Add to ORKGCalpain cleavage within dysferlin exon 40a releases a synaptotagmin-like module for membrane repai
<p><b>A.</b> Human GFAP was undigested or digested with calpain (Capn), resolved on SDS-PAGE, staine...
Calpain 3 (CAPN3) is a cysteine protease that when mutated causes Limb Girdle Muscular Dystrophy 2A....
Calpain 3 (CAPN3) is a calcium-dependent protease, mutations in which cause limb girdle muscular dys...
Dysferlin and calpain are important mediators of the emergency response to repair plasma membrane in...
International audienceDysferlinopathies are a group of muscular dystrophies caused by recessive muta...
Dysferlin is proposed as a key mediator of calcium-dependent muscle membrane repair, although its pr...
Mutations in the dysferlin gene cause a group of inherited muscular dystrophies, collectively known ...
Dysferlin is proposed as a key mediator of calcium-dependent muscle membrane repair, although its pr...
Drosophila calpain (Dm-calpain) produced in Escherichia coli has a distinct Ca2+-depen-dent activity...
Dysferlin is proposed as a key mediator of calcium-dependent muscle membrane repair, although its pr...
Calpain 3 (C3) is the only muscle-specific member of the calcium-dependent protease family. Although...
Calpain-mediated cleavage of neuronal targets has long been associated with excitotoxicity and synap...
Dysferlin (Dysf) and mitsugumin53 (MG53) are two key proteins involved in membrane repair of muscle ...
Contains fulltext : 110705.pdf (publisher's version ) (Closed access)Exocytosis of...
<div><p>Dysferlin (Dysf) and mitsugumin53 (MG53) are two key proteins involved in membrane repair of...
<p><b>A.</b> Human GFAP was undigested or digested with calpain (Capn), resolved on SDS-PAGE, staine...
Calpain 3 (CAPN3) is a cysteine protease that when mutated causes Limb Girdle Muscular Dystrophy 2A....
Calpain 3 (CAPN3) is a calcium-dependent protease, mutations in which cause limb girdle muscular dys...
Dysferlin and calpain are important mediators of the emergency response to repair plasma membrane in...
International audienceDysferlinopathies are a group of muscular dystrophies caused by recessive muta...
Dysferlin is proposed as a key mediator of calcium-dependent muscle membrane repair, although its pr...
Mutations in the dysferlin gene cause a group of inherited muscular dystrophies, collectively known ...
Dysferlin is proposed as a key mediator of calcium-dependent muscle membrane repair, although its pr...
Drosophila calpain (Dm-calpain) produced in Escherichia coli has a distinct Ca2+-depen-dent activity...
Dysferlin is proposed as a key mediator of calcium-dependent muscle membrane repair, although its pr...
Calpain 3 (C3) is the only muscle-specific member of the calcium-dependent protease family. Although...
Calpain-mediated cleavage of neuronal targets has long been associated with excitotoxicity and synap...
Dysferlin (Dysf) and mitsugumin53 (MG53) are two key proteins involved in membrane repair of muscle ...
Contains fulltext : 110705.pdf (publisher's version ) (Closed access)Exocytosis of...
<div><p>Dysferlin (Dysf) and mitsugumin53 (MG53) are two key proteins involved in membrane repair of...
<p><b>A.</b> Human GFAP was undigested or digested with calpain (Capn), resolved on SDS-PAGE, staine...
Calpain 3 (CAPN3) is a cysteine protease that when mutated causes Limb Girdle Muscular Dystrophy 2A....
Calpain 3 (CAPN3) is a calcium-dependent protease, mutations in which cause limb girdle muscular dys...