Published in J Membr Biol on September 25, 1978
Size-selective loosening of the blood-brain barrier in claudin-5-deficient mice. J Cell Biol (2003) 5.74
Normal variation of magnetic resonance T1 relaxation times in the human population at 1.5 T using ShMOLLI. J Cardiovasc Magn Reson (2013) 1.60
Diffusional water permeability of human erythrocytes and their ghosts. J Gen Physiol (1982) 1.14
Proton nuclear magnetic resonance measurement of diffusional water permeability in suspended renal proximal tubules. Biophys J (1987) 1.07
Water permeability through biological membranes by isotopic effects of fluorescence and light scattering. Biophys J (1984) 1.00
Abnormal hyperintensity within the subarachnoid space evaluated by fluid-attenuated inversion-recovery MR imaging: a spectrum of central nervous system diseases. Eur Radiol (2003) 0.98
Water permeability of capillaries in the subfornical organ of rats determined by Gd-DTPA(2-) enhanced 1H magnetic resonance imaging. J Physiol (2002) 0.91
Water permeability of acinar cell membranes in the isolated perfused rabbit mandibular salivary gland. J Physiol (1990) 0.86
Two-site exchange revisited: a new method for extracting exchange parameters in biological systems. Biophys J (1989) 0.75
Relaxation rates of blood with osmotically modified red cell volume: application of the two-compartment fast exchange model. MAGMA (1998) 0.75
Correction of sickle cell disease in transgenic mouse models by gene therapy. Science (2001) 3.25
Hematologically and genetically distinct forms of sickle cell anemia in Africa. The Senegal type and the Benin type. N Engl J Med (1985) 1.90
Common haplotype dependency of high G gamma-globin gene expression and high Hb F levels in beta-thalassemia and sickle cell anemia patients. Proc Natl Acad Sci U S A (1985) 1.85
Microvascular sites and characteristics of sickle cell adhesion to vascular endothelium in shear flow conditions: pathophysiological implications. Proc Natl Acad Sci U S A (1989) 1.79
Intrasomatic injection of radioactive precursors for studying transmitter synthesis in identified neurons of Aplysia californica. Proc Natl Acad Sci U S A (1973) 1.66
Impaired nitric oxide-mediated vasodilation in transgenic sickle mouse. Am J Physiol Heart Circ Physiol (2000) 1.63
Heterogeneity of red cells in the sickler: a characteristic with practical clinical and pathophysiological implications. Blood Cells (1982) 1.49
Erythrocytes in sickle cell anemia are heterogeneous in their rheological and hemodynamic characteristics. J Clin Invest (1983) 1.48
Nuclear magnetic relaxation dispersion in protein solutions. IV. Proton relaxation at the active site of carbonic anhydrase. J Biol Chem (1970) 1.32
The hematologic characteristics of sickle cell anemia bearing the Bantu haplotype: the relationship between G gamma and HbF level. Blood (1987) 1.29
An objective sign in painful crisis in sickle cell anemia: the concomitant reduction of high density red cells. Blood (1984) 1.27
Water exchange between red cells and plasma. Measurement by nuclear magnetic relaxation. Biophys J (1975) 1.25
SC erythrocytes have an abnormally high intracellular hemoglobin concentration. Pathophysiological consequences. J Clin Invest (1982) 1.18
Transgenic mice expressing human fetal globin are protected from malaria by a novel mechanism. Blood (1998) 1.18
Axonal transport of newly synthesized acetylcholine in an identified neuron of Aplysia. Brain Res (1972) 1.16
In vivo demonstration of red cell-endothelial interaction, sickling and altered microvascular response to oxygen in the sickle transgenic mouse. J Clin Invest (1995) 1.15
Effect of magnetic susceptibility on nuclear magnetic resonance signals arising from red cells: a warning. Biochemistry (1983) 1.14
Volume-stimulated, Cl(-)-dependent K+ efflux is highly expressed in young human red cells containing normal hemoglobin or HbS. J Membr Biol (1987) 1.10
On the mechanism for the red-cell accumulation of mefloquine, an antimalarial drug. Biochim Biophys Acta (1984) 1.09
