-
1
-
-
36248966518
-
Induction of pluripotent stem cells from adult human fibroblasts by defined factors
-
Takahashi K, Tanabe K, Ohnuki M, 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
-
2
-
-
77953879152
-
Pluripotent stem cells in neurodegenerative and neurodevelopmental diseases
-
Marchetto MC, Winner B, Gage FH,. Pluripotent stem cells in neurodegenerative and neurodevelopmental diseases. Hum Mol Genet 2010; 19: R71-R76.
-
(2010)
Hum Mol Genet
, vol.19
, pp. R71-R76
-
-
Marchetto, M.C.1
Winner, B.2
Gage, F.H.3
-
3
-
-
84874817493
-
An efficient nonviral method to generate integration-free human-induced pluripotent stem cells from cord blood and peripheral blood cells
-
Okita K, Yamakawa T, Matsumura Y, et al., An efficient nonviral method to generate integration-free human-induced pluripotent stem cells from cord blood and peripheral blood cells. Stem Cells 2013; 31: 458-466.
-
(2013)
Stem Cells
, vol.31
, pp. 458-466
-
-
Okita, K.1
Yamakawa, T.2
Matsumura, Y.3
-
4
-
-
79953021243
-
Development of defective and persistent Sendai virus vector a unique gene delivery/expression system ideal for cell reprogramming
-
Nishimura K, Sano M, Ohtaka M, et al., Development of defective and persistent Sendai virus vector a unique gene delivery/expression system ideal for cell reprogramming. J Biol Chem 2011; 286: 4760-4771.
-
(2011)
J Biol Chem
, vol.286
, pp. 4760-4771
-
-
Nishimura, K.1
Sano, M.2
Ohtaka, M.3
-
5
-
-
79955634826
-
A more efficient method to generate integration-free human iPS cells
-
Okita K, Matsumura Y, Sato Y, et al., A more efficient method to generate integration-free human iPS cells. Nat Methods 2011; 8: 409-412.
-
(2011)
Nat Methods
, vol.8
, pp. 409-412
-
-
Okita, K.1
Matsumura, Y.2
Sato, Y.3
-
6
-
-
58949094552
-
Telomeres acquire embryonic stem cell characteristics in induced pluripotent stem cells
-
Marion RM, Strati K, Li H, et al., Telomeres acquire embryonic stem cell characteristics in induced pluripotent stem cells. Cell Stem Cell 2009; 4: 141-154.
-
(2009)
Cell Stem Cell
, vol.4
, pp. 141-154
-
-
Marion, R.M.1
Strati, K.2
Li, H.3
-
7
-
-
84901414493
-
Stem cells on the brain: Modeling neurodevelopmental and neurodegenerative diseases using human induced pluripotent stem cells
-
Srikanth P, Young-Pearse TL,. Stem cells on the brain: Modeling neurodevelopmental and neurodegenerative diseases using human induced pluripotent stem cells. J Neurogenet 2014; 28: 5-29.
-
(2014)
J Neurogenet
, vol.28
, pp. 5-29
-
-
Srikanth, P.1
Young-Pearse, T.L.2
-
8
-
-
84884288934
-
Double nicking by RNA-guided CRISPR Cas9 for enhanced genome editing specificity
-
Ran FA, Hsu PD, Lin C-Y, et al., Double nicking by RNA-guided CRISPR Cas9 for enhanced genome editing specificity. Cell 2013; 154: 1380-1389.
-
(2013)
Cell
, vol.154
, pp. 1380-1389
-
-
Ran, F.A.1
Hsu, P.D.2
Lin, C.-Y.3
-
9
-
-
84890033064
-
Functional repair of CFTR by CRISPR/Cas9 in intestinal stem cell organoids of cystic fibrosis patients
-
Schwank G, Koo B-K, Sasselli V, et al., Functional repair of CFTR by CRISPR/Cas9 in intestinal stem cell organoids of cystic fibrosis patients. Cell Stem Cell 2013; 13: 653-658.
-
(2013)
Cell Stem Cell
, vol.13
, pp. 653-658
-
-
Schwank, G.1
Koo, B.-K.2
Sasselli, V.3
-
10
-
-
84895528015
-
Isolation of single-base genome-edited human iPS cells without antibiotic selection
-
Miyaoka Y, Chan AH, Judge LM, et al., Isolation of single-base genome-edited human iPS cells without antibiotic selection. Nat Methods 2014; 11: 291-293.
