These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
164 related articles for article (PubMed ID: 12183387)
61. Membrane skeleton hyperstability due to a novel alternatively spliced 4.1R can account for ellipsoidal camelid red cells with decreased deformability. Chen Y; Miyazono K; Otsuka Y; Kanamori M; Yamashita A; Arashiki N; Matsumoto T; Takada K; Sato K; Mohandas N; Inaba M J Biol Chem; 2023 Feb; 299(2):102877. PubMed ID: 36621628 [TBL] [Abstract][Full Text] [Related]
62. Molecular analysis of insertion/deletion mutations in protein 4.1 in elliptocytosis. II. Determination of molecular genetic origins of rearrangements. Conboy J; Marchesi S; Kim R; Agre P; Kan YW; Mohandas N J Clin Invest; 1990 Aug; 86(2):524-30. PubMed ID: 2384598 [TBL] [Abstract][Full Text] [Related]
63. Gene disruption of dematin causes precipitous loss of erythrocyte membrane stability and severe hemolytic anemia. Lu Y; Hanada T; Fujiwara Y; Nwankwo JO; Wieschhaus AJ; Hartwig J; Huang S; Han J; Chishti AH Blood; 2016 Jul; 128(1):93-103. PubMed ID: 27073223 [TBL] [Abstract][Full Text] [Related]
64. [Molecular interactions of membrane proteins and erythrocyte deformability]. Boivin P Pathol Biol (Paris); 1984 Jun; 32(6):717-35. PubMed ID: 6235477 [TBL] [Abstract][Full Text] [Related]
65. Possible roles for the membrane cytoskeleton in regulating red cell stability and deformability. Shohet SB Scand J Clin Lab Invest Suppl; 1981; 156():123-30. PubMed ID: 6459641 [TBL] [Abstract][Full Text] [Related]
67. Band 4.2 Komatsu: 523 GAT-->TAT (175 Asp-->Tyr) in exon 4 of the band 4.2 gene associated with total deficiency of band 4.2, hemolytic anemia with ovalostomatocytosis and marked disruption of the cytoskeletal network. Kanzaki A; Yawata Y; Yawata A; Inoue T; Okamoto N; Wada H; Harano T; Harano K; Wilmotte R; Hayette S Int J Hematol; 1995 Jun; 61(4):165-78. PubMed ID: 8547605 [TBL] [Abstract][Full Text] [Related]
68. [Disorders of the membrane skeleton of erythrocytes in hereditary spherocytosis and elliptocytosis: significance of the molecular defect for pathogenesis and clinical severity]. Eber SW Klin Padiatr; 1991; 203(4):284-95. PubMed ID: 1942935 [TBL] [Abstract][Full Text] [Related]
69. What do mouse gene knockouts tell us about the structure and function of the red cell membrane? Mohandas N; Gascard P Baillieres Best Pract Res Clin Haematol; 1999 Dec; 12(4):605-20. PubMed ID: 10895255 [TBL] [Abstract][Full Text] [Related]
70. A nonsense mutation in zebrafish gata1 causes the bloodless phenotype in vlad tepes. Lyons SE; Lawson ND; Lei L; Bennett PE; Weinstein BM; Liu PP Proc Natl Acad Sci U S A; 2002 Apr; 99(8):5454-9. PubMed ID: 11960002 [TBL] [Abstract][Full Text] [Related]
71. Functional characterization of spectrin-actin-binding domains in 4.1 family of proteins. Gimm JA; An X; Nunomura W; Mohandas N Biochemistry; 2002 Jun; 41(23):7275-82. PubMed ID: 12044158 [TBL] [Abstract][Full Text] [Related]
72. Red cell membrane alteration involving protein 4.1 and protein 3 in a case of recessively inherited haemolytic anaemia. Morlé L; Pothier B; Alloisio N; Ducluzeau MT; Marques S; Olim G; Martins e Silva J; Féo C; Garbarz M; Chaveroche I Eur J Haematol; 1987 May; 38(5):447-55. PubMed ID: 3653367 [TBL] [Abstract][Full Text] [Related]
73. [Molecular pathology of the erythrocyte membrane. Erythrocyte membrane defects as a cause of congenital hemolytic anemia]. Schröter W; Eber SW Monatsschr Kinderheilkd; 1989 Jul; 137(7):368-79. PubMed ID: 2677683 [TBL] [Abstract][Full Text] [Related]
74. The molecular basis of disorders of the red cell membrane. McMullin MF J Clin Pathol; 1999 Apr; 52(4):245-8. PubMed ID: 10474512 [No Abstract] [Full Text] [Related]
75. Protein 4.1R-dependent multiprotein complex: new insights into the structural organization of the red blood cell membrane. Salomao M; Zhang X; Yang Y; Lee S; Hartwig JH; Chasis JA; Mohandas N; An X Proc Natl Acad Sci U S A; 2008 Jun; 105(23):8026-31. PubMed ID: 18524950 [TBL] [Abstract][Full Text] [Related]
76. A deep intronic mutation in the ankyrin-1 gene causes diminished protein expression resulting in hemolytic anemia in mice. Huang H; Zhao P; Arimatsu K; Tabeta K; Yamazaki K; Krieg L; Fu E; Zhang T; Du X G3 (Bethesda); 2013 Oct; 3(10):1687-95. PubMed ID: 23934996 [TBL] [Abstract][Full Text] [Related]
77. 4.1R proteins associate with interphase microtubules in human T cells: a 4.1R constitutive region is involved in tubulin binding. Pérez-Ferreiro CM; Luque CM; Correas I J Biol Chem; 2001 Nov; 276(48):44785-91. PubMed ID: 11579097 [TBL] [Abstract][Full Text] [Related]
78. Beta spectrin kissimmee: a spectrin variant associated with autosomal dominant hereditary spherocytosis and defective binding to protein 4.1. Becker PS; Tse WT; Lux SE; Forget BG J Clin Invest; 1993 Aug; 92(2):612-6. PubMed ID: 8102379 [TBL] [Abstract][Full Text] [Related]
79. Molecular cloning and characterization of dystrophin and Dp71, two products of the Duchenne Muscular Dystrophy gene, in zebrafish. Bolaños-Jiménez F; Bordais A; Behra M; Strähle U; Mornet D; Sahel J; Rendón A Gene; 2001 Aug; 274(1-2):217-26. PubMed ID: 11675014 [TBL] [Abstract][Full Text] [Related]
80. Expression of specific isoforms of protein 4.1 in erythroid and non-erythroid tissues. Tang TK; Leto TL; Marchesi VT; Benz EJ Adv Exp Med Biol; 1988; 241():81-95. PubMed ID: 3223413 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]