360 related articles for article (PubMed ID: 28597987)
1. Trafficking and localisation to the plasma membrane of Na
Dulsat G; Palomeras S; Cortada E; Riuró H; Brugada R; Vergés M
Biol Cell; 2017 Jul; 109(7):273-291. PubMed ID: 28597987
[TBL] [Abstract][Full Text] [Related]
2.
Cortada E; Brugada R; Verges M
J Biol Chem; 2019 Nov; 294(44):16123-16140. PubMed ID: 31511323
[TBL] [Abstract][Full Text] [Related]
3. A missense mutation in the sodium channel β2 subunit reveals SCN2B as a new candidate gene for Brugada syndrome.
Riuró H; Beltran-Alvarez P; Tarradas A; Selga E; Campuzano O; Vergés M; Pagans S; Iglesias A; Brugada J; Brugada P; Vázquez FM; Pérez GJ; Scornik FS; Brugada R
Hum Mutat; 2013 Jul; 34(7):961-6. PubMed ID: 23559163
[TBL] [Abstract][Full Text] [Related]
4. Trafficking and Function of the Voltage-Gated Sodium Channel β2 Subunit.
Cortada E; Brugada R; Verges M
Biomolecules; 2019 Oct; 9(10):. PubMed ID: 31614896
[TBL] [Abstract][Full Text] [Related]
5. Electrophysiological and trafficking defects of the SCN5A T353I mutation in Brugada syndrome are rescued by alpha-allocryptopine.
Zhang J; Chen Y; Yang J; Xu B; Wen Y; Xiang G; Wei G; Zhu C; Xing Y; Li Y
Eur J Pharmacol; 2015 Jan; 746():333-43. PubMed ID: 25261036
[TBL] [Abstract][Full Text] [Related]
6. Mechanistic insights into the interaction of the MOG1 protein with the cardiac sodium channel Na
Yu G; Liu Y; Qin J; Wang Z; Hu Y; Wang F; Li Y; Chakrabarti S; Chen Q; Wang QK
J Biol Chem; 2018 Nov; 293(47):18207-18217. PubMed ID: 30282806
[TBL] [Abstract][Full Text] [Related]
7. Inter-Regulation of K
Clatot J; Neyroud N; Cox R; Souil C; Huang J; Guicheney P; Antzelevitch C
Int J Mol Sci; 2020 Jul; 21(14):. PubMed ID: 32709127
[TBL] [Abstract][Full Text] [Related]
8. Brugada syndrome disease phenotype explained in apparently benign sodium channel mutations.
Hoshi M; Du XX; Shinlapawittayatorn K; Liu H; Chai S; Wan X; Ficker E; Deschênes I
Circ Cardiovasc Genet; 2014 Apr; 7(2):123-31. PubMed ID: 24573164
[TBL] [Abstract][Full Text] [Related]
9. Scn2b Deletion in Mice Results in Ventricular and Atrial Arrhythmias.
Bao Y; Willis BC; Frasier CR; Lopez-Santiago LF; Lin X; Ramos-Mondragón R; Auerbach DS; Chen C; Wang Z; Anumonwo J; Valdivia HH; Delmar M; Jalife J; Isom LL
Circ Arrhythm Electrophysiol; 2016 Dec; 9(12):. PubMed ID: 27932425
[TBL] [Abstract][Full Text] [Related]
10. Myotonic dystrophy type 1 mimics and exacerbates Brugada phenotype induced by Nav1.5 sodium channel loss-of-function mutation.
Pambrun T; Mercier A; Chatelier A; Patri S; Schott JJ; Le Scouarnec S; Chahine M; Degand B; Bois P
Heart Rhythm; 2014 Aug; 11(8):1393-400. PubMed ID: 24768612
[TBL] [Abstract][Full Text] [Related]
11. Mutant voltage-gated Na
Clatot J; Zheng Y; Girardeau A; Liu H; Laurita KR; Marionneau C; Deschênes I
Am J Physiol Heart Circ Physiol; 2018 Nov; 315(5):H1250-H1257. PubMed ID: 30118344
[TBL] [Abstract][Full Text] [Related]
