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45. Erythrocyte membrane in myotonic dystrophy. A study with acetylcholinesterase. Igisu H; Antoku Y; Mawatari S; Kuroiwa Y J Neurol Sci; 1981 Aug; 51(2):199-205. PubMed ID: 7276973 [TBL] [Abstract][Full Text] [Related]
46. Acetylcholinesterase activity of normal and diabetic human erythrocyte membranes: the effect of oxidative agents. Krajewska E; Zavodnik I; Kluska B; Szosland K; Bryszewska M Biochem Mol Biol Int; 1997 Jun; 42(1):203-10. PubMed ID: 9192101 [TBL] [Abstract][Full Text] [Related]
47. Interaction of human red cell membrane acetylcholinesterase with phospholipids. Di Francesco C; Brodbeck U Biochim Biophys Acta; 1981 Jan; 640(1):359-64. PubMed ID: 7213691 [TBL] [Abstract][Full Text] [Related]
48. [Importance of erythrocyte adenosine triphosphatase in some physiopathological conditions in childhood]. De Luca R; Gemelli M Minerva Pediatr; 1971 Aug; 23(33):1369-72. PubMed ID: 4256390 [No Abstract] [Full Text] [Related]
49. [Pathogenesis and treatment of anemias with decreased erythrocyte acetylcholinesterase activity]. Savina LS; Ivanpva IV Voen Med Zh; 1980 Nov; (11):54-5. PubMed ID: 7445464 [No Abstract] [Full Text] [Related]
51. [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]
52. Differences between the red cell acetylcholinesterase defects of paroxysmal nocturnal hemoglobinuria and of ABO hemolytic disease. Herz F; Kaplan E; Scheye ES Acta Haematol; 1968; 39(2):85-90. PubMed ID: 4969265 [No Abstract] [Full Text] [Related]
53. Absence of phosphorylation-induced gelation of erythrocyte membrane skeletons: a diagnostic tool for hereditary spherocytosis. Armbrust R; Eber SW; Schröter W Ann Hematol; 1992 Feb; 64(2):93-6. PubMed ID: 1554801 [TBL] [Abstract][Full Text] [Related]
54. A review: human erythrocyte acetylcholinesterase. Herz F; Kaplan E Pediatr Res; 1973 Apr; 7(4):204-14. PubMed ID: 4581727 [No Abstract] [Full Text] [Related]
55. Acetylcholine esterase as a probe for erythrocyte-membrane intactness. Aloni B; Livne A Biochim Biophys Acta; 1974 Mar; 339(3):359-66. PubMed ID: 4834674 [No Abstract] [Full Text] [Related]
56. [Acetylcholinesterase in aging of human erythrocytes]. Kamyshentsev MV; Blinov MN Biull Eksp Biol Med; 1976 Oct; 82(10):1198-200. PubMed ID: 1029501 [TBL] [Abstract][Full Text] [Related]
57. [Erythrocyte membrane protein abnormalities in hereditary hemolytic anemias]. Boivin P; Galand C Nouv Rev Fr Hematol Blood Cells; 1977; 18(1):95-116. PubMed ID: 197487 [TBL] [Abstract][Full Text] [Related]
58. [Anomalies in erythrocyte membrane lipids during congenital hemolytic anemia]. Chap H; Douste-Blazy L Nouv Rev Fr Hematol Blood Cells; 1977; 18(1):139-50. PubMed ID: 408790 [No Abstract] [Full Text] [Related]
59. Lipid-protein interactions in human erythrocyte-membrane acetylcholinesterase. Modulation of enzyme activity by lipids. Frenkel EJ; Roelofsen B; Brodbeck U; van Deenen LL; Ott P Eur J Biochem; 1980 Aug; 109(2):377-82. PubMed ID: 7408889 [TBL] [Abstract][Full Text] [Related]
60. Peroxidation of lipid from paroxysmal nocturnal haemoglobinuria-like erythrocytes. Meriwether WD; Mengel CE Nature; 1967 Oct; 216(5110):85-6. PubMed ID: 6050685 [No Abstract] [Full Text] [Related] [Previous] [Next] [New Search]