about
Association of polymorphisms of IGF1R and genes in the transforming growth factor- beta /bone morphogenetic protein pathway with bacteremia in sickle cell anemiaBCL11A represses HBG transcription in K562 cellsGenetic dissection and prognostic modeling of overt stroke in sickle cell anemiaEffects of alpha-thalassemia and sickle polymerization tendency on the urine-concentrating defect of individuals with sickle cell traitGenomic approaches to identifying targets for treating β hemoglobinopathiesThe paradox of hemoglobin SC diseaseDifferential modulation of endotoxin responsiveness by human caspase-12 polymorphismsGenetic signatures of exceptional longevity in humansGenetic determinants of haemolysis in sickle cell anaemia.Sickle Cell Disease.Learning Bayesian Networks from Correlated DataSickle cell anemia is associated with reduced nitric oxide bioactivity in peripheral conduit and resistance vessels.Identification of oxidative post-translational modification of serum albumin in patients with idiopathic pulmonary arterial hypertension and pulmonary hypertension of sickle cell anemia.Sickle cell bone disease: response to vitamin D and calcium.A hierarchical and modular approach to the discovery of robust associations in genome-wide association studies from pooled DNA samples.Chronic hyper-hemolysis in sickle cell anemia: association of vascular complications and mortality with less frequent vasoocclusive painImputation of missing genotypes: an empirical evaluation of IMPUTE.Climatic and geographic temporal patterns of pain in the Multicenter Study of Hydroxyurea.RNA editing genes associated with extreme old age in humans and with lifespan in C. elegans.Management of sickle cell disease.Fetal hemoglobin in sickle cell anemia: genome-wide association studies suggest a regulatory region in the 5' olfactory receptor gene clusterClustering by genetic ancestry using genome-wide SNP data.Sickle cell disease in Saudi Arabia: the phenotype in adults with the Arab-Indian haplotype is not benign.Pathophysiology of sickle cell disease.Clinical and radiologic findings of inner ear involvement in sickle cell disease.Fetal haemoglobin levels and haematological characteristics of compound heterozygotes for haemoglobin S and deletional hereditary persistence of fetal haemoglobin.Neuropsychiatric symptoms in dementia patients with and without a history of traumatic brain injury.RETRACTED: Genetic signatures of exceptional longevity in humans.Effect of hydroxyurea on mortality and morbidity in adult sickle cell anemia: risks and benefits up to 9 years of treatment.Leg ulcers in sickle cell diseaseTwo missense mutations in the beta-globin gene can cause severe beta thalassemia. Hemoglobin Medicine Lake (beta 32[B14]leucine-->glutamine; 98 [FG5] valine-->methionine).A genome-wide association study of total bilirubin and cholelithiasis risk in sickle cell anemia.The aryl hydrocarbon receptor directs hematopoietic progenitor cell expansion and differentiation.Pharmacologic modulation of fetal hemoglobin.Deconstructing sickle cell disease: reappraisal of the role of hemolysis in the development of clinical subphenotypes.Fetal hemoglobin in sickle cell anemia: genetic studies of the Arab-Indian haplotypeDeveloping treatment for sickle cell disease.Fetal hemoglobin in sickle cell anemia: Bayesian modeling of genetic associations.A GCH1 haplotype confers sex-specific susceptibility to pain crises and altered endothelial function in adults with sickle cell anemia.Severe sickle cell anemia is associated with increased plasma levels of TNF-R1 and VCAM-1
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P50
description
hulumtues
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researcher
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Martin H Steinberg
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Martin H Steinberg
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Martin H Steinberg
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Martin H Steinberg
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Martin H Steinberg
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type
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Martin H Steinberg
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Martin H Steinberg
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Martin H Steinberg
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Martin H Steinberg
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Martin H Steinberg
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Martin Steinberg
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Martin H Steinberg
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Martin H Steinberg
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Martin H Steinberg
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Martin H Steinberg
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Martin H Steinberg
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P106
P21
P31
P496
0000-0001-8800-8020