12. SCN5A variant that blocks fibroblast growth factor homologous factor regulation causes human arrhythmia.
Musa H; Kline CF; Sturm AC; Murphy N; Adelman S; Wang C; Yan H; Johnson BL; Csepe TA; Kilic A; Higgins RS; Janssen PM; Fedorov VV; Weiss R; Salazar C; Hund TJ; Pitt GS; Mohler PJ
Proc Natl Acad Sci U S A; 2015 Oct; 112(40):12528-33. PubMed ID: 26392562
[TBL] [Abstract][Full Text] [Related]
13. Patient-Specific and Genome-Edited Induced Pluripotent Stem Cell-Derived Cardiomyocytes Elucidate Single-Cell Phenotype of Brugada Syndrome.
Liang P; Sallam K; Wu H; Li Y; Itzhaki I; Garg P; Zhang Y; Vermglinchan V; Lan F; Gu M; Gong T; Zhuge Y; He C; Ebert AD; Sanchez-Freire V; Churko J; Hu S; Sharma A; Lam CK; Scheinman MM; Bers DM; Wu JC
J Am Coll Cardiol; 2016 Nov; 68(19):2086-2096. PubMed ID: 27810048
[TBL] [Abstract][Full Text] [Related]
14. Contribution of Cardiac Sodium Channel β-Subunit Variants to Brugada Syndrome.
Peeters U; Scornik F; Riuró H; Pérez G; Komurcu-Bayrak E; Van Malderen S; Pappaert G; Tarradas A; Pagans S; Daneels D; Breckpot K; Brugada P; Bonduelle M; Brugada R; Van Dooren S
Circ J; 2015; 79(10):2118-29. PubMed ID: 26179811
[TBL] [Abstract][Full Text] [Related]
15. A novel gain-of-function sodium channel β2 subunit mutation in idiopathic small fiber neuropathy.
Alsaloum M; Labau JIR; Sosniak D; Zhao P; Almomani R; Gerrits M; Hoeijmakers JGJ; Lauria G; Faber CG; Waxman SG; Dib-Hajj S
J Neurophysiol; 2021 Sep; 126(3):827-839. PubMed ID: 34320850
[TBL] [Abstract][Full Text] [Related]
16. Sodium channel current loss of function in induced pluripotent stem cell-derived cardiomyocytes from a Brugada syndrome patient.
Selga E; Sendfeld F; Martinez-Moreno R; Medine CN; Tura-Ceide O; Wilmut SI; Pérez GJ; Scornik FS; Brugada R; Mills NL
J Mol Cell Cardiol; 2018 Jan; 114():10-19. PubMed ID: 29024690
[TBL] [Abstract][Full Text] [Related]
17. Investigations of the Navβ1b sodium channel subunit in human ventricle; functional characterization of the H162P Brugada syndrome mutant.
Yuan L; Koivumäki JT; Liang B; Lorentzen LG; Tang C; Andersen MN; Svendsen JH; Tfelt-Hansen J; Maleckar M; Schmitt N; Olesen MS; Jespersen T
Am J Physiol Heart Circ Physiol; 2014 Apr; 306(8):H1204-12. PubMed ID: 24561865
[TBL] [Abstract][Full Text] [Related]
18. hiPSC-derived cardiomyocytes from Brugada Syndrome patients without identified mutations do not exhibit clear cellular electrophysiological abnormalities.
Veerman CC; Mengarelli I; Guan K; Stauske M; Barc J; Tan HL; Wilde AA; Verkerk AO; Bezzina CR
Sci Rep; 2016 Aug; 6():30967. PubMed ID: 27485484
[TBL] [Abstract][Full Text] [Related]
19. Alterations of Nedd4-2-binding capacity in PY-motif of Na
Wang Y; Du Y; Luo L; Hu P; Yang G; Li T; Han X; Ma A; Wang T
Acta Physiol (Oxf); 2020 Jun; 229(2):e13438. PubMed ID: 31900993
[TBL] [Abstract][Full Text] [Related]
20. The voltage-gated sodium channel β2 subunit associates with lipid rafts by S-palmitoylation.
Cortada E; Serradesanferm R; Brugada R; Verges M
J Cell Sci; 2021 Mar; 134(6):. PubMed ID: 33602743
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
