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Results: 1-9 |
Results: 9

Authors: Solis, C Aizencang, GI Astrin, KH Bishop, DF Desnick, R
Citation: C. Solis et al., Uroporphyrinogen III synthase erythroid promoter mutations in adjacent GATA1 and CP2 elements cause congenital erythropoietic porphyria, J CLIN INV, 107(6), 2001, pp. 753-762

Authors: Chen, BY Utgikar, VP Harmon, SM Tabak, HH Bishop, DF Govind, R
Citation: By. Chen et al., Studies on biosorption of zinc(II) and copper(II) on Desulfovibrio desulfuricans, INT BIO BIO, 46(1), 2000, pp. 11-18

Authors: Utgikar, V Chen, BY Tabak, HH Bishop, DF Govind, R
Citation: V. Utgikar et al., Treatment of acid mine drainage: I. Equilibrium biosorption of zinc and copper on non-viable activated sludge, INT BIO BIO, 46(1), 2000, pp. 19-28

Authors: Aizencang, G Solis, C Bishop, DF Warner, C Desnick, RJ
Citation: G. Aizencang et al., Human uroporphyrinogen-III synthase: Genomic organization, alternative promoters, and erythroid-specific expression, GENOMICS, 70(2), 2000, pp. 223-231

Authors: Mihopoulos, PG Sayles, GD Suidan, MT Shah, J Bishop, DF
Citation: Pg. Mihopoulos et al., Vapor phase treatment of PCE in a soil column by lab-scale anaerobic bioventing, WATER RES, 34(12), 2000, pp. 3231-3237

Authors: Aizencang, GI Bishop, DF Forrest, D Astrin, KH Desnick, RJ
Citation: Gi. Aizencang et al., Uroporphyrinogen III synthase - An alternative promoter controls erythroid-specific expression in the murine gene, J BIOL CHEM, 275(4), 2000, pp. 2295-2304

Authors: Bekri, S Kispal, G Lange, H Fitzsimons, E Tolmie, J Lill, R Bishop, DF
Citation: S. Bekri et al., Human ABC7 transporter: gene structure and mutation causing X-linked sideroblastic anemia with ataxia with disruption of cytosolic iron-sulfur protein maturation, BLOOD, 96(9), 2000, pp. 3256-3264

Authors: Cazzola, M May, A Bergamaschi, G Cerani, P Rosti, V Bishop, DF
Citation: M. Cazzola et al., Familial-skewed X-chromosome inactivation as a predisposing factor for late-onset X-linked sideroblastic anemia in carrier females, BLOOD, 96(13), 2000, pp. 4363-4365

Authors: Cotter, PD May, A Li, LP Al-Sabah, AI Fitzsimons, EJ Cazzola, M Bishop, DF
Citation: Pd. Cotter et al., Four new mutations in the erythroid-specific 5-aminolevulinate synthase (ALAS2) gene causing X-linked sideroblastic anemia: Increased pyridoxine responsiveness after removal of iron overload by phlebotomy and coinheritance of hereditary hemochromatosis, BLOOD, 93(5), 1999, pp. 1757-1769
Risultati: 1-9 |