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Peng-Peng Zhu

National Institutes of Health

29

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2099

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Hereditary spastic paraplegia SPG8 mutations impair CAV1-dependent, integrin-mediated cell adhesion

2020 Science Signaling
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Mammalian Knock Out Cells Reveal Prominent Roles for Atlastin GTPases in ER Network Morphology.

2016 Experimental Cell Research
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Pharmacologic rescue of axon growth defects in a human iPSC model of hereditary spastic paraplegia SPG3A

2014 Human Molecular Genetics
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Hereditary spastic paraplegia type 43 (SPG43) is caused by mutation in C19orf12

2013 Human Mutation
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Targeted High-Throughput Sequencing Identifies Mutations in atlastin-1 as a Cause of Hereditary Sensory Neuropathy Type I

2011 American Journal of Human Genetics
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Hereditary spastic paraplegia proteins REEP1, spastin, and atlastin-1 coordinate microtubule interactions with the tubular ER network

2010 Journal of Clinical Investigation
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A Class of Dynamin-like GTPases Involved in the Generation of the Tubular ER Network

2009 Cell
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Atlastin GTPases are required for Golgi apparatus and ER morphogenesis

2008 Human Molecular Genetics
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SPG3A protein atlastin-1 is enriched in growth cones and promotes axon elongation during neuronal development

2006 Human Molecular Genetics
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Structure of phosphorylated enzyme I, the phosphoenolpyruvate:sugar phosphotransferase system sugar translocation signal protein.

2006 Proceedings of the National Academy of Sciences of the United States of America
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Citations (63)