148 related articles for article (PubMed ID: 33973684)
1. New insights into the role of endoplasmic reticulum-associated degradation in Bartter Syndrome Type 1.
Shaukat I; Bakhos-Douaihy D; Zhu Y; Seaayfan E; Demaretz S; Frachon N; Weber S; Kömhoff M; Vargas-Poussou R; Laghmani K
Hum Mutat; 2021 Aug; 42(8):947-968. PubMed ID: 33973684
[TBL] [Abstract][Full Text] [Related]
2. OS9 Protein Interacts with Na-K-2Cl Co-transporter (NKCC2) and Targets Its Immature Form for the Endoplasmic Reticulum-associated Degradation Pathway.
Seaayfan E; Defontaine N; Demaretz S; Zaarour N; Laghmani K
J Biol Chem; 2016 Feb; 291(9):4487-502. PubMed ID: 26721884
[TBL] [Abstract][Full Text] [Related]
3. AUP1 Regulates the Endoplasmic Reticulum-Associated Degradation and Polyubiquitination of NKCC2.
Frachon N; Demaretz S; Seaayfan E; Chelbi L; Bakhos-Douaihy D; Laghmani K
Cells; 2024 Feb; 13(5):. PubMed ID: 38474353
[TBL] [Abstract][Full Text] [Related]
4. Differential Effects of STCH and Stress-Inducible Hsp70 on the Stability and Maturation of NKCC2.
Bakhos-Douaihy D; Seaayfan E; Demaretz S; Komhoff M; Laghmani K
Int J Mol Sci; 2021 Feb; 22(4):. PubMed ID: 33672238
[TBL] [Abstract][Full Text] [Related]
5. Golgi Alpha1,2-Mannosidase IA Promotes Efficient Endoplasmic Reticulum-Associated Degradation of NKCC2.
Demaretz S; Seaayfan E; Bakhos-Douaihy D; Frachon N; Kömhoff M; Laghmani K
Cells; 2021 Dec; 11(1):. PubMed ID: 35011665
[TBL] [Abstract][Full Text] [Related]
6. Protein Quality Control of NKCC2 in Bartter Syndrome and Blood Pressure Regulation.
Laghmani K
Cells; 2024 May; 13(10):. PubMed ID: 38786040
[TBL] [Abstract][Full Text] [Related]
7. A highly conserved motif at the COOH terminus dictates endoplasmic reticulum exit and cell surface expression of NKCC2.
Zaarour N; Demaretz S; Defontaine N; Mordasini D; Laghmani K
J Biol Chem; 2009 Aug; 284(32):21752-64. PubMed ID: 19535327
[TBL] [Abstract][Full Text] [Related]
8. Diacidic Motifs in the Carboxyl Terminus Are Required for ER Exit and Translocation to the Plasma Membrane of NKCC2.
Bakhos-Douaihy D; Seaayfan E; Frachon N; Demaretz S; Kömhoff M; Laghmani K
Int J Mol Sci; 2022 Oct; 23(21):. PubMed ID: 36361553
[TBL] [Abstract][Full Text] [Related]
9. Multiple evolutionarily conserved Di-leucine like motifs in the carboxyl terminus control the anterograde trafficking of NKCC2.
Zaarour N; Demaretz S; Defontaine N; Zhu Y; Laghmani K
J Biol Chem; 2012 Dec; 287(51):42642-53. PubMed ID: 23105100
[TBL] [Abstract][Full Text] [Related]
10. NKCC2 activity is inhibited by the Bartter's syndrome type 5 gain-of-function CaR-A843E mutant in renal cells.
Carmosino M; Gerbino A; Hendy GN; Torretta S; Rizzo F; Debellis L; Procino G; Svelto M
Biol Cell; 2015 Apr; 107(4):98-110. PubMed ID: 25631355
[TBL] [Abstract][Full Text] [Related]
11. Endoplasmic reticulum-associated degradation of the renal potassium channel, ROMK, leads to type II Bartter syndrome.
