335 related articles for article (PubMed ID: 8640229)
21. Ankyrin gene mutations in japanese patients with hereditary spherocytosis.
Nakanishi H; Kanzaki A; Yawata A; Yamada O; Yawata Y
Int J Hematol; 2001 Jan; 73(1):54-63. PubMed ID: 11372755
[TBL] [Abstract][Full Text] [Related]
22. [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]
23. Hereditary spherocytosis--defects in proteins that connect the membrane skeleton to the lipid bilayer.
Eber S; Lux SE
Semin Hematol; 2004 Apr; 41(2):118-41. PubMed ID: 15071790
[TBL] [Abstract][Full Text] [Related]
24. Characterization of the underlying molecular defect in hereditary spherocytosis associated with spectrin deficiency.
Hassoun H; Vassiliadis JN; Murray J; Njolstad PR; Rogus JJ; Ballas SK; Schaffer F; Jarolim P; Brabec V; Palek J
Blood; 1997 Jul; 90(1):398-406. PubMed ID: 9207476
[TBL] [Abstract][Full Text] [Related]
25. Hereditary spherocytosis and related disorders.
Becker PS; Lux SE
Clin Haematol; 1985 Feb; 14(1):15-43. PubMed ID: 3886234
[TBL] [Abstract][Full Text] [Related]
26. Characterization of 13 novel band 3 gene defects in hereditary spherocytosis with band 3 deficiency.
Jarolim P; Murray JL; Rubin HL; Taylor WM; Prchal JT; Ballas SK; Snyder LM; Chrobak L; Melrose WD; Brabec V; Palek J
Blood; 1996 Dec; 88(11):4366-74. PubMed ID: 8943874
[TBL] [Abstract][Full Text] [Related]
27. Ankyrin deficiency is the most common defect in dominant and non dominant hereditary spherocytosis.
Lanciotti M; Perutelli P; Valetto A; Di Martino D; Mori PG
Haematologica; 1997; 82(4):460-2. PubMed ID: 9299863
[No Abstract] [Full Text] [Related]
28. Defective anion transport and marked spherocytosis with membrane instability caused by hereditary total deficiency of red cell band 3 in cattle due to a nonsense mutation.
Inaba M; Yawata A; Koshino I; Sato K; Takeuchi M; Takakuwa Y; Manno S; Yawata Y; Kanzaki A; Sakai J; Ban A; Ono K; Maede Y
J Clin Invest; 1996 Apr; 97(8):1804-17. PubMed ID: 8621763
[TBL] [Abstract][Full Text] [Related]
29. Apparently normal ankyrin content in unsplenectomized hereditary spherocytosis patients with the inactivation of one ankyrin (ANK1) allele.
Miraglia del Giudice E; Francese M; Polito R; Nobili B; Iolascon A; Perrotta S
Haematologica; 1997; 82(3):332-3. PubMed ID: 9234582
[TBL] [Abstract][Full Text] [Related]
30. Linkage of dominant hereditary spherocytosis to the gene for the erythrocyte membrane-skeleton protein ankyrin.
Costa FF; Agre P; Watkins PC; Winkelmann JC; Tang TK; John KM; Lux SE; Forget BG
N Engl J Med; 1990 Oct; 323(15):1046-50. PubMed ID: 1977081
[No Abstract] [Full Text] [Related]
31. Combined spectrin and ankyrin deficiency is common in autosomal dominant hereditary spherocytosis.
Savvides P; Shalev O; John KM; Lux SE
Blood; 1993 Nov; 82(10):2953-60. PubMed ID: 8219186
[TBL] [Abstract][Full Text] [Related]
32. Band 3 and its alterations in health and disease.
Kay MM
Cell Mol Biol (Noisy-le-grand); 2004 Mar; 50(2):117-38. PubMed ID: 15095783
[TBL] [Abstract][Full Text] [Related]
33. Comparison of the ankyrin (AC)n microsatellites in genomic DNA and mRNA reveals absence of one ankyrin mRNA allele in 20% of patients with hereditary spherocytosis.
Jarolim P; Rubin HL; Brabec V; Palek J
Blood; 1995 Jun; 85(11):3278-82. PubMed ID: 7756660
[TBL] [Abstract][Full Text] [Related]
34. Heterogenous band 3 deficiency in hereditary spherocytosis related to different band 3 gene defects.
Dhermy D; Galand C; Bournier O; Boulanger L; Cynober T; Schismanoff PO; Bursaux E; Tchernia G; Boivin P; Garbarz M
Br J Haematol; 1997 Jul; 98(1):32-40. PubMed ID: 9233560
[TBL] [Abstract][Full Text] [Related]
35. Simultaneous (AC)n microsatellite polymorphism analysis and single-stranded conformation polymorphism screening is an efficient strategy for detecting ankyrin-1 mutations in dominant hereditary spherocytosis.
Ozcan R; Jarolim P; Lux SE; Ungewickell E; Eber SW
Br J Haematol; 2003 Aug; 122(4):669-77. PubMed ID: 12899723
[TBL] [Abstract][Full Text] [Related]
36. [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]
37. Hematologically important mutations: spectrin and ankyrin variants in hereditary spherocytosis.
Gallagher PG; Forget BG
Blood Cells Mol Dis; 1998 Dec; 24(4):539-43. PubMed ID: 9887280
[No Abstract] [Full Text] [Related]
38. A recurrent frameshift mutation of the ankyrin gene associated with severe hereditary spherocytosis.
Gallagher PG; Ferreira JD; Costa FF; Saad ST; Forget BG
Br J Haematol; 2000 Dec; 111(4):1190-3. PubMed ID: 11167760
[TBL] [Abstract][Full Text] [Related]
39. Alport syndrome. Molecular genetic aspects.
Hertz JM
Dan Med Bull; 2009 Aug; 56(3):105-52. PubMed ID: 19728970
[TBL] [Abstract][Full Text] [Related]
40. Ankyrin-linked hereditary spherocytosis in an African-American kindred.
Sangerman J; Maksimova Y; Edelman EJ; Morrow JS; Forget BG; Gallagher PG
Am J Hematol; 2008 Oct; 83(10):789-94. PubMed ID: 18704959
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