-
(2014)
Nat Methods
, vol.11
, pp. 291-293
-
-
Miyaoka, Y.1
Chan, A.H.2
Judge, L.M.3
-
11
-
-
33846604242
-
How common are the "common" neurologic disorders?
-
Hirtz D, Thurman D, Gwinn-Hardy K, et al., How common are the "common" neurologic disorders? Neurology 2007; 68: 326-337.
-
(2007)
Neurology
, vol.68
, pp. 326-337
-
-
Hirtz, D.1
Thurman, D.2
Gwinn-Hardy, K.3
-
12
-
-
24944576673
-
Incidence of unprovoked seizures and epilepsy in Iceland and assessment of the epilepsy syndrome classification: A prospective study
-
Olafsson E, Ludvigsson P, Hesdorffer D, et al., Incidence of unprovoked seizures and epilepsy in Iceland and assessment of the epilepsy syndrome classification: A prospective study. Lancet Neurol 2005; 4: 627-634.
-
(2005)
Lancet Neurol
, vol.4
, pp. 627-634
-
-
Olafsson, E.1
Ludvigsson, P.2
Hesdorffer, D.3
-
13
-
-
84911966458
-
Sudden unexpected death in epilepsy: Assessing the public health burden
-
Thurman DJ, Hesdorffer DC, French JA,. Sudden unexpected death in epilepsy: Assessing the public health burden. Epilepsia 2014; 55: 1479-1485.
-
(2014)
Epilepsia
, vol.55
, pp. 1479-1485
-
-
Thurman, D.J.1
Hesdorffer, D.C.2
French, J.A.3
-
14
-
-
0025368281
-
Myoclonic epilepsy and ragged-red fiber disease (MERRF) is associated with a mitochondrial DNA tRNA Lys mutation
-
Shoffner JM, Lott MT, Lezza AM, et al., Myoclonic epilepsy and ragged-red fiber disease (MERRF) is associated with a mitochondrial DNA tRNA Lys mutation. Cell 1990; 61: 931-937.
-
(1990)
Cell
, vol.61
, pp. 931-937
-
-
Shoffner, J.M.1
Lott, M.T.2
Lezza, A.M.3
-
15
-
-
84923698562
-
Pathway-driven discovery of epilepsy genes
-
Noebels J,. Pathway-driven discovery of epilepsy genes. Nat Neurosci 2015; 18: 344-350.
-
(2015)
Nat Neurosci
, vol.18
, pp. 344-350
-
-
Noebels, J.1
-
16
-
-
79953685960
-
The pharmacologic treatment of Dravet syndrome
-
Chiron C, Dulac O,. The pharmacologic treatment of Dravet syndrome. Epilepsia 2011; 52: 72-75.
-
(2011)
Epilepsia
, vol.52
, pp. 72-75
-
-
Chiron, C.1
Dulac, O.2
-
17
-
-
84879684377
-
Targeted resequencing in epileptic encephalopathies identifies de novo mutations in CHD2 and SYNGAP1
-
Carvill GL, Heavin SB, Yendle SC, et al., Targeted resequencing in epileptic encephalopathies identifies de novo mutations in CHD2 and SYNGAP1. Nat Genet 2013; 45: 825-830.
-
(2013)
Nat Genet
, vol.45
, pp. 825-830
-
-
Carvill, G.L.1
Heavin, S.B.2
Yendle, S.C.3
-
18
-
-
84893440324
-
Sodium channel SCN8A (Nav1. 6): Properties and de novo mutations in epileptic encephalopathy and intellectual disability
-
O'Brien JE, Meisler MH,. Sodium channel SCN8A (Nav1. 6): Properties and de novo mutations in epileptic encephalopathy and intellectual disability. Front Genet 2013; 4.
-
(2013)
Front Genet
, vol.4
-
-
O'Brien, J.E.1
Meisler, M.H.2
-
19
-
-
84884130368
-
De novo mutations in epileptic encephalopathies
-
Phenome E, Consortium EK,. De novo mutations in epileptic encephalopathies. Nature 2013; 501: 217-221.
