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MeSH Review

Sickle Cell Trait

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Disease relevance of Sickle Cell Trait


High impact information on Sickle Cell Trait


Chemical compound and disease context of Sickle Cell Trait


Biological context of Sickle Cell Trait


Anatomical context of Sickle Cell Trait


Gene context of Sickle Cell Trait


Analytical, diagnostic and therapeutic context of Sickle Cell Trait


  1. Treatment of sickle cell trait hematuria with oral urea. Pariser, S., Katz, A. J. Urol. (1994) [Pubmed]
  2. Textural differences between AA and SS blood specimens as detected by image analysis. Robinson, R.D., Benjamin, L.J., Cosgriff, J.M., Cox, C., Lapets, O.P., Rowley, P.T., Yatco, E., Wheeless, L.L. Cytometry. (1994) [Pubmed]
  3. NADH-methemoglobin reductase (cytochrome b5 reductase) levels in two groups of American blacks and whites. Mansouri, A., Nandy, I. J. Investig. Med. (1998) [Pubmed]
  4. Postoperative coma in a child with carnitine palmitoyltransferase I deficiency. Neuvonen, P.T., van den Berg, A.A. Anesth. Analg. (2001) [Pubmed]
  5. Etilefrine for the prevention of priapism in adult sickle cell disease. Okpala, I., Westerdale, N., Jegede, T., Cheung, B. Br. J. Haematol. (2002) [Pubmed]
  6. Clinical implications of sickle-cell trait and glucose-6-phosphate dehydrogenase deficiency in hospitalized black male patients. Heller, P., Best, W.R., Nelson, R.B., Becktel, J. N. Engl. J. Med. (1979) [Pubmed]
  7. Sodium-potassium pump, ion fluxes, and cellular dehydration in sickle cell anemia. Izumo, H., Lear, S., Williams, M., Rosa, R., Epstein, F.H. J. Clin. Invest. (1987) [Pubmed]
  8. Antenatal diagnosis of sickle-cell anaemia by D.N.A. analysis of amniotic-fluid cells. Kan, Y.W., Dozy, A.M. Lancet (1978) [Pubmed]
  9. Pulmonary function in sickle cell trait. Dillard, T.A., Kark, J.A., Rajagopal, K.R., Key, J.A., Canik, J.J., Ruehle, C.J. Ann. Intern. Med. (1987) [Pubmed]
  10. Fetal hemoglobin levels and beta (s) globin haplotypes in an Indian populations with sickle cell disease. Kulozik, A.E., Kar, B.C., Satapathy, R.K., Serjeant, B.E., Serjeant, G.R., Weatherall, D.J. Blood (1987) [Pubmed]
  11. Renal acidification in sickle cell trait. Oster, J.R., Lee, S.M., Lespier, L.E., Pellegrini, E.L., Vaamonde, C.A. Arch. Intern. Med. (1976) [Pubmed]
  12. Direct and continuous measurement of hydroperoxide-induced oxidative stress on the membrane of intact erythrocytes. van den Berg, J.J., Kuypers, F.A., Lubin, B.H., Roelofsen, B., Op den Kamp, J.A. Free Radic. Biol. Med. (1991) [Pubmed]
  13. Blood lactate concentrations during incremental exercise in subjects with sickle cell trait. Bile, A., Le Gallais, D., Mercier, B., Martinez, P., Ahmaidi, S., Prefaut, C., Mercier, J. Medicine and science in sports and exercise. (1998) [Pubmed]
  14. Decreased insulin response to glucose in sickle cell trait. Saad, M.J., Saad, S.T., Braga, G.S. Diabète & métabolisme. (1991) [Pubmed]
  15. Sickle cell and thiamine deficiency: case report of a fetal death. Multon, O., Sibony, O., Carbillon, L., Guerin, J.M., Nessman, C., Blot, P. Fetal. Diagn. Ther. (1994) [Pubmed]
  16. Malaria infection and morbidity in infants in relation to genetic polymorphisms in Tanzania. Stirnadel, H.A., Stöckle, M., Felger, I., Smith, T., Tanner, M., Beck, H.P. Trop. Med. Int. Health (1999) [Pubmed]
  17. Blood pressure and other cardiovascular disease risk factors in black adults with sickle cell trait or glucose-6-phosphate dehydrogenase deficiency. Nwankwo, M.U., Bunker, C.H., Ukoli, F.A., Omene, J.A., Freeman, D.T., Vergis, E.N., Yeh, L.L., Kuller, L.H. Genet. Epidemiol. (1990) [Pubmed]
  18. Increased expression in erythrocytic Ii antigens in sickle cell disease and sickle cell trait. Maniatis, A., Frieman, B., Bertles, J.F. Vox Sang. (1977) [Pubmed]
  19. Genetic studies in a black family with autosomal dominant polycystic kidney disease and sickle-cell trait. Kimberling, W.J., Yium, J.J., Johnson, A.M., Gabow, P.A., Martinez-Maldonado, M. Nephron (1996) [Pubmed]
  20. Fast-track cardiac anesthesia in patients with sickle cell abnormalities. Djaiani, G.N., Cheng, D.C., Carroll, J.A., Yudin, M., Karski, J.M. Anesth. Analg. (1999) [Pubmed]
  21. Family analysis of malaria infection in Dienga, Gabon. Domarle, O., Migot-Nabias, F., Pilkington, H., Elissa, N., Touré, F.S., Mayombo, J., Cot, M., Deloron, P. Am. J. Trop. Med. Hyg. (2002) [Pubmed]
  22. A new gene deletion in the alpha-like globin gene cluster as the molecular basis for the rare alpha-thalassemia-1(--/alpha alpha) in blacks: HbH disease in sickle cell trait. Steinberg, M.H., Coleman, M.B., Adams, J.G., Hartmann, R.C., Saba, H., Anagnou, N.P. Blood (1986) [Pubmed]
  23. Association of haptoglobin levels with age, parasite density, and haptoglobin genotype in a malaria-endemic area of Gabon. Fowkes, F.J., Imrie, H., Migot-Nabias, F., Michon, P., Justice, A., Deloron, P., Luty, A.J., Day, K.P. Am. J. Trop. Med. Hyg. (2006) [Pubmed]
  24. Trisomy 4 in a fetus with cyclopia and other anomalies. Van Allen, M.I., Ritchie, S., Toi, A., Fong, K., Winsor, E. Am. J. Med. Genet. (1993) [Pubmed]
  25. Distribution of IgG subclass antibodies specific for Plasmodium falciparum glutamate-rich-protein molecule in sickle cell trait children with asymptomatic infections. Matondo Maya, D.W., Mavoungou, E., Deloron, P., Theisen, M., Ntoumi, F. Exp. Parasitol. (2006) [Pubmed]
  26. Folic acid deficiency in sickle cell anaemia. Liu, Y.K. Scandinavian journal of haematology. (1975) [Pubmed]
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