231 related articles for article (PubMed ID: 18216024)
1. Congenital chloride-losing diarrhea causing mutations in the STAS domain result in misfolding and mistrafficking of SLC26A3.
Dorwart MR; Shcheynikov N; Baker JM; Forman-Kay JD; Muallem S; Thomas PJ
J Biol Chem; 2008 Mar; 283(13):8711-22. PubMed ID: 18216024
[TBL] [Abstract][Full Text] [Related]
2. Acute regulation of the SLC26A3 congenital chloride diarrhoea anion exchanger (DRA) expressed in Xenopus oocytes.
Chernova MN; Jiang L; Shmukler BE; Schweinfest CW; Blanco P; Freedman SD; Stewart AK; Alper SL
J Physiol; 2003 May; 549(Pt 1):3-19. PubMed ID: 12651923
[TBL] [Abstract][Full Text] [Related]
3. Effect of SLC26 anion transporter disease-causing mutations on the stability of the homologous STAS domain of E. coli DauA (YchM).
Bai X; Moraes TF; Reithmeier RA
Biochem J; 2016 Mar; 473(5):615-26. PubMed ID: 26635355
[TBL] [Abstract][Full Text] [Related]
4. SLC26A3 mutations in congenital chloride diarrhea.
Mäkelä S; Kere J; Holmberg C; Höglund P
Hum Mutat; 2002 Dec; 20(6):425-38. PubMed ID: 12442266
[TBL] [Abstract][Full Text] [Related]
5. Molecular analysis of human solute carrier SLC26 anion transporter disease-causing mutations using 3-dimensional homology modeling.
Rapp C; Bai X; Reithmeier RAF
Biochim Biophys Acta Biomembr; 2017 Dec; 1859(12):2420-2434. PubMed ID: 28941661
[TBL] [Abstract][Full Text] [Related]
6. Regulation of intestinal Cl-/HCO3- exchanger SLC26A3 by intracellular pH.
Hayashi H; Suruga K; Yamashita Y
Am J Physiol Cell Physiol; 2009 Jun; 296(6):C1279-90. PubMed ID: 19321737
[TBL] [Abstract][Full Text] [Related]
7. Identification of SLC26A3 mutations in a Korean patient with congenital chloride diarrhea.
Lee ES; Cho AR; Ki CS
Ann Lab Med; 2012 Jul; 32(4):312-5. PubMed ID: 22779076
[TBL] [Abstract][Full Text] [Related]
8. SLC26A3 and congenital chloride diarrhoea.
Höglund P
Novartis Found Symp; 2006; 273():74-86; discussion 86-90, 261-4. PubMed ID: 17120762
[TBL] [Abstract][Full Text] [Related]
9. Slc26a9 is inhibited by the R-region of the cystic fibrosis transmembrane conductance regulator via the STAS domain.
Chang MH; Plata C; Sindic A; Ranatunga WK; Chen AP; Zandi-Nejad K; Chan KW; Thompson J; Mount DB; Romero MF
J Biol Chem; 2009 Oct; 284(41):28306-28318. PubMed ID: 19643730
[TBL] [Abstract][Full Text] [Related]
10. Update on SLC26A3 mutations in congenital chloride diarrhea.
Wedenoja S; Pekansaari E; Höglund P; Mäkelä S; Holmberg C; Kere J
Hum Mutat; 2011 Jul; 32(7):715-22. PubMed ID: 21394828
[TBL] [Abstract][Full Text] [Related]
11. Expression of SLC26A3, CFTR and NHE3 in the human male reproductive tract: role in male subfertility caused by congenital chloride diarrhoea.
Hihnala S; Kujala M; Toppari J; Kere J; Holmberg C; Höglund P
Mol Hum Reprod; 2006 Feb; 12(2):107-11. PubMed ID: 16421216
[TBL] [Abstract][Full Text] [Related]
12. Slc26a3 deficiency is associated with epididymis dysplasia and impaired sperm fertilization potential in the mouse.
El Khouri E; Whitfield M; Stouvenel L; Kini A; Riederer B; Lores P; Roemermann D; di Stefano G; Drevet JR; Saez F; Seidler U; Touré A
Mol Reprod Dev; 2018 Aug; 85(8-9):682-695. PubMed ID: 30118583
[TBL] [Abstract][Full Text] [Related]
13. A missense mutation in SLC26A3 is associated with human male subfertility and impaired activation of CFTR.
Wedenoja S; Khamaysi A; Shimshilashvili L; Anbtawe-Jomaa S; Elomaa O; Toppari J; Höglund P; Aittomäki K; Holmberg C; Hovatta O; Tapanainen JS; Ohana E; Kere J
Sci Rep; 2017 Oct; 7(1):14208. PubMed ID: 29079751
[TBL] [Abstract][Full Text] [Related]
14. Downregulated in adenoma gene encodes a chloride transporter defective in congenital chloride diarrhea.
Moseley RH; Höglund P; Wu GD; Silberg DG; Haila S; de la Chapelle A; Holmberg C; Kere J
Am J Physiol; 1999 Jan; 276(1):G185-92. PubMed ID: 9886994
[TBL] [Abstract][Full Text] [Related]
15. Identification of seven novel mutations including the first two genomic rearrangements in SLC26A3 mutated in congenital chloride diarrhea.
Höglund P; Sormaala M; Haila S; Socha J; Rajaram U; Scheurlen W; Sinaasappel M; de Jonge H; Holmberg C; Yoshikawa H; Kere J
Hum Mutat; 2001 Sep; 18(3):233-42. PubMed ID: 11524734
[TBL] [Abstract][Full Text] [Related]
16. Significance of molecular testing for congenital chloride diarrhea.
Lechner S; Ruemmele FM; Zankl A; Lausch E; Huber WD; Mihatsch W; Phillips AD; Lewindon P; Querfeld U; Heinz-Erian P; Müller T; Janecke AR
J Pediatr Gastroenterol Nutr; 2011 Jul; 53(1):48-54. PubMed ID: 21694535
[TBL] [Abstract][Full Text] [Related]
17. A novel de novo SLC26A3 mutation causing congenital chloride diarrhea in a Japanese neonate.
Konishi KI; Mizuochi T; Honma H; Etani Y; Morikawa K; Wada K; Yamamoto K
Mol Genet Genomic Med; 2020 Nov; 8(11):e1505. PubMed ID: 32951339
[TBL] [Abstract][Full Text] [Related]
18. Congenital chloride diarrhea in patient with SLC26A2 mutation - analysis of the clinical phenotype and differential diagnosis.
Sun M; Tao N; Liu X; Yang Y; Su Y; Xu F
Pediatr Endocrinol Diabetes Metab; 2021; 27(1):51-56. PubMed ID: 33599438
[TBL] [Abstract][Full Text] [Related]
19. SLC26A3 inhibitor identified in small molecule screen blocks colonic fluid absorption and reduces constipation.
Haggie PM; Cil O; Lee S; Tan JA; Rivera AA; Phuan PW; Verkman AS
JCI Insight; 2018 Jul; 3(14):. PubMed ID: 30046015
[TBL] [Abstract][Full Text] [Related]
20. Congenital chloride diarrhea and Pendred syndrome: case report of siblings with two rare recessive disorders of SLC26 family genes.
Lindberg E; Moller C; Kere J; Wedenoja S; Anderzén-Carlsson A
BMC Med Genet; 2020 Apr; 21(1):79. PubMed ID: 32295532
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
