| scholarly article | Q13442814 |
| P2093 | author name string | David R Hampson | |
| Berge A Minassian | |||
| Yosuke Niibori | |||
| Shiron J Lee | |||
| P2860 | cites work | Altered cardiac electrophysiology and SUDEP in a model of Dravet syndrome | Q21089741 |
| Dissecting the phenotypes of Dravet syndrome by gene deletion | Q27303721 | ||
| A novel epilepsy mutation in the sodium channel SCN1A identifies a cytoplasmic domain for beta subunit interaction | Q28291611 | ||
| Structure and function of the beta 2 subunit of brain sodium channels, a transmembrane glycoprotein with a CAM motif | Q28579493 | ||
| Nav1.1 localizes to axons of parvalbumin-positive inhibitory interneurons: a circuit basis for epileptic seizures in mice carrying an Scn1a gene mutation | Q28587835 | ||
| Modulation of voltage-gated K+ channels by the sodium channel β1 subunit | Q30460758 | ||
| Preferential inactivation of Scn1a in parvalbumin interneurons increases seizure susceptibility | Q30542513 | ||
| Mapping genetic modifiers of survival in a mouse model of Dravet syndrome | Q30572370 | ||
| Generalized epilepsy with febrile seizures plus-associated sodium channel beta1 subunit mutations severely reduce beta subunit-mediated modulation of sodium channel function. | Q34650291 | ||
| Action potential initiation in neocortical inhibitory interneurons. | Q35244419 | ||
| The sodium channel accessory subunit Navβ1 regulates neuronal excitability through modulation of repolarizing voltage-gated K⁺ channels. | Q35944812 | ||
| Estradiol acutely suppresses inhibition in the hippocampus through a sex-specific endocannabinoid and mGluR-dependent mechanism | Q36025493 | ||
| Incidence of Dravet Syndrome in a US Population | Q36210601 | ||
| Autistic-like behaviour in Scn1a+/- mice and rescue by enhanced GABA-mediated neurotransmission. | Q36252621 | ||
| Optimizing the Diagnosis and Management of Dravet Syndrome: Recommendations From a North American Consensus Panel | Q36305239 | ||
| β1-C121W Is Down But Not Out: Epilepsy-Associated Scn1b-C121W Results in a Deleterious Gain-of-Function | Q36985341 | ||
| Age- and gender-related differences in GABAA receptor-mediated postsynaptic currents in GABAergic neurons of the substantia nigra reticulata in the rat | Q37311718 | ||
| Strain- and age-dependent hippocampal neuron sodium currents correlate with epilepsy severity in Dravet syndrome mice | Q37670832 | ||
| A viral strategy for targeting and manipulating interneurons across vertebrate species. | Q37696772 | ||
| Dravet syndrome: seizure control and gait in adults with different SCN1A mutations | Q38025195 | ||
| The role of non-pore-forming β subunits in physiology and pathophysiology of voltage-gated sodium channels. | Q38204926 | ||
| Adeno-Associated Virus-Based Gene Therapy for CNS Diseases. | Q38856794 | ||
| Clinical and genetic factors predicting Dravet syndrome in infants with SCN1A mutations | Q38959338 | ||
| Methylphenidate improves learning impairments and hyperthermia-induced seizures caused by an Scn1a mutation | Q40195437 | ||
| Persistent Expression of Dopamine-Synthesizing Enzymes 15 Years After Gene Transfer in a Primate Model of Parkinson's Disease | Q40299515 | ||
| Dravet syndrome in Sweden: a population-based study | Q41220933 | ||
| Autism and behavior in adult patients with Dravet syndrome (DS). | Q41719406 | ||
| Expecting the Unexpected: Lack of In Vivo Network Defects in an Scn1a Model of Dravet Syndrome | Q41889830 | ||
| Reduced dendritic arborization and hyperexcitability of pyramidal neurons in a Scn1b-based model of Dravet syndrome | Q42655726 | ||
| Retrospective multiinstitutional study of the prevalence of early death in Dravet syndrome. | Q45918638 | ||
| Quality of life and comorbidities associated with Dravet syndrome severity: a multinational cohort survey. | Q47549947 | ||
