• 1868 Citations
  • 20 h-Index
1991 …2019
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Fingerprint Dive into the research topics where Weichun Lin is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

  • 3 Similar Profiles
Neuromuscular Junction Medicine & Life Sciences
Synapses Medicine & Life Sciences
Muscles Medicine & Life Sciences
Cholinergic Receptors Medicine & Life Sciences
Motor Neurons Medicine & Life Sciences
Schwann Cells Medicine & Life Sciences
Skeletal Muscle Medicine & Life Sciences
Neurotransmitter Agents Medicine & Life Sciences

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Research Output 1991 2019

  • 1868 Citations
  • 20 h-Index
  • 33 Article
  • 1 Chapter
1 Citation (Scopus)
R-SNARE Proteins
Vesicle-Associated Membrane Protein 2
Synaptic Transmission
Synapses
Neurotransmitter Agents

Blocking skeletal muscle DHPRs/Ryr1 prevents neuromuscular synapse loss in mutant mice deficient in type III Neuregulin 1 (CRD-Nrg1)

Liu, Y., Sugiura, Y., Chen, F., Lee, K. F., Ye, Q. & Lin, W., Mar 1 2019, In : PLoS genetics. 15, 3, p. e1007857

Research output: Contribution to journalArticle

Open Access
Neuregulin-1
ryanodine receptors
Ryanodine Receptor Calcium Release Channel
Muscle Denervation
Schwann Cells
1 Citation (Scopus)

Glial cells maintain synapses by inhibiting an activity-dependent retrograde protease signal

Gould, T. W., Dominguez, B., de Winter, F., Yeo, G. W., Liu, P., Sundararaman, B., Stark, T., Vu, A., Degen, J. L., Lin, W. & Lee, K. F., Mar 1 2019, In : PLoS genetics. 15, 3, p. e1007948

Research output: Contribution to journalArticle

Open Access
neuroglia
synapse
Schwann cells
Neuroglia
Synapses
5 Citations (Scopus)

MACF1 links rapsyn to microtubule- and actin-binding proteins to maintain neuromuscular synapses

Oury, J., Liu, Y., Töpf, A., Todorovic, S., Hoedt, E., Preethish-Kumar, V., Neubert, T. A., Lin, W., Lochmüller, H. & Burden, S. J., May 1 2019, In : Journal of Cell Biology. 218, 5, p. 1686-1705 20 p.

Research output: Contribution to journalArticle

Open Access
Microfilament Proteins
Microtubules
Synapses
Actins
Cholinergic Receptors
12 Citations (Scopus)

Homozygous mutations in VAMP1 cause a presynaptic congenital myasthenic syndrome

SYNAPS Study Group & Liu, Y., Apr 1 2017, In : Annals of Neurology. 81, 4, p. 597-603 7 p.

Research output: Contribution to journalArticle

Vesicle-Associated Membrane Protein 1
Congenital Myasthenic Syndromes
Neuromuscular Junction
Mutation
Exome