Weichun Lin, Ph.D.
Affiliations: | University of Texas Southwestern Medical Center, Dallas, TX, United States |
Area:
synapse developmentGoogle:
"Weichun Lin"Mean distance: 17.13 (cluster 31) | S | N | B | C | P |
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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 |