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Summary Expression Phenotypes Gene Literature (12) GO Terms (5) Nucleotides (46) Proteins (24) Interactants (26) Wiki
XB--994627

Papers associated with scn1b

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Splicing misregulation of SCN5A contributes to cardiac-conduction delay and heart arrhythmia in myotonic dystrophy., Freyermuth F, Rau F, Kokunai Y, Linke T, Sellier C, Nakamori M, Kino Y, Arandel L, Jollet A, Thibault C, Philipps M, Vicaire S, Jost B, Udd B, Day JW, Duboc D, Wahbi K, Matsumura T, Fujimura H, Mochizuki H, Deryckere F, Kimura T, Nukina N, Ishiura S, Lacroix V, Campan-Fournier A, Navratil V, Chautard E, Auboeuf D, Horie M, Imoto K, Lee KY, Swanson MS, de Munain AL, Inada S, Itoh H, Nakazawa K, Ashihara T, Wang E, Zimmer T, Furling D, Takahashi MP, Charlet-Berguerand N., Nat Commun. April 11, 2016; 7 11067.              


Modulation of voltage-gated K+ channels by the sodium channel β1 subunit., Nguyen HM, Miyazaki H, Hoshi N, Smith BJ, Nukina N, Goldin AL, Chandy KG., Proc Natl Acad Sci U S A. November 6, 2012; 109 (45): 18577-82.


A functional null mutation of SCN1B in a patient with Dravet syndrome., Patino GA, Claes LR, Lopez-Santiago LF, Slat EA, Dondeti RS, Chen C, O'Malley HA, Gray CB, Miyazaki H, Nukina N, Oyama F, De Jonghe P, Isom LL., J Neurosci. August 26, 2009; 29 (34): 10764-78.


Cloning and expression of a zebrafish SCN1B ortholog and identification of a species-specific splice variant., Fein AJ, Meadows LS, Chen C, Slat EA, Isom LL., BMC Genomics. July 10, 2007; 8 226.                      


An epilepsy mutation in the sodium channel SCN1A that decreases channel excitability., Barela AJ, Waddy SP, Lickfett JG, Hunter J, Anido A, Helmers SL, Goldin AL, Escayg A., J Neurosci. March 8, 2006; 26 (10): 2714-23.


Mutations linked to generalized epilepsy in humans reduce GABA(A) receptor current., Macdonald RL, Bianchi MT, Bianch MT, Feng H., Exp Neurol. November 1, 2003; 184 Suppl 1 S58-67.


Functional and biochemical analysis of a sodium channel beta1 subunit mutation responsible for generalized epilepsy with febrile seizures plus type 1., Meadows LS, Malhotra J, Loukas A, Thyagarajan V, Kazen-Gillespie KA, Koopman MC, Kriegler S, Isom LL, Ragsdale DS., J Neurosci. December 15, 2002; 22 (24): 10699-709.


Modulation of sodium current in mammalian cells by an epilepsy-correlated beta 1-subunit mutation., Tammaro P, Conti F, Moran O., Biochem Biophys Res Commun. March 8, 2002; 291 (4): 1095-101.


The sodium channel beta-subunit SCN3b modulates the kinetics of SCN5a and is expressed heterogeneously in sheep heart., Fahmi AI, Patel M, Stevens EB, Fowden AL, John JE, Lee K, Pinnock R, Morgan K, Jackson AP, Vandenberg JI., J Physiol. December 15, 2001; 537 (Pt 3): 693-700.


Skeletal muscle sodium channel is affected by an epileptogenic beta1 subunit mutation., Moran O, Conti F., Biochem Biophys Res Commun. March 23, 2001; 282 (1): 55-9.


Febrile seizures and generalized epilepsy associated with a mutation in the Na+-channel beta1 subunit gene SCN1B., Wallace RH, Wang DW, Singh R, Scheffer IE, George AL, Phillips HA, Saar K, Reis A, Johnson EW, Sutherland GR, Berkovic SF, Mulley JC., Nat Genet. August 1, 1998; 19 (4): 366-70.


A single B1 subunit mapped to mouse chromosome 7 may be a common component of Na channel isoforms from brain, skeletal muscle and heart., Tong J, Potts JF, Rochelle JM, Seldin MF, Agnew WS., Biochem Biophys Res Commun. September 15, 1993; 195 (2): 679-85.

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