell , vol.8 , pp. 688-694
    • Liu, G.H.1    Suzuki, K.2    Qu, J.3    Sancho-Martinez, I.4    Yi, F.5    Li, M.6
  • 28
    • 80155144126 scopus 로고    scopus 로고
    • Induced pluripotent stem cells (iPSCs) and neurological disease modeling: Progress and promises
    • Marchetto M.C., Brennand K.J., Boyer L.F., Gage F.H. Induced pluripotent stem cells (iPSCs) and neurological disease modeling: Progress and promises. Human Molecular Genetics 2011, 20:R109-R115.
    • (2011) Human Molecular Genetics , vol.20
    • Marchetto, M.C.1    Brennand, K.J.2    Boyer, L.F.3    Gage, F.H.4
  • 29
    • 78149488365 scopus 로고    scopus 로고
    • A model for neural development and treatment of Rett syndrome using human induced pluripotent stem cells
    • Marchetto M.C., Carromeu C., Acab A., Yu D., Yeo G.W., Mu Y., et al. A model for neural development and treatment of Rett syndrome using human induced pluripotent stem cells. Cell 2010, 143:527-539.
    • (2010) Cell , vol.143 , pp. 527-539
    • Marchetto, M.C.1    Carromeu, C.2    Acab, A.3    Yu, D.4    Yeo, G.W.5    Mu, Y.6
  • 30
    • 77953879152 scopus 로고    scopus 로고
    • Pluripotent stem cells in neurodegenerative and neurodevelopmental diseases
    • Marchetto M.C., Winner B., Gage F.H. Pluripotent stem cells in neurodegenerative and neurodevelopmental diseases. Human Molecular Genetics 2010, 19:R71-R76.
    • (2010) Human Molecular Genetics , vol.19
    • Marchetto, M.C.1    Winner, B.2    Gage, F.H.3
  • 32
    • 31544441632 scopus 로고    scopus 로고
    • Derivation of human embryonic stem cell lines from embryos obtained after IVF and after PGD for monogenic disorders
    • Mateizel I., De Temmerman N., Ullmann U., Cauffman G., Sermon K., Van de Velde H., et al. Derivation of human embryonic stem cell lines from embryos obtained after IVF and after PGD for monogenic disorders. Human Reproduction 2006, 21:503-511.
    • (2006) Human Reproduction , vol.21 , pp. 503-511
    • Mateizel, I.1    De Temmerman, N.2    Ullmann, U.3    Cauffman, G.4    Sermon, K.5    Van de Velde, H.6
  • 33
    • 77957334627 scopus 로고    scopus 로고
    • Identification and classification of chromosomal aberrations in human induced pluripotent stem cells
    • Mayshar Y., Ben-David U., Lavon N., Biancotti J.C., Yakir B., Clark A.T., et al. Identification and classification of chromosomal aberrations in human induced pluripotent stem cells. Cell Stem Cell 2010, 7:521-531.
    • (2010) Cell Stem Cell , vol.7 , pp. 521-531
    • Mayshar, Y.1    Ben-David, U.2    Lavon, N.3    Biancotti, J.C.4    Yakir, B.5    Clark, A.T.6
  • 34
    • 56049091987 scopus 로고    scopus 로고
    • Modeling epilepsy with pluripotent human cells
    • Muotri A.R. Modeling epilepsy with pluripotent human cells. Epilepsy Behavior 2009, 14:81-85.
    • (2009) Epilepsy Behavior , vol.14 , pp. 81-85
    • Muotri, A.R.1
  • 35
    • 20544466648 scopus 로고    scopus 로고
    • Somatic mosaicism in neuronal precursor cells mediated by L1 retrotransposition
    • Muotri A.R., Chu V.T., Marchetto M.C., Deng W., Moran J.V., Gage F.H. Somatic mosaicism in neuronal precursor cells mediated by L1 retrotransposition. Nature 2005, 435:903-910.
