Polymerization in erythrocytes containing S and non-S hemoglobinsNOGUCHI, C. T.Biophysical journal. 1984, Vol 45, Num 6, pp 1153-1158, issn 0006-3495Article

In vitro differential expression of human globin genesWADA, Y; NOGUCHI, C. T.The Journal of biological chemistry (Print). 1988, Vol 263, Num 24, pp 12142-12146, issn 0021-9258Article

Activation of globin gene expression by cDNAs from induced K562 cells : evidence for involvement of ferritin in globin gene expressionYONGJI WU; NOGUCHI, C. T.The Journal of biological chemistry (Print). 1991, Vol 266, Num 26, pp 17566-17572, issn 0021-9258Article

Is there a role for selective vasodilation in the management of sickle cell disease?RODGERS, G. P; ROY, M. S; NOGUCHI, C. T et al.Blood. 1988, Vol 71, Num 3, pp 597-602, issn 0006-4971Article

Conjunctival sign in sickle cell anaemia: an in-vivo correlate of the extent of red cell heterogeneityROY, M. S; RODGERS, G. P; PODGOR, M. J et al.British journal of ophthalmology. 1985, Vol 69, Num 8, pp 629-632, issn 0007-1161Article

Microcirculatory adaptations in sickle cell anemia: reactive hyperemia responseRODGERS, G. P; SCHECHTER, A. N; NOGUCHI, C. T et al.American journal of physiology. Heart and circulatory physiology. 1990, Vol 27, Num 1, pp H113-H120, issn 0363-6135Article

Periodic microcirculatory flow in patients with sickle-cell diseaseRODGERS, G. P; SCHECHTER, A. N; NOGUCHI, C. T et al.The New England journal of medicine. 1984, Vol 311, Num 24, pp 1534-1538, issn 0028-4793Article

Intracellular polymerization of sickle hemoglobinNOGUCHI, C. T; TORCHIA, D. A; SCHECHTER, A. N et al.The Journal of clinical investigation. 1983, Vol 72, Num 3, pp 846-852, issn 0021-9738Article

Contributions of sickle hemoglobin polymer and sickle cell membranes to impaired filterabilityHIRUMA, H; NOGUCHI, C. T; UYESAKA, N et al.American journal of physiology. Heart and circulatory physiology. 1995, Vol 37, Num 5, pp H2003-H2008, issn 0363-6135Article

Filterability of mixtures of sickle and normal erythrocytesHASEGAWA, S; HIRUMA, H; UYESAKA, N et al.American journal of hematology. 1995, Vol 50, Num 2, pp 91-97, issn 0361-8609Article

Hemin-induced acceleration of hemoglobin production in immature cultured erythroid cells : preferential enhancement of fetal hemoglobinFIBACH, E; KOLLIA, P; SCHECHTER, A. N et al.Blood. 1995, Vol 85, Num 10, pp 2967-2974, issn 0006-4971Conference Paper

Erythropoietin receptor mRNA expression in human endothelial cellsATHANASIUS ANAGNOSTOU; ZIYAO LIU; STEINER, M et al.Proceedings of the National Academy of Sciences of the United States of America. 1994, Vol 91, Num 9, pp 3974-3978, issn 0027-8424Article

Sickle cell disease pathophysiologyNOGUCHI, C. T; SCHECHTER, A. N; RODGERS, G. P et al.Baillière's clinical haematology. 1993, Vol 6, Num 1, pp 57-91, issn 0950-3536Article

Renal pathology in hemizygous sickle cell miceDIWAN, B. A; GLADWIN, M. T; NOGUCHI, C. T et al.Toxicologic pathology. 2002, Vol 30, Num 2, pp 254-262, issn 0192-6233Article

A minimal cytoplasmic subdomain of the erythropoietin receptor mediates erythroid and megakaryocytic cell developmentMILLER, C. P; LIU, Z. Y; NOGUCHI, C. T et al.Blood. 1999, Vol 94, Num 10, pp 3381-3387, issn 0006-4971Article

Hemoglobin S polymerization: primary determinant of the hemolytic and clinical severity of the sickling syndromesBRITTENHAM, G. M; SCHECHTER, A. N; NOGUCHI, C. T et al.Blood. 1985, Vol 65, Num 1, pp 183-189, issn 0006-4971Article

Sickle hemoglobin polymerization in solution and in cellsNOGUCHI, C. T; SCHECHTER, A. N.Annual review of biophysics and bioengineering. 1985, Vol 14, pp 239-263, issn 0084-6589Article

Irreversibly sickled erythrocytes in sickle cell anemia: a quantitative reappraisalRODGERS, G. P; NOGUCHI, C. T; SCHECHTER, A. N et al.American journal of hematology. 1985, Vol 20, Num 1, pp 17-23, issn 0361-8609Article

5-Azacytidine increases γ-globin synthesis and reduces the proportion of dense cells in patients with sickle cell anemiaLEY, T. J; DESIMONE, J; NOGUCHI, C. T et al.Blood. 1983, Vol 62, Num 2, pp 370-380, issn 0006-4971Article

Augmentation by erythropoietin of the fetal-hemoglobin response to hydroxyurea in sickle cell diseaseRODGERS, G. P; DOVER, G. J; UYESAKA, N et al.The New England journal of medicine. 1993, Vol 328, Num 2, pp 73-80, issn 0028-4793Article

Hydroxyurea increases fetal hemoglobin in cultured erythroid cells derived from normal individuals and patients with sickle cell anemia or β-thalassemiaFIBACH, E; BURKE, L. P; SCHECHTER, A. N et al.Blood. 1993, Vol 81, Num 6, pp 1630-1635, issn 0006-4971Article

Sparing effect of hemoglobin F and hemoglobin A₂ on the polymerization of hemoglobin S at physiologic ligand saturationsPOILLON, W. N; KIM, B. C; RODGERS, G. P et al.Proceedings of the National Academy of Sciences of the United States of America. 1993, Vol 90, Num 11, pp 5039-5043, issn 0027-8424Article

Hemoglobin aggregation and psueodiskling in vitro of hemoglobin setif-containing erythrocytesNOGUCHI, C. T; MOHANDAS, N; BLANCHETTE-MACKIE, J et al.American journal of hematology. 1991, Vol 36, Num 2, pp 131-139, issn 0361-8609, 9 p.Article

Cloning of the human erythropoietin receptor geneNOGUCHI, C. T; BAE, K. S; KYUNG CHIN et al.Blood. 1991, Vol 78, Num 10, pp 2548-2556, issn 0006-4971Article

Effects of α-thalassemia and sickle polymerization tendency on the urine-concentring defect of individuals with sickle cell traitGUPTA, A. K; KIRCHNER, K. A; NICHOLSON, R et al.The Journal of clinical investigation. 1991, Vol 88, Num 6, pp 1963-1968, issn 0021-9738Article