-
1
-
-
80053143413
-
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
-
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
-
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
-
4
-
-
79952120621
-
Derivation of Huntington's disease-affected human embryonic stem cell lines
-
Bradley C.K., Scott H.A., Chami O., Peura T.T., Dumevska B., Schmidt U., et al. Derivation of Huntington's disease-affected human embryonic stem cell lines. Stem Cells and Development 2011, 20:495-502.
-
(2011)
Stem Cells and Development
, vol.20
, pp. 495-502
-
-
Bradley, C.K.1
Scott, H.A.2
Chami, O.3
Peura, T.T.4
Dumevska, B.5
Schmidt, U.6
-
5
-
-
79955884485
-
Modelling schizophrenia using human induced pluripotent stem cells
-
Brennand K.J., Simone A., Jou J., Gelboin-Burkhart C., Tran N., Sangar S., et al. Modelling schizophrenia using human induced pluripotent stem cells. Nature 2011, 473:221-225.
-
(2011)
Nature
, vol.473
, pp. 221-225
-
-
Brennand, K.J.1
Simone, A.2
Jou, J.3
Gelboin-Burkhart, C.4
Tran, N.5
Sangar, S.6
-
6
-
-
67651233780
-
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
-
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
-
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
-
9
-
-
69349096044
-
L1 retrotransposition in human neural progenitor cells
-
Coufal N.G., Garcia-Perez J.L., Peng G.E., Yeo G.W., Mu Y., Lovci M.T., et al. L1 retrotransposition in human neural progenitor cells. Nature 2009, 460:1127-1131.
-
(2009)
Nature
, vol.460
, pp. 1127-1131
-
-
Coufal, N.G.1
Garcia-Perez, J.L.2
Peng, G.E.3
Yeo, G.W.4
Mu, Y.5
Lovci, M.T.6
-
10
-
-
48749089453
-
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
-
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
-
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
-
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
-
-
1842684068
-
Genome sequence of the Brown Norway rat yields insights into mammalian evolution
-
Gibbs R.A., Weinstock G.M., Metzker M.L., Muzny D.M., Sodergren E.J., Scherer S., et al. Genome sequence of the Brown Norway rat yields insights into mammalian evolution. Nature 2004, 428:493-521.
-
(2004)
Nature
, vol.428
, pp. 493-521
-
-
Gibbs, R.A.1
Weinstock, G.M.2
Metzker, M.L.3
Muzny, D.M.4
Sodergren, E.J.5
Scherer, S.6
-
15
-
-
79958035893
-
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
-
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
-
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
-
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
-
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
-
20
-
-
77749279749
-
Neural differentiation of human induced pluripotent stem cells follows developmental principles but with variable potency
-
Hu B.Y., Weick J.P., Yu J., Ma L.X., Zhang X.Q., Thomson J.A., et al. Neural differentiation of human induced pluripotent stem cells follows developmental principles but with variable potency. Proceedings of the National Academy of Sciences of the United States of America 2010, 107:4335-4340.
-
(2010)
Proceedings of the National Academy of Sciences of the United States of America
, vol.107
, pp. 4335-4340
-
-
Hu, B.Y.1
Weick, J.P.2
Yu, J.3
Ma, L.X.4
Zhang, X.Q.5
Thomson, J.A.6
-
21
-
-
42649084334
-
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
-
22
-
-
80052155858
-
Neuronal maturation defect in induced pluripotent stem cells from patients with Rett syndrome
-
Kim K.Y., Hysolli E., Park I.H. Neuronal maturation defect in induced pluripotent stem cells from patients with Rett syndrome. Proceedings of the National Academy of Sciences of the United States of America 2011, 108:14,169-14,174.
-
(2011)
Proceedings of the National Academy of Sciences of the United States of America
, vol.108
, pp. 14169-14174
-
-
Kim, K.Y.1
Hysolli, E.2
Park, I.H.3
-
23
-
-
2042437650
-
Initial sequencing and analysis of the human genome
-
Lander E.S., Linton L.M., Birren B., Nusbaum C., Zody M.C., Baldwin J., et al. Initial sequencing and analysis of the human genome. Nature 2001, 409:860-921.
