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91 related items for PubMed ID: 10462704
21. Cellular dehydration and immunoglobulin binding in senescent neonatal erythrocytes. Lane PA, Galili U, Iarocci TA, Shew RL, Mentzer WC. Pediatr Res; 1988 Mar; 23(3):288-92. PubMed ID: 3353175 [Abstract] [Full Text] [Related]
22. Surface ultrastructure of pyruvate kinase-deficient erythrocytes in the Basenji dog. Chandler FW, Prasse KW, Callaway CS. Am J Vet Res; 1975 Oct; 36(10):1477-80. PubMed ID: 1190589 [Abstract] [Full Text] [Related]
23. Association of lipid peroxidation and polymerization of membrane proteins with erythrocyte aging. Hochstein P, Jain SK. Fed Proc; 1981 Feb; 40(2):183-8. PubMed ID: 6257558 [Abstract] [Full Text] [Related]
25. Molecular cloning and expression of a chloride channel-associated protein pICln in human young red blood cells: association with actin. Schwartz RS, Rybicki AC, Nagel RL. Biochem J; 1997 Oct 15; 327 ( Pt 2)(Pt 2):609-16. PubMed ID: 9359436 [Abstract] [Full Text] [Related]
26. Erythrocyte age-dependent changes of membrane protein 4.1: studies in transient erythroblastopenia. Ravindranath Y, Brohn F, Johnson RM. Pediatr Res; 1987 Mar 15; 21(3):275-8. PubMed ID: 3104874 [Abstract] [Full Text] [Related]
27. [Progress in research on red cell membrane disorders: from the genome to the postgenome era]. Yawata Y. Rinsho Ketsueki; 2001 May 15; 42(5):343-51. PubMed ID: 11452448 [No Abstract] [Full Text] [Related]
28. Differential effect of neuraminidase-treatment on the surface charge-associated properties of rat reticulocytes and erythrocytes. Studies by partitioning in two-polymer aqueous phases. Walter H, Krob EJ, Pedram A. Biochim Biophys Acta; 1983 Jun 23; 731(3):487-90. PubMed ID: 6860666 [Abstract] [Full Text] [Related]
29. Ankyrin and the hemolytic anemia mutation, nb, map to mouse chromosome 8: presence of the nb allele is associated with a truncated erythrocyte ankyrin. White RA, Birkenmeier CS, Lux SE, Barker JE. Proc Natl Acad Sci U S A; 1990 Apr 23; 87(8):3117-21. PubMed ID: 2139228 [Abstract] [Full Text] [Related]
30. An isoform-specific mutation in the protein 4.1 gene results in hereditary elliptocytosis and complete deficiency of protein 4.1 in erythrocytes but not in nonerythroid cells. Conboy JG, Chasis JA, Winardi R, Tchernia G, Kan YW, Mohandas N. J Clin Invest; 1993 Jan 23; 91(1):77-82. PubMed ID: 8423235 [Abstract] [Full Text] [Related]
33. Monitoring of an experimental red blood cell pathology with gravitational field-flow fractionation. Merino-Dugay A, Cardot PJ, Czok M, Guernet M, Andreux JP. J Chromatogr; 1992 Aug 07; 579(1):73-83. PubMed ID: 1447352 [Abstract] [Full Text] [Related]
34. The "b" mutated gene in heterozygous Belgrade anemic rat. Popović ZB, Rajić NV, Savković SD, Glisin VR. Exp Hematol; 1993 Jan 07; 21(1):21-4. PubMed ID: 8417956 [Abstract] [Full Text] [Related]
35. Increased adsorption of cytoplasmic proteins to the erythrocyte membrane in ATP-depleted normal and pyruvate kinase-deficient mature cells and reticulocytes. Allen DW, Groat JD, Finkel B, Rank BH, Wood PA, Eaton JW. Am J Hematol; 1983 Feb 07; 14(1):11-25. PubMed ID: 6837565 [Abstract] [Full Text] [Related]
36. Evidence for and consequences of chronic heme deficiency in Belgrade rat reticulocytes. Garrick MD, Scott D, Kulju D, Romano MA, Dolan KG, Garrick LM. Biochim Biophys Acta; 1999 Mar 08; 1449(2):125-36. PubMed ID: 10082971 [Abstract] [Full Text] [Related]
37. Folate activity in reticulocytes and the incorporation of triated pteroylglutamic acid into red cells. Izak G, Rachmilewitz M, Grossowicz N, Galewski K, Kraus S. Br J Haematol; 1968 Apr 08; 14(4):447-52. PubMed ID: 5689348 [No Abstract] [Full Text] [Related]