Published in Hemoglobin on May 01, 2000
Tracing European founder lineages in the Near Eastern mtDNA pool. Am J Hum Genet (2000) 7.06
Unstable beta-globin mRNA in mRNA-deficient beta o thalassemia. Cell (1981) 3.80
Jewish and Middle Eastern non-Jewish populations share a common pool of Y-chromosome biallelic haplotypes. Proc Natl Acad Sci U S A (2000) 3.10
A unique natural human IgG antibody with anti-alpha-galactosyl specificity. J Exp Med (1984) 3.07
Non-specific serum iron in thalassaemia: an abnormal serum iron fraction of potential toxicity. Br J Haematol (1978) 2.07
The present status of the heterogeneity of fetal hemoglobin in beta-thalassemia: an attempt to unify some observations in thalassemia and related conditions. Ann N Y Acad Sci (1974) 1.99
Bacterial chitobiase structure provides insight into catalytic mechanism and the basis of Tay-Sachs disease. Nat Struct Biol (1996) 1.98
Proliferation and maturation of human erythroid progenitors in liquid culture. Blood (1989) 1.78
Origin and spread of the glucose-6-phosphate dehydrogenase variant (G6PD-Mediterranean) in the Middle East. Am J Hum Genet (1990) 1.75
The Y chromosome pool of Jews as part of the genetic landscape of the Middle East. Am J Hum Genet (2001) 1.74
Retroregulation: control of gene expression from sites distal to the gene. Cell (1982) 1.65
High-resolution Y chromosome haplotypes of Israeli and Palestinian Arabs reveal geographic substructure and substantial overlap with haplotypes of Jews. Hum Genet (2000) 1.61
Role of the cro gene in bacteriophage lambda development. J Mol Biol (1973) 1.58
The effects of protein conformation on the heme symmetry in high spin ferric heme proteins as studied by electron paramagnetic resonance. J Biol Chem (1971) 1.57
Adding fresh frozen plasma to rituximab for the treatment of patients with refractory advanced CLL. QJM (2008) 1.56
Initiation points for DNA replication in nontransformed and simian virus 40-transformed Chinese hamster lung cells. Cell (1977) 1.52
Brief report: tumor lysis syndrome following treatment with 2-chlorodeoxyadenosine for refractory chronic lymphocytic leukemia. N Engl J Med (1993) 1.51
Ovarian tissue banking in patients with Hodgkin's disease: is it safe? Fertil Steril (1998) 1.46
Evaluation of triage decisions for intensive care admission. Crit Care Med (1999) 1.44
Activation of the lambda int gene by the cii and ciii gene products. Virology (1976) 1.44
Demonstration of a natural antigalactosyl IgG antibody on thalassemic red blood cells. Blood (1983) 1.41
Activated oxygen and haemolysis. Br J Haematol (1975) 1.41
Efficient transduction of human hematopoietic cells with the human multidrug resistance gene 1 via SV40 pseudovirions. Hum Gene Ther (1998) 1.41
Studies on the stability of oxyhemoglobin A and its constituent chains and their derivatives. J Biol Chem (1971) 1.38
Cardiopulmonary assessment in beta-thalassemia major. Chest (1990) 1.26
Oxidative denaturation of red blood cells in thalassemia. Semin Hematol (1990) 1.24
Rapid detection of the common Mediterranean alpha-globin deletions/rearrangements using PCR. Am J Hematol (1998) 1.23
Trend of mortality from cancer of the breast. JAMA (1965) 1.23
Self-assembly and protein-protein interactions between the SV40 capsid proteins produced in insect cells. Virology (1997) 1.20
Lipid membrane peroxidation in beta-thalassemia major. Blood (1976) 1.18
Denaturation of the normal and abnormal hemoglobin molecule. Semin Hematol (1974) 1.17
Role of haemichromes in the formation of inclusion bodies in haemoglobin H disease. Nature (1969) 1.12
DNA methylation pattern is determined by the intracellular level of the methylase. Proc Natl Acad Sci U S A (1984) 1.11
Evolution of a genetic disease in an ethnic isolate: beta-thalassemia in the Jews of Kurdistan. Proc Natl Acad Sci U S A (1991) 1.11
