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Results: 1-16 |
Results: 16

Authors: Nagel, RL Steinberg, MH
Citation: Rl. Nagel et Mh. Steinberg, Role of epistatic (modifier) genes in the modulation of the phenotypic diversity of sickle cell anemia, PEDIAT PATH, 20(2), 2001, pp. 123-136

Authors: Mitchell, T Plonczynski, M McCollum, A Hardy, CL Safaya, S Steinberg, MH
Citation: T. Mitchell et al., Gene expression profiling during erythroid differentiation of K562 cells, BL CELL M D, 27(1), 2001, pp. 309-319

Authors: Steinberg, MH
Citation: Mh. Steinberg, Modulation of fetal hemoglobin in sickle cell anemia, HEMOGLOBIN, 25(2), 2001, pp. 195-211

Authors: Qu, GZ Elkins, S Steinberg, MH
Citation: Gz. Qu et al., Thalassemia intermedia and extramedullary hematopoiesis associated with compound heterozygosity for the 532 bp deletion of the beta-globin gene and gene deletion hereditary persistence of fetal hemoglobin, HEMOGLOBIN, 25(1), 2001, pp. 91-96

Authors: Steinberg, MH Rodgers, GP
Citation: Mh. Steinberg et Gp. Rodgers, Pathophysiology of sickle cell disease: Role of cellular and genetic modifiers, SEM HEMATOL, 38(4), 2001, pp. 299-306

Authors: Steinberg, MH Rodgers, GP
Citation: Mh. Steinberg et Gp. Rodgers, Pharmacologic modulation of fetal hemoglobin, MEDICINE, 80(5), 2001, pp. 328-344

Authors: Iyer, R Baliga, R Nagel, RL Brugnara, C Kirchner, K Hogan, S Steinberg, MH
Citation: R. Iyer et al., Maximum urine concentrating ability in children with Hb SC disease: Effects of hydroxyurea, AM J HEMAT, 64(1), 2000, pp. 47-52

Authors: Steinberg, MH
Citation: Mh. Steinberg, Southern Society for Clinical Investigation Founders Medal recipient's address, AM J MED SC, 320(3), 2000, pp. 161-162

Authors: Kanter, AS Spencer, DC Steinberg, MH Soltysik, R Yarnold, PR Graham, NM
Citation: As. Kanter et al., Supplemental vitamin B and progression to AIDS and death in black South African patients infected with HIV, J ACQ IMM D, 21(3), 1999, pp. 252-253

Authors: Plonczynski, M Hardy, CL Safaya, S Harrell, A McCoy, L Brinson, A Agwarangbo, L Steinberg, MH
Citation: M. Plonczynski et al., Induction of globin synthesis in K562 cells is associated with differential expression of transcription factor genes, BL CELL M D, 25(10), 1999, pp. 156-165

Authors: Li, J Wilson, D Plonczynski, M Harrell, A Cook, CB Scheer, WD Zeng, YT Coleman, MB Steinberg, MH
Citation: J. Li et al., Genetic studies suggest a multicentric origin for Hb G-Coushatta [beta 22(B4)Glu -> Ala], HEMOGLOBIN, 23(1), 1999, pp. 57-67

Authors: Steinberg, MH
Citation: Mh. Steinberg, Management of sickle cell disease, N ENG J MED, 340(13), 1999, pp. 1021-1030

Authors: Belcher, JD Marker, PH Geiger, P Girotti, AW Steinberg, MH Hebbel, RP Vercellotti, GM
Citation: Jd. Belcher et al., Low-density lipoprotein susceptibility to oxidation and cytotoxicity to endothelium in sickle cell anemia, J LA CL MED, 133(6), 1999, pp. 605-612

Authors: Solovey, A Gui, LZ Ramakrishnan, S Steinberg, MH Hebbel, RP
Citation: A. Solovey et al., Sickle cell anemia as a possible state of enhanced anti-apoptotic tone: Survival effect of vascular endothelial growth factor on circulating and unanchored endothelial cells, BLOOD, 93(11), 1999, pp. 3824-3830

Authors: Rhodes, SL Plonczynski, M Harrell, A Li, J Safaya, S Files, JC Steinberg, MH
Citation: Sl. Rhodes et al., Double heterozygosity for the codon beta 39 C-to-T nonsense mutation and atriplicate alpha-globin gene locus can cause "dominantly" inherited beta-thalassemia intermedia, AM J MED SC, 317(5), 1999, pp. 341-345

Authors: Steinberg, MH
Citation: Mh. Steinberg, Pathophysiology of sickle cell disease, BAIL CLIN H, 11(1), 1998, pp. 163-184
Risultati: 1-16 |