Year |
Citation |
Score |
2023 |
Sebastian R, Jin K, Pavon N, Bansal R, Potter A, Song Y, Babu J, Gabriel R, Sun Y, Aronow B, Pak C. Schizophrenia-associated NRXN1 deletions induce developmental-timing- and cell-type-specific vulnerabilities in human brain organoids. Nature Communications. 14: 3770. PMID 37355690 DOI: 10.1038/s41467-023-39420-6 |
0.308 |
|
2023 |
McSweeney D, English J, Howell E, Ribbe F, Pak C. Measuring Neuronal Network Activity Using Human Induced Neuronal Cells. Methods in Molecular Biology (Clifton, N.J.). 2683: 235-245. PMID 37300780 DOI: 10.1007/978-1-0716-3287-1_19 |
0.305 |
|
2023 |
English J, McSweeney D, Ribbe F, Howell E, Pak C. Generation and Co-culture of Cortical Glutamatergic and GABAergic-Induced Neuronal Cells. Methods in Molecular Biology (Clifton, N.J.). 2683: 21-37. PMID 37300764 DOI: 10.1007/978-1-0716-3287-1_3 |
0.36 |
|
2022 |
Wang L, Mirabella VR, Dai R, Su X, Xu R, Jadali A, Bernabucci M, Singh I, Chen Y, Tian J, Jiang P, Kwan KY, Pak C, Liu C, Comoletti D, et al. Analyses of the autism-associated neuroligin-3 R451C mutation in human neurons reveal a gain-of-function synaptic mechanism. Molecular Psychiatry. PMID 36280753 DOI: 10.1038/s41380-022-01834-x |
0.388 |
|
2022 |
McSweeney D, Gabriel R, Jin K, Pang ZP, Aronow B, Pak C. loss of function differentially regulates neuronal maturation and synaptic function in human induced cortical excitatory neurons. Iscience. 25: 105187. PMID 36262316 DOI: 10.1016/j.isci.2022.105187 |
0.408 |
|
2021 |
Pak C, Danko T, Mirabella VR, Wang J, Liu Y, Vangipuram M, Grieder S, Zhang X, Ward T, Huang YA, Jin K, Dexheimer P, Bardes E, Mitelpunkt A, Ma J, et al. Cross-platform validation of neurotransmitter release impairments in schizophrenia patient-derived -mutant neurons. Proceedings of the National Academy of Sciences of the United States of America. 118. PMID 34035170 DOI: 10.1073/pnas.2025598118 |
0.369 |
|
2019 |
Purmann C, Zhang X, Pak C, Huang Y, Pattni R, Grieder S, Wernig M, Levinson D, Aronow B, Sudhof T, Urban A. M12 Approaches To Transcriptome Analysis Of Human Induced Neurons In Co-Culture With Murine Glia To Model Functional Synapses European Neuropsychopharmacology. 29. DOI: 10.1016/J.Euroneuro.2019.08.112 |
0.376 |
|
2018 |
Pak C, Grieder S, Yang N, Zhang Y, Wernig M, Sudhof T. Rapid generation of functional and homogeneous excitatory human forebrain neurons using Neurogenin-2 (Ngn2) Protocol Exchange. DOI: 10.1038/Protex.2018.082 |
0.446 |
|
2017 |
Bienkowski RS, Banerjee A, Rounds JC, Rha J, Omotade OF, Gross C, Morris KJ, Leung SW, Pak C, Jones SK, Santoro MR, Warren ST, Zheng JQ, Bassell GJ, Corbett AH, et al. The Conserved, Disease-Associated RNA Binding Protein dNab2 Interacts with the Fragile X Protein Ortholog in Drosophila Neurons. Cell Reports. 20: 1372-1384. PMID 28793261 DOI: 10.1016/J.Celrep.2017.07.038 |
0.69 |
|
2016 |
Lee SJ, Wei M, Zhang C, Maxeiner S, Pak C, Calado Botelho S, Trotter J, Sterky FH, Südhof TC. Presynaptic neuronal pentraxin receptor organizes excitatory and inhibitory synapses. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. PMID 27986928 DOI: 10.1523/Jneurosci.2768-16.2016 |