New apparatus for mass screening in mammography. Am J Roentgenol Radium Ther Nucl Med (1968) 1.10
Acute promyelocytic leukaemia with t(15;17) following treatment of Hodgkin's disease--a report of 4 cases. Ann Oncol (1995) 1.09
Microsatellite instability and p53 mutations in therapy-related leukemia suggest mutator phenotype. Blood (1996) 1.08
beta 0-Thalassemia complicated by autoimmune hemolytic anemia. Globin synthesis during immunosuppressive therapy. Acta Haematol (1980) 1.06
Haplogroup-specific deviation from the stepwise mutation model at the microsatellite loci DYS388 and DYS392. Eur J Hum Genet (2001) 1.05
The natural anti-alpha-galactosyl IgG on human normal senescent red blood cells. Br J Haematol (1986) 1.05
Optic atrophy following treatment with cobalt chloride in a patient with pancytopenia and hypercellular marrow. Isr J Med Sci (1972) 1.05
Expression of beta-globin in primary erythroid progenitors of beta-thalassemia patients using an SV40-based gene delivery system. J Hematother Stem Cell Res (1999) 1.05
Essential cryofibrinogenemia. Clinical, pathological and immunological studies. Isr J Med Sci (1970) 1.05
Gonadotrophin, thyrotrophin and prolactin reserve in beta thalassaemia. Clin Endocrinol (Oxf) (1978) 1.04
A new polymorphism in the human beta-globin gene useful in antenatal diagnosis. J Clin Invest (1981) 1.02
In-vivo platelet activation correlates with red cell anionic phospholipid exposure in patients with beta-thalassaemia major. Br J Haematol (1997) 1.02
Erythropoietin triggers a burst of GATA-1 in normal human erythroid cells differentiating in tissue culture. Nucleic Acids Res (1993) 1.00
Absence of beta mRNA in beta0-thalassemia in Kurdish Jews. Blood (1978) 1.00
Erythrocyte membrane skeleton abnormalities in severe beta-thalassemia. Blood (1987) 0.99
Novel treatment options in the severe beta-globin disorders. Br J Haematol (1995) 0.99
The demonstration of ferrihemochrome intermediates in heinz body formation following the reduction of oxyhemoglobin A by acetylphenylhydrazone. Biochim Biophys Acta (1975) 0.99
Blood group phenotypes and hemoglobin S. An anthropologic study in two Israeli Arab communities. Acta Haematol (1976) 0.98
Superoxide dismutase in red blood cells: method of assay and enzyme content in normal subjects and in patients with beta-thalassemia (major and intermedia). J Lab Clin Med (1976) 0.98
Mean corpuscular volume of heterozygotes for beta-thalassemia correlates with the severity of mutations. Blood (1992) 0.98
The two-step liquid culture: a novel procedure for studying maturation of human normal and pathological erythroid precursors. Stem Cells (1993) 0.97
Quantitative studies of ferritinlike iron in erythrocytes of thalassemia, sickle-cell anemia, and hemoglobin Hammersmith with Mössbauer spectroscopy. Proc Natl Acad Sci U S A (1979) 0.96
Promoter resurrection by activators--a minireview. Gene (1993) 0.96
Phosphatidylserine in the outer leaflet of red blood cells from beta-thalassemia patients may explain the chronic hypercoagulable state and thrombotic episodes. Am J Hematol (1993) 0.96
Juvenile leg ulceration in beta-thalassemia major and intermedia. Plast Reconstr Surg (1982) 0.96
Objective-type dark-field illumination for scattering from microbeads. Appl Opt (2001) 0.96
In vitro assembly of SV40 virions and pseudovirions: vector development for gene therapy. Hum Gene Ther (1997) 0.96
Blood group phenotypes and the origin of sickle cell hemoglobin in Sicilians. Acta Haematol (1978) 0.94
Hypomethylation of DNA derived from purified human erythroid cells correlates with gene activity of the beta-globin cluster. Blood (1985) 0.94
Visceral leishmaniasis: a difficult diagnosis and unusual causative agent. J Infect Dis (1991) 0.94
