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Results: 1-25 | 26-28
Results: 1-25/28
Lack of germline transmission of vector sequences following systemic administration of recombinant AAV-2 vector in males
Authors: Arruda, VR Fields, PA Milner, R Wainwright, L De Miguel, MP Donovan, PJ Herzog, RW Nichols, TC Biegel, JA Razavi, M Dake, M Huff, D Flake, AW Couto, L Kay, MA High, KA
Citation: Vr. Arruda et al., Lack of germline transmission of vector sequences following systemic administration of recombinant AAV-2 vector in males, MOL THER, 4(6), 2001, pp. 586-592
Muscle-directed gene transfer and transient immune suppression result in sustained partial correction of canine hemophilia B caused by a null mutation
Authors: Herzog, RW Mount, JD Arruda, VR High, KA Lothrop, CD
Citation: Rw. Herzog et al., Muscle-directed gene transfer and transient immune suppression result in sustained partial correction of canine hemophilia B caused by a null mutation, MOL THER, 4(3), 2001, pp. 192-200
Risk and prevention of anti-factor IX formation in AAV-mediated gene transfer in the context of a large deletion of F9
Authors: Fields, PA Arruda, VR Armstrong, E Chu, K Mingozzi, F Hagstrom, JN Herzog, RW High, KA
Citation: Pa. Fields et al., Risk and prevention of anti-factor IX formation in AAV-mediated gene transfer in the context of a large deletion of F9, MOL THER, 4(3), 2001, pp. 201-210
Intravenous administration of an E1/E3-deleted adenoviral vector induces tolerance to factor IX in C57BL/6 mice
Authors: Fields, PA Armstrong, E Hagstrom, JN Arruda, VR Murphy, ML Farrell, JP High, KA Herzog, RW
Citation: Pa. Fields et al., Intravenous administration of an E1/E3-deleted adenoviral vector induces tolerance to factor IX in C57BL/6 mice, GENE THER, 8(5), 2001, pp. 354-361
Increased risk for acute myeloid leukaemia in individuals with glutathioneS-transferase mu 1 (GSTM1) and theta 1 (GSTT1) gene defects
Authors: Arruda, VR Lima, CSP Grignoli, CRE de Melo, MB Lorand-Metze, I Alberto, FL Saad, STO Costa, FF
Citation: Vr. Arruda et al., Increased risk for acute myeloid leukaemia in individuals with glutathioneS-transferase mu 1 (GSTM1) and theta 1 (GSTT1) gene defects, EUR J HAEMA, 66(6), 2001, pp. 383-388
Detection of somatic mutations of the PIG-A gene in Brazilian patients with paroxysmal nocturnal hemoglobinuria
Authors: de Carvalho, RF Arruda, VR Saad, STO Costa, FF
Citation: Rf. De Carvalho et al., Detection of somatic mutations of the PIG-A gene in Brazilian patients with paroxysmal nocturnal hemoglobinuria, BRAZ J MED, 34(6), 2001, pp. 763-766
Posttranslational modifications of recombinant myotube-synthesized human factor IX
Authors: Arruda, VR Hagstrom, JN Deitch, J Heiman-Patterson, T Camire, RM Chu, K Fields, PA Herzog, RW Couto, LB Larson, PJ High, KA
Citation: Vr. Arruda et al., Posttranslational modifications of recombinant myotube-synthesized human factor IX, BLOOD, 97(1), 2001, pp. 130-138
Role of vector in activation of T cell subsets in immune responses againstthe secreted transgene product factor IX
Authors: Fields, PA Kowalczyk, DW Arruda, VR Armstrong, E McCleland, ML Hagstrom, JN Pasi, KJ Ertl, HCJ Herzog, RW High, KA
Citation: Pa. Fields et al., Role of vector in activation of T cell subsets in immune responses againstthe secreted transgene product factor IX, MOL THER, 1(3), 2000, pp. 225-235
C282Y mutation in the HLA-H gene is not a risk factor for patients with myocardial infarction
Authors: Annichino-Bizzacchi, JM Saad, STO Arruda, VR Ramires, JAF Siqueira, LH Chiaparini, LC Mansur, AP
Citation: Jm. Annichino-bizzacchi et al., C282Y mutation in the HLA-H gene is not a risk factor for patients with myocardial infarction, J CARD RISK, 7(1), 2000, pp. 37-40
The impact of the search for thrombophilia risk factors among antiphospholipid syndrome patients with thrombosis
Authors: Torresan, M Machado, TFGS Siqueira, LH Ozelo, MC Arruda, VR Annichino-Bizzacchi, JM
Citation: M. Torresan et al., The impact of the search for thrombophilia risk factors among antiphospholipid syndrome patients with thrombosis, BL COAG FIB, 11(7), 2000, pp. 679-682
beta(0)-thalassemia resulting from a novel mutation: beta 66/u -> stop codon
Authors: Grignoli, CRE Carvalho, MH Kimura, EM Sonati, MF Arruda, VR Saad, STO Costa, FF
Citation: Cre. Grignoli et al., beta(0)-thalassemia resulting from a novel mutation: beta 66/u -> stop codon, EUR J HAEMA, 64(2), 2000, pp. 137-138
Cytoplasmic overexpression of p53 and p21(ras) in megaloblastic anemia
Authors: Schulz, E Arruda, VR Costa, FF Saad, STO
Citation: E. Schulz et al., Cytoplasmic overexpression of p53 and p21(ras) in megaloblastic anemia, HAEMATOLOG, 85(8), 2000, pp. 874-875
Identification of one novel and three other point mutations in the proteinC gene of five unrelated Brazilian patients with hereditary protein C deficiency
Authors: Singh, YS Arruda, VR Ozello, MC Machado, TFGS Annichino-Bizzachi, JM
Citation: Ys. Singh et al., Identification of one novel and three other point mutations in the proteinC gene of five unrelated Brazilian patients with hereditary protein C deficiency, HAEMATOLOG, 85(8), 2000, pp. 891-893
beta-thalassemia trait might increase the severity of hemochromatosis in subjects with the C282Y mutation in the HFE gene
Authors: Arruda, VR Agostinho, MF Cancado, R Costa, FF Saad