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MeSH Review

Spherocytes

 
 
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Disease relevance of Spherocytes

 

High impact information on Spherocytes

  • However, propranolol hydrochloride, a cationic anesthetic that does not prevent ATP depletion, inhibited fragmentation and the appearance of myelin forms in both hereditary spherocytes and xerocytes [2].
  • Transfusion medicine illustrated. A surfeit of spherocytes [3].
  • The quantitation of spherocytes in ABO hemolytic disease [4].
  • We aimed to clarify the role of EPO in the response to enhanced spherocyte destruction, and to look for a linkage with the broad clinical spectra of HS [5].
  • Therefore in spectrin deficient erythrocytes the induction of cytoskeletal damage, specifically recognized by PCMT type II, could be one of the splenic steps producing conditioned spherocytes [6].
 

Biological context of Spherocytes

 

Associations of Spherocytes with chemical compounds

 

Gene context of Spherocytes

  • The activation required both extracellular Ca2+ and A23187, and was accompanied by the degradation of some membrane proteins and morphological changes in erythrocyte shape from discocytes to echinodisks, echinocytes, and spherocytes [14].
  • Fresh hereditary spherocytes were very resistant to lysis by phospholipase C, but, like normal erythrocytes, became progressively more susceptible to lysis upon storage [15].

References

  1. The presence of an anti-erythrocyte autoantibody in C3HeB/FeJ mice after lymphocytic choriomeningitis virus infection. Vella, A.T., Pfau, C.J. Autoimmunity (1991) [Pubmed]
  2. Fragmentation and myelin formation in hereditary xerocytosis and other hemolytic anemias. Snyder, L.M., Lutz, H.U., Sauberman, N., Jacobs, J., Fortier, N.L. Blood (1978) [Pubmed]
  3. Transfusion medicine illustrated. A surfeit of spherocytes. So, C.C., Wong, K.F. Transfusion (2003) [Pubmed]
  4. The quantitation of spherocytes in ABO hemolytic disease. Zipursky, A., Chintu, C., Brown, E., Brown, E.J. J. Pediatr. (1979) [Pubmed]
  5. Erythropoietin levels in the different clinical forms of hereditary spherocytosis. Rocha, S., Costa, E., Catarino, C., Belo, L., Castro, E.M., Barbot, J., Quintanilha, A., Santos-Silva, A. Br. J. Haematol. (2005) [Pubmed]
  6. Cytoskeletal behaviour in spectrin and in band 3 deficient spherocytic red cells: evidence for differentiated splenic conditioning role. Ingrosso, D., D'Angelo, S., Perrotta, S., d'Urzo, G., Iolascon, A., Perna, A.F., Galletti, P., Zappia, V., Miraglia del Giudice, E. Br. J. Haematol. (1996) [Pubmed]
  7. Hypertonic cryohemolysis: a diagnostic test for hereditary spherocytosis. Streichman, S., Gesheidt, Y., Tatarsky, I. Am. J. Hematol. (1990) [Pubmed]
  8. Hemolysis and morphological changes in rat erythrocytes with mercurials. Tanaka, R., Nakai, K. Jpn. J. Pharmacol. (1977) [Pubmed]
  9. Abnormal hemoglobins found in Hunan. Lu, Y., Liu, J. Chin. Med. J. (2003) [Pubmed]
  10. Autolytic changes in blood cells of human cadavers. II. Morphological studies. Penttilä, A., Laiho, K. Forensic Sci. Int. (1981) [Pubmed]
  11. Effect of progesterone and its 17 alpha-hydroxyl derivative on human erythrocyte membrane. Kaya, H., Saito, T. Jpn. J. Pharmacol. (1985) [Pubmed]
  12. The in vitro effect of primaquine on red cell phospholipid metabolism. Miller, A., Smith, H.C. J. Lab. Clin. Med. (1976) [Pubmed]
  13. Effects of bilirubin and phototherapy on osmotic fragility and haematoporphyrin-induced photohaemolysis of normal erythrocytes and spherocytes. Roll, E.B., Christensen, T., Gederaas, O.A. Acta Paediatr. (2005) [Pubmed]
  14. Activation of intracellular calcium-activated neutral proteinase in erythrocytes and its inhibition by exogenously added inhibitors. Hayashi, M., Inomata, M., Saito, Y., Ito, H., Kawashima, S. Biochim. Biophys. Acta (1991) [Pubmed]
  15. Ageing of blood in hereditary spherocytosis. Little, C., Rumsby, M.G. Scandinavian journal of haematology. (1980) [Pubmed]
 
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