Pages that link to "Q28506321"
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The following pages link to Mice lacking sodium channel beta1 subunits display defects in neuronal excitability, sodium channel expression, and nodal architecture (Q28506321):
Displaying 50 items.
- Altered cardiac electrophysiology and SUDEP in a model of Dravet syndrome (Q21089741) (← links)
- Contactin associated protein-like 1 (Q21499302) (← links)
- Potassium voltage-gated channel, shaker-related subfamily, member 2 (Q21987572) (← links)
- Sodium channel, voltage-gated, type I, beta (Q21991611) (← links)
- Sodium channel Scn1b null mice exhibit prolonged QT and RR intervals (Q24294528) (← links)
- Sodium channel β1 subunit mutations associated with Brugada syndrome and cardiac conduction disease in humans (Q24310498) (← links)
- SCN4B-encoded sodium channel beta4 subunit in congenital long-QT syndrome (Q24314276) (← links)
- Scn3b knockout mice exhibit abnormal ventricular electrophysiological properties (Q24651316) (← links)
- Trafficking regulates the subcellular distribution of voltage-gated sodium channels in primary sensory neurons (Q26783929) (← links)
- Trafficking mechanisms underlying neuronal voltage-gated ion channel localization at the axon initial segment (Q26829715) (← links)
- Pathogenesis and new candidate treatments for infantile spasms and early life epileptic encephalopathies: A view from preclinical studies (Q27308052) (← links)
- On the multiple roles of the voltage gated sodium channel β1 subunit in genetic diseases (Q28080803) (← links)
- Mechanisms of sudden unexplained death in epilepsy (Q28081176) (← links)
- Sodium channel β subunits: emerging targets in channelopathies (Q28082122) (← links)
- An update on transcriptional and post-translational regulation of brain voltage-gated sodium channels (Q28087661) (← links)
- Contactin associates with sodium channel Nav1.3 in native tissues and increases channel density at the cell surface (Q28277714) (← links)
- A novel epilepsy mutation in the sodium channel SCN1A identifies a cytoplasmic domain for beta subunit interaction (Q28291611) (← links)
- Voltage-gated Na+ channel beta1 subunit-mediated neurite outgrowth requires Fyn kinase and contributes to postnatal CNS development in vivo (Q28510216) (← links)
- Nodes of Ranvier and axon initial segments are ankyrin G-dependent domains that assemble by distinct mechanisms (Q28582251) (← links)
- Tyrosine-phosphorylated and nonphosphorylated sodium channel beta1 subunits are differentially localized in cardiac myocytes (Q28589427) (← links)
- Persistent Sodium Current and Its Role in Epilepsy (Q29396058) (← links)
- The ataxia3 mutation in the N-terminal cytoplasmic domain of sodium channel Na(v)1.6 disrupts intracellular trafficking (Q30487520) (← links)
- Altered function of the SCN1A voltage-gated sodium channel leads to gamma-aminobutyric acid-ergic (GABAergic) interneuron abnormalities (Q30493834) (← links)
- BACE1 deficiency causes altered neuronal activity and neurodegeneration (Q30495458) (← links)
- Axon initial segment dysfunction in a mouse model of genetic epilepsy with febrile seizures plus (Q30495760) (← links)
- RING finger protein 121 facilitates the degradation and membrane localization of voltage-gated sodium channels (Q30625607) (← links)
- Cloning and expression of a zebrafish SCN1B ortholog and identification of a species-specific splice variant (Q33290469) (← links)
- Molecular cloning and analysis of zebrafish voltage-gated sodium channel beta subunit genes: implications for the evolution of electrical signaling in vertebrates (Q33290470) (← links)
- Effect of Seizures on the Developing Brain and Cognition (Q33618960) (← links)
- Functional reciprocity between Na+ channel Nav1.6 and beta1 subunits in the coordinated regulation of excitability and neurite outgrowth (Q33719761) (← links)
- Inherited disorders of voltage-gated sodium channels (Q33905815) (← links)
- The alpha-amino-3-hydroxyl-5-methyl-4-isoxazolepropionate receptor trafficking regulator "stargazin" is related to the claudin family of proteins by Its ability to mediate cell-cell adhesion (Q34081801) (← links)
- Localization of the paranodal protein Caspr in the mammalian retina (Q34208147) (← links)
- Mechanisms of epileptogenesis: a convergence on neural circuit dysfunction. (Q34339959) (← links)
- More than a pore: ion channel signaling complexes (Q34491609) (← links)
- The roles of sodium channels in nociception: Implications for mechanisms of pain (Q34674268) (← links)
- Na+ channel Scn1b gene regulates dorsal root ganglion nociceptor excitability in vivo (Q35067709) (← links)
- Na Channel β Subunits: Overachievers of the Ion Channel Family (Q35235909) (← links)
- Voltage-gated Na+ channel β1B: a secreted cell adhesion molecule involved in human epilepsy (Q35538368) (← links)
- Regulatory Role of Voltage-Gated Na Channel β Subunits in Sensory Neurons (Q35564862) (← links)
- Regulation of Nav1.6 and Nav1.8 peripheral nerve Na+ channels by auxiliary β-subunits (Q35810868) (← links)
- Association of common genetic variants in GPCPD1 with scaling of visual cortical surface area in humans (Q35844926) (← links)
- The sodium channel accessory subunit Navβ1 regulates neuronal excitability through modulation of repolarizing voltage-gated K⁺ channels. (Q35944812) (← links)
- An emerging role for voltage-gated Na+ channels in cellular migration: regulation of central nervous system development and potentiation of invasive cancers (Q36049612) (← links)
- betaIV spectrin is recruited to axon initial segments and nodes of Ranvier by ankyrinG. (Q36117801) (← links)
- Voltage-Gated Na+ Channel Isoforms and Their mRNA Expression Levels and Protein Abundance in Three Electric Organs and the Skeletal Muscle of the Electric Eel Electrophorus electricus (Q36210192) (← links)
- Sodium channel mutations in epilepsy and other neurological disorders (Q36216288) (← links)
- Neonatal epilepsy syndromes and GEFS+: mechanistic considerations (Q36344256) (← links)
- Voltage-gated sodium channels and metastatic disease. (Q36430239) (← links)
- Na(+) current in human ventricle: implications for sodium loading and homeostasis (Q36474141) (← links)