262 related articles for article (PubMed ID: 8567957)
21. [Polymorphism analysis of G199A, Ncol in ANK1 and Memphis I in SLC4A1 genes in Mexican healthy individuals and subjects affected with hereditary spherocytosis].
Camacho-Torres AL; Sánchez-López JY; Mesa-Cornejo VM; Ibarra B; Perea-Díaz FJ
Gac Med Mex; 2006; 142(5):435-7. PubMed ID: 17128827
[TBL] [Abstract][Full Text] [Related]
22. Partial pyruvate kinase deficiency aggravates the phenotypic expression of band 3 deficiency in a family with hereditary spherocytosis.
van Zwieten R; van Oirschot BA; Veldthuis M; Dobbe JG; Streekstra GJ; van Solinge WW; Schutgens RE; van Wijk R
Am J Hematol; 2015 Mar; 90(3):E35-9. PubMed ID: 25388786
[TBL] [Abstract][Full Text] [Related]
23. Uniquely higher incidence of isolated or combined deficiency of band 3 and/or band 4.2 as the pathogenesis of autosomal dominantly inherited hereditary spherocytosis in the Japanese population.
Inoue T; Kanzaki A; Yawata A; Wada H; Okamoto N; Takahashi M; Sugihara T; Yamada O; Yawata Y
Int J Hematol; 1994 Dec; 60(4):227-38. PubMed ID: 7894027
[TBL] [Abstract][Full Text] [Related]
24. [Hereditary spherocytosis: one year study of erythrocyte membrane proteins].
Tshilolo L; Kagambega F; Sztern B; Vertongen F; Gulbis B
Rev Med Brux; 1998 Oct; 19(5 Pt 1):417-23. PubMed ID: 9844481
[TBL] [Abstract][Full Text] [Related]
25. A variant of the EPB3 gene of the anti-Lepore type in hereditary spherocytosis.
Bianchi P; Zanella A; Alloisio N; Barosi G; Bredi E; Pelissero G; Zappa M; Vercellati C; Baronciani L; Delaunay J; Sirchia G
Br J Haematol; 1997 Aug; 98(2):283-8. PubMed ID: 9266920
[TBL] [Abstract][Full Text] [Related]
26. Band 3 mutations, renal tubular acidosis and South-East Asian ovalocytosis in Malaysia and Papua New Guinea: loss of up to 95% band 3 transport in red cells.
Bruce LJ; Wrong O; Toye AM; Young MT; Ogle G; Ismail Z; Sinha AK; McMaster P; Hwaihwanje I; Nash GB; Hart S; Lavu E; Palmer R; Othman A; Unwin RJ; Tanner MJ
Biochem J; 2000 Aug; 350 Pt 1(Pt 1):41-51. PubMed ID: 10926824
[TBL] [Abstract][Full Text] [Related]
27. Band 3 Cape Town (E90K) causes severe hereditary spherocytosis in combination with band 3 Prague III.
Bracher NA; Lyons CA; Wessels G; Mansvelt E; Coetzer TL
Br J Haematol; 2001 Jun; 113(3):689-93. PubMed ID: 11380459
[TBL] [Abstract][Full Text] [Related]
28. 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]
29. 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]
30. Alport syndrome. Molecular genetic aspects.
Hertz JM
Dan Med Bull; 2009 Aug; 56(3):105-52. PubMed ID: 19728970
[TBL] [Abstract][Full Text] [Related]
31. [Erythrocyte membrane and hereditary spherocytosis].
Ideguchi H
Rinsho Byori; 1990 Apr; 38(4):360-4. PubMed ID: 2195190
[TBL] [Abstract][Full Text] [Related]
32. Hereditary spherocytosis due to band 3 deficiency: 15 novel mutations in SLC4A1.
Van Zwieten R; François JJ; Van Leeuwen K; Van Wesel AC; Van Bruggen R; Van Solinge WW; Roos D; Verhoeven AJ; Van Wijk R
Am J Hematol; 2013 Feb; 88(2):159-60. PubMed ID: 23255290
[No Abstract] [Full Text] [Related]
33. Membrane protein band 3 alteration associated with neurologic disease and tissue-reactive antibodies.
Kay MM; Goodman J; Goodman S; Lawrence C
Exp Clin Immunogenet; 1990; 7(3):181-99. PubMed ID: 2383405
[TBL] [Abstract][Full Text] [Related]
34. Hereditary spherocytosis: identification of several HS families with ankyrin and band 3 deficiency in a population of southwestern Poland.
Bogusławska DM; Heger E; Chorzalska A; Nierzwicka M; Hołojda J; Swiderska A; Straburzyńska A; Paździor G; Langner M; Sikorski AF
Ann Hematol; 2004 Jan; 83(1):28-33. PubMed ID: 14517693
[TBL] [Abstract][Full Text] [Related]
35. Band 3 Chur: a variant associated with band 3-deficient hereditary spherocytosis and substitution in a highly conserved position of transmembrane segment 11.
Maillet P; Vallier A; Reinhart WH; Wyss EJ; Ott P; Texier P; Baklouti F; Tanner MJ; Delaunay J; Alloisio N
Br J Haematol; 1995 Dec; 91(4):804-10. PubMed ID: 8547122
[TBL] [Abstract][Full Text] [Related]
36. Association of hereditary spherocytosis with familial adenomatous polyposis in a pedigree: a new syndrome or coincidence?
Hirata K; Matsumoto K; Gondo K; Matsuzaki K; Akahane K; Higure A; Nakayama Y; Okamoto K; Konishi T; Nagata N; Itoh H
J Gastroenterol; 2003; 38(1):79-81. PubMed ID: 12560926
[TBL] [Abstract][Full Text] [Related]
37. Defects in processing and trafficking of the AE1 Cl-/HCO3- exchanger associated with inherited distal renal tubular acidosis.
Shayakul C; Alper SL
Clin Exp Nephrol; 2004 Mar; 8(1):1-11. PubMed ID: 15067510
[TBL] [Abstract][Full Text] [Related]
38. Hematologically important mutations: ankyrin variants in hereditary spherocytosis.
Gallagher PG
Blood Cells Mol Dis; 2005; 35(3):345-7. PubMed ID: 16223590
[TBL] [Abstract][Full Text] [Related]
39. Erythrocyte-specific overproduction of adenosine deaminase: molecular genetic studies.
Chottiner EG; Gribbin TE; Ginsburg D; Mitchell BS
Prog Clin Biol Res; 1989; 319():55-64; discussion 65-8. PubMed ID: 2622927
[TBL] [Abstract][Full Text] [Related]
40. A de novo band 3 mutation in hereditary spherocytosis.
Bogardus HH; Maksimova YD; Forget BG; Gallagher PG
Pediatr Blood Cancer; 2012 Jun; 58(6):1004. PubMed ID: 22170767
[No Abstract] [Full Text] [Related]
[Previous] [Next] [New Search]