0.391 |
|
2016 |
Yi F, Danko T, Botelho SC, Patzke C, Pak C, Wernig M, Südhof TC. Autism-associated SHANK3 haploinsufficiency causes Ih channelopathy in human neurons. Science (New York, N.Y.). 352: aaf2669. PMID 26966193 DOI: 10.1126/Science.Aaf2669 |
0.432 |
|
2015 |
Pak C, Danko T, Zhang Y, Aoto J, Anderson G, Maxeiner S, Yi F, Wernig M, Südhof TC. Human Neuropsychiatric Disease Modeling using Conditional Deletion Reveals Synaptic Transmission Defects Caused by Heterozygous Mutations in NRXN1. Cell Stem Cell. 17: 316-28. PMID 26279266 DOI: 10.1016/J.Stem.2015.07.017 |
0.448 |
|
2014 |
Chanda S, Ang CE, Davila J, Pak C, Mall M, Lee QY, Ahlenius H, Jung SW, Südhof TC, Wernig M. Generation of induced neuronal cells by the single reprogramming factor ASCL1. Stem Cell Reports. 3: 282-96. PMID 25254342 DOI: 10.1016/J.Stemcr.2014.05.020 |
0.45 |
|
2014 |
Kelly SM, Leung SW, Pak C, Banerjee A, Moberg KH, Corbett AH. A conserved role for the zinc finger polyadenosine RNA binding protein, ZC3H14, in control of poly(A) tail length. Rna (New York, N.Y.). 20: 681-8. PMID 24671764 DOI: 10.1261/Rna.043984.113 |
0.692 |
|
2013 |
Zhang Y, Pak C, Han Y, Ahlenius H, Zhang Z, Chanda S, Marro S, Patzke C, Acuna C, Covy J, Xu W, Yang N, Danko T, Chen L, Wernig M, et al. Rapid single-step induction of functional neurons from human pluripotent stem cells. Neuron. 78: 785-98. PMID 23764284 DOI: 10.1016/J.Neuron.2013.05.029 |
0.344 |
|
2012 |
Kelly S, Pak C, Garshasbi M, Kuss A, Corbett AH, Moberg K. New kid on the ID block: neural functions of the Nab2/ZC3H14 class of Cys₃His tandem zinc-finger polyadenosine RNA binding proteins. Rna Biology. 9: 555-62. PMID 22614829 DOI: 10.4161/Rna.20187 |
0.676 |
|
2011 |
Pak C, Garshasbi M, Kahrizi K, Gross C, Apponi LH, Noto JJ, Kelly SM, Leung SW, Tzschach A, Behjati F, Abedini SS, Mohseni M, Jensen LR, Hu H, Huang B, et al. Mutation of the conserved polyadenosine RNA binding protein, ZC3H14/dNab2, impairs neural function in Drosophila and humans. Proceedings of the National Academy of Sciences of the United States of America. 108: 12390-5. PMID 21734151 DOI: 10.1073/Pnas.1107103108 |
0.691 |
|
2010 |
Bamburg JR, Bernstein BW, Davis RC, Flynn KC, Goldsbury C, Jensen JR, Maloney MT, Marsden IT, Minamide LS, Pak CW, Shaw AE, Whiteman I, Wiggan O. ADF/Cofilin-actin rods in neurodegenerative diseases. Current Alzheimer Research. 7: 241-50. PMID 20088812 DOI: 10.2174/156720510791050902 |
0.306 |
|
2008 |
Allan AM, Liang X, Luo Y, Pak C, Li X, Szulwach KE, Chen D, Jin P, Zhao X. The loss of methyl-CpG binding protein 1 leads to autism-like behavioral deficits. Human Molecular Genetics. 17: 2047-57. PMID 18385101 DOI: 10.1093/Hmg/Ddn102 |
0.366 |
|
2007 |
Zhao X, Pak C, Smrt RD, Jin P. Epigenetics and Neural developmental disorders: Washington DC, September 18 and 19, 2006. Epigenetics. 2: 126-34. PMID 17965627 DOI: 10.4161/Epi.2.2.4236 |
0.424 |
|
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