O'Donnell BM; Mackie TD; Subramanya AR; Brodsky JL
J Biol Chem; 2017 Aug; 292(31):12813-12827. PubMed ID: 28630040
[TBL] [Abstract][Full Text] [Related]
12. Late-onset manifestation of antenatal Bartter syndrome as a result of residual function of the mutated renal Na+-K+-2Cl- co-transporter.
Pressler CA; Heinzinger J; Jeck N; Waldegger P; Pechmann U; Reinalter S; Konrad M; Beetz R; Seyberth HW; Waldegger S
J Am Soc Nephrol; 2006 Aug; 17(8):2136-42. PubMed ID: 16807401
[TBL] [Abstract][Full Text] [Related]
13. [Functional characterization of SLC12A1 gene variants in 3 patients with Bartter syndrome type Ⅰ].
Sha YG; Wang CL; Du ZW; Zheng BX; Zhou W; Zhao F; Ding GX; Zhang A
Zhonghua Er Ke Za Zhi; 2022 Feb; 60(2):129-133. PubMed ID: 35090230
[No Abstract] [Full Text] [Related]
14. Genome mining yields new disease-associated ROMK variants with distinct defects.
Nguyen NH; Sarangi S; McChesney EM; Sheng S; Porter AW; Kleyman TR; Pitluk ZW; Brodsky JL
bioRxiv; 2023 May; ():. PubMed ID: 37214976
[TBL] [Abstract][Full Text] [Related]
15. Secretory carrier membrane protein 2 regulates exocytic insertion of NKCC2 into the cell membrane.
Zaarour N; Defontaine N; Demaretz S; Azroyan A; Cheval L; Laghmani K
J Biol Chem; 2011 Mar; 286(11):9489-502. PubMed ID: 21205824
[TBL] [Abstract][Full Text] [Related]
16. Impaired phosphorylation of Na(+)-K(+)-2Cl(-) cotransporter by oxidative stress-responsive kinase-1 deficiency manifests hypotension and Bartter-like syndrome.
Lin SH; Yu IS; Jiang ST; Lin SW; Chu P; Chen A; Sytwu HK; Sohara E; Uchida S; Sasaki S; Yang SS
Proc Natl Acad Sci U S A; 2011 Oct; 108(42):17538-43. PubMed ID: 21972418
[TBL] [Abstract][Full Text] [Related]
17. Genome mining yields putative disease-associated ROMK variants with distinct defects.
Nguyen NH; Sarangi S; McChesney EM; Sheng S; Durrant JD; Porter AW; Kleyman TR; Pitluk ZW; Brodsky JL
PLoS Genet; 2023 Nov; 19(11):e1011051. PubMed ID: 37956218
[TBL] [Abstract][Full Text] [Related]
18. Mutation of the Na(+)-K(+)-2Cl(-) cotransporter NKCC2 in mice is associated with severe polyuria and a urea-selective concentrating defect without hyperreninemia.
Kemter E; Rathkolb B; Bankir L; Schrewe A; Hans W; Landbrecht C; Klaften M; Ivandic B; Fuchs H; Gailus-Durner V; Hrabé de Angelis M; Wolf E; Wanke R; Aigner B
Am J Physiol Renal Physiol; 2010 Jun; 298(6):F1405-15. PubMed ID: 20219826
[TBL] [Abstract][Full Text] [Related]
19. Na+-K+-2Cl- cotransporter type 2 trafficking and activity: the role of interacting proteins.
Carmosino M; Procino G; Svelto M
Biol Cell; 2012 Apr; 104(4):201-12. PubMed ID: 22211456
[TBL] [Abstract][Full Text] [Related]
20. Unraveling the function of Arabidopsis thaliana OS9 in the endoplasmic reticulum-associated degradation of glycoproteins.
Hüttner S; Veit C; Schoberer J; Grass J; Strasser R
Plant Mol Biol; 2012 May; 79(1-2):21-33. PubMed ID: 22328055
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]