Pages that link to "Q22008052"
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The following pages link to Exon organization, coding sequence, physical mapping, and polymorphic intragenic markers for the human neuronal sodium channel gene SCN8A (Q22008052):
Displaying 47 items.
- Sodium voltage-gated channel alpha subunit 8 (Q21135479) (← links)
- Sodium channel, voltage-gated, type VIII, alpha (Q21985728) (← links)
- Identification of a novel human voltage-gated sodium channel alpha subunit gene, SCN12A (Q22011020) (← links)
- Characterization of a de novo SCN8A mutation in a patient with epileptic encephalopathy (Q24304239) (← links)
- Neuronal sodium-channel alpha1-subunit mutations in generalized epilepsy with febrile seizures plus. (Q24536353) (← links)
- Characterization of 5' untranslated regions of the voltage-gated sodium channels SCN1A, SCN2A, and SCN3A and identification of cis-conserved noncoding sequences (Q24656272) (← links)
- Two tetrodotoxin-resistant sodium channels in human dorsal root ganglion neurons (Q28139065) (← links)
- Genomic structures of SCN2A and SCN3A - candidate genes for deafness at the DFNA16 locus (Q28204578) (← links)
- Comparative distribution of voltage-gated sodium channel proteins in human brain (Q28211443) (← links)
- Structure of the sodium channel gene SCN11A: evidence for intron-to-exon conversion model and implications for gene evolution (Q28214636) (← links)
- Alternative splicing in the voltage-gated sodium channel DmNav regulates activation, inactivation, and persistent current. (Q30379170) (← links)
- Voltage-gated potassium channel KCNV2 (Kv8.2) contributes to epilepsy susceptibility (Q30499291) (← links)
- Fine mapping of an epilepsy modifier gene on mouse Chromosome 19. (Q33583837) (← links)
- AT-AC pre-mRNA splicing mechanisms and conservation of minor introns in voltage-gated ion channel genes (Q33595931) (← links)
- Diversity of mammalian voltage-gated sodium channels. (Q33691479) (← links)
- Is there a role for voltage-gated Na+ channels in the aggressiveness of breast cancer? (Q33777055) (← links)
- Alternative splicing of Na(V)1.7 exon 5 increases the impact of the painful PEPD mutant channel I1461T. (Q33796526) (← links)
- Use-dependent potentiation of the Nav1.6 sodium channel (Q34188077) (← links)
- Sodium channels and neurological disease: insights from Scn8a mutations in the mouse (Q34331937) (← links)
- Sodium channel SCN8A (Nav1.6): properties and de novo mutations in epileptic encephalopathy and intellectual disability (Q34382820) (← links)
- Multiple transcripts of sodium channel SCN8A (Na(V)1.6) with alternative 5'- and 3'-untranslated regions and initial characterization of the SCN8A promoter (Q34388928) (← links)
- Regulation of membrane excitability: a convergence on voltage-gated sodium conductance. (Q35024719) (← links)
- Voltage-gated Na+ channels: multiplicity of expression, plasticity, functional implications and pathophysiological aspects (Q35667228) (← links)
- Subunit dependence of Na channel slow inactivation and open channel block in cerebellar neurons (Q35774461) (← 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)
- Regulation of sodium channel activity by phosphorylation (Q36176745) (← links)
- Voltage-gated sodium channels: action players with many faces (Q36652537) (← links)
- Novel isoforms of the sodium channels Nav1.8 and Nav1.5 are produced by a conserved mechanism in mouse and rat. (Q37304434) (← links)
- Cardiac arrhythmia in a mouse model of sodium channel SCN8A epileptic encephalopathy (Q37417878) (← links)
- Cerebellum-related characteristics of Scn8a-mutant mice (Q37474494) (← links)
- The association of bacterial C9-based TTX-like compounds with Prorocentrum minimum opens new uncertainties about shellfish seafood safety. (Q37595332) (← links)
- Molecular Characterization of Voltage-Gated Sodium Channels and Their Relations with Paralytic Shellfish Toxin Bioaccumulation in the Pacific Oyster Crassostrea gigas. (Q37628651) (← links)
- Biophysical properties of human Na v1.7 splice variants and their regulation by protein kinase A. (Q40003069) (← links)
- Molecular cloning, distribution and functional analysis of the NA(V)1.6. Voltage-gated sodium channel from human brain (Q40719915) (← links)
- Novel mRNA isoforms of the sodium channels Na(v)1.2, Na(v)1.3 and Na(v)1.7 encode predicted two-domain, truncated proteins (Q42065325) (← links)
- Activity-dependent alternative splicing increases persistent sodium current and promotes seizure (Q42243377) (← links)
- Expression profiles of voltage-gated Na(+) channel alpha-subunit genes in rat and human prostate cancer cell lines (Q42508363) (← links)
- Heterozygosity for a protein truncation mutation of sodium channel SCN8A in a patient with cerebellar atrophy, ataxia, and mental retardation (Q43168798) (← links)
- D1/D5 dopamine receptor activation differentially modulates rapidly inactivating and persistent sodium currents in prefrontal cortex pyramidal neurons. (Q43551102) (← links)
- De novo variants in the alternative exon 5 of SCN8A cause epileptic encephalopathy (Q47625623) (← links)
- Na(v)1.7 and Na(v)1.3 are the only tetrodotoxin-sensitive sodium channels expressed by the adult guinea pig enteric nervous system (Q48090925) (← links)
- A role for phosphorylation in the maintenance of resurgent sodium current in cerebellar purkinje neurons. (Q48635183) (← links)
- Floxed allele for conditional inactivation of the voltage-gated sodium channel Scn8a (NaV1.6). (Q50283127) (← links)
- Gene duplications and evolution of vertebrate voltage-gated sodium channels. (Q51938135) (← links)
- Genetic modifiers affecting severity of epilepsy caused by mutation of sodium channel Scn2a. (Q54634416) (← links)
- Radiation hybrid mapping of 18 positional and physiological candidate genes for arthrogryposis multiplex congenita on porcine chromosome 5 (Q56601692) (← links)
- Distribution of voltage-gated sodium channel ?-subunit and ?-subunit mRNAs in human hippocampal formation, cortex, and cerebellum (Q60513667) (← links)