-
(2013)
Nature
, vol.501
, pp. 217-221
-
-
Phenome, E.1
Consortium, E.K.2
-
20
-
-
0344672944
-
Mutations of sodium channel α subunit type 1 (SCN1A) in intractable childhood epilepsies with frequent generalized tonic-clonic seizures
-
Fujiwara T, Sugawara T, Mazaki-Miyazaki E, et al., Mutations of sodium channel α subunit type 1 (SCN1A) in intractable childhood epilepsies with frequent generalized tonic-clonic seizures. Brain 2003; 126: 531-546.
-
(2003)
Brain
, vol.126
, pp. 531-546
-
-
Fujiwara, T.1
Sugawara, T.2
Mazaki-Miyazaki, E.3
-
21
-
-
84929502090
-
The SCN1A mutation database: Updating information and analysis of the relationships among genotype, functional alteration, and phenotype
-
Meng H, Xu HQ, Yu L, et al., The SCN1A mutation database: Updating information and analysis of the relationships among genotype, functional alteration, and phenotype. Hum Mutat 2015; 36: 573-580.
-
(2015)
Hum Mutat
, vol.36
, pp. 573-580
-
-
Meng, H.1
Xu, H.Q.2
Yu, L.3
-
22
-
-
84859744583
-
Large-scale cellular-resolution gene profiling in human neocortex reveals species-specific molecular signatures
-
Zeng H, Shen EH, Hohmann JG, et al., Large-scale cellular-resolution gene profiling in human neocortex reveals species-specific molecular signatures. Cell 2012; 149: 483-496.
-
(2012)
Cell
, vol.149
, pp. 483-496
-
-
Zeng, H.1
Shen, E.H.2
Hohmann, J.G.3
-
23
-
-
84876223311
-
Rett syndrome and epilepsy: An update for child neurologists
-
Dolce A, Ben-Zeev B, Naidu S, et al., Rett syndrome and epilepsy: An update for child neurologists. Pediatr Neurol 2013; 48: 337-345.
-
(2013)
Pediatr Neurol
, vol.48
, pp. 337-345
-
-
Dolce, A.1
Ben-Zeev, B.2
Naidu, S.3
-
24
-
-
78149488365
-
A model for neural development and treatment of Rett syndrome using human induced pluripotent stem cells
-
Marchetto MC, Carromeu C, Acab A, 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
-
25
-
-
79955602167
-
Isolation of MECP2-null Rett Syndrome patient hiPS cells and isogenic controls through X-chromosome inactivation
-
Cheung AY, Horvath LM, Grafodatskaya D, et al., Isolation of MECP2-null Rett Syndrome patient hiPS cells and isogenic controls through X-chromosome inactivation. Hum Mol Genet 2011; 20: 2103-2115.
-
(2011)
Hum Mol Genet
, vol.20
, pp. 2103-2115
-
-
Cheung, A.Y.1
Horvath, L.M.2
Grafodatskaya, D.3
-
26
-
-
65549144456
-
Rett syndrome astrocytes are abnormal and spread MeCP2 deficiency through gap junctions
-
Maezawa I, Swanberg S, Harvey D, et al., Rett syndrome astrocytes are abnormal and spread MeCP2 deficiency through gap junctions. J Neurosci 2009; 29: 5051-5061.
-
(2009)
J Neurosci
, vol.29
, pp. 5051-5061
-
-
Maezawa, I.1
Swanberg, S.2
Harvey, D.3
-
27
-
-
84865773360
-
CDKL5 ensures excitatory synapse stability by reinforcing NGL-1-PSD95 interaction in the postsynaptic compartment and is impaired in patient iPSC-derived neurons
-
Ricciardi S, Ungaro F, Hambrock M, et al., CDKL5 ensures excitatory synapse stability by reinforcing NGL-1-PSD95 interaction in the postsynaptic compartment and is impaired in patient iPSC-derived neurons. Nat Cell Biol 2012; 14: 911-923.
-
(2012)
Nat Cell Biol
, vol.14
, pp. 911-923
-
-
Ricciardi, S.1
Ungaro, F.2
Hambrock, M.3
-
28
-
-
84921411214
-
GluD1 is a common altered player in neuronal differentiation from both MECP2-mutated and CDKL5-mutated iPS cells
-
Livide G, Patriarchi T, Amenduni M, et al., GluD1 is a common altered player in neuronal differentiation from both MECP2-mutated and CDKL5-mutated iPS cells. Eur J Hum Genet 2015; 23: 195-201.
