Chien-Ping Ko
Affiliations: | University of Southern California, Los Angeles, CA, United States |
Area:
Schwann cells, Neuromuscular junctionsGoogle:
"Chien-Ping Ko"Mean distance: 14.25 (cluster 6) | S | N | B | C | P |
Children
Sign in to add traineeSamir Koirala | grad student | 2002 | USC |
Guan Cao | grad student | 2004 | USC |
Linga V. Reddy | grad student | 2004 | USC |
Zhihua Feng | grad student | 2007 | USC |
Young-Eun Yoo | grad student | 2010 | USC |
Ming-Yi Lin | grad student | 2011 | USC |
Kar Y. Ling | grad student | 2011 | USC |
Chiara Mazzasette | grad student | 2010-2016 | USC |
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Publications
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Gould TW, Ko CP, Willison H, et al. (2024) Perisynaptic Schwann Cells: Guardians of Neuromuscular Junction Integrity and Function in Health and Disease. Cold Spring Harbor Perspectives in Biology |
Miller N, Xu Z, Quinlan KA, et al. (2023) Mitigating aberrant Cdk5 activation alleviates mitochondrial defects and motor neuron disease symptoms in spinal muscular atrophy. Proceedings of the National Academy of Sciences of the United States of America. 120: e2300308120 |
Kim JK, Jha NN, Awano T, et al. (2023) A spinal muscular atrophy modifier implicates the SMN protein in SNARE complex assembly at neuromuscular synapses. Neuron |
Zhao X, Feng Z, Risher N, et al. (2021) SMN protein is required throughout life to prevent spinal muscular atrophy disease progression. Human Molecular Genetics |
Feng Z, Lam S, Tenn ES, et al. (2021) Activation of Muscle-Specific Kinase (MuSK) Reduces Neuromuscular Defects in the Delta7 Mouse Model of Spinal Muscular Atrophy (SMA). International Journal of Molecular Sciences. 22 |
Feng Z, Ling KKY, Zhao X, et al. (2020) Corrigendum to: Pharmacologically-induced mouse model of adult spinal muscular atrophy to evaluate effectiveness of therapeutics after disease onset. Human Molecular Genetics |
Osman EY, Van Alstyne M, Yen PF, et al. (2020) Minor snRNA gene delivery improves the loss of proprioceptive synapses on SMA motor neurons. Jci Insight |
Kim JK, Jha NN, Feng Z, et al. (2020) Muscle-specific SMN reduction reveals motor neuron-independent disease in spinal muscular atrophy models. The Journal of Clinical Investigation |
Rimer M, Seaberg BL, Yen PF, et al. (2019) Nerve sprouting capacity in a pharmacologically induced mouse model of spinal muscular atrophy. Scientific Reports. 9: 7799 |
Morini E, Gao D, Montgomery CM, et al. (2019) ELP1 Splicing Correction Reverses Proprioceptive Sensory Loss in Familial Dysautonomia. American Journal of Human Genetics |