94 related articles for article (PubMed ID: 10352215)
21. Immunohistochemical comparison of a case of inherited distal renal tubular acidosis (with a unique AE1 mutation) with an acquired case secondary to autoimmune disease.
Walsh S; Turner CM; Toye A; Wagner C; Jaeger P; Laing C; Unwin R
Nephrol Dial Transplant; 2007 Mar; 22(3):807-12. PubMed ID: 17205967
[No Abstract] [Full Text] [Related]
22. 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]
23. Molecular basis of proximal renal tubular acidosis.
Igarashi T; Sekine T; Watanabe H
J Nephrol; 2002; 15 Suppl 5():S135-41. PubMed ID: 12027212
[TBL] [Abstract][Full Text] [Related]
24. A Novel Compound Heterozygous Mutation in SLC4A1 Gene Causing Severe Hereditary Spherocytosis and Distal Renal Tubular Acidosis.
Tang X; Guo X; Gao J
Indian J Pediatr; 2020 Mar; 87(3):233-234. PubMed ID: 31933135
[No Abstract] [Full Text] [Related]
25. Distal renal tubular acidosis with hereditary spherocytosis.
Sinha R; Agarwal I; Bawazir WM; Bruce LJ
Indian Pediatr; 2013 Jul; 50(7):693-5. PubMed ID: 23942433
[TBL] [Abstract][Full Text] [Related]
26. [Hereditary kidney tubular diseases].
Sasaki S
Nihon Jinzo Gakkai Shi; 2007; Suppl 50th Ann():107-11. PubMed ID: 17899836
[No Abstract] [Full Text] [Related]
27. Compound mutations in human anion exchanger 1 are associated with complete distal renal tubular acidosis and hereditary spherocytosis.
Chang YH; Shaw CF; Jian SH; Hsieh KH; Chiou YH; Lu PJ
Kidney Int; 2009 Oct; 76(7):774-83. PubMed ID: 19625994
[TBL] [Abstract][Full Text] [Related]
28. Distal renal tubular acidosis and the potassium enigma.
Batlle D; Moorthi KM; Schlueter W; Kurtzman N
Semin Nephrol; 2006 Nov; 26(6):471-8. PubMed ID: 17275585
[TBL] [Abstract][Full Text] [Related]
29. Transport enzymes and renal tubular acidosis.
Mujais SK
Semin Nephrol; 1998 Jan; 18(1):74-82. PubMed ID: 9459290
[TBL] [Abstract][Full Text] [Related]
30. 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]
31. A novel SLC4A1 mutation in a child with hereditary spherocytosis and distal renal tubular acidosis.
Giovanni Raimondo P; Ilaria P; Andrea S; Pierangela C; Fabio P; Tommaso M; Marco Z; Enrico F
Pediatr Blood Cancer; 2022 Nov; 69(11):e29729. PubMed ID: 35441494
[No Abstract] [Full Text] [Related]
32. Dominant and recessive distal renal tubular acidosis mutations of kidney anion exchanger 1 induce distinct trafficking defects in MDCK cells.
Cordat E; Kittanakom S; Yenchitsomanus PT; Li J; Du K; Lukacs GL; Reithmeier RA
Traffic; 2006 Feb; 7(2):117-28. PubMed ID: 16420521
[TBL] [Abstract][Full Text] [Related]
33. Familial pure proximal renal tubular acidosis--a clinical and genetic study.
Katzir Z; Dinour D; Reznik-Wolf H; Nissenkorn A; Holtzman E
Nephrol Dial Transplant; 2008 Apr; 23(4):1211-5. PubMed ID: 17881426
[TBL] [Abstract][Full Text] [Related]
34. Severe hereditary spherocytosis and distal renal tubular acidosis associated with the total absence of band 3.
Ribeiro ML; Alloisio N; Almeida H; Gomes C; Texier P; Lemos C; Mimoso G; Morlé L; Bey-Cabet F; Rudigoz RC; Delaunay J; Tamagnini G
Blood; 2000 Aug; 96(4):1602-4. PubMed ID: 10942416
[TBL] [Abstract][Full Text] [Related]
35. The red blood cell band 3 variant (band 3Biceêtrel:R490C) associated with dominant hereditary spherocytosis causes defective membrane targeting of the molecule and a dominant negative effect.
Dhermy D; Burnier O; Bourgeois M; Grandchamp B
Mol Membr Biol; 1999; 16(4):305-12. PubMed ID: 10766130
[TBL] [Abstract][Full Text] [Related]
36. Vacuolar H+ -ATPase B1 subunit mutations that cause inherited distal renal tubular acidosis affect proton pump assembly and trafficking in inner medullary collecting duct cells.
Yang Q; Li G; Singh SK; Alexander EA; Schwartz JH
J Am Soc Nephrol; 2006 Jul; 17(7):1858-66. PubMed ID: 16769747
[TBL] [Abstract][Full Text] [Related]
37. 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]
38. The AE gene family of Cl/HCO3- exchangers.
Alper SL; Darman RB; Chernova MN; Dahl NK
J Nephrol; 2002; 15 Suppl 5():S41-53. PubMed ID: 12027221
[TBL] [Abstract][Full Text] [Related]
39. 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]
40. Kidney collecting duct acid-base "regulon".
Cheval L; Morla L; Elalouf JM; Doucet A
Physiol Genomics; 2006 Nov; 27(3):271-81. PubMed ID: 16868073
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