Initiation points for DNA replication in nontransformed and simian virus 40-transformed BALB/c 3T3 cells. J Virol (1978) 0.93
Sex identification of archaeological human remains based on amplification of the X and Y amelogenin alleles. Gene (1995) 0.93
A chronic hypercoagulable state in patients with beta-thalassaemia major is already present in childhood. Br J Haematol (1999) 0.93
Two mutations in the beta-globin polyadenylylation signal reveal extended transcripts and new RNA polyadenylylation sites. Proc Natl Acad Sci U S A (1992) 0.92
Enhanced generation of monocyte tissue factor and increased plasma prothrombin fragment1+2 levels in patients with polycythemia vera: mechanism of activation of blood coagulation. Am J Hematol (1997) 0.91
Differing erythrocyte membrane skeletal protein defects in alpha and beta thalassemia. J Clin Invest (1989) 0.91
Interaction of cII, cIII, and cro gene products in the regulation of early and late functions of phage lambda. Virology (1977) 0.91
Nonspecific serum iron in thalassemia: quantitation and chemical reactivity. Am J Hematol (1979) 0.91
Expression of granulocytic functions by leukemic promyelocytic HL-60 cells: differential induction by dimethylsulfoxide and retinoic acid. Cell Differ (1987) 0.90
Homozygous beta0- and beta+ - thalassemia in Kurdish Jews and Arabs. Hemoglobin (1977) 0.90
In vivo platelet activation in beta-thalassemia major reflected by increased platelet-thromboxane urinary metabolites. Blood (1991) 0.90
Regulation of protein synthesis in bacteriophage lambda. Restoration of gene expression in lambda N-strains by mutations in the cro gene. Virology (1977) 0.90
Ultrastructural studies in -thalassaemia major. Br J Haematol (1973) 0.89
The interaction of hemoglobin O Arab with Hb S and beta+ thalassemia among Israeli Arabs. Hum Genet (1985) 0.89
Formation of hemichromes from oxidized hemoglobin subunits. Ann N Y Acad Sci (1969) 0.89
Mechanism of desferrioxamine-induced iron excretion in thalassaemia. Br J Haematol (1979) 0.88
Cross-sectional and longitudinal study of the pituitary-thyroid axis in patients with thalassaemia major. Clin Endocrinol (Oxf) (1993) 0.88
Self-renewal and commitment to differentiation of human leukemic promyelocytic cells (HL-60). J Cell Physiol (1982) 0.88
Thromboembolic complications in beta thalassemia major. Acta Haematol (1992) 0.87
Relief of pruritus by cholestyramine in chronic liver disease. Isr J Med Sci (1965) 0.87
Protective effects of tea polyphenols against oxidative damage to red blood cells. Biochem Pharmacol (1997) 0.87
Phagocytosis of nucleated and mature beta thalassaemic red blood cells by mouse macrophages in vitro. Br J Haematol (1979) 0.87
High-resolution analysis of Y-chromosomal polymorphisms reveals signatures of population movements from Central Asia and West Asia into India. J Genet (2001) 0.87
Effect of magnesium given 1 hour after head trauma on brain edema and neurological outcome. J Neurosurg (1996) 0.87
Improved single-step PCR assay for sex identification post-allogeneic sex-mismatched BMT. Bone Marrow Transplant (1996) 0.86
Left ventricular function in beta-thalassemia and the effect of multiple transfusions. Am Heart J (1978) 0.86
Splenectomy in homozygous beta thalassaemia: a retrospective study of 30 patients. Br J Haematol (1975) 0.86
Genetic and molecular diversity in nondeletion Hb H disease. Proc Natl Acad Sci U S A (1981) 0.86
The simian virus 40 packaging signal ses is composed of redundant DNA elements which are partly interchangeable. J Mol Biol (1996) 0.86
Adult and neonatal patterns of human globin gene expression are recapitulated in liquid cultures. Exp Hematol (1992) 0.86
Cross-linking of red blood cell membrane proteins induced by oxidative stress in beta thalassemia. FEBS Lett (1978) 0.86