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Results: 1 to 20 of 120

Similar articles for PubMed (Select 21209359)

1.

Functional characterization and modified rescue of novel AE1 mutation R730C associated with overhydrated cation leak stomatocytosis.

Stewart AK, Kedar PS, Shmukler BE, Vandorpe DH, Hsu A, Glader B, Rivera A, Brugnara C, Alper SL.

Am J Physiol Cell Physiol. 2011 May;300(5):C1034-46. doi: 10.1152/ajpcell.00447.2010. Epub 2011 Jan 5.

2.

The GPA-dependent, spherostomatocytosis mutant AE1 E758K induces GPA-independent, endogenous cation transport in amphibian oocytes.

Stewart AK, Vandorpe DH, Heneghan JF, Chebib F, Stolpe K, Akhavein A, Edelman EJ, Maksimova Y, Gallagher PG, Alper SL.

Am J Physiol Cell Physiol. 2010 Feb;298(2):C283-97. doi: 10.1152/ajpcell.00444.2009. Epub 2009 Nov 11.

3.

Rapid Cl⁻/HCO⁻₃exchange kinetics of AE1 in HEK293 cells and hereditary stomatocytosis red blood cells.

Frumence E, Genetet S, Ripoche P, Iolascon A, Andolfo I, Le Van Kim C, Colin Y, Mouro-Chanteloup I, Lopez C.

Am J Physiol Cell Physiol. 2013 Sep 15;305(6):C654-62. doi: 10.1152/ajpcell.00142.2013. Epub 2013 Jul 10.

4.

Mouse Ae1 E699Q mediates SO42-i/anion-o exchange with [SO42-]i-dependent reversal of wild-type pHo sensitivity.

Chernova MN, Stewart AK, Barry PN, Jennings ML, Alper SL.

Am J Physiol Cell Physiol. 2008 Aug;295(2):C302-12. doi: 10.1152/ajpcell.00109.2008. Epub 2008 May 14.

5.

Electrogenic sulfate/chloride exchange in Xenopus oocytes mediated by murine AE1 E699Q.

Chernova MN, Jiang L, Crest M, Hand M, Vandorpe DH, Strange K, Alper SL.

J Gen Physiol. 1997 Mar;109(3):345-60.

6.

A novel erythroid anion exchange variant (Gly796Arg) of hereditary stomatocytosis associated with dyserythropoiesis.

Iolascon A, De Falco L, Borgese F, Esposito MR, Avvisati RA, Izzo P, Piscopo C, Guizouarn H, Biondani A, Pantaleo A, De Franceschi L.

Haematologica. 2009 Aug;94(8):1049-59. doi: 10.3324/haematol.2008.002873.

7.

Cation-leak stomatocytosis in standard schnauzers does not cosegregate with coding mutations in the RhAG, SLC4A1, or GLUT1 genes associated with human disease.

Shmukler BE, Rivera A, Vandorpe DH, Alves J, Bonfanti U, Paltrinieri S, Alper SL.

Blood Cells Mol Dis. 2012 Apr 15;48(4):219-25. doi: 10.1016/j.bcmd.2012.02.003. Epub 2012 Mar 9.

8.

Loss-of-function and gain-of-function phenotypes of stomatocytosis mutant RhAG F65S.

Stewart AK, Shmukler BE, Vandorpe DH, Rivera A, Heneghan JF, Li X, Hsu A, Karpatkin M, O'Neill AF, Bauer DE, Heeney MM, John K, Kuypers FA, Gallagher PG, Lux SE, Brugnara C, Westhoff CM, Alper SL.

Am J Physiol Cell Physiol. 2011 Dec;301(6):C1325-43. doi: 10.1152/ajpcell.00054.2011. Epub 2011 Aug 17.

9.

Cation transport activity of anion exchanger 1 mutations found in inherited distal renal tubular acidosis.

Walsh S, Borgese F, Gabillat N, Unwin R, Guizouarn H.

Am J Physiol Renal Physiol. 2008 Aug;295(2):F343-50. doi: 10.1152/ajprenal.00587.2007. Epub 2008 Jun 4.

10.

Novel AE1 mutations in recessive distal renal tubular acidosis. Loss-of-function is rescued by glycophorin A.

Tanphaichitr VS, Sumboonnanonda A, Ideguchi H, Shayakul C, Brugnara C, Takao M, Veerakul G, Alper SL.

J Clin Invest. 1998 Dec 15;102(12):2173-9.

11.

Interactions of mouse glycophorin A with the dRTA-related mutant G719D of the mouse Cl-/HCO3- exchanger Ae1.

Stewart AK, Chebib FT, Akbar SW, Salas MJ, Sonik RA, Shmukler BE, Alper SL.

Biochem Cell Biol. 2011 Apr;89(2):224-35. doi: 10.1139/o10-147.

PMID:
21455273
12.

Autosomal dominant distal renal tubular acidosis is associated in three families with heterozygosity for the R589H mutation in the AE1 (band 3) Cl-/HCO3- exchanger.

Jarolim P, Shayakul C, Prabakaran D, Jiang L, Stuart-Tilley A, Rubin HL, Simova S, Zavadil J, Herrin JT, Brouillette J, Somers MJ, Seemanova E, Brugnara C, Guay-Woodford LM, Alper SL.

J Biol Chem. 1998 Mar 13;273(11):6380-8.

13.

Multiple transport functions of a red blood cell anion exchanger, tAE1: its role in cell volume regulation.

Guizouarn H, Gabillat N, Motais R, Borgese F.

J Physiol. 2001 Sep 1;535(Pt 2):497-506.

14.

Monovalent cation leaks in human red cells caused by single amino-acid substitutions in the transport domain of the band 3 chloride-bicarbonate exchanger, AE1.

Bruce LJ, Robinson HC, Guizouarn H, Borgese F, Harrison P, King MJ, Goede JS, Coles SE, Gore DM, Lutz HU, Ficarella R, Layton DM, Iolascon A, Ellory JC, Stewart GW.

Nat Genet. 2005 Nov;37(11):1258-63. Epub 2005 Oct 9.

PMID:
16227998
15.

Deficient HCO3- transport in an AE1 mutant with normal Cl- transport can be rescued by carbonic anhydrase II presented on an adjacent AE1 protomer.

Dahl NK, Jiang L, Chernova MN, Stuart-Tilley AK, Shmukler BE, Alper SL.

J Biol Chem. 2003 Nov 7;278(45):44949-58. Epub 2003 Aug 21.

16.

Reduced DIDS-sensitive chloride conductance in Ae1-/- mouse erythrocytes.

Alper SL, Vandorpe DH, Peters LL, Brugnara C.

Blood Cells Mol Dis. 2008 Jul-Aug;41(1):22-34. doi: 10.1016/j.bcmd.2008.01.002. Epub 2008 Mar 10.

17.

Role of nonconserved charged residues of the AE2 transmembrane domain in regulation of anion exchange by pH.

Stewart AK, Kurschat CE, Alper SL.

Pflugers Arch. 2007 Jun;454(3):373-84. Epub 2007 Feb 16.

PMID:
17492309
18.

The substrate anion selectivity filter in the human erythrocyte Cl-/HCO3- exchange protein, AE1.

Zhu Q, Casey JR.

J Biol Chem. 2004 May 28;279(22):23565-73. Epub 2004 Mar 24.

19.

Pig reticulocytes. V. Development of Rb+ influx during in vitro maturation.

Lauf PK, Zeidler RB, Kim HD.

J Cell Physiol. 1984 Nov;121(2):284-90.

PMID:
6490727
20.
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