Water exchange between red cells and plasma. Measurement by nuclear magnetic relaxation.

Autor Fabry, M E, Eisenstadt, M
Vydáno 1975

Microvascular sites and characteristics of sickle cell adhesion to vascular endothelium in shear flow conditions: pathophysiological implications.

Autor Kaul, D K, Fabry, M E, Nagel, R L
Vydáno 1989

High expression of human beta S- and alpha-globins in transgenic mice: hemoglobin composition and hematological consequences.

Autor Fabry, M E, Nagel, R L, Pachnis, A, Suzuka, S M, Costantini, F
Vydáno 1992

Erythrocytes in sickle cell anemia are heterogeneous in their rheological and hemodynamic characteristics.

Autor Kaul, D K, Fabry, M E, Windisch, P, Baez, S, Nagel, R L
Vydáno 1983

In vivo demonstration of red cell-endothelial interaction, sickling and altered microvascular response to oxygen in the sickle transgenic mouse.

Autor Kaul, D K, Fabry, M E, Costantini, F, Rubin, E M, Nagel, R L
Vydáno 1995

SC erythrocytes have an abnormally high intracellular hemoglobin concentration. Pathophysiological consequences.

Autor Fabry, M E, Kaul, D K, Raventos-Suarez, C, Chang, H, Nagel, R L
Vydáno 1982

Some aspects of the pathophysiology of homozygous Hb CC erythrocytes.

Autor Fabry, M E, Kaul, D K, Raventos, C, Baez, S, Rieder, R, Nagel, R L
Vydáno 1981

High levels of human gamma-globin gene expression in adult mice carrying a transgene of deletion-type hereditary persistence of fetal hemoglobin.

Autor Arcasoy, M O, Romana, M, Fabry, M E, Skarpidi, E, Nagel, R L, Forget, B G
Vydáno 1997

Retinal and choroidal neovascularization in a transgenic mouse model of sickle cell disease.

Autor Lutty, G. A., McLeod, D. S., Pachnis, A., Costantini, F., Fabry, M. E., Nagel, R. L.
Vydáno 1994

Modeling sickle cell vasoocclusion in the rat leg: quantification of trapped sickle cells and correlation with 31P metabolic and 1H magnetic resonance imaging changes.

Autor Fabry, M E, Rajanayagam, V, Fine, E, Holland, S, Gore, J C, Nagel, R L, Kaul, D K
Vydáno 1989

High expression of human beta S- and alpha-globins in transgenic mice: erythrocyte abnormalities, organ damage, and the effect of hypoxia.

Autor Fabry, M E, Costantini, F, Pachnis, A, Suzuka, S M, Bank, N, Aynedjian, H S, Factor, S M, Nagel, R L
Vydáno 1992

Magnetic resonance evidence of hypoxia in a homozygous alpha-knockout of a transgenic mouse model for sickle cell disease.

Autor Fabry, M E, Kennan, R P, Paszty, C, Costantini, F, Rubin, E M, Gore, J C, Nagel, R L
Vydáno 1996

Common haplotype dependency of high G gamma-globin gene expression and high Hb F levels in beta-thalassemia and sickle cell anemia patients.

Autor Labie, D, Pagnier, J, Lapoumeroulie, C, Rouabhi, F, Dunda-Belkhodja, O, Chardin, P, Beldjord, C, Wajcman, H, Fabry, M E, Nagel, R L
Vydáno 1985