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 *

182 related articles for article (PubMed ID: 38862622)

  • 21. Confirmation of an epilepsy modifier locus on mouse chromosome 11 and candidate gene analysis by RNA-Seq.
    Hawkins NA; Kearney JA
    Genes Brain Behav; 2012 Jun; 11(4):452-60. PubMed ID: 22471526
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Genetic therapeutic advancements for Dravet Syndrome.
    Chilcott E; Díaz JA; Bertram C; Berti M; Karda R
    Epilepsy Behav; 2022 Jul; 132():108741. PubMed ID: 35653814
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Mouse with Nav1.1 haploinsufficiency, a model for Dravet syndrome, exhibits lowered sociability and learning impairment.
    Ito S; Ogiwara I; Yamada K; Miyamoto H; Hensch TK; Osawa M; Yamakawa K
    Neurobiol Dis; 2013 Jan; 49():29-40. PubMed ID: 22986304
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Antisense oligonucleotides increase
    Han Z; Chen C; Christiansen A; Ji S; Lin Q; Anumonwo C; Liu C; Leiser SC; Meena ; Aznarez I; Liau G; Isom LL
    Sci Transl Med; 2020 Aug; 12(558):. PubMed ID: 32848094
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Selective Na
    Richards KL; Milligan CJ; Richardson RJ; Jancovski N; Grunnet M; Jacobson LH; Undheim EAB; Mobli M; Chow CY; Herzig V; Csoti A; Panyi G; Reid CA; King GF; Petrou S
    Proc Natl Acad Sci U S A; 2018 Aug; 115(34):E8077-E8085. PubMed ID: 30076230
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Dravet syndrome as part of the clinical and genetic spectrum of sodium channel epilepsies and encephalopathies.
    Mei D; Cetica V; Marini C; Guerrini R
    Epilepsia; 2019 Dec; 60 Suppl 3():S2-S7. PubMed ID: 31904125
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Life-span characterization of epilepsy and comorbidities in Dravet syndrome mice carrying a targeted deletion of exon 1 of the Scn1a gene.
    Gerbatin RR; Augusto J; Boutouil H; Reschke CR; Henshall DC
    Exp Neurol; 2022 Aug; 354():114090. PubMed ID: 35487274
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Behavioral phenotyping of young Scn1a haploinsufficient mice.
    Reiber M; Miljanovic N; Schönhoff K; Palme R; Potschka H
    Epilepsy Behav; 2022 Nov; 136():108903. PubMed ID: 36240579
    [TBL] [Abstract][Full Text] [Related]  

  • 29. 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]  

  • 30. Targeted Molecular Strategies for Genetic Neurodevelopmental Disorders: Emerging Lessons from Dravet Syndrome.
    Lersch R; Jannadi R; Grosse L; Wagner M; Schneider MF; von Stülpnagel C; Heinen F; Potschka H; Borggraefe I
    Neuroscientist; 2023 Dec; 29(6):732-750. PubMed ID: 35414300
    [TBL] [Abstract][Full Text] [Related]  

  • 31. A high seizure burden increases several prostaglandin species in the hippocampus of a Scn1a
    Zhou C; Satpute V; Yip KL; Anderson LL; Hawkins N; Kearney J; Arnold JC
    Prostaglandins Other Lipid Mediat; 2024 Jun; 172():106836. PubMed ID: 38599513
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Hlf is a genetic modifier of epilepsy caused by voltage-gated sodium channel mutations.
    Hawkins NA; Kearney JA
    Epilepsy Res; 2016 Jan; 119():20-3. PubMed ID: 26656780
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Rescuing epileptic and behavioral alterations in a Dravet syndrome mouse model by inhibiting eukaryotic elongation factor 2 kinase (eEF2K).
    Beretta S; Gritti L; Ponzoni L; Scalmani P; Mantegazza M; Sala M; Verpelli C; Sala C
    Mol Autism; 2022 Jan; 13(1):1. PubMed ID: 34980259
    [TBL] [Abstract][Full Text] [Related]  

  • 34. 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]  

  • 35. 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]  

  • 36. Genetic exploration of Dravet syndrome: two case report.
    Triono A; Herini ES; Gunadi
    J Med Case Rep; 2024 Apr; 18(1):215. PubMed ID: 38649973
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Generation of a human iPSC line (UUIGPi015-A) from a patient with Dravet syndrome and a 2.9 Mb deletion spanning SCN1A on chromosome 2.
    Schuster J; de Guidi C; Tripathi R; Klar J; Dahl N
    Stem Cell Res; 2022 Apr; 60():102712. PubMed ID: 35203050
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Rare variants of small effect size in neuronal excitability genes influence clinical outcome in Japanese cases of SCN1A truncation-positive Dravet syndrome.
    Hammer MF; Ishii A; Johnstone L; Tchourbanov A; Lau B; Sprissler R; Hallmark B; Zhang M; Zhou J; Watkins J; Hirose S
    PLoS One; 2017; 12(7):e0180485. PubMed ID: 28686619
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Aberrant regulation of a poison exon caused by a non-coding variant in a mouse model of Scn1a-associated epileptic encephalopathy.
    Voskobiynyk Y; Battu G; Felker SA; Cochran JN; Newton MP; Lambert LJ; Kesterson RA; Myers RM; Cooper GM; Roberson ED; Barsh GS
    PLoS Genet; 2021 Jan; 17(1):e1009195. PubMed ID: 33411788
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Dravet Syndrome: A Developmental and Epileptic Encephalopathy.
    Lopez-Santiago L; Isom LL
    Epilepsy Curr; 2019 Jan; 19(1):51-53. PubMed ID: 30838929
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 10.