-
(2015)
Eur J Hum Genet
, vol.23
, pp. 195-201
-
-
Livide, G.1
Patriarchi, T.2
Amenduni, M.3
-
29
-
-
77649209695
-
22q13. 3 deletion syndrome: Clinical and molecular analysis using array CGH
-
Dhar S, Del Gaudio D, German J, et al., 22q13. 3 deletion syndrome: Clinical and molecular analysis using array CGH. Am J Med Genet Part A 2010; 152: 573-581.
-
(2010)
Am J Med Genet Part A
, vol.152
, pp. 573-581
-
-
Dhar, S.1
Del Gaudio, D.2
German, J.3
-
30
-
-
84887627330
-
SHANK3 and IGF1 restore synaptic deficits in neurons from 22q13 deletion syndrome patients
-
Shcheglovitov A, Shcheglovitova O, Yazawa M, et al., SHANK3 and IGF1 restore synaptic deficits in neurons from 22q13 deletion syndrome patients. Nature 2013; 503: 267-271.
-
(2013)
Nature
, vol.503
, pp. 267-271
-
-
Shcheglovitov, A.1
Shcheglovitova, O.2
Yazawa, M.3
-
31
-
-
1642295079
-
Psychopharmacology in fragile X syndrome - Present and future
-
Berry-Kravis E, Potanos K,. Psychopharmacology in fragile X syndrome-Present and future. Ment Retard Dev Disabil Res Rev 2004; 10: 42-48.
-
(2004)
Ment Retard Dev Disabil Res Rev
, vol.10
, pp. 42-48
-
-
Berry-Kravis, E.1
Potanos, K.2
-
32
-
-
84865064735
-
Signaling defects in iPSC-derived fragile X premutation neurons
-
Liu J, Kos̈cielska KA, Cao Z, et al., Signaling defects in iPSC-derived fragile X premutation neurons. Hum Mol Genet 2012: dds207.
-
(2012)
Hum Mol Genet
, pp. dds207
-
-
Liu, J.1
Kos̈cielska, K.A.2
Cao, Z.3
-
33
-
-
84920815607
-
Molecular mechanisms regulating the defects in fragile X syndrome neurons derived from human pluripotent stem cells
-
Halevy T, Czech C, Benvenisty N,. Molecular mechanisms regulating the defects in fragile X syndrome neurons derived from human pluripotent stem cells. Stem Cell Rep 2015; 4: 37-46.
-
(2015)
Stem Cell Rep
, vol.4
, pp. 37-46
-
-
Halevy, T.1
Czech, C.2
Benvenisty, N.3
-
34
-
-
79952438377
-
Using induced pluripotent stem cells to investigate cardiac phenotypes in Timothy syndrome
-
Yazawa M, Hsueh B, Jia X, et al., Using induced pluripotent stem cells to investigate cardiac phenotypes in Timothy syndrome. Nature 2011; 471: 230-234.
-
(2011)
Nature
, vol.471
, pp. 230-234
-
-
Yazawa, M.1
Hsueh, B.2
Jia, X.3
-
35
-
-
84856088804
-
Using iPSC-derived neurons to uncover cellular phenotypes associated with Timothy syndrome
-
Paşca SP, Portmann T, Voineagu I, et al., Using iPSC-derived neurons to uncover cellular phenotypes associated with Timothy syndrome. Nat Med 2011; 17: 1657-1662.
-
(2011)
Nat Med
, vol.17
, pp. 1657-1662
-
-
Paşca, S.P.1
Portmann, T.2
Voineagu, I.3
-
36
-
-
84876839257
-
A human Dravet syndrome model from patient induced pluripotent stem cells
-
Higurashi N, Uchida T, Lossin C, et al., A human Dravet syndrome model from patient induced pluripotent stem cells. Mol Brain 2013; 6: 19.
-
(2013)
Mol Brain
, vol.6
, pp. 19
-
-
Higurashi, N.1
Uchida, T.2
Lossin, C.3
-
37
-
-
84885724899
-
Modeling Dravet syndrome using induced pluripotent stem cells (iPSCs) and directly converted neurons
-
Jiao J, Yang Y, Shi Y, et al., Modeling Dravet syndrome using induced pluripotent stem cells (iPSCs) and directly converted neurons. Hum Mol Genet 2013; 22: 4241-4252.