    • (2005) Nature , vol.435 , pp. 903-910
    • Muotri, A.R.1    Chu, V.T.2    Marchetto, M.C.3    Deng, W.4    Moran, J.V.5    Gage, F.H.6
  • 36
    • 33745593721 scopus 로고    scopus 로고
    • Generation of neuronal variability and complexity
    • Muotri A.R., Gage F.H. Generation of neuronal variability and complexity. Nature 2006, 441:1087-1093.
    • (2006) Nature , vol.441 , pp. 1087-1093
    • Muotri, A.R.1    Gage, F.H.2
  • 40
    • 84856088804 scopus 로고    scopus 로고
    • Using iPSC-derived neurons to uncover cellular phenotypes associated with Timothy syndrome
    • Pasca S.P., Portmann T., Voineagu I., Yazawa M., Shcheglovitov A., Pasca A.M., et al. Using iPSC-derived neurons to uncover cellular phenotypes associated with Timothy syndrome. Nature Medicine 2011, 17:1657-1662.
    • (2011) Nature Medicine , vol.17 , pp. 1657-1662
    • Pasca, S.P.1    Portmann, T.2    Voineagu, I.3    Yazawa, M.4    Shcheglovitov, A.5    Pasca, A.M.6
  • 41
    • 14944386646 scopus 로고    scopus 로고
    • Generation of a human embryonic stem cell line encoding the cystic fibrosis mutation deltaF508, using preimplantation genetic diagnosis
    • Pickering S.J., Minger S.L., Patel M., Taylor H., Black C., Burns C.J., et al. Generation of a human embryonic stem cell line encoding the cystic fibrosis mutation deltaF508, using preimplantation genetic diagnosis. Reproductive Biomedicine Online 2005, 10:390-397.
    • (2005) Reproductive Biomedicine Online , vol.10 , pp. 390-397
    • Pickering, S.J.1    Minger, S.L.2    Patel, M.3    Taylor, H.4    Black, C.5    Burns, C.J.6
  • 42
    • 84856007232 scopus 로고    scopus 로고
    • The promise of induced pluripotent stem cells in research and therapy
    • Robinton D.A., Daley G.Q. The promise of induced pluripotent stem cells in research and therapy. Nature 2012, 481:295-305.
    • (2012) Nature , vol.481 , pp. 295-305
    • Robinton, D.A.1    Daley, G.Q.2
  • 43
    • 79958074870 scopus 로고    scopus 로고
    • Multiple recurrent de novo CNVs, including duplications of the 7q11.23 Williams syndrome region, are strongly associated with autism
    • Sanders S.J., Ercan-Sencicek A.G., Hus V., Luo R., Murtha M.T., Moreno-De-Luca D., et al. Multiple recurrent de novo CNVs, including duplications of the 7q11.23 Williams syndrome region, are strongly associated with autism. Neuron 2011, 70:863-885.
    • (2011) Neuron , vol.70 , pp. 863-885
    • Sanders, S.J.1    Ercan-Sencicek, A.G.2    Hus, V.3    Luo, R.4    Murtha, M.T.5    Moreno-De-Luca, D.6
  • 45
    • 16044373524 scopus 로고    scopus 로고
    • Secreted amyloid beta-protein similar to that in the senile plaques of alzheimer's disease is increased in vivo by the presenilin 1 and 2 and APP mutations linked to familial Alzheimer's disease
    • Scheuner D., Eckman C., Jensen M., Song X., Citron M., Suzuki N., et al. Secreted amyloid beta-protein similar to that in the senile plaques of alzheimer's disease is increased in vivo by the presenilin 1 and 2 and APP mutations linked to familial Alzheimer's disease. Nature Medicine 1996, 2:864-870.
    • (1996) Nature Medicine , vol.2 , pp. 864-870
    • Scheuner, D.1    Eckman, C.2    Jensen, M.3    Song, X.4    Citron, M.5    Suzuki, N.6
  • 47
    • 79960833952 scopus 로고    scopus 로고
    • Generation of isogenic pluripotent stem cells differing exclusively at two early onset Parkinson point mutations
    • Soldner F., Laganiere J., Cheng A.W., Hockemeyer D., Gao Q., Alagappan R., et al. Generation of isogenic pluripotent stem cells differing exclusively at two early onset Parkinson point mutations. Cell 2011, 146:318-331.
    • (2011) Cell , vol.146 , pp. 318-331
    • Soldner, F.1    Laganiere, J.2    Cheng, A.W.3    Hockemeyer, D.4    Gao, Q.5    Alagappan, R.6
  • 48
    • 5344223383 scopus 로고    scopus 로고
    • Ca(V)1.2 calcium channel dysfunction causes a multisystem disorder including arrhythmia and autism
    • Splawski I., Timothy K.W., Sharpe L.M., Decher N., Kumar P., Bloise R., et al. Ca(V)1.2 calcium channel dysfunction causes a multisystem disorder including arrhythmia and autism. Cell 2004, 119:19-31.
    • (2004) Cell , vol.119 , pp. 19-31
    • Splawski, I.1    Timothy, K.W.2    Sharpe, L.M.3    Decher, N.4    Kumar, P.5    Bloise, R.6
  • 50
    • 82255192290 scopus 로고    scopus 로고
    • The conundrums of understanding genetic risks for autism spectrum disorders
    • State M.W., Levitt P. The conundrums of understanding genetic risks for autism spectrum disorders. Nature Neuroscience 2011.
    • (2011) Nature Neuroscience
    • State, M.W.1    Levitt, P.2
  • 51
    • 33747195353 scopus 로고    scopus 로고
    • Induction of pluripotent stem cells from mouse embryonic and adult fibroblast cultures by defined factors
    • Takahashi K., Yamanaka S. Induction of pluripotent stem cells from mouse embryonic and adult fibroblast cultures by defined factors. Cell 2006, 126:663-676.
    • (2006) Cell , vol.126 , pp. 663-676
    • Takahashi, K.1    Yamanaka, S.2
  • 52
    • 36248966518 scopus 로고    scopus 로고
    • Induction of pluripotent stem cells from adult human fibroblasts by defined factors
    • Takahashi K., Tanabe K., Ohnuki M., Narita M., Ichisaka T., Tomoda K., et al. Induction of pluripotent stem cells from adult human fibroblasts by defined factors. Cell 2007, 131:861-872.
    • (2007) Cell , vol.131 , pp. 861-872
    • Takahashi, K.1    Tanabe, K.2    Ohnuki, M.3    Narita, M.4    Ichisaka, T.5    Tomoda, K.6
  • 55
    • 77956214743 scopus 로고    scopus 로고
    • Differential modeling of fragile X syndrome by human embryonic stem cells and induced pluripotent stem cells
    • Urbach A., Bar-Nur O., Daley G.Q., Benvenisty N. Differential modeling of fragile X syndrome by human embryonic stem cells and induced pluripotent stem cells. Cell Stem Cell 2010, 6:407-411.
    • (2010) Cell Stem Cell , vol.6 , pp. 407-411
    • Urbach, A.1    Bar-Nur, O.2    Daley, G.Q.3    Benvenisty, N.4
  • 56
    • 3543030995 scopus 로고    scopus 로고
    • Modeling for Lesch-Nyhan disease by gene targeting in human embryonic stem cells
    • Urbach A., Schuldiner M., Benvenisty N. Modeling for Lesch-Nyhan disease by gene targeting in human embryonic stem cells. Stem Cells 2004, 22:635-641.
    • (2004) Stem Cells , vol.22 , pp. 635-641
    • Urbach, A.1    Schuldiner, M.2    Benvenisty, N.3
  • 58
    • 80054726357 scopus 로고    scopus 로고
    • Direct lineage conversions: Unnatural but useful?
    • Vierbuchen T., Wernig M. Direct lineage conversions: Unnatural but useful?. Nature Biotechnology 2011, 29:892-907.
    • (2011) Nature Biotechnology , vol.29 , pp. 892-907
    • Vierbuchen, T.1    Wernig, M.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.