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 *

194 related articles for article (PubMed ID: 12374766)

  • 1. Molecular and pathological effects of a modifier gene on deficiency of the sodium channel Scn8a (Na(v)1.6).
    Kearney JA; Buchner DA; De Haan G; Adamska M; Levin SI; Furay AR; Albin RL; Jones JM; Montal M; Stevens MJ; Sprunger LK; Meisler MH
    Hum Mol Genet; 2002 Oct; 11(22):2765-75. PubMed ID: 12374766
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Dystonia associated with mutation of the neuronal sodium channel Scn8a and identification of the modifier locus Scnm1 on mouse chromosome 3.
    Sprunger LK; Escayg A; Tallaksen-Greene S; Albin RL; Meisler MH
    Hum Mol Genet; 1999 Mar; 8(3):471-9. PubMed ID: 9949206
    [TBL] [Abstract][Full Text] [Related]  

  • 3. SCNM1, a putative RNA splicing factor that modifies disease severity in mice.
    Buchner DA; Trudeau M; Meisler MH
    Science; 2003 Aug; 301(5635):967-9. PubMed ID: 12920299
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Single amino acid deletion in transmembrane segment D4S6 of sodium channel Scn8a (Nav1.6) in a mouse mutant with a chronic movement disorder.
    Jones JM; Dionne L; Dell'Orco J; Parent R; Krueger JN; Cheng X; Dib-Hajj SD; Bunton-Stasyshyn RK; Sharkey LM; Dowling JJ; Murphy GG; Shakkottai VG; Shrager P; Meisler MH
    Neurobiol Dis; 2016 May; 89():36-45. PubMed ID: 26807988
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A targeted deleterious allele of the splicing factor SCNM1 in the mouse.
    Howell VM; de Haan G; Bergren S; Jones JM; Culiat CT; Michaud EJ; Frankel WN; Meisler MH
    Genetics; 2008 Nov; 180(3):1419-27. PubMed ID: 18791226
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Mutation detection in the med and medJ alleles of the sodium channel Scn8a. Unusual splicing due to a minor class AT-AC intron.
    Kohrman DC; Harris JB; Meisler MH
    J Biol Chem; 1996 Jul; 271(29):17576-81. PubMed ID: 8663325
    [TBL] [Abstract][Full Text] [Related]  

  • 7. The voltage-gated sodium channel Scn8a is a genetic modifier of severe myoclonic epilepsy of infancy.
    Martin MS; Tang B; Papale LA; Yu FH; Catterall WA; Escayg A
    Hum Mol Genet; 2007 Dec; 16(23):2892-9. PubMed ID: 17881658
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Normal audiogram but poor sensitivity to brief sounds in mice with compromised voltage-gated sodium channels (Scn8a
    Heffner RS; Koay G; Heffner HE
    Hear Res; 2019 Mar; 374():1-4. PubMed ID: 30669034
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Impaired firing and cell-specific compensation in neurons lacking nav1.6 sodium channels.
    Van Wart A; Matthews G
    J Neurosci; 2006 Jul; 26(27):7172-80. PubMed ID: 16822974
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Paranodal interactions regulate expression of sodium channel subtypes and provide a diffusion barrier for the node of Ranvier.
    Rios JC; Rubin M; St Martin M; Downey RT; Einheber S; Rosenbluth J; Levinson SR; Bhat M; Salzer JL
    J Neurosci; 2003 Aug; 23(18):7001-11. PubMed ID: 12904461
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Heterozygous mutations of the voltage-gated sodium channel SCN8A are associated with spike-wave discharges and absence epilepsy in mice.
    Papale LA; Beyer B; Jones JM; Sharkey LM; Tufik S; Epstein M; Letts VA; Meisler MH; Frankel WN; Escayg A
    Hum Mol Genet; 2009 May; 18(9):1633-41. PubMed ID: 19254928
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Reduced expression of Na(v)1.6 sodium channels and compensation by Na(v)1.2 channels in mice heterozygous for a null mutation in Scn8a.
    Vega AV; Henry DL; Matthews G
    Neurosci Lett; 2008 Sep; 442(1):69-73. PubMed ID: 18601978
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Floxed allele for conditional inactivation of the voltage-gated sodium channel Scn8a (NaV1.6).
    Levin SI; Meisler MH
    Genesis; 2004 Aug; 39(4):234-9. PubMed ID: 15286995
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Mutations of voltage-gated sodium channels in movement disorders and epilepsy.
    Meisler MH; Kearney JA; Sprunger LK; MacDonald BT; Buchner DA; Escayg A
    Novartis Found Symp; 2002; 241():72-81; discussion 82-6, 226-32. PubMed ID: 11771652
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Differential expression of exon 5 splice variants of sodium channel alpha subunit mRNAs in the developing mouse brain.
    Gazina EV; Richards KL; Mokhtar MB; Thomas EA; Reid CA; Petrou S
    Neuroscience; 2010 Mar; 166(1):195-200. PubMed ID: 20006674
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Three ENU-induced neurological mutations in the pore loop of sodium channel Scn8a (Na(v)1.6) and a genetically linked retinal mutation, rd13.
    Buchner DA; Seburn KL; Frankel WN; Meisler MH
    Mamm Genome; 2004 May; 15(5):344-51. PubMed ID: 15170223
    [TBL] [Abstract][Full Text] [Related]  

  • 17. High-resolution mapping of the sodium channel modifier Scnm1 on mouse chromosome 3 and identification of a 1.3-kb recombination hot spot.
    Buchner DA; Trudeau M; George AL; Sprunger LK; Meisler MH
    Genomics; 2003 Oct; 82(4):452-9. PubMed ID: 13679025
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Pathological and genetic analysis of the degenerating muscle (dmu) mouse: a new allele of Scn8a.
    De Repentigny Y; Côté PD; Pool M; Bernier G; Girard S; Vidal SM; Kothary R
    Hum Mol Genet; 2001 Aug; 10(17):1819-27. PubMed ID: 11532991
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Unique role of dystroglycan in peripheral nerve myelination, nodal structure, and sodium channel stabilization.
    Saito F; Moore SA; Barresi R; Henry MD; Messing A; Ross-Barta SE; Cohn RD; Williamson RA; Sluka KA; Sherman DL; Brophy PJ; Schmelzer JD; Low PA; Wrabetz L; Feltri ML; Campbell KP
    Neuron; 2003 Jun; 38(5):747-58. PubMed ID: 12797959
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Allelic mutations of the sodium channel SCN8A reveal multiple cellular and physiological functions.
    Meisler MH; Plummer NW; Burgess DL; Buchner DA; Sprunger LK
    Genetica; 2004 Sep; 122(1):37-45. PubMed ID: 15619959
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.