-
(2013)
Hum Mol Genet
, vol.22
, pp. 4241-4252
-
-
Jiao, J.1
Yang, Y.2
Shi, Y.3
-
38
-
-
84883302304
-
Dravet syndrome patient-derived neurons suggest a novel epilepsy mechanism
-
Liu Y, Lopez-Santiago LF, Yuan Y, et al., Dravet syndrome patient-derived neurons suggest a novel epilepsy mechanism. Ann Neurol 2013; 74: 128-139.
-
(2013)
Ann Neurol
, vol.74
, pp. 128-139
-
-
Liu, Y.1
Lopez-Santiago, L.F.2
Yuan, Y.3
-
39
-
-
79952446402
-
Modelling the long QT syndrome with induced pluripotent stem cells
-
Itzhaki I, Maizels L, Huber I, et al., Modelling the long QT syndrome with induced pluripotent stem cells. Nature 2011; 471: 225-229.
-
(2011)
Nature
, vol.471
, pp. 225-229
-
-
Itzhaki, I.1
Maizels, L.2
Huber, I.3
-
40
-
-
84863213874
-
Cardiomyocytes derived from pluripotent stem cells recapitulate electrophysiological characteristics of an overlap syndrome of cardiac sodium channel disease
-
Davis RP, Casini S, van den Berg CW, et al., Cardiomyocytes derived from pluripotent stem cells recapitulate electrophysiological characteristics of an overlap syndrome of cardiac sodium channel disease. Circulation 2012; 125: 3079-3091.
-
(2012)
Circulation
, vol.125
, pp. 3079-3091
-
-
Davis, R.P.1
Casini, S.2
Van Den Berg, C.W.3
-
41
-
-
77957729169
-
Patient-specific induced pluripotent stem-cell models for long-QT syndrome
-
Moretti A, Bellin M, Welling A, et al., Patient-specific induced pluripotent stem-cell models for long-QT syndrome. N Engl J Med 2010; 363: 1397-1409.
-
(2010)
N Engl J Med
, vol.363
, pp. 1397-1409
-
-
Moretti, A.1
Bellin, M.2
Welling, A.3
-
42
-
-
77749279749
-
Neural differentiation of human induced pluripotent stem cells follows developmental principles but with variable potency
-
Hu B-Y, Weick JP, Yu J, et al., Neural differentiation of human induced pluripotent stem cells follows developmental principles but with variable potency. Proc Natl Acad Sci USA 2010; 107: 4335-4340.
-
(2010)
Proc Natl Acad Sci USA
, vol.107
, pp. 4335-4340
-
-
Hu, B.-Y.1
Weick, J.P.2
Yu, J.3
-
43
-
-
77955449906
-
Epigenetic memory in induced pluripotent stem cells
-
Kim K, Doi A, Wen B, et al., Epigenetic memory in induced pluripotent stem cells. Nature 2010; 467: 285-290.
-
(2010)
Nature
, vol.467
, pp. 285-290
-
-
Kim, K.1
Doi, A.2
Wen, B.3
-
44
-
-
79953267538
-
A bioinformatic assay for pluripotency in human cells
-
Müller F-J, Schuldt BM, Williams R, et al., A bioinformatic assay for pluripotency in human cells. Nat Methods 2011; 8: 315-317.
-
(2011)
Nat Methods
, vol.8
, pp. 315-317
-
-
Müller, F.-J.1
Schuldt, B.M.2
Williams, R.3
-
45
-
-
84885850258
-
Opportunities and challenges of pluripotent stem cell neurodegenerative disease models
-
Sandoe J, Eggan K,. Opportunities and challenges of pluripotent stem cell neurodegenerative disease models. Nat Neurosci 2013; 16: 780-789.
-
(2013)
Nat Neurosci
, vol.16
, pp. 780-789
-
-
Sandoe, J.1
Eggan, K.2
-
46
-
-
84877301288
-
Functional maturation of hPSC-derived forebrain interneurons requires an extended timeline and mimics human neural development
-
Nicholas CR, Chen J, Tang Y, et al., Functional maturation of hPSC-derived forebrain interneurons requires an extended timeline and mimics human neural development. Cell Stem Cell 2013; 12: 573-586.
-
(2013)
Cell Stem Cell
, vol.12
, pp. 573-586
-
-
Nicholas, C.R.1
Chen, J.2
Tang, Y.3
-
47
-
-
84879403017
-
Astroglial cells regulate the developmental timeline of human neurons differentiated from induced pluripotent stem cells
-
Tang X, Zhou L, Wagner AM, et al., Astroglial cells regulate the developmental timeline of human neurons differentiated from induced pluripotent stem cells. Stem Cell Res 2013; 11: 743-757.
