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.
Pubmed for Handhelds
PUBMED FOR HANDHELDS
Journal Abstract Search
71 related items for PubMed ID: 93915
1. Study of spectrin phosphorylation and polymerization in normal and spherocytic red blood-cells [proceedings]. Devogel M, Vincentelli J, Polastro E, Schnek G, Léonis J. Arch Int Physiol Biochim; 1979 Oct; 87(4):805-7. PubMed ID: 93915 [No Abstract] [Full Text] [Related]
2. Unchanged binding of 99molybdenum to red cell membrane proteins in hereditary spherocytosis. Marík T, Kselíková M, Bíbr B, Brabec V, Lener J. Folia Haematol Int Mag Klin Morphol Blutforsch; 1983 Oct; 110(1):81-5. PubMed ID: 6192057 [Abstract] [Full Text] [Related]
4. Red cell membrane protein phosphorylation in hemolytic anemias and muscular dystrophies. Tsung PK, Palek J. Muscle Nerve; 1980 Oct; 3(1):55-69. PubMed ID: 6246419 [Abstract] [Full Text] [Related]
5. The spectrin phosphorylation reaction in human erythrocytes. Greenquist AC, Wyatt JL, Guatelli JC, Shohet SB. Prog Clin Biol Res; 1978 Oct; 20():1-24. PubMed ID: 652813 [Abstract] [Full Text] [Related]
6. The molecular basis of the defect in phosphorylation of spectrin in human hereditary spherocytosis. Thompson S, Maddy AH. Biochim Biophys Acta; 1981 Nov 20; 649(1):38-44. PubMed ID: 6796120 [Abstract] [Full Text] [Related]
8. Abnormal binding of spectrin to the membrane of erythrocytes in some cases of hereditary spherocytosis. Sheehy R, Ralston GB. Blut; 1978 Mar 15; 36(3):145-8. PubMed ID: 638266 [Abstract] [Full Text] [Related]
9. The abnormal phosphorylation of spectrin in human hereditary spherocytosis. Thompson S, Maddy AH. Biochim Biophys Acta; 1981 Nov 20; 649(1):31-7. PubMed ID: 6272858 [Abstract] [Full Text] [Related]