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Blood|July 27, 2001
Direct intracellular measurement of deoxygenated hemoglobin S solubilityM E Fabry, L Desrosiers, S M SuzukaProceedings of the National Academy of Sciences of the United States of America|December 15, 1992
High expression of human beta S- and alpha-globins in transgenic mice: hemoglobin composition and hematological consequencesM E Fabry, R L Nagel, A Pachnis, et al.The Journal of Membrane Biology|June 1, 1990
Na+/H+ exchange is increased in sickle cell anemia and young normal red cellsM Canessa, M E Fabry, S M Suzuka, et al.Blood Cells, Molecules & Diseases|May 19, 2001
K:Cl cotransport activity is inhibited by HCO3- in knockout mouse red cells expressing human HbCJ R Romero, S M Suzuka, G V Romero-González, et al.American Journal of Hematology|June 1, 1997
K:Cl cotransport in red cells of transgenic mice expressing high levels of human hemoglobin SJ R Romero, M E Fabry, S M Suzuka, et al.Blood|July 1, 1991
Rapid increase in red blood cell density driven by K:Cl cotransport in a subset of sickle cell anemia reticulocytes and discocytesM E Fabry, J R Romero, I D Buchanan, et al.Current Eye Research|April 30, 1998
Nonperfusion of retina and choroid in transgenic mouse models of sickle cell diseaseG A Lutty, C Merges, D S McLeod, et al.Proceedings of the National Academy of Sciences of the United States of America|December 15, 1992
High expression of human beta S- and alpha-globins in transgenic mice: erythrocyte abnormalities, organ damage, and the effect of hypoxiaM E Fabry, F Costantini, A Pachnis, et al.Blood|January 12, 2001
Second generation knockout sickle mice: the effect of HbFM E Fabry, S M Suzuka, R S Weinberg, et al.Blood|December 3, 1998
HbS-oman heterozygote: a new dominant sickle syndromeR L Nagel, S Daar, J R Romero, et al.Pageof 2