Pages that link to "Q28584895"
The following pages link to Distinct phenotypes of mutant mice lacking agrin, MuSK, or rapsyn (Q28584895):
Displaying 46 items.
- Muscle, skeletal, receptor tyrosine kinase (Q21983870) (← links)
- Form and function: the laminin family of heterotrimers (Q22254277) (← links)
- Muscle-like nicotinic receptor accessory molecules in sensory hair cells of the inner ear (Q24322879) (← links)
- Distinct domains of MuSK mediate its abilities to induce and to associate with postsynaptic specializations (Q24680337) (← links)
- Alterations of cAMP-dependent signaling in dystrophic skeletal muscle (Q27003221) (← links)
- Induction, assembly, maturation and maintenance of a postsynaptic apparatus (Q28206352) (← links)
- Reduced glycosaminoglycan sulfation diminishes the agrin signal transduction pathway (Q28290198) (← links)
- Motoneuron survival is enhanced in the absence of neuromuscular junction formation in embryos (Q28510890) (← links)
- Assembling the presynaptic active zone: a characterization of an active one precursor vesicle (Q28571859) (← links)
- Asparagine of z8 insert is critical for the affinity, conformation, and acetylcholine receptor-clustering activity of neural agrin (Q28579476) (← links)
- Mutations in MUSK causing congenital myasthenic syndrome impair MuSK-Dok-7 interaction (Q28589320) (← links)
- Agrin isoforms with distinct amino termini: differential expression, localization, and function (Q28592146) (← links)
- Altered properties of quantal neurotransmitter release at endplates of mice lacking P/Q-type Ca2+ channels (Q28594746) (← links)
- Heparan sulphate proteoglycans fine-tune mammalian physiology (Q29619329) (← links)
- Induction of myasthenia by immunization against muscle-specific kinase (Q30476990) (← links)
- A genomic view of the sea urchin nervous system (Q30499627) (← links)
- Still more complexity in mammalian basement membranes (Q34035427) (← links)
- Tissue inhibitor of metalloproteinase-2(TIMP-2)-deficient mice display motor deficits. (Q34546831) (← links)
- Heparan sulfate proteoglycans (Q35059448) (← links)
- Differential requirement for MuSK and dystroglycan in generating patterns of neuromuscular innervation (Q35844450) (← links)
- Sodium nitrate decreases agrin-induced acetylcholine receptor clustering (Q36004467) (← links)
- Nerve-independent formation of a topologically complex postsynaptic apparatus. (Q36321935) (← links)
- The role of chronic inflammation in obesity-associated cancers (Q36931512) (← links)
- Receptor-associated proteins and synaptic plasticity (Q37123934) (← links)
- The lens capsule (Q37171354) (← links)
- Interactions between heparan sulfate and proteins-design and functional implications (Q37543699) (← links)
- Dual roles for Wnt signalling during the formation of the vertebrate neuromuscular junction. (Q37873575) (← links)
- Functional innervation of cultured human skeletal muscle proceeds by two modes with regard to agrin effects (Q38494033) (← links)
- The role of semaphorin3A in myogenic regeneration and the formation of functional neuromuscular junctions on new fibres (Q38863834) (← links)
- Functional Roles of the Interaction of APP and Lipoprotein Receptors. (Q39180867) (← links)
- A role for the juxtamembrane domain of beta-dystroglycan in agrin-induced acetylcholine receptor clustering. (Q40676604) (← links)
- Differential Vicia villosa agglutinin reactivity identifies three distinct dystroglycan complexes in skeletal muscle (Q40791672) (← links)
- MuSK frizzled-like domain is critical for mammalian neuromuscular junction formation and maintenance. (Q41157669) (← links)
- Tissue inhibitor of metalloproteinase-2 (TIMP-2) regulates neuromuscular junction development via a beta1 integrin-mediated mechanism. (Q42361671) (← links)
- Maturation and maintenance of the neuromuscular synapse: genetic evidence for roles of the dystrophin--glycoprotein complex (Q42485105) (← links)
- Overexpression of muscle specific kinase increases the transcription and aggregation of acetylcholine receptors in Xenopus embryos. (Q43814016) (← links)
- Neuromuscular synapses mediate motor axon branching and motoneuron survival during the embryonic period of programmed cell death (Q44413786) (← links)
- Common founder effect of rapsyn N88K studied using intragenic markers (Q44977772) (← links)
- Congenital myasthenic syndromes due to mutations in the rapsyn gene (Q44990074) (← links)
- The role of agrin, Lrp4 and MuSK during dendritic arborization and synaptogenesis in cultured embryonic CNS neurons (Q58596724) (← links)
- Cytoskeleton and Adhesion in Myogenesis (Q59048948) (← links)
- Promotion of motoneuron survival and branching in rapsyn-deficient mice (Q73209814) (← links)
- Nerve terminals form but fail to mature when postsynaptic differentiation is blocked: in vivo analysis using mammalian nerve-muscle chimeras (Q74139732) (← links)
- Fast and slow-twitching muscles are differentially affected by reduced cholinergic transmission in mice deficient for VAChT: A mouse model for congenital myasthenia (Q90024304) (← links)
- Inferring novel genes related to colorectal cancer via random walk with restart algorithm (Q91903963) (← links)
- Evolution and Functional Differentiation of the Diaphragm Muscle of Mammals (Q92378287) (← links)