Pages that link to "Q28141226"
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The following pages link to Evolution and diversity of mammalian sodium channel genes (Q28141226):
Displaying 50 items.
- Ion channel clustering at the axon initial segment and node of Ranvier evolved sequentially in early chordates (Q21145023) (← links)
- Overview of the voltage-gated sodium channel family (Q21999779) (← links)
- Identification of a novel human voltage-gated sodium channel alpha subunit gene, SCN12A (Q22011020) (← links)
- Mutations of SCN1A, encoding a neuronal sodium channel, in two families with GEFS+2 (Q22253421) (← links)
- A common ankyrin-G-based mechanism retains KCNQ and NaV channels at electrically active domains of the axon (Q24307090) (← links)
- Neuronal sodium-channel alpha1-subunit mutations in generalized epilepsy with febrile seizures plus. (Q24536353) (← links)
- A novel SCN1A mutation associated with generalized epilepsy with febrile seizures plus--and prevalence of variants in patients with epilepsy (Q24536363) (← links)
- Coding and noncoding variation of the human calcium-channel beta4-subunit gene CACNB4 in patients with idiopathic generalized epilepsy and episodic ataxia (Q24540213) (← links)
- Genetic architecture of a feeding adaptation: garter snake (Thamnophis) resistance to tetrodotoxin bearing prey (Q24605305) (← links)
- A missense mutation of the Na+ channel alpha II subunit gene Na(v)1.2 in a patient with febrile and afebrile seizures causes channel dysfunction (Q24626279) (← links)
- Tetrodotoxin sensitivity of the vertebrate cardiac Na+ current (Q24632919) (← links)
- Channelopathy pathogenesis in autism spectrum disorders (Q26864726) (← links)
- Identifying the promoter region of the human brain sodium channel subtype II gene (SCN2A) (Q28139329) (← links)
- Nomenclature of voltage-gated sodium channels (Q28141860) (← links)
- A locus for febrile seizures (FEB3) maps to chromosome 2q23-24 (Q28145631) (← links)
- Genomic structures of SCN2A and SCN3A - candidate genes for deafness at the DFNA16 locus (Q28204578) (← links)
- Sodium channel beta subunits: anything but auxiliary (Q28210938) (← links)
- Sodium channels SCN1A, SCN2A and SCN3A in familial autism (Q28212831) (← links)
- Structure of the sodium channel gene SCN11A: evidence for intron-to-exon conversion model and implications for gene evolution (Q28214636) (← links)
- Evolutionary diversification of TTX-resistant sodium channels in a predator-prey interaction (Q28243909) (← links)
- SCN1A mutations and epilepsy (Q28249270) (← links)
- A novel epilepsy mutation in the sodium channel SCN1A identifies a cytoplasmic domain for beta subunit interaction (Q28291611) (← links)
- Behavioral audiograms of homozygous med(J) mutant mice with sodium channel deficiency and unaffected controls (Q28506561) (← links)
- Vasa recta voltage-gated Na+ channel Nav1.3 is regulated by calmodulin (Q28565378) (← links)
- Cloning and expression of the two new variants of Nav1.5/SCN5A in rat brain (Q28581127) (← links)
- Neuronal death and perinatal lethality in voltage-gated sodium channel alpha(II)-deficient mice (Q28592196) (← links)
- The VGL-Chanome: A Protein Superfamily Specialized for Electrical Signaling and Ionic Homeostasis (Q29032115) (← links)
- Metabolic energy cost of action potential velocity (Q30439834) (← 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)
- Excitability constraints on voltage-gated sodium channels (Q33300128) (← links)
- Phylogenetic and chromosomal analyses of multiple gene families syntenic with vertebrate Hox clusters (Q33370668) (← links)
- First record of a new member of Anopheles Hyrcanus Group from Iran: molecular identification, diagnosis, phylogeny, status of kdr resistance and Plasmodium infection (Q33505381) (← links)
- Evolutionary dynamics of U12-type spliceosomal introns (Q33531915) (← links)
- Structure-based assessment of disease-related mutations in human voltage-gated sodium channels (Q33729032) (← links)
- Selection and evaluation of tagging SNPs in the neuronal-sodium-channel gene SCN1A: implications for linkage-disequilibrium gene mapping (Q33906328) (← links)
- Voltage-gated sodium channels as therapeutic targets (Q33925684) (← links)
- Genetic predictors of the maximum doses patients receive during clinical use of the anti-epileptic drugs carbamazepine and phenytoin (Q33936573) (← links)
- Epilepsy genes: the link between molecular dysfunction and pathophysiology (Q34099226) (← links)
- The human Hox-bearing chromosome regions did arise by block or chromosome (or even genome) duplications (Q34162705) (← links)
- Phylogeny of ion channels: clues to structure and function (Q34241477) (← links)
- Sodium channels and neurological disease: insights from Scn8a mutations in the mouse (Q34331937) (← links)
- Transcriptional channelopathies: an emerging class of disorders (Q34354397) (← 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)
- Mechanisms of pyrethroid neurotoxicity: implications for cumulative risk assessment (Q34506845) (← links)
- "Paleogenomics": looking in the past to the future (Q34508010) (← links)
- A genome-wide survey of human short-term memory (Q34538809) (← links)
- Expansion of voltage-dependent Na+ channel gene family in early tetrapods coincided with the emergence of terrestriality and increased brain complexity (Q34683283) (← links)
- The voltage-gated sodium channel nav1.8 is expressed in human sperm (Q35006187) (← links)
- Functional ion channels in human pulmonary artery smooth muscle cells: Voltage-dependent cation channels (Q35214857) (← links)
- De novo exon duplication in a new allele of mouse Glra1 (spasmodic) (Q35221560) (← links)