Pages that link to "Q28257712"
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The following pages link to Interaction of Muscle and Brain Sodium Channels with Multiple Members of the Syntrophin Family of Dystrophin-Associated Proteins (Q28257712):
Displaying 50 items.
- Stress-activated protein kinase-3 interacts with the PDZ domain of alpha1-syntrophin. A mechanism for specific substrate recognition (Q22009443) (← links)
- alpha-actinin-2 couples to cardiac Kv1.5 channels, regulating current density and channel localization in HEK cells (Q22254099) (← links)
- Spectrin and ankyrin-based pathways: metazoan inventions for integrating cells into tissues (Q24291372) (← links)
- Selectivity and promiscuity of the first and second PDZ domains of PSD-95 and synapse-associated protein 102 (Q24293430) (← links)
- DAMAGE, a Novel α-Dystrobrevin-associated MAGE Protein in Dystrophin Complexes (Q24299985) (← links)
- Cardiac sodium channel Na(v)1.5 interacts with and is regulated by the protein tyrosine phosphatase PTPH1 (Q24300624) (← links)
- Biochemical characterization of MLC1 protein in astrocytes and its association with the dystrophin-glycoprotein complex (Q24305215) (← links)
- The phosphoinositol 3,4-bisphosphate-binding protein TAPP1 interacts with syntrophins and regulates actin cytoskeletal organization (Q24306862) (← links)
- Blood pressure is regulated by an alpha1D-adrenergic receptor/dystrophin signalosome (Q24311297) (← links)
- Modulation of the cardiac sodium channel Nav1.5 by fibroblast growth factor homologous factor 1B (Q24313401) (← links)
- Dephosphorylation of beta2-syntrophin and Ca2 /mu-calpain-mediated cleavage of ICA512 upon stimulation of insulin secretion (Q24550152) (← links)
- Sarcospan-deficient mice maintain normal muscle function (Q24554300) (← links)
- Syntrophin-dependent expression and localization of Aquaporin-4 water channel protein (Q24555081) (← links)
- Diacylglycerol Kinase-ζ Localization in Skeletal Muscle Is Regulated by Phosphorylation and Interaction with Syntrophins (Q24644928) (← links)
- alpha-1-syntrophin mutation and the long-QT syndrome: a disease of sodium channel disruption (Q24651586) (← links)
- The neuregulin receptor ErbB-4 interacts with PDZ-containing proteins at neuronal synapses (Q24676816) (← links)
- AnkyrinG is required for clustering of voltage-gated Na channels at axon initial segments and for normal action potential firing (Q24682474) (← links)
- Different dystrophin-like complexes are expressed in neurons and glia (Q24684826) (← links)
- In vivo requirement of the alpha-syntrophin PDZ domain for the sarcolemmal localization of nNOS and aquaporin-4 (Q24685543) (← links)
- Absence of alpha-syntrophin leads to structurally aberrant neuromuscular synapses deficient in utrophin (Q24685703) (← links)
- Dystrophins and dystrobrevins (Q24805434) (← links)
- The biochemical and mass spectrometric profiling of the dystrophin complexome from skeletal muscle (Q26770343) (← links)
- Physiological and Pathophysiological Insights of Nav1.4 and Nav1.5 Comparison (Q26772794) (← links)
- Defective interactions of protein partner with ion channels and transporters as alternative mechanisms of membrane channelopathies (Q26866107) (← links)
- Proteomic profiling of the dystrophin-deficient mdx phenocopy of dystrophinopathy-associated cardiomyopathy (Q27006945) (← links)
- β2-Syntrophin is a Cdk5 substrate that restrains the motility of insulin secretory granules (Q27319464) (← links)
- Interactions between beta 2-syntrophin and a family of microtubule-associated serine/threonine kinases (Q28139505) (← links)
- Alternative splicing of dystrobrevin regulates the stoichiometry of syntrophin binding to the dystrophin protein complex (Q28143244) (← links)
- Deficiency of the syntrophins and alpha-dystrobrevin in patients with inherited myopathy (Q28191769) (← links)
- N-terminal PDZ-binding domain in Kv1 potassium channels (Q28215123) (← links)
- Dystrobrevin dynamics in muscle-cell signalling: a possible target for therapeutic intervention in Duchenne muscular dystrophy? (Q28220007) (← links)
- Cardiac sodium channel Na(v)1.5 and interacting proteins: Physiology and pathophysiology (Q28258096) (← links)
- CRIPT, a novel postsynaptic protein that binds to the third PDZ domain of PSD-95/SAP90 (Q28270363) (← links)
- α1-Syntrophin Variant Identified in Drug-Induced Long QT Syndrome Increases Late Sodium Current (Q28551060) (← links)
- Learning from Heterogeneous Data Sources: An Application in Spatial Proteomics (Q28552061) (← links)
- Consensus Substrate Sequence for Protein-tyrosine Phosphatase Receptor Type Z (Q28566366) (← links)
- Voltage-gated sodium channels and ankyrinG occupy a different postsynaptic domain from acetylcholine receptors from an early stage of neuromuscular junction maturation in rats (Q28574440) (← links)
- Slick (Slo2.1), a rapidly-gating sodium-activated potassium channel inhibited by ATP (Q28574688) (← links)
- Temporal and spatial localization of nectin-1 and l-afadin during synaptogenesis in hippocampal neurons (Q28580414) (← links)
- Distribution of proteins implicated in excitation-contraction coupling in rat ventricular myocytes (Q28581347) (← links)
- Characterization of human alpha-dystrobrevin isoforms in HL-60 human promyelocytic leukemia cells undergoing granulocytic differentiation. (Q30873797) (← links)
- Profound human/mouse differences in alpha-dystrobrevin isoforms: a novel syntrophin-binding site and promoter missing in mouse and rat. (Q30954335) (← links)
- Chronic hypoxia impairs muscle function in the Drosophila model of Duchenne's muscular dystrophy (DMD). (Q30990789) (← links)
- Digenic inheritance novel mutations in SCN5a and SNTA1 increase late I(Na) contributing to LQT syndrome (Q33162328) (← links)
- Convergent evolution with combinatorial peptides (Q33180988) (← links)
- Role of mental retardation-associated dystrophin-gene product Dp71 in excitatory synapse organization, synaptic plasticity and behavioral functions (Q33489556) (← links)
- The company they keep: ion channels and their intracellular regulatory partners. (Q33602343) (← links)
- Characteristics of skeletal muscle in mdx mutant mice (Q33644573) (← links)
- β1-Syntrophin Modulation by miR-222 in mdx Mice (Q33697991) (← links)
- Therapeutic targeting of signaling pathways in muscular dystrophy (Q33707964) (← links)