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Summary Expression Phenotypes Gene Literature (7) GO Terms (8) Nucleotides (86) Proteins (41) Interactants (51) Wiki
XB-GENEPAGE-854456

Papers associated with chrnb2



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Sleep-related hypermotor epilepsy associated mutations uncover important kinetic roles of α4β2- nicotinic acetylcholine receptor intracellular structures., Weltzin MM, George AA, Lukas RJ, Whiteaker P., PLoS One. March 3, 2021; 16 (3): e0247825.                      

Genomic Takeover by Transposable Elements in the Strawberry Poison Frog., Rogers RL, Zhou L, Chu C, Márquez R, Corl A, Linderoth T, Freeborn L, MacManes MD, Xiong Z, Zheng J, Guo C, Xun X, Kronforst MR, Summers K, Wu Y, Yang H, Richards-Zawacki CL, Zhang G, Nielsen R., Mol Biol Evol. December 1, 2018; 35 (12): 2913-2927.              

Heparanase 2, mutated in urofacial syndrome, mediates peripheral neural development in Xenopus., Roberts NA, Woolf AS, Stuart HM, Thuret R, McKenzie EA, Newman WG, Hilton EN., Hum Mol Genet. August 15, 2014; 23 (16): 4302-14.                              

Pleiotropic functional effects of the first epilepsy-associated mutation in the human CHRNA2 gene., Hoda JC, Wanischeck M, Bertrand D, Steinlein OK., FEBS Lett. May 19, 2009; 583 (10): 1599-604.

Human nocturnal frontal lobe epilepsy: pharmocogenomic profiles of pathogenic nicotinic acetylcholine receptor beta-subunit mutations outside the ion channel pore., Hoda JC, Gu W, Friedli M, Phillips HA, Bertrand S, Antonarakis SE, Goudie D, Roberts R, Scheffer IE, Marini C, Patel J, Berkovic SF, Mulley JC, Steinlein OK, Bertrand D., Mol Pharmacol. August 1, 2008; 74 (2): 379-91.

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.

CHRNB2 is the second acetylcholine receptor subunit associated with autosomal dominant nocturnal frontal lobe epilepsy., Phillips HA, Favre I, Kirkpatrick M, Zuberi SM, Goudie D, Heron SE, Scheffer IE, Sutherland GR, Berkovic SF, Bertrand D, Mulley JC., Am J Hum Genet. January 1, 2001; 68 (1): 225-31.

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