238 related articles for article (PubMed ID: 9922149)
1. Regulation of band 3 rotational mobility by ankyrin in intact human red cells.
Cho MR; Eber SW; Liu SC; Lux SE; Golan DE
Biochemistry; 1998 Dec; 37(51):17828-35. PubMed ID: 9922149
[TBL] [Abstract][Full Text] [Related]
2. Splenectomy prolongs in vivo survival of erythrocytes differently in spectrin/ankyrin- and band 3-deficient hereditary spherocytosis.
Reliene R; Mariani M; Zanella A; Reinhart WH; Ribeiro ML; del Giudice EM; Perrotta S; Iolascon A; Eber S; Lutz HU
Blood; 2002 Sep; 100(6):2208-15. PubMed ID: 12200387
[TBL] [Abstract][Full Text] [Related]
3. [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]
4. Ankyrin-1 mutations are a major cause of dominant and recessive hereditary spherocytosis.
Eber SW; Gonzalez JM; Lux ML; Scarpa AL; Tse WT; Dornwell M; Herbers J; Kugler W; Ozcan R; Pekrun A; Gallagher PG; Schröter W; Forget BG; Lux SE
Nat Genet; 1996 Jun; 13(2):214-8. PubMed ID: 8640229
[TBL] [Abstract][Full Text] [Related]
5. Red cell membranes of ankyrin-deficient nb/nb mice lack band 3 tetramers but contain normal membrane skeletons.
Yi SJ; Liu SC; Derick LH; Murray J; Barker JE; Cho MR; Palek J; Golan DE
Biochemistry; 1997 Aug; 36(31):9596-604. PubMed ID: 9236006
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. Combined ankyrin and spectrin deficiency in hereditary spherocytosis.
Pekrun A; Eber SW; Kuhlmey A; Schröter W
Ann Hematol; 1993 Aug; 67(2):89-93. PubMed ID: 8347735
[TBL] [Abstract][Full Text] [Related]
8. Both ankyrin and band 4.1 are required to restrict the rotational mobility of band 3 in the human erythrocyte membrane.
Wyatt K; Cherry RJ
Biochim Biophys Acta; 1992 Jan; 1103(2):327-30. PubMed ID: 1531931
[TBL] [Abstract][Full Text] [Related]
9. Restriction by ankyrin of band 3 rotational mobility in human erythrocyte membranes and reconstituted lipid vesicles.
Che A; Morrison IE; Pan R; Cherry RJ
Biochemistry; 1997 Aug; 36(31):9588-95. PubMed ID: 9236005
[TBL] [Abstract][Full Text] [Related]
10. Increased rotational mobility and extractability of band 3 from protein 4.2-deficient erythrocyte membranes: evidence of a role for protein 4.2 in strengthening the band 3-cytoskeleton linkage.
Rybicki AC; Schwartz RS; Hustedt EJ; Cobb CE
Blood; 1996 Oct; 88(7):2745-53. PubMed ID: 8839871
[TBL] [Abstract][Full Text] [Related]
11. Search for the candidate genes in dominant hereditary spherocytosis using linkage analysis.
Garbarz M; Bibas D; Cynober T; Galand C; Bournier O; Devaux I; Tchernia G; Dhermy D
C R Acad Sci III; 1996 Oct; 319(10):913-9. PubMed ID: 8977772
[TBL] [Abstract][Full Text] [Related]
12. Abnormalities of erythrocyte membrane proteins in Korean patients with hereditary spherocytosis.
Lee YK; Cho HI; Park SS; Lee YJ; Ra E; Chang YH; Hur M; Shin HY; Ahn HS
J Korean Med Sci; 2000 Jun; 15(3):284-8. PubMed ID: 10895969
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. Red cell membrane protein abnormalities in hereditary spherocytosis in Brazil.
Saad ST; Costa FF; Vicentim DL; Salles TS; Pranke PH
Br J Haematol; 1994 Oct; 88(2):295-9. PubMed ID: 7803273
[TBL] [Abstract][Full Text] [Related]
15. Differential control of band 3 lateral and rotational mobility in intact red cells.
Corbett JD; Agre P; Palek J; Golan DE
J Clin Invest; 1994 Aug; 94(2):683-8. PubMed ID: 8040322
[TBL] [Abstract][Full Text] [Related]
16. Characteristic features of the genotype and phenotype of hereditary spherocytosis in the Japanese population.
Yawata Y; Kanzaki A; Yawata A; Doerfler W; Ozcan R; Eber SW
Int J Hematol; 2000 Feb; 71(2):118-35. PubMed ID: 10745622
[TBL] [Abstract][Full Text] [Related]
17. Control of band 3 lateral and rotational mobility by band 4.2 in intact erythrocytes: release of band 3 oligomers from low-affinity binding sites.
Golan DE; Corbett JD; Korsgren C; Thatte HS; Hayette S; Yawata Y; Cohen CM
Biophys J; 1996 Mar; 70(3):1534-42. PubMed ID: 8785311
[TBL] [Abstract][Full Text] [Related]
18. Hereditary spherocytosis associated with deletion of human erythrocyte ankyrin gene on chromosome 8.
Lux SE; Tse WT; Menninger JC; John KM; Harris P; Shalev O; Chilcote RR; Marchesi SL; Watkins PC; Bennett V
Nature; 1990 Jun; 345(6277):736-9. PubMed ID: 2141669
[TBL] [Abstract][Full Text] [Related]
19. Membrane cation and anion transport activities in erythrocytes of hereditary spherocytosis: effects of different membrane protein defects.
De Franceschi L; Olivieri O; Miraglia del Giudice E; Perrotta S; Sabato V; Corrocher R; Iolascon A
Am J Hematol; 1997 Jul; 55(3):121-8. PubMed ID: 9256290
[TBL] [Abstract][Full Text] [Related]
20. Severe Ankyrin-R deficiency results in impaired surface retention and lysosomal degradation of RhAG in human erythroblasts.
Satchwell TJ; Bell AJ; Hawley BR; Pellegrin S; Mordue KE; van Deursen CT; Braak NH; Huls G; Leers MP; Overwater E; Tamminga RY; van der Zwaag B; Fermo E; Bianchi P; van Wijk R; Toye AM
Haematologica; 2016 Sep; 101(9):1018-27. PubMed ID: 27247322
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]