128 related articles for article (PubMed ID: 8160710)
1. Band 4.2 abnormalities in human red cells.
Yawata Y
Am J Med Sci; 1994 Mar; 307(3):190-203. PubMed ID: 8160710
[TBL] [Abstract][Full Text] [Related]
2. Red cell membrane protein band 4.2: phenotypic, genetic and electron microscopic aspects.
Yawata Y
Biochim Biophys Acta; 1994 Feb; 1204(2):131-48. PubMed ID: 8142452
[TBL] [Abstract][Full Text] [Related]
3. Mechanical properties of the red cell membrane in relation to molecular structure and genetic defects.
Mohandas N; Evans E
Annu Rev Biophys Biomol Struct; 1994; 23():787-818. PubMed ID: 7919799
[No Abstract] [Full Text] [Related]
4. Human erythrocyte membrane protein band 4.2 (pallidin).
Cohen CM; Dotimas E; Korsgren C
Semin Hematol; 1993 Apr; 30(2):119-37. PubMed ID: 8480187
[No Abstract] [Full Text] [Related]
5. [The complete band4.2 deficiency in human red cells].
Kanzaki A; Inoue T; Wada H; Yawata Y
Nihon Rinsho; 1996 Sep; 54(9):2492-501. PubMed ID: 8890584
[TBL] [Abstract][Full Text] [Related]
6. Electron microscopic evidence of impaired intramembrane particles and instability of the cytoskeletal network in band 4.2 deficiency in human red cells.
Yawata Y; Yawata A; Kanzaki A; Inoue T; Okamoto N; Uehira K; Yasunaga M; Nakamura Y
Cell Motil Cytoskeleton; 1996; 33(2):95-105. PubMed ID: 8635206
[TBL] [Abstract][Full Text] [Related]
7. Electron microscopic and physicobiochemical studies on disorganization of the cytoskeletal network and integral protein (band 3) in red cells of band 4.2 deficiency with a mutation (codon 142: GCT-->ACT).
Inoue T; Kanzaki A; Yawata A; Tsuji A; Ata K; Okamoto N; Wada H; Higo I; Sugihara T; Yamada O
Int J Hematol; 1994 Apr; 59(3):157-75. PubMed ID: 8011986
[TBL] [Abstract][Full Text] [Related]
8. Molecular maps of red cell deformation: hidden elasticity and in situ connectivity.
Discher DE; Mohandas N; Evans EA
Science; 1994 Nov; 266(5187):1032-5. PubMed ID: 7973655
[TBL] [Abstract][Full Text] [Related]
9. [Approach of hematology. Red cell deformability and membrane protein].
Nakashima K
Rinsho Byori; 1984 Aug; 32(8):856-61. PubMed ID: 6502984
[No Abstract] [Full Text] [Related]
10. [Drug-induced severe hemolytic crisis in a patient with hemolytic hereditary elliptocytosis with complete deficiency of red cell membrane protein band 4.2].
Fukuda M; Komatsu M; Inaba R; Kanzaki A; Hashimoto M; Ikeda A; Takahara M; Yawata Y
Rinsho Ketsueki; 1988 Apr; 29(4):559-64. PubMed ID: 3404671
[No Abstract] [Full Text] [Related]
11. Clinical expression and laboratory detection of red blood cell membrane protein mutations.
Palek J; Jarolim P
Semin Hematol; 1993 Oct; 30(4):249-83. PubMed ID: 8266114
[No Abstract] [Full Text] [Related]
12. Red cell membrane disorders in the Japanese population: clinical, biochemical, electron microscopic, and genetic studies.
Yawata Y; Kanzaki A; Inoue T; Ata K; Wada H; Okamoto N; Higo I; Yawata A; Sugihara T; Yamada O
Int J Hematol; 1994 Jul; 60(1):23-38. PubMed ID: 7919236
[TBL] [Abstract][Full Text] [Related]
13. An overview about erythrocyte membrane.
de Oliveira S; Saldanha C
Clin Hemorheol Microcirc; 2010; 44(1):63-74. PubMed ID: 20134094
[TBL] [Abstract][Full Text] [Related]
14. [Application of 2 electrophoresis techniques to the analysis of erythrocyte membrane proteins in hereditary spherocytosis].
Ferrándiz F; Ródenas S; Villegas A
Sangre (Barc); 1993 Oct; 38(5):393-7. PubMed ID: 8140503
[TBL] [Abstract][Full Text] [Related]
15. [Study on the relation of human red cell membrane protein band 4.2 to red cell aging--in cases of obstructive jaundice].
Hashimoto E; Kageoka T
Rinsho Byori; 1993 Aug; 41(8):930-6. PubMed ID: 8371509
[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. 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]
18. Minor red cell surface proteins associated with red cell dysfunction.
Anstee DJ
Baillieres Clin Haematol; 1993 Jun; 6(2):445-63. PubMed ID: 8043934
[No Abstract] [Full Text] [Related]
19. Molecular pathology of inherited erythrocyte membrane disorders: hereditary spherocytosis and elliptocytosis.
Iolascon A; Miraglia del Giudice E; Camaschella C
Haematologica; 1992; 77(1):60-72. PubMed ID: 1356891
[TBL] [Abstract][Full Text] [Related]
20. Homozygous missense mutation (band 3 Fukuoka: G130R): a mild form of hereditary spherocytosis with near-normal band 3 content and minimal changes of membrane ultrastructure despite moderate protein 4.2 deficiency.
Inoue T; Kanzaki A; Kaku M; Yawata A; Takezono M; Okamoto N; Wada H; Sugihara T; Yamada O; Katayama Y; Nagata N; Yawata Y
Br J Haematol; 1998 Sep; 102(4):932-9. PubMed ID: 9734643
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