| Severe peri-ictal respiratory dysfunction is common in Dravet syndrome. | Q47658294 | ||
| Voltage-gated sodium channel β subunits: The power outside the pore in brain development and disease | Q47776524 | ||
| Is phenotype difference in severe myoclonic epilepsy in infancy related to SCN1A mutations? | Q48197553 | ||
| Adult motor phenotype differentiates Dravet syndrome from Lennox-Gastaut syndrome and links SCN1A to early onset parkinsonian features. | Q48253368 | ||
| Biosynthesis and processing of the alpha subunit of the voltage-sensitive sodium channel in rat brain neurons | Q48319338 | ||
| Sodium channel β1 subunit localizes to axon initial segments of excitatory and inhibitory neurons and shows regional heterogeneity in mouse brain. | Q48448358 | ||
| GABA(A) receptor alpha4 subunit suppression prevents withdrawal properties of an endogenous steroid | Q48472565 | ||
| Cross-kingdom auxiliary subunit modulation of a voltage-gated Sodium channel | Q48502710 | ||
| Sex differences in the activity of gamma-aminobutyric acidergic neurons in the rat hypothalamus | Q48557561 | ||
| Supraventricular Tachycardia During Status Epilepticus in Dravet Syndrome: A Link Between Brain and Heart? | Q48953043 | ||
| Changes in GABA(A) receptor subunit expression in the midbrain during the oestrous cycle in Wistar rats. | Q49053852 | ||
| Developmental and Regulatory Functions of Na(+) Channel Non-pore-forming β Subunits. | Q50489790 | ||
| Increased risk of sudden unexpected death in epilepsy in females using lamotrigine: a nested, case-control study. | Q51382080 | ||
| Recent progress and considerations for AAV gene therapies targeting the central nervous system. | Q54206545 | ||
| Viral Vectors for Gene Transfer | Q59349759 | ||
| Incidence and mechanisms of cardiorespiratory arrests in epilepsy monitoring units (MORTEMUS): a retrospective study | Q60148932 | ||
| Functional Access to Neuron Subclasses in Rodent and Primate Forebrain | Q64061634 | ||
| A Transient Developmental Window of Fast-Spiking Interneuron Dysfunction in a Mouse Model of Dravet Syndrome. | Q64967262 | ||
| Differential subcellular localization of the RI and RII Na+ channel subtypes in central neurons | Q69366003 | ||
| Sex differences in GABA turnover and glutamic acid decarboxylase (GAD(65) and GAD(67)) mRNA in the rat hypothalamus | Q74340277 | ||
| Spectrum of SCN1A gene mutations associated with Dravet syndrome: analysis of 333 patients | Q79639496 | ||
| Reduced axonal surface expression and phosphoinositide sensitivity in Kv7 channels disrupts their function to inhibit neuronal excitability in Kcnq2 epileptic encephalopathy | Q90217319 | ||
| Safe and Sustained Expression of Human Iduronidase After Intrathecal Administration of Adeno-Associated Virus Serotype 9 in Infant Rhesus Monkeys | Q90264049 | ||
| Sexually dimorphic behavior, neuronal activity, and gene expression in Chd8-mutant mice | Q90929313 | ||
| A more efficient conditional mouse model of Dravet syndrome: Implications for epigenetic selection and sex-dependent behaviors | Q91555726 | ||
| Scn1b deletion in adult mice results in seizures and SUDEP | Q92842110 | ||
| P4510 | describes a project that uses | ImageJ | Q1659584 |
| P433 | issue | 5-6 | |
| P921 | main subject | Dravet syndrome | Q1255956 |
| P304 | page(s) | 339-351 | |
| P577 | publication date | 2020-01-16 | |
| P1433 | published in | Human Gene Therapy | Q15757580 |
| P1476 | title | Sexually Divergent Mortality and Partial Phenotypic Rescue After Gene Therapy in a Mouse Model of Dravet Syndrome | |
| P478 | volume | 31 |
| Q110699053 | A zebrafish-centric approach to antiepileptic drug development | cites work | P2860 |
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