Vaso-occlusion by sickle cells: evidence for selective trapping of dense red cells. Blood (1986) 1.09
Deoxygenation inhibits the volume-stimulated, Cl(-)-dependent K+ efflux in SS and young AA cells: a cytosolic Mg2+ modulation. Blood (1987) 1.07
The pathophysiology of vascular obstruction in the sickle syndromes. Blood Rev (1996) 1.06
Transgenic mice expressing human sickle hemoglobin are partially resistant to rodent malaria. Blood (1993) 1.04
Renal nitric oxide synthases in transgenic sickle cell mice. Kidney Int (1996) 1.04
The effect of deoxygenation on red cell density: significance for the pathophysiology of sickle cell anemia. Blood (1982) 1.03
HbS-oman heterozygote: a new dominant sickle syndrome. Blood (1998) 1.03
Some aspects of the pathophysiology of homozygous Hb CC erythrocytes. J Clin Invest (1981) 1.02
The Senegal DNA haplotype is associated with the amelioration of anemia in African-American sickle cell anemia patients. Blood (1991) 1.02
Acute priapism associated with the use of sildenafil in a patient with sickle cell trait. Blood (2000) 1.01
The percentage of dense red cells does not predict incidence of sickle cell painful crisis. Blood (1986) 1.01
Erythrocytic and vascular factors influencing the microcirculatory behavior of blood in sickle cell anemia. Ann N Y Acad Sci (1989) 0.99
The unique red cell heterogeneity of SC disease: crystal formation, dense reticulocytes, and unusual morphology. Blood (1991) 0.96
Impairment of the growth of Plasmodium falciparum in HbEE erythrocytes. J Clin Invest (1981) 0.95
Peroxynitrite formation and apoptosis in transgenic sickle cell mouse kidneys. Kidney Int (1998) 0.95
F reticulocyte response in sickle cell anemia treated with recombinant human erythropoietin: a double-blind study. Blood (1993) 0.94
Turnover of hepatic collagen in reversible and irreversible fibrosis. Experientia (1970) 0.93
High levels of human gamma-globin gene expression in adult mice carrying a transgene of deletion-type hereditary persistence of fetal hemoglobin. Mol Cell Biol (1997) 0.92
Dense cells in sickle cell anemia: the effects of gene interaction. Blood (1984) 0.91
The panoply of animal models for sickle cell anaemia. Br J Haematol (2001) 0.91
Senegal haplotype is associated with higher HbF than Benin and Cameroon haplotypes in African children with sickle cell anemia. Am J Hematol (1993) 0.91
Velocity measurements of normal and sickle red blood cells in the rat retinal and choroidal vasculatures. Microvasc Res (2000) 0.90
Paradoxical increase of painful crises in sickle cell patients with alpha-thalassemia. Blood (1995) 0.89
Pulmonary entrapment of sickle cells: the role of regional alveolar hypoxia. J Appl Physiol (1985) (1996) 0.89
Red cell distribution width parallels dense red cell disappearance during painful crises in sickle cell anemia. J Lab Clin Med (1985) 0.87
Retinal and choroidal neovascularization in a transgenic mouse model of sickle cell disease. Am J Pathol (1994) 0.87
A rat model for sickle cell-mediated vaso-occlusion in retina. Microvasc Res (1996) 0.85
Inhibition of TNF-alpha-induced sickle RBC retention in retina by a VLA-4 antagonist. Invest Ophthalmol Vis Sci (2001) 0.84
Sickle cell painful crises: a multifactorial event. Prog Clin Biol Res (1987) 0.84
Two distinct pathways mediate the formation of intermediate density cells and hyperdense cells from normal density sickle red blood cells. Blood (1998) 0.84
Rate of activation and deactivation of K:Cl cotransport by changes in cell volume in hemoglobin SS, CC and AA red cells. J Membr Biol (1994) 0.83
Anti-beta s-ribozyme reduces beta s mRNA levels in transgenic mice: potential application to the gene therapy of sickle cell anemia. Blood Cells Mol Dis (1999) 0.83
Hemoglobin distribution width: a rapid assessment of dense red cells in the steady state and during painful crisis in sickle cell anemia. J Lab Clin Med (1988) 0.81
Immunohistochemical localization of hepatic nitric oxide synthase in normal and transgenic sickle cell mice: the effect of hypoxia. Blood (1996) 0.81