-
(2001)
Nature
, vol.409
, pp. 860-921
-
-
Lander, E.S.1
Linton, L.M.2
Birren, B.3
Nusbaum, C.4
Zody, M.C.5
Baldwin, J.6
-
24
-
-
78650971216
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
31
-
-
70349445082
-
Transcriptional signature and memory retention of human-induced pluripotent stem cells
-
Marchetto M.C., Yeo G.W., Kainohana O., Marsala M., Gage F.H., Muotri A.R. Transcriptional signature and memory retention of human-induced pluripotent stem cells. PLoS ONE 2009, 4:e7076.
-
(2009)
PLoS ONE
, vol.4
-
-
Marchetto, M.C.1
Yeo, G.W.2
Kainohana, O.3
Marsala, M.4
Gage, F.H.5
Muotri, A.R.6
-
32
-
-
31544441632
-
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
-
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
-
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
-
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
-
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
-
37
-
-
29444439070
-
Development of functional human embryonic stem cell-derived neurons in mouse brain
-
Muotri A.R., Nakashima K., Toni N., Sandler V.M., Gage F.H. Development of functional human embryonic stem cell-derived neurons in mouse brain. Proceedings of the National Academy of Sciences of the United States of America 2005, 102:18,644-18,648.
-
(2005)
Proceedings of the National Academy of Sciences of the United States of America
, vol.102
, pp. 18644-18648
-
-
Muotri, A.R.1
Nakashima, K.2
Toni, N.3
Sandler, V.M.4
Gage, F.H.5
-
38
-
-
78549247463
-
L1 retrotransposition in neurons is modulated by MeCP2
-
Muotri A.R., Marchetto M.C., Coufal N.G., Oefner R., Yeo G., Nakashima K., Gage F.H. L1 retrotransposition in neurons is modulated by MeCP2. Nature 2010, 468:443-446.
-
(2010)
Nature
, vol.468
, pp. 443-446
-
-
Muotri, A.R.1
Marchetto, M.C.2
Coufal, N.G.3
Oefner, R.4
Yeo, G.5
Nakashima, K.6
Gage, F.H.7
-
39
-
-
79960854285
-
Induction of human neuronal cells by defined transcription factors
-
Pang Z.P., Yang N., Vierbuchen T., Ostermeier A., Fuentes D.R., Yang T.Q., et al. Induction of human neuronal cells by defined transcription factors. Nature 2011, 476:220-223.
-
(2011)
Nature
, vol.476
, pp. 220-223
-
-
Pang, Z.P.1
Yang, N.2
Vierbuchen, T.3
Ostermeier, A.4
Fuentes, D.R.5
Yang, T.Q.6
-
40
-
-
84856088804
-
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
-
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
-
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
-
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
-
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
-
46
-
-
77953800799
-
Behavioral phenotyping assays for mouse models of autism
-
Silverman J.L., Yang M., Lord C., Crawley J.N. Behavioral phenotyping assays for mouse models of autism. Nature Reviews Neuroscience 2010, 11:490-502.
-
(2010)
Nature Reviews Neuroscience
, vol.11
, pp. 490-502
-
-
Silverman, J.L.1
Yang, M.2
Lord, C.3
Crawley, J.N.4
-
47
-
-
79960833952
-
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
-
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
-
49
-
-
33746805846
-
CACNA1H mutations in autism spectrum disorders
-
Splawski I., Yoo D.S., Stotz S.C., Cherry A., Clapham D.E., Keating M.T. CACNA1H mutations in autism spectrum disorders. Journal of Biological Chemistry 2006, 281:22,085-22,091.
-
(2006)
Journal of Biological Chemistry
, vol.281
, pp. 22085-22091
-
-
Splawski, I.1
Yoo, D.S.2
Stotz, S.C.3
Cherry, A.4
Clapham, D.E.5
Keating, M.T.6
-
50
-
-
82255192290
-
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
-
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
-
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
-
53
-
-
0032491416
-
Embryonic stem cell lines derived from human blastocysts
-
Thomson J.A., Itskovitz-Eldor J., Shapiro S.S., Waknitz M.A., Swiergiel J.J., Marshall V.S., et al. Embryonic stem cell lines derived from human blastocysts. Science 1998, 282:1145-1147.
