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 *

711 related articles for article (PubMed ID: 17537961)

  • 21. Sodium channel dysfunction in intractable childhood epilepsy with generalized tonic-clonic seizures.
    Rhodes TH; Vanoye CG; Ohmori I; Ogiwara I; Yamakawa K; George AL
    J Physiol; 2005 Dec; 569(Pt 2):433-45. PubMed ID: 16210358
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Severe epilepsy resulting from genetic interaction between Scn2a and Kcnq2.
    Kearney JA; Yang Y; Beyer B; Bergren SK; Claes L; Dejonghe P; Frankel WN
    Hum Mol Genet; 2006 Mar; 15(6):1043-8. PubMed ID: 16464983
    [TBL] [Abstract][Full Text] [Related]  

  • 23. dCas9-Based Scn1a Gene Activation Restores Inhibitory Interneuron Excitability and Attenuates Seizures in Dravet Syndrome Mice.
    Colasante G; Lignani G; Brusco S; Di Berardino C; Carpenter J; Giannelli S; Valassina N; Bido S; Ricci R; Castoldi V; Marenna S; Church T; Massimino L; Morabito G; Benfenati F; Schorge S; Leocani L; Kullmann DM; Broccoli V
    Mol Ther; 2020 Jan; 28(1):235-253. PubMed ID: 31607539
    [TBL] [Abstract][Full Text] [Related]  

  • 24. 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]  

  • 25. A selective Na
    Chow CY; Chin YKY; Ma L; Undheim EAB; Herzig V; King GF
    Biochem Pharmacol; 2020 Nov; 181():113991. PubMed ID: 32335140
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Epilepsy-associated dysfunction in the voltage-gated neuronal sodium channel SCN1A.
    Lossin C; Rhodes TH; Desai RR; Vanoye CG; Wang D; Carniciu S; Devinsky O; George AL
    J Neurosci; 2003 Dec; 23(36):11289-95. PubMed ID: 14672992
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Interneuron Dysfunction in a New Mouse Model of SCN1A GEFS.
    Das A; Zhu B; Xie Y; Zeng L; Pham AT; Neumann JC; Safrina O; Benavides DR; MacGregor GR; Schutte SS; Hunt RF; O'Dowd DK
    eNeuro; 2021; 8(2):. PubMed ID: 33658306
    [TBL] [Abstract][Full Text] [Related]  

  • 28. 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]  

  • 29. K
    Gertler TS; Cherian S; DeKeyser JM; Kearney JA; George AL
    Neurobiol Dis; 2022 Jun; 168():105713. PubMed ID: 35346832
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Molecular correlates of age-dependent seizures in an inherited neonatal-infantile epilepsy.
    Liao Y; Deprez L; Maljevic S; Pitsch J; Claes L; Hristova D; Jordanova A; Ala-Mello S; Bellan-Koch A; Blazevic D; Schubert S; Thomas EA; Petrou S; Becker AJ; De Jonghe P; Lerche H
    Brain; 2010 May; 133(Pt 5):1403-14. PubMed ID: 20371507
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Genetic background modulates impaired excitability of inhibitory neurons in a mouse model of Dravet syndrome.
    Rubinstein M; Westenbroek RE; Yu FH; Jones CJ; Scheuer T; Catterall WA
    Neurobiol Dis; 2015 Jan; 73():106-17. PubMed ID: 25281316
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Nav1.1 channels with mutations of severe myoclonic epilepsy in infancy display attenuated currents.
    Sugawara T; Tsurubuchi Y; Fujiwara T; Mazaki-Miyazaki E; Nagata K; Montal M; Inoue Y; Yamakawa K
    Epilepsy Res; 2003 May; 54(2-3):201-7. PubMed ID: 12837571
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Preservation of perisomatic inhibitory input of granule cells in the epileptic human dentate gyrus.
    Wittner L; Maglóczky Z; Borhegyi Z; Halász P; Tóth S; Eross L; Szabó Z; Freund TF
    Neuroscience; 2001; 108(4):587-600. PubMed ID: 11738496
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Somatostatin-Positive Interneurons Contribute to Seizures in
    Wengert ER; Miralles RM; Wedgwood KCA; Wagley PK; Strohm SM; Panchal PS; Idrissi AM; Wenker IC; Thompson JA; Gaykema RP; Patel MK
    J Neurosci; 2021 Nov; 41(44):9257-9273. PubMed ID: 34544834
    [No Abstract]   [Full Text] [Related]  

  • 35. Enhanced inactivation and acceleration of activation of the sodium channel associated with epilepsy in man.
    Alekov AK; Rahman MM; Mitrovic N; Lehmann-Horn F; Lerche H
    Eur J Neurosci; 2001 Jun; 13(11):2171-6. PubMed ID: 11422459
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Aberrant Sodium Channel Currents and Hyperexcitability of Medial Entorhinal Cortex Neurons in a Mouse Model of
    Ottolini M; Barker BS; Gaykema RP; Meisler MH; Patel MK
    J Neurosci; 2017 Aug; 37(32):7643-7655. PubMed ID: 28676574
    [No Abstract]   [Full Text] [Related]  

  • 37. Impaired inactivation gate stabilization predicts increased persistent current for an epilepsy-associated SCN1A mutation.
    Kahlig KM; Misra SN; George AL
    J Neurosci; 2006 Oct; 26(43):10958-66. PubMed ID: 17065438
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Neddylation stabilizes Nav1.1 to maintain interneuron excitability and prevent seizures in murine epilepsy models.
    Chen W; Luo B; Gao N; Li H; Wang H; Li L; Cui W; Zhang L; Sun D; Liu F; Dong Z; Ren X; Zhang H; Su H; Xiong WC; Mei L
    J Clin Invest; 2021 Apr; 131(8):. PubMed ID: 33651714
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Interneuron Desynchronization Precedes Seizures in a Mouse Model of Dravet Syndrome.
    Tran CH; Vaiana M; Nakuci J; Somarowthu A; Goff KM; Goldstein N; Murthy P; Muldoon SF; Goldberg EM
    J Neurosci; 2020 Mar; 40(13):2764-2775. PubMed ID: 32102923
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Regionalized loss of parvalbumin interneurons in the cerebral cortex of mice with deficits in GFRalpha1 signaling.
    Canty AJ; Dietze J; Harvey M; Enomoto H; Milbrandt J; Ibáñez CF
    J Neurosci; 2009 Aug; 29(34):10695-705. PubMed ID: 19710321
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 36.