The crisis in clinical research: Endangering the half-century national institutes of health consensusSCHECHTER, A. N.JAMA, the journal of the American Medical Association. 1998, Vol 280, Num 16, pp 1440-1442, issn 0098-7484Article

Genetic diseases of hemoglobin: diagnostic methods for elucidating β-thalassemia mutationsTUZMEN, S; SCHECHTER, A. N.Blood reviews. 2001, Vol 15, Num 1, pp 19-29, issn 0268-960XArticle

Nuclease hypersensitivity in the β-globin gene region of K562 cellsSHI-XIAN CAO; SCHECHTER, A. N.European journal of biochemistry (Print). 1988, Vol 173, Num 3, pp 517-522, issn 0014-2956Article

The development of a filtration system for evaluating flow characteristics of erythrocytesACQUAYE, C; WALKER, E. C; SCHECHTER, A. N et al.Microvascular research (Print). 1987, Vol 33, Num 1, pp 1-14, issn 0026-2862Article

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

Influence of sickle hemoglobin polymerization and membrane properties on deformability of sickle erythrocytes in the microcirculationCHENG DONG; CHADWICK, R. S; SCHECHTER, A. N et al.Biophysical journal. 1992, Vol 63, Num 3, pp 774-783, issn 0006-3495Article

Chemical potential measurements of deoxyhemoglobin S polymerization determination of the phase diagram of an assembling proteinPROUTY, M. S; SCHECHTER, A. N.Journal of molecular biology. 1985, Vol 184, Num 3, pp 517-528, issn 0022-2836Article

Hydroxyurea increases hemoglobin F levels and improves the effectiveness of erythropoiesis in β-thalassemia/hemoglobin E diseaseFUCHAROEN, S; SIRITANARATKUL, N; PIANKJAGUM, A et al.Blood. 1996, Vol 87, Num 3, pp 887-892, issn 0006-4971Article

Causal role of dense microspherocytes in the anemia of hereditary spherocytosis: clinical importance of filterability measurements through 3-μM poresHASEGAWA, S; NOMURA, T; IINO, M et al.Clinical hemorheology. 1994, Vol 14, Num 4, pp 571-584, issn 0271-5198Article

Brain glucose metabolism in neurologically normal patients with sickle cell disease: regional alterationsRODGERS, G. P; CLARK, C. M; LARSON, S. M et al.Archives of neurology (Chicago). 1988, Vol 45, Num 1, pp 78-82, issn 0003-9942Article

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

The acute chest syndrome in Sickle cell disease : Possible role of nitric oxide in its pathophysiology and treatmentGLADWIN, M. T; SCHECHTER, A. N; SHELHAMER, J. H et al.American journal of respiratory and critical care medicine. 1999, Vol 159, Num 5, pp 1368-1376, issn 1073-449X, 1Article

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

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

A β-globin gene, inactive in the K562 leukemic cell, functions normally in a heterologous expression systemFORDIS, C. M; ANAGNOU, N. P; DEAN, A et al.Proceedings of the National Academy of Sciences of the United States of America. Biological sciences. 1984, Vol 81, Num 14, pp 4485-4489, issn 0273-1134Article

The delta-globin RNA transcript level in beta-thalassemia carriersHUANG, S.-Z; ZENG, F.-Y; CHEN, M.-J et al.Acta haematologica. 1999, Vol 102, Num 1, pp 1-6, issn 0001-5792Article

Diagnosis of thalassemia using cDNA amplification of circulating erythroid cell mRNA with the polymerase chain reactionSHU-ZHEN HUANG; RODGERS, G. P; FAN-YI ZENG et al.Blood. 1991, Vol 78, Num 9, pp 2433-2437, issn 0006-4971Article

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

A common protein binds to two silencers 5' to the human β-globin geneBERG, P. E; WILLIAMS, D. M; RUO-LAN QIAN et al.Nucleic acids research. 1989, Vol 17, Num 21, pp 8833-8852, issn 0305-1048Article

Use of selective vasodilation in treatment of sickle cell diseaseRODGERS, G. P; ROY, M. S; TOM NOGUCHI, C et al.The American journal of pediatric hematology/oncology. 1988, Vol 10, Num 4, pp 351-356, issn 0192-8562Article

Control of oxygen affinity of hemoglobin in K562 cells induced by heminWU, Y; DEAN, A; EGAN, W et al.Blood. 1984, Vol 63, Num 6, pp 1447-1452, issn 0006-4971Article

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