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List of works by William Daniel Phillips
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Faculty Opinions recommendation of Ablation of All Synaptobrevin vSNAREs Blocks Evoked But Not Spontaneous Neurotransmitter Release at Neuromuscular Synapses.
Faculty Opinions recommendation of Adenosine receptors and muscarinic receptors cooperate in acetylcholine release modulation in the neuromuscular synapse.
Faculty Opinions recommendation of Branched fibers from old fast-twitch dystrophic muscles are the sites of terminal damage in muscular dystrophy.
Faculty Opinions recommendation of Characterization of neuromuscular synapse function abnormalities in multiple Duchenne muscular dystrophy mouse models.
Faculty Opinions recommendation of Continuous administration of pyridostigmine improves immobilization-induced neuromuscular weakness.
Faculty Opinions recommendation of Cross-disease comparison of amyotrophic lateral sclerosis and spinal muscular atrophy reveals conservation of selective vulnerability but differential neuromuscular junction pathology.
Faculty Opinions recommendation of DOK7 gene therapy enhances motor activity and life span in ALS model mice.
Faculty Opinions recommendation of Development of abnormalities at the neuromuscular junction in the SOD1-G93A mouse model of ALS: dysfunction then disruption of postsynaptic structure precede overt motor symptoms.
Faculty Opinions recommendation of Interaction between ROR1 and MuSK activation complex in myogenic cells.
Faculty Opinions recommendation of Membraneless condensates by Rapsn phase separation as a platform for neuromuscular junction formation.
Faculty Opinions recommendation of MuSK is a BMP co-receptor that shapes BMP responses and calcium signaling in muscle cells.
Faculty Opinions recommendation of MuSK myasthenia gravis monoclonal antibodies.
Faculty Opinions recommendation of Overexpression of Dok-7 in skeletal muscle enhances neuromuscular transmission with structural alterations of neuromuscular junctions: Implications in robustness of neuromuscular transmission.
Faculty Opinions recommendation of Ryanodine- and CaMKII-dependent release of endogenous CGRP induces an increase in acetylcholine quantal size in neuromuscular junctions of mice.
Faculty Opinions recommendation of Single SERCA2a Therapy Ameliorated Dilated Cardiomyopathy for 18 Months in a Mouse Model of Duchenne Muscular Dystrophy.
Faculty Opinions recommendation of Terminal Schwann cells participate in the competition underlying neuromuscular synapse elimination.
Faculty Opinions recommendation of The cell polarity protein Vangl2 in the muscle shapes the neuromuscular synapse by binding to and regulating the tyrosine kinase MuSK.
Faculty Opinions recommendation of The synaptic receptor Lrp4 promotes peripheral nerve regeneration.
Faculty Opinions recommendation of β-dystroglycan is regulated by a balance between WWP1-mediated degradation and protection from WWP1 by dystrophin and utrophin.