268 related articles for article (PubMed ID: 23431407)
1. Distinct roles of molecular chaperones HSP90α and HSP90β in the biogenesis of KCNQ4 channels.
Gao Y; Yechikov S; Vazquez AE; Chen D; Nie L
PLoS One; 2013; 8(2):e57282. PubMed ID: 23431407
[TBL] [Abstract][Full Text] [Related]
2. Impaired surface expression and conductance of the KCNQ4 channel lead to sensorineural hearing loss.
Gao Y; Yechikov S; Vázquez AE; Chen D; Nie L
J Cell Mol Med; 2013 Jul; 17(7):889-900. PubMed ID: 23750663
[TBL] [Abstract][Full Text] [Related]
3. Specific Binding of Tetratricopeptide Repeat Proteins to Heat Shock Protein 70 (Hsp70) and Heat Shock Protein 90 (Hsp90) Is Regulated by Affinity and Phosphorylation.
Assimon VA; Southworth DR; Gestwicki JE
Biochemistry; 2015 Dec; 54(48):7120-31. PubMed ID: 26565746
[TBL] [Abstract][Full Text] [Related]
4. Hsp70 and Hsp90 multichaperone complexes sequentially regulate thiazide-sensitive cotransporter endoplasmic reticulum-associated degradation and biogenesis.
Donnelly BF; Needham PG; Snyder AC; Roy A; Khadem S; Brodsky JL; Subramanya AR
J Biol Chem; 2013 May; 288(18):13124-35. PubMed ID: 23482560
[TBL] [Abstract][Full Text] [Related]
5. Restoration of ion channel function in deafness-causing KCNQ4 mutants by synthetic channel openers.
Leitner MG; Feuer A; Ebers O; Schreiber DN; Halaszovich CR; Oliver D
Br J Pharmacol; 2012 Apr; 165(7):2244-59. PubMed ID: 21951272
[TBL] [Abstract][Full Text] [Related]
6. Role of the cytosolic chaperones Hsp70 and Hsp90 in maturation of the cardiac potassium channel HERG.
Ficker E; Dennis AT; Wang L; Brown AM
Circ Res; 2003 Jun; 92(12):e87-100. PubMed ID: 12775586
[TBL] [Abstract][Full Text] [Related]
7. Alterations of the Hsp70/Hsp90 chaperone and the HOP/CHIP co-chaperone system in cancer.
Ruckova E; Muller P; Nenutil R; Vojtesek B
Cell Mol Biol Lett; 2012 Sep; 17(3):446-58. PubMed ID: 22669480
[TBL] [Abstract][Full Text] [Related]
8. A novel KCNQ4 pore-region mutation (p.G296S) causes deafness by impairing cell-surface channel expression.
Mencía A; González-Nieto D; Modamio-Høybjør S; Etxeberría A; Aránguez G; Salvador N; Del Castillo I; Villarroel A; Moreno F; Barrio L; Moreno-Pelayo MA
Hum Genet; 2008 Feb; 123(1):41-53. PubMed ID: 18030493
[TBL] [Abstract][Full Text] [Related]
9. Chaperone Activity and Dimerization Properties of Hsp90
Morishima Y; Mehta RK; Yoshimura M; Lau M; Southworth DR; Lawrence TS; Pratt WB; Nyati MK; Osawa Y
Mol Pharmacol; 2018 Sep; 94(3):984-991. PubMed ID: 29941666
[TBL] [Abstract][Full Text] [Related]
10. A recurrent mutation in KCNQ4 in Korean families with nonsyndromic hearing loss and rescue of the channel activity by KCNQ activators.
Shin DH; Jung J; Koh YI; Rim JH; Lee JS; Choi HJ; Joo SY; Yu S; Cha DH; Lee SY; Lee JH; Lee MG; Choi JY; Gee HY
Hum Mutat; 2019 Mar; 40(3):335-346. PubMed ID: 30556268
[TBL] [Abstract][Full Text] [Related]
11. Regulation of CLC-1 chloride channel biosynthesis by FKBP8 and Hsp90β.
Peng YJ; Huang JJ; Wu HH; Hsieh HY; Wu CY; Chen SC; Chen TY; Tang CY
Sci Rep; 2016 Sep; 6():32444. PubMed ID: 27580824
[TBL] [Abstract][Full Text] [Related]
12. C-terminal phosphorylation of Hsp70 and Hsp90 regulates alternate binding to co-chaperones CHIP and HOP to determine cellular protein folding/degradation balances.
Muller P; Ruckova E; Halada P; Coates PJ; Hrstka R; Lane DP; Vojtesek B
Oncogene; 2013 Jun; 32(25):3101-10. PubMed ID: 22824801
[TBL] [Abstract][Full Text] [Related]
13. Rare KCNQ4 variants found in public databases underlie impaired channel activity that may contribute to hearing impairment.
Jung J; Lin H; Koh YI; Ryu K; Lee JS; Rim JH; Choi HJ; Lee HJ; Kim HY; Yu S; Jin H; Lee JH; Lee MG; Namkung W; Choi JY; Gee HY
Exp Mol Med; 2019 Aug; 51(8):1-12. PubMed ID: 31434872
[TBL] [Abstract][Full Text] [Related]
14. Recruitment of a cytoplasmic chaperone relay by the A2A adenosine receptor.
Bergmayr C; Thurner P; Keuerleber S; Kudlacek O; Nanoff C; Freissmuth M; Gruber CW
J Biol Chem; 2013 Oct; 288(40):28831-44. PubMed ID: 23965991
[TBL] [Abstract][Full Text] [Related]
15. CHIP: A Co-chaperone for Degradation by the Proteasome and Lysosome.
Chakraborty A; Edkins AL
Subcell Biochem; 2023; 101():351-387. PubMed ID: 36520313
[TBL] [Abstract][Full Text] [Related]
16. Regulation of ClC-2 Chloride Channel Proteostasis by Molecular Chaperones: Correction of Leukodystrophy-Associated Defect.
Fu SJ; Hu MC; Hsiao CT; Cheng AT; Chen TY; Jeng CJ; Tang CY
Int J Mol Sci; 2021 May; 22(11):. PubMed ID: 34070744
[TBL] [Abstract][Full Text] [Related]
17. Valproic Acid Inhibits Progressive Hereditary Hearing Loss in a KCNQ4 Variant Model through HDAC1 Suppression.
Nam YS; Choi YM; Lee S; Cho HH
Int J Mol Sci; 2023 Mar; 24(6):. PubMed ID: 36982769
[TBL] [Abstract][Full Text] [Related]
18. A novel pore-region mutation, c.887G > A (p.G296D) in KCNQ4, causing hearing loss in a Chinese family with autosomal dominant non-syndromic deafness 2.
Huang B; Liu Y; Gao X; Xu J; Dai P; Zhu Q; Yuan Y
BMC Med Genet; 2017 Mar; 18(1):36. PubMed ID: 28340560
[TBL] [Abstract][Full Text] [Related]
19. Blind cavefish and heat shock protein chaperones: a novel role for hsp90alpha in lens apoptosis.
Hooven TA; Yamamoto Y; Jeffery WR
Int J Dev Biol; 2004; 48(8-9):731-8. PubMed ID: 15558465
[TBL] [Abstract][Full Text] [Related]
20. KCNQ4 mutations associated with nonsyndromic progressive sensorineural hearing loss.
Nie L
Curr Opin Otolaryngol Head Neck Surg; 2008 Oct; 16(5):441-4. PubMed ID: 18797286
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]