-
(2013)
Stem Cell Res
, vol.11
, pp. 743-757
-
-
Tang, X.1
Zhou, L.2
Wagner, A.M.3
-
48
-
-
84904753399
-
Expression of astrocyte-related receptors in cortical dysplasia with intractable epilepsy
-
Sukigara S, Dai H, Nabatame S, et al., Expression of astrocyte-related receptors in cortical dysplasia with intractable epilepsy. J Neuropathol Exp Neurol 2014; 73: 798-806.
-
(2014)
J Neuropathol Exp Neurol
, vol.73
, pp. 798-806
-
-
Sukigara, S.1
Dai, H.2
Nabatame, S.3
-
49
-
-
67651100884
-
Electrical excitability of early neurons in the human cerebral cortex during the second trimester of gestation
-
Moore AR, Filipovic R, Mo Z, et al., Electrical excitability of early neurons in the human cerebral cortex during the second trimester of gestation. Cereb Cortex 2009; 19: 1795-1805.
-
(2009)
Cereb Cortex
, vol.19
, pp. 1795-1805
-
-
Moore, A.R.1
Filipovic, R.2
Mo, Z.3
-
50
-
-
84929428248
-
Neuronal medium that supports basic synaptic functions and activity of human neurons in vitro
-
Bardy C, van den Hurk M, Eames T, et al., Neuronal medium that supports basic synaptic functions and activity of human neurons in vitro. Proc Natl Acad Sci 2015: 201504393.
-
(2015)
Proc Natl Acad Sci
, pp. 201504393
-
-
Bardy, C.1
Van Den Hurk, M.2
Eames, T.3
-
51
-
-
84898034713
-
Intrinsic membrane hyperexcitability of amyotrophic lateral sclerosis patient-derived motor neurons
-
Wainger BJ, Kiskinis E, Mellin C, et al., Intrinsic membrane hyperexcitability of amyotrophic lateral sclerosis patient-derived motor neurons. Cell Rep 2014; 7: 1-11.
-
(2014)
Cell Rep
, vol.7
, pp. 1-11
-
-
Wainger, B.J.1
Kiskinis, E.2
Mellin, C.3
-
52
-
-
84867233159
-
Evaluation of multi-well microelectrode arrays for neurotoxicity screening using a chemical training set
-
McConnell ER, McClain MA, Ross J, et al., Evaluation of multi-well microelectrode arrays for neurotoxicity screening using a chemical training set. Neurotoxicology 2012; 33: 1048-1057.
-
(2012)
Neurotoxicology
, vol.33
, pp. 1048-1057
-
-
McConnell, E.R.1
McClain, M.A.2
Ross, J.3
-
53
-
-
84884414984
-
Cerebral organoids model human brain development and microcephaly
-
Lancaster MA, Renner M, Martin C-A, et al., Cerebral organoids model human brain development and microcephaly. Nature 2013; 501: 373-379.
-
(2013)
Nature
, vol.501
, pp. 373-379
-
-
Lancaster, M.A.1
Renner, M.2
Martin, C.-A.3
-
54
-
-
84873282055
-
Pyramidal neurons derived from human pluripotent stem cells integrate efficiently into mouse brain circuits in vivo
-
Espuny-Camacho I, Michelsen KA, Gall D, et al., Pyramidal neurons derived from human pluripotent stem cells integrate efficiently into mouse brain circuits in vivo. Neuron 2013; 77: 440-456.
-
(2013)
Neuron
, vol.77
, pp. 440-456
-
-
Espuny-Camacho, I.1
Michelsen, K.A.2
Gall, D.3
-
55
-
-
84922639322
-
HPSC-derived maturing GABAergic interneurons ameliorate seizures and abnormal behavior in epileptic mice
-
Cunningham M, Cho J-H, Leung A, et al., hPSC-derived maturing GABAergic interneurons ameliorate seizures and abnormal behavior in epileptic mice. Cell Stem Cell 2014; 15: 559-573.
-
(2014)
Cell Stem Cell
, vol.15
, pp. 559-573
-
-
Cunningham, M.1
Cho, J.-H.2
Leung, A.3
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