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Items: 1 to 20 of 34

1.

Pendrin, encoded by the Pendred syndrome gene, resides in the apical region of renal intercalated cells and mediates bicarbonate secretion.

Royaux IE, Wall SM, Karniski LP, Everett LA, Suzuki K, Knepper MA, Green ED.

Proc Natl Acad Sci U S A. 2001 Mar 27;98(7):4221-6.

2.

Cloning and characterization of SLC26A6, a novel member of the solute carrier 26 gene family.

Waldegger S, Moschen I, Ramirez A, Smith RJ, Ayadi H, Lang F, Kubisch C.

Genomics. 2001 Feb 15;72(1):43-50. Erratum in: Genomics 2001 Sep;77(1-2):115.

PMID:
11247665
3.

Pendrin: an apical Cl-/OH-/HCO3- exchanger in the kidney cortex.

Soleimani M, Greeley T, Petrovic S, Wang Z, Amlal H, Kopp P, Burnham CE.

Am J Physiol Renal Physiol. 2001 Feb;280(2):F356-64.

4.

Active (9.6 s) and inactive (21 s) oligomers of NHE3 in microdomains of the renal brush border.

Biemesderfer D, DeGray B, Aronson PS.

J Biol Chem. 2001 Mar 30;276(13):10161-7. Epub 2000 Dec 18.

5.

Mapping of five new putative anion transporter genes in human and characterization of SLC26A6, a candidate gene for pancreatic anion exchanger.

Lohi H, Kujala M, Kerkelä E, Saarialho-Kere U, Kestilä M, Kere J.

Genomics. 2000 Nov 15;70(1):102-12.

PMID:
11087667
6.

Prestin is the motor protein of cochlear outer hair cells.

Zheng J, Shen W, He DZ, Long KB, Madison LD, Dallos P.

Nature. 2000 May 11;405(6783):149-55.

PMID:
10821263
7.

Role of Na(+)/H(+) exchanger NHE3 in nephron function: micropuncture studies with S3226, an inhibitor of NHE3.

Vallon V, Schwark JR, Richter K, Hropot M.

Am J Physiol Renal Physiol. 2000 Mar;278(3):F375-9.

8.

Human pendrin expressed in Xenopus laevis oocytes mediates chloride/formate exchange.

Scott DA, Karniski LP.

Am J Physiol Cell Physiol. 2000 Jan;278(1):C207-11.

9.

Mechanism of proximal tubule bicarbonate absorption in NHE3 null mice.

Wang T, Yang CL, Abbiati T, Schultheis PJ, Shull GE, Giebisch G, Aronson PS.

Am J Physiol. 1999 Aug;277(2 Pt 2):F298-302.

10.

The Pendred syndrome gene encodes a chloride-iodide transport protein.

Scott DA, Wang R, Kreman TM, Sheffield VC, Karniski LP.

Nat Genet. 1999 Apr;21(4):440-3.

PMID:
10192399
11.

Renal and intestinal absorptive defects in mice lacking the NHE3 Na+/H+ exchanger.

Schultheis PJ, Clarke LL, Meneton P, Miller ML, Soleimani M, Gawenis LR, Riddle TM, Duffy JJ, Doetschman T, Wang T, Giebisch G, Aronson PS, Lorenz JN, Shull GE.

Nat Genet. 1998 Jul;19(3):282-5.

PMID:
9662405
12.

Pendred syndrome is caused by mutations in a putative sulphate transporter gene (PDS).

Everett LA, Glaser B, Beck JC, Idol JR, Buchs A, Heyman M, Adawi F, Hazani E, Nassir E, Baxevanis AD, Sheffield VC, Green ED.

Nat Genet. 1997 Dec;17(4):411-22.

PMID:
9398842
13.

Mechanisms of chloride transport in the proximal tubule.

Aronson PS, Giebisch G.

Am J Physiol. 1997 Aug;273(2 Pt 2):F179-92. Review.

PMID:
9277578
14.

Role of NHE3 in mediating renal brush border Na+-H+ exchange. Adaptation to metabolic acidosis.

Wu MS, Biemesderfer D, Giebisch G, Aronson PS.

J Biol Chem. 1996 Dec 20;271(51):32749-52.

15.

Mutations of the Down-regulated in adenoma (DRA) gene cause congenital chloride diarrhoea.

Höglund P, Haila S, Socha J, Tomaszewski L, Saarialho-Kere U, Karjalainen-Lindsberg ML, Airola K, Holmberg C, de la Chapelle A, Kere J.

Nat Genet. 1996 Nov;14(3):316-9.

PMID:
8896562
16.

Pathways for oxalate transport in rabbit renal microvillus membrane vesicles.

Kuo SM, Aronson PS.

J Biol Chem. 1996 Jun 28;271(26):15491-7.

17.

Expression of NHE-3 in the apical membrane of rat renal proximal tubule and thick ascending limb.

Amemiya M, Loffing J, Lötscher M, Kaissling B, Alpern RJ, Moe OW.

Kidney Int. 1995 Oct;48(4):1206-15.

18.

Functional expression cloning of the canalicular sulfate transport system of rat hepatocytes.

Bissig M, Hagenbuch B, Stieger B, Koller T, Meier PJ.

J Biol Chem. 1994 Jan 28;269(4):3017-21.

19.
20.

NHE3: a Na+/H+ exchanger isoform of renal brush border.

Biemesderfer D, Pizzonia J, Abu-Alfa A, Exner M, Reilly R, Igarashi P, Aronson PS.

Am J Physiol. 1993 Nov;265(5 Pt 2):F736-42.

PMID:
8238556

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