Zobrazeno 1 - 10
of 37
pro vyhledávání: '"M E, Fabry"'
Publikováno v:
Magnetic Resonance in Medicine
A half-volume quadrature head transverse electromagnetic (TEM) coil has been constructed for 4 T imaging applications. This coil produces a sufficiently large homogeneous B(1) field region for the use as a volume coil. It provides superior transmissi
Publikováno v:
Molecular and Cellular Biology. 17:2076-2089
Persistent expression of the gamma-globin genes in adults with deletion types of hereditary persistence of fetal hemoglobin (HPFH) is thought to be mediated by enhancer-like effects of DNA sequences at the 3' breakpoints of the deletions. A transgeni
Publikováno v:
Blood. 78:2104-2112
Knowledge concerning SS (homozygous for the beta s gene) red blood cell (RBC) heterogeneity has been useful for understanding the pathophysiology of sickle cell anemia. No equivalent information exists for RBCs of the compound heterozygote for the be
Autor:
M E, Fabry, J R, Romero, I D, Buchanan, S M, Suzuka, G, Stamatoyannopoulos, R L, Nagel, M, Canessa
Publikováno v:
Blood. 78:217-225
We have previously demonstrated that young normal (AA) and sickle cell anemia (SS) red blood cells are capable of a volume regulatory decrease response (VRD) driven by a K:Cl cotransporter that is activated by low pH or hypotonic conditions. We now r
Autor:
G A, Lutty, M, Taomoto, J, Cao, D S, McLeod, P, Vanderslice, B W, McIntyre, M E, Fabry, R L, Nagel
Publikováno v:
Investigative ophthalmologyvisual science. 42(6)
Patients with sickle cell disease have elevated circulating levels of cytokines including tumor necrosis factor (TNF) alpha. TNF-alpha stimulates expression by endothelial cells of adhesion molecules, including vascular cell adhesion molecule (VCAM)
Autor:
R L, Nagel, M E, Fabry
Publikováno v:
British journal of haematology. 112(1)
Publikováno v:
British journal of haematology. 107(3)
To test the hypothesis that HbOARAB induces an increase in red cell mean corpuscular haemoglobin concentration (MCHC), we studied members of four Tunisian families who were either homo- or heterozygous for HbOARAB or were double heterozygotes for HbS
Publikováno v:
Blood. 92(12)
In sickle cell anemia (SS), some red blood cells dehydrate, forming a hyperdense (HD) cell fraction (1.114 g/mL; mean corpuscular hemoglobin concentration [MCHC],46 g/dL) that contains many irreversibly sickled cells (ISCs), whereas other SS red bloo
Autor:
R L, Nagel, S, Daar, J R, Romero, S M, Suzuka, D, Gravell, E, Bouhassira, R S, Schwartz, M E, Fabry, R, Krishnamoorthy
Publikováno v:
Blood. 92(11)
Hemoglobin (Hb) S-Oman has two mutations in the beta-chains. In addition to the classic betaS mutation (beta6 Glu --Val), it contains a second mutation in the same chain (beta121 Glu --Lys) identical to that of HbOARAB. We have studied a pedigree of
Autor:
H L, Shear, L, Grinberg, J, Gilman, M E, Fabry, G, Stamatoyannopoulos, D E, Goldberg, R L, Nagel
Publikováno v:
Blood. 92(7)
Studies in vitro by Pasvol et al (Nature, 270:171, 1977) have indicated that the growth of Plasmodium falciparum in cells containing fetal hemoglobin (HbF = alpha2gamma2) is retarded, but invasion is increased, at least in newborn cells. Normal neona