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.
24. Mice harboring the T316N variant in the GABA Jiang YL; Xia L; Zhao JJ; Zhou HM; Mi D; Wang X; Wang YY; Song CG; Jiang W Exp Neurol; 2024 Jun; 376():114775. PubMed ID: 38604438 [TBL] [Abstract][Full Text] [Related]
25. L-type Calcium Channel Blockers Enhance Trafficking and Function of Epilepsy-associated α1(D219N) Subunits of GABA(A) Receptors. Han DY; Guan BJ; Wang YJ; Hatzoglou M; Mu TW ACS Chem Biol; 2015 Sep; 10(9):2135-48. PubMed ID: 26168288 [TBL] [Abstract][Full Text] [Related]
26. The human epilepsy mutation GABRG2(Q390X) causes chronic subunit accumulation and neurodegeneration. Kang JQ; Shen W; Zhou C; Xu D; Macdonald RL Nat Neurosci; 2015 Jul; 18(7):988-96. PubMed ID: 26005849 [TBL] [Abstract][Full Text] [Related]
27. Inhibition of SMG-8, a subunit of SMG-1 kinase, ameliorates nonsense-mediated mRNA decay-exacerbated mutant phenotypes without cytotoxicity. Usuki F; Yamashita A; Shiraishi T; Shiga A; Onodera O; Higuchi I; Ohno S Proc Natl Acad Sci U S A; 2013 Sep; 110(37):15037-42. PubMed ID: 23983263 [TBL] [Abstract][Full Text] [Related]
28. A nonsense mutation of the sodium channel gene SCN2A in a patient with intractable epilepsy and mental decline. Kamiya K; Kaneda M; Sugawara T; Mazaki E; Okamura N; Montal M; Makita N; Tanaka M; Fukushima K; Fujiwara T; Inoue Y; Yamakawa K J Neurosci; 2004 Mar; 24(11):2690-8. PubMed ID: 15028761 [TBL] [Abstract][Full Text] [Related]
29. Why does fever trigger febrile seizures? GABAA receptor gamma2 subunit mutations associated with idiopathic generalized epilepsies have temperature-dependent trafficking deficiencies. Kang JQ; Shen W; Macdonald RL J Neurosci; 2006 Mar; 26(9):2590-7. PubMed ID: 16510738 [TBL] [Abstract][Full Text] [Related]
30. GABRG2 mutations in genetic epilepsy with febrile seizures plus: structure, roles, and molecular genetics. Li X; Guo S; Sun Y; Ding J; Chen C; Wu Y; Li P; Sun T; Wang X J Transl Med; 2024 Aug; 22(1):767. PubMed ID: 39143639 [TBL] [Abstract][Full Text] [Related]
32. Functional genomics of epilepsy-associated mutations in the GABA Absalom NL; Ahring PK; Liao VW; Balle T; Jiang T; Anderson LL; Arnold JC; McGregor IS; Bowen MT; Chebib M J Biol Chem; 2019 Apr; 294(15):6157-6171. PubMed ID: 30728247 [TBL] [Abstract][Full Text] [Related]
33. Deleterious Rare Variants Reveal Risk for Loss of GABAA Receptor Function in Patients with Genetic Epilepsy and in the General Population. Hernandez CC; Klassen TL; Jackson LG; Gurba K; Hu N; Noebels JL; Macdonald RL PLoS One; 2016; 11(9):e0162883. PubMed ID: 27622563 [TBL] [Abstract][Full Text] [Related]
34. Altered cortical GABAA receptor composition, physiology, and endocytosis in a mouse model of a human genetic absence epilepsy syndrome. Zhou C; Huang Z; Ding L; Deel ME; Arain FM; Murray CR; Patel RS; Flanagan CD; Gallagher MJ J Biol Chem; 2013 Jul; 288(29):21458-21472. PubMed ID: 23744069 [TBL] [Abstract][Full Text] [Related]
35. Differential inflammation responses determine the variable phenotypes of epilepsy induced by GABRG2 mutations. Sui J; Zhan L; Ji S; Wu W; Chen Y; Yun F; Liang W; Wang J; Cao M; Shen D; Zhang Q CNS Neurosci Ther; 2024 Feb; 30(2):e14583. PubMed ID: 38357846 [TBL] [Abstract][Full Text] [Related]
36. Endoplasmic reticulum retention and degradation of a mutation in SLC6A1 associated with epilepsy and autism. Wang J; Poliquin S; Mermer F; Eissman J; Delpire E; Wang J; Shen W; Cai K; Li BM; Li ZY; Xu D; Nwosu G; Flamm C; Liao WP; Shi YW; Kang JQ Mol Brain; 2020 May; 13(1):76. PubMed ID: 32398021 [TBL] [Abstract][Full Text] [Related]
37. Mutations in GABAA receptor subunits associated with genetic epilepsies. Macdonald RL; Kang JQ; Gallagher MJ J Physiol; 2010 Jun; 588(Pt 11):1861-9. PubMed ID: 20308251 [TBL] [Abstract][Full Text] [Related]
38. A new paradigm of channelopathy in epilepsy syndromes: intracellular trafficking abnormality of channel molecules. Hirose S Epilepsy Res; 2006 Aug; 70 Suppl 1():S206-17. PubMed ID: 16860540 [TBL] [Abstract][Full Text] [Related]