<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>7(1)</volume><submitter>Bernadzki KM</submitter><pubmed_abstract>Neuromuscular junctions (NMJs) are specialized synapses that connect motor neurons to skeletal muscle fibers and orchestrate proper signal transmission from the nervous system to muscles. The efficient formation and maintenance of the postsynaptic machinery that contains acetylcholine receptors (AChR) are indispensable for proper NMJ function. Abnormalities in the organization of synaptic components often cause severe neuromuscular disorders, such as muscular dystrophy. The dystrophin-associated glycoprotein complex (DGC) was shown to play an important role in NMJ development. We recently identified liprin-α-1 as a novel binding partner for one of the cytoplasmic DGC components, α-dystrobrevin-1. In the present study, we performed a detailed analysis of localization and function of liprin-</pubmed_abstract><journal>Scientific reports</journal><pagination>9116</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC5567263</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Liprin-α-1 is a novel component of the murine neuromuscular junction and is involved in the organization of the postsynaptic machinery.</pubmed_title><pmcid>PMC5567263</pmcid><pubmed_authors>Niewiadomski P</pubmed_authors><pubmed_authors>Redowicz MJ</pubmed_authors><pubmed_authors>Proszynski TJ</pubmed_authors><pubmed_authors>Mazurek P</pubmed_authors><pubmed_authors>Pezinski M</pubmed_authors><pubmed_authors>Bernadzki KM</pubmed_authors><pubmed_authors>Gawor M</pubmed_authors></additional><is_claimable>false</is_claimable><name>Liprin-α-1 is a novel component of the murine neuromuscular junction and is involved in the organization of the postsynaptic machinery.</name><description>Neuromuscular junctions (NMJs) are specialized synapses that connect motor neurons to skeletal muscle fibers and orchestrate proper signal transmission from the nervous system to muscles. The efficient formation and maintenance of the postsynaptic machinery that contains acetylcholine receptors (AChR) are indispensable for proper NMJ function. Abnormalities in the organization of synaptic components often cause severe neuromuscular disorders, such as muscular dystrophy. The dystrophin-associated glycoprotein complex (DGC) was shown to play an important role in NMJ development. We recently identified liprin-α-1 as a novel binding partner for one of the cytoplasmic DGC components, α-dystrobrevin-1. In the present study, we performed a detailed analysis of localization and function of liprin-</description><dates><release>2017-01-01T00:00:00Z</release><publication>2017 Aug</publication><modification>2025-04-26T01:29:01.051Z</modification><creation>2019-03-27T02:54:11Z</creation></dates><accession>S-EPMC5567263</accession><cross_references><pubmed>28831123</pubmed><doi>10.1038/s41598-017-09590-7</doi></cross_references></HashMap>