These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

259 related articles for article (PubMed ID: 31282864)

  • 21. Dissecting the phenotypes of Dravet syndrome by gene deletion.
    Rubinstein M; Han S; Tai C; Westenbroek RE; Hunker A; Scheuer T; Catterall WA
    Brain; 2015 Aug; 138(Pt 8):2219-33. PubMed ID: 26017580
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Developmental alterations in firing properties of hippocampal CA1 inhibitory and excitatory neurons in a mouse model of Dravet syndrome.
    Almog Y; Fadila S; Brusel M; Mavashov A; Anderson K; Rubinstein M
    Neurobiol Dis; 2021 Jan; 148():105209. PubMed ID: 33271326
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Sexually Divergent Mortality and Partial Phenotypic Rescue After Gene Therapy in a Mouse Model of Dravet Syndrome.
    Niibori Y; Lee SJ; Minassian BA; Hampson DR
    Hum Gene Ther; 2020 Mar; 31(5-6):339-351. PubMed ID: 31830809
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Preferential inactivation of Scn1a in parvalbumin interneurons increases seizure susceptibility.
    Dutton SB; Makinson CD; Papale LA; Shankar A; Balakrishnan B; Nakazawa K; Escayg A
    Neurobiol Dis; 2013 Jan; 49():211-20. PubMed ID: 22926190
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Corticohippocampal circuit dysfunction in a mouse model of Dravet syndrome.
    Mattis J; Somarowthu A; Goff KM; Jiang E; Yom J; Sotuyo N; Mcgarry LM; Feng H; Kaneko K; Goldberg EM
    Elife; 2022 Feb; 11():. PubMed ID: 35212623
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Strain- and age-dependent hippocampal neuron sodium currents correlate with epilepsy severity in Dravet syndrome mice.
    Mistry AM; Thompson CH; Miller AR; Vanoye CG; George AL; Kearney JA
    Neurobiol Dis; 2014 May; 65():1-11. PubMed ID: 24434335
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Unexpected Efficacy of a Novel Sodium Channel Modulator in Dravet Syndrome.
    Anderson LL; Hawkins NA; Thompson CH; Kearney JA; George AL
    Sci Rep; 2017 May; 7(1):1682. PubMed ID: 28490751
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Preictal dysfunctions of inhibitory interneurons paradoxically lead to their rebound hyperactivity and to low-voltage-fast onset seizures in Dravet syndrome.
    Capitano F; Kuchenbuch M; Lavigne J; Chaptoukaev H; Zuluaga MA; Lorenzi M; Nabbout R; Mantegazza M
    Proc Natl Acad Sci U S A; 2024 Jun; 121(23):e2316364121. PubMed ID: 38809712
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Atypical myelinogenesis and reduced axon caliber in the Scn1a variant model of Dravet syndrome: An electron microscopy pilot study of the developing and mature mouse corpus callosum.
    Richards K; Jancovski N; Hanssen E; Connelly A; Petrou S
    Brain Res; 2021 Jan; 1751():147157. PubMed ID: 33069731
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Astrocyte Ca
    Uchino K; Tanaka Y; Ikezawa W; Deshimaru M; Kubota K; Watanabe T; Katsurabayashi S; Iwasaki K; Hirose S
    Biochem Biophys Res Commun; 2023 Feb; 643():169-174. PubMed ID: 36610382
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Functional and structural deficits of the dentate gyrus network coincide with emerging spontaneous seizures in an Scn1a mutant Dravet Syndrome model during development.
    Tsai MS; Lee ML; Chang CY; Fan HH; Yu IS; Chen YT; You JY; Chen CY; Chang FC; Hsiao JH; Khorkova O; Liou HH; Yanagawa Y; Lee LJ; Lin SW
    Neurobiol Dis; 2015 May; 77():35-48. PubMed ID: 25725421
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Impairments in social novelty recognition and spatial memory in mice with conditional deletion of Scn1a in parvalbumin-expressing cells.
    Tatsukawa T; Ogiwara I; Mazaki E; Shimohata A; Yamakawa K
    Neurobiol Dis; 2018 Apr; 112():24-34. PubMed ID: 29337050
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Upregulation of Haploinsufficient Gene Expression in the Brain by Targeting a Long Non-coding RNA Improves Seizure Phenotype in a Model of Dravet Syndrome.
    Hsiao J; Yuan TY; Tsai MS; Lu CY; Lin YC; Lee ML; Lin SW; Chang FC; Liu Pimentel H; Olive C; Coito C; Shen G; Young M; Thorne T; Lawrence M; Magistri M; Faghihi MA; Khorkova O; Wahlestedt C
    EBioMedicine; 2016 Jul; 9():257-277. PubMed ID: 27333023
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Sleep impairment and reduced interneuron excitability in a mouse model of Dravet Syndrome.
    Kalume F; Oakley JC; Westenbroek RE; Gile J; de la Iglesia HO; Scheuer T; Catterall WA
    Neurobiol Dis; 2015 May; 77():141-54. PubMed ID: 25766678
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Chronic partial TrkB activation reduces seizures and mortality in a mouse model of Dravet syndrome.
    Gu F; Parada I; Yang T; Longo FM; Prince DA
    Proc Natl Acad Sci U S A; 2022 Feb; 119(7):. PubMed ID: 35165147
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Functional Investigation of a Neuronal Microcircuit in the CA1 Area of the Hippocampus Reveals Synaptic Dysfunction in Dravet Syndrome Mice.
    Almog Y; Mavashov A; Brusel M; Rubinstein M
    Front Mol Neurosci; 2022; 15():823640. PubMed ID: 35370551
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Molecular basis of severe myoclonic epilepsy in infancy.
    Yamakawa K
    Brain Dev; 2009 May; 31(5):401-4. PubMed ID: 19203854
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Nav1.1 haploinsufficiency in excitatory neurons ameliorates seizure-associated sudden death in a mouse model of Dravet syndrome.
    Ogiwara I; Iwasato T; Miyamoto H; Iwata R; Yamagata T; Mazaki E; Yanagawa Y; Tamamaki N; Hensch TK; Itohara S; Yamakawa K
    Hum Mol Genet; 2013 Dec; 22(23):4784-804. PubMed ID: 23922229
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Cell-Selective Adeno-Associated Virus-Mediated
    Tanenhaus A; Stowe T; Young A; McLaughlin J; Aeran R; Lin IW; Li J; Hosur R; Chen M; Leedy J; Chou T; Pillay S; Vila MC; Kearney JA; Moorhead M; Belle A; Tagliatela S
    Hum Gene Ther; 2022 Jun; 33(11-12):579-597. PubMed ID: 35435735
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Mapping genetic modifiers of survival in a mouse model of Dravet syndrome.
    Miller AR; Hawkins NA; McCollom CE; Kearney JA
    Genes Brain Behav; 2014 Feb; 13(2):163-72. PubMed ID: 24152123
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 13.