Atypical haplotypes linked to the beta S gene in Africa are likely to be the product of recombination. Am J Hematol (1988) 0.81
Detection of hemoglobin S polymerization in intact red cells by P-31 NMR. Biochem Biophys Res Commun (1980) 0.81
Protection from lethal malaria in transgenic mice expressing sickle hemoglobin. Blood (1996) 0.81
NMR relaxation of protein and water protons in methemoglobin solutions. Biophys J (1981) 0.80
In vivo quantitation of water content in muscle tissues by NMR imaging. Magn Reson Imaging (1991) 0.80
Open half-volume quadrature transverse electromagnetic coil for high-field magnetic resonance imaging. Magn Reson Med (2005) 0.80
An animal model for sickle cell vaso-occlusion: a study using NMR and technetium imaging. Prog Clin Biol Res (1987) 0.79
K:Cl cotransport in red cells of transgenic mice expressing high levels of human hemoglobin S. Am J Hematol (1997) 0.79
Compound heterozygosity for hemoglobin C and Korle-Bu: moderate microcytic hemolytic anemia and acceleration of crystal formation [corrected]. Blood (1993) 0.79
NMR relaxation of protein and water protons in diamagnetic hemoglobin solutions. Biochemistry (1985) 0.79
Red blood cells of a transgenic mouse expressing high levels of human hemoglobin S exhibit deoxy-stimulated cation flux. J Membr Biol (1997) 0.79
Linkage-disequilibrium of the senegal haplotype with the beta S gene in the republic of guinea. Am J Hematol (1995) 0.79
The mechanism of water proton nuclear magnetic resonance relaxation in the presence of mammalian and Aplysia metmyoglobin fluoride. J Biol Chem (1974) 0.78
K:Cl cotransport activity is inhibited by HCO3- in knockout mouse red cells expressing human HbC. Blood Cells Mol Dis (2001) 0.78
Roles of alpha 114 and beta 87 amino acid residues in the polymerization of hemoglobin S: implications for gene therapy. J Mol Biol (1996) 0.78
Na+/H+ exchange is increased in sickle cell anemia and young normal red cells. J Membr Biol (1990) 0.78
Erythrocyte sedimentation rate during steady state and painful crisis in sickle cell anemia. Am J Med (1986) 0.78
Sickle cell anemia as a multigenetic disease: new insights into the mechanism of painful crisis. Prog Clin Biol Res (1984) 0.78
Evolution of laboratory parameters during sickle cell painful crisis: evidence compatible with dense red cell sequestration without thrombosis. Am J Med Sci (1988) 0.78
Known and potential sources for epistatic effects in sickle cell anemia. Ann N Y Acad Sci (1989) 0.76
The erythrocyte effects of haemoglobin O(ARAB). Br J Haematol (1999) 0.76
The many pathophysiologies of sickle cell anemia. Am J Hematol (1985) 0.76
Pentoxifylline (Trental) has no significant effect on laboratory parameters in sickle cell disease. Nouv Rev Fr Hematol (1989) 0.75
Molecular interactions between Hb alpha-G Philadelphia, HbC, and HbS: phenotypic implications for SC alpha-G Philadelphia disease. Blood (1997) 0.75
The structure and formation of the glucose 6-phosphate adduct of hemoglobin A: a 31P-NMR study. Biochim Biophys Acta (1987) 0.75
Red cell density is sex and race dependent in the adult. J Lab Clin Med (1988) 0.75
Dielectrophoresis of macromolecules. Biopolymers (1973) 0.75
Activation of a K:C1 cotransporter by cell swelling in HbAA and HbSS red cells. Prog Clin Biol Res (1987) 0.75
Megalophallus as a sequela of priapism in sickle cell anemia: use of blood oxygen level-dependent magnetic resonance imaging. Urology (2000) 0.75
Dielectrophoresis of macromolecules: determination of the diffusion constant of poly- -benzyl-L-glutamate. Science (1972) 0.75
Nonperfusion of retina and choroid in transgenic mouse models of sickle cell disease. Curr Eye Res (1998) 0.75
Calculating number of offenses and victims of juvenile sexual offending: the role of posttreatment disclosures. Sex Abuse (2001) 0.75
Objective indices of sickle cell painful crisis: decrease in RDW and percent dense cells and increase in ESR and fibrinogen. Prog Clin Biol Res (1987) 0.75
The effect of buffers on nuclear magnetic relaxation of water protons by bovine and human-B cobalt carbonic anhydrase. J Biol Chem (1978) 0.75