213 related articles for article (PubMed ID: 21039340)
1. Protein 4.2 interaction with hereditary spherocytosis mutants of the cytoplasmic domain of human anion exchanger 1.
Bustos SP; Reithmeier RA
Biochem J; 2011 Jan; 433(2):313-22. PubMed ID: 21039340
[TBL] [Abstract][Full Text] [Related]
2. Structure and stability of hereditary spherocytosis mutants of the cytosolic domain of the erythrocyte anion exchanger 1 protein.
Bustos SP; Reithmeier RA
Biochemistry; 2006 Jan; 45(3):1026-34. PubMed ID: 16411779
[TBL] [Abstract][Full Text] [Related]
3. Ubiquitylation-independent ER-associated degradation of an AE1 mutant associated with dominant hereditary spherocytosis in cattle.
Ito D; Koshino I; Arashiki N; Adachi H; Tomihari M; Tamahara S; Kurogi K; Amano T; Ono K; Inaba M
J Cell Sci; 2006 Sep; 119(Pt 17):3602-12. PubMed ID: 16912075
[TBL] [Abstract][Full Text] [Related]
4. Trafficking defects of the Southeast Asian ovalocytosis deletion mutant of anion exchanger 1 membrane proteins.
Cheung JC; Cordat E; Reithmeier RA
Biochem J; 2005 Dec; 392(Pt 3):425-34. PubMed ID: 16107207
[TBL] [Abstract][Full Text] [Related]
5. Dominant-negative effect of Southeast Asian ovalocytosis anion exchanger 1 in compound heterozygous distal renal tubular acidosis.
Kittanakom S; Cordat E; Reithmeier RA
Biochem J; 2008 Mar; 410(2):271-81. PubMed ID: 17941824
[TBL] [Abstract][Full Text] [Related]
6. Trafficking defect of mutant kidney anion exchanger 1 (kAE1) proteins associated with distal renal tubular acidosis and Southeast Asian ovalocytosis.
Sawasdee N; Udomchaiprasertkul W; Noisakran S; Rungroj N; Akkarapatumwong V; Yenchitsomanus PT
Biochem Biophys Res Commun; 2006 Nov; 350(3):723-30. PubMed ID: 17027918
[TBL] [Abstract][Full Text] [Related]
7. Impaired trafficking of human kidney anion exchanger (kAE1) caused by hetero-oligomer formation with a truncated mutant associated with distal renal tubular acidosis.
Quilty JA; Cordat E; Reithmeier RA
Biochem J; 2002 Dec; 368(Pt 3):895-903. PubMed ID: 12227829
[TBL] [Abstract][Full Text] [Related]
8. Lumenal localization in the endoplasmic reticulum of the C-terminal tail of an AE1 mutant responsible for hereditary spherocytosis in cattle.
Ito D; Otsuka Y; Koshino I; Inaba M
Jpn J Vet Res; 2007 Feb; 54(4):191-7. PubMed ID: 17405356
[TBL] [Abstract][Full Text] [Related]
9. Human kanadaptin and kidney anion exchanger 1 (kAE1) do not interact in transfected HEK 293 cells.
Kittanakom S; Keskanokwong T; Akkarapatumwong V; Yenchitsomanus PT; Reithmeier RA
Mol Membr Biol; 2004; 21(6):395-402. PubMed ID: 15764369
[TBL] [Abstract][Full Text] [Related]
10. Expression and interaction of two compound heterozygous distal renal tubular acidosis mutants of kidney anion exchanger 1 in epithelial cells.
Cordat E; Reithmeier RA
Am J Physiol Renal Physiol; 2006 Dec; 291(6):F1354-61. PubMed ID: 16849697
[TBL] [Abstract][Full Text] [Related]
11. Trafficking and folding defects in hereditary spherocytosis mutants of the human red cell anion exchanger.
Quilty JA; Reithmeier RA
Traffic; 2000 Dec; 1(12):987-98. PubMed ID: 11208088
[TBL] [Abstract][Full Text] [Related]
12. Impaired trafficking of distal renal tubular acidosis mutants of the human kidney anion exchanger kAE1.
Quilty JA; Li J; Reithmeier RA
Am J Physiol Renal Physiol; 2002 May; 282(5):F810-20. PubMed ID: 11934690
[TBL] [Abstract][Full Text] [Related]
13. Interaction of anion exchanger 1 and glycophorin A in human erythroleukaemic K562 cells.
Pang AJ; Reithmeier RA
Biochem J; 2009 Jul; 421(3):345-56. PubMed ID: 19438409
[TBL] [Abstract][Full Text] [Related]
14. Band 3 Edmonton I, a novel mutant of the anion exchanger 1 causing spherocytosis and distal renal tubular acidosis.
Chu C; Woods N; Sawasdee N; Guizouarn H; Pellissier B; Borgese F; Yenchitsomanus PT; Gowrishankar M; Cordat E
Biochem J; 2010 Feb; 426(3):379-88. PubMed ID: 20028337
[TBL] [Abstract][Full Text] [Related]
15. Regions of human kidney anion exchanger 1 (kAE1) required for basolateral targeting of kAE1 in polarised kidney cells: mis-targeting explains dominant renal tubular acidosis (dRTA).
Toye AM; Banting G; Tanner MJ
J Cell Sci; 2004 Mar; 117(Pt 8):1399-410. PubMed ID: 14996906
[TBL] [Abstract][Full Text] [Related]
16. Impaired trafficking and intracellular retention of mutant kidney anion exchanger 1 proteins (G701D and A858D) associated with distal renal tubular acidosis.
Ungsupravate D; Sawasdee N; Khositseth S; Udomchaiprasertkul W; Khoprasert S; Li J; Reithmeier RA; Yenchitsomanus PT
Mol Membr Biol; 2010 Apr; 27(2-3):92-103. PubMed ID: 20151848
[TBL] [Abstract][Full Text] [Related]
17. Molecular physiology of SLC4 anion exchangers.
Alper SL
Exp Physiol; 2006 Jan; 91(1):153-61. PubMed ID: 16239253
[TBL] [Abstract][Full Text] [Related]
18. [Band 3 deficiency as a cause of hereditary spherocytosis].
Wada H; Suemori S; Nakanishi H; Sugihara T
Rinsho Ketsueki; 2015 Jul; 56(7):837-45. PubMed ID: 26251147
[TBL] [Abstract][Full Text] [Related]
19. Structural characterization of the cytosolic domain of kidney chloride/bicarbonate anion exchanger 1 (kAE1).
Pang AJ; Bustos SP; Reithmeier RA
Biochemistry; 2008 Apr; 47(15):4510-7. PubMed ID: 18358003
[TBL] [Abstract][Full Text] [Related]
20. Glycophorin A: Band 3 aid.
Williamson RC; Toye AM
Blood Cells Mol Dis; 2008; 41(1):35-43. PubMed ID: 18304844
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