-
(1998)
Science
, vol.282
, pp. 1145-1147
-
-
Thomson, J.A.1
Itskovitz-Eldor, J.2
Shapiro, S.S.3
Waknitz, M.A.4
Swiergiel, J.J.5
Marshall, V.S.6
-
54
-
-
60549115413
-
Partial reversal of Rett syndrome-like symptoms in MeCP2 mutant mice
-
Tropea D., Giacometti E., Wilson N.R., Beard C., McCurry C., Fu D.D., et al. Partial reversal of Rett syndrome-like symptoms in MeCP2 mutant mice. Proceedings of the National Academy of Sciences of the United States of America 2009, 106:2029-2034.
-
(2009)
Proceedings of the National Academy of Sciences of the United States of America
, vol.106
, pp. 2029-2034
-
-
Tropea, D.1
Giacometti, E.2
Wilson, N.R.3
Beard, C.4
McCurry, C.5
Fu, D.D.6
-
55
-
-
77956214743
-
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
-
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
-
57
-
-
11944264980
-
Human embryonic stem cell lines with genetic disorders
-
Verlinsky Y., Strelchenko N., Kukharenko V., Rechitsky S., Verlinsky O., Galat V., et al. Human embryonic stem cell lines with genetic disorders. Reproductive Biomedicine Online 2005, 10:105-110.
-
(2005)
Reproductive Biomedicine Online
, vol.10
, pp. 105-110
-
-
Verlinsky, Y.1
Strelchenko, N.2
Kukharenko, V.3
Rechitsky, S.4
Verlinsky, O.5
Galat, V.6
-
58
-
-
80054726357
-
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
-
59
-
-
77649162059
-
Direct conversion of fibroblasts to functional neurons by defined factors
-
Vierbuchen, T., Ostermeier, A., Pang, Z.P., Kokubu, Y., Sudhof, T.C., Wernig, M., 2010 Direct conversion of fibroblasts to functional neurons by defined factors. Nature.
-
(2010)
Nature
-
-
Vierbuchen, T.1
Ostermeier, A.2
Pang, Z.P.3
Kokubu, Y.4
Sudhof, T.C.5
Wernig, M.6
-
60
-
-
1542563409
-
Initial sequencing and comparative analysis of the mouse genome
-
Waterston R.H., Lindblad-Toh K., Birney E., Rogers J., Abril J.F., Agarwal P., et al. Initial sequencing and comparative analysis of the mouse genome. Nature 2002, 420:520-562.
-
(2002)
Nature
, vol.420
, pp. 520-562
-
-
Waterston, R.H.1
Lindblad-Toh, K.2
Birney, E.3
Rogers, J.4
Abril, J.F.5
Agarwal, P.6
-
61
-
-
39049163023
-
Association between microdeletion and microduplication at 16p11.2 and autism
-
Weiss L.A., Shen Y., Korn J.M., Arking D.E., Miller D.T., Fossdal R., et al. Association between microdeletion and microduplication at 16p11.2 and autism. New England Journal of Medicine 2008, 358:667-675.
-
(2008)
New England Journal of Medicine
, vol.358
, pp. 667-675
-
-
Weiss, L.A.1
Shen, Y.2
Korn, J.M.3
Arking, D.E.4
Miller, D.T.5
Fossdal, R.6
-
62
-
-
36749043230
-
Induced pluripotent stem cell lines derived from human somatic cells
-
Yu J., Vodyanik M.A., Smuga-Otto K., Antosiewicz-Bourget J., Frane J.L., Tian S., et al. Induced pluripotent stem cell lines derived from human somatic cells. Science 2007, 318:1917-1920.
-
(2007)
Science
, vol.318
, pp. 1917-1920
-
-
Yu, J.1
Vodyanik, M.A.2
Smuga-Otto, K.3
Antosiewicz-Bourget, J.4
Frane, J.L.5
Tian, S.6
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