Weichun Lin, Ph.D.

Affiliations: 
University of Texas Southwestern Medical Center, Dallas, TX, United States 
Area:
synapse development
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"Weichun Lin"
Mean distance: 17.13 (cluster 31)
 
SNBCP

Parents

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Ben G. Szaro grad student 1991-1996 SUNY Albany
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Publications

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Liu Y, Sugiura Y, Südhof TC, et al. (2019) Ablation of all synaptobrevin vSNAREs blocks evoked but not spontaneous neurotransmitter release at neuromuscular synapses. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience
Liu Y, Sugiura Y, Chen F, et al. (2019) Blocking skeletal muscle DHPRs/Ryr1 prevents neuromuscular synapse loss in mutant mice deficient in type III Neuregulin 1 (CRD-Nrg1). Plos Genetics. 15: e1007857
Gould TW, Dominguez B, de Winter F, et al. (2019) Glial cells maintain synapses by inhibiting an activity-dependent retrograde protease signal. Plos Genetics. 15: e1007948
Oury J, Liu Y, Töpf A, et al. (2019) MACF1 links Rapsyn to microtubule- and actin-binding proteins to maintain neuromuscular synapses. The Journal of Cell Biology
Chen Z, Donnelly CR, Dominguez B, et al. (2017) p75 Is Required for the Establishment of Postnatal Sensory Neuron Diversity by Potentiating Ret Signaling. Cell Reports. 21: 707-720
Salpietro V, Lin W, Delle Vedove A, et al. (2017) Homozygous mutations in VAMP1 cause a presynaptic congenital myasthenic syndrome. Annals of Neurology. 81: 597-603
Anderson DM, Cannavino J, Li H, et al. (2016) Severe muscle wasting and denervation in mice lacking the RNA-binding protein ZFP106. Proceedings of the National Academy of Sciences of the United States of America
Liu Y, Li H, Sugiura Y, et al. (2015) Ubiquitin-Synaptobrevin Fusion Protein Causes Degeneration of Presynaptic Motor Terminals in Mice. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 35: 11514-31
May-Simera HL, Petralia RS, Montcouquiol M, et al. (2015) Ciliary proteins Bbs8 and Ift20 promote planar cell polarity in the cochlea. Development (Cambridge, England). 142: 555-66
Choi HY, Liu Y, Tennert C, et al. (2013) APP interacts with LRP4 and agrin to coordinate the development of the neuromuscular junction in mice. Elife. 2: e00220
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