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
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
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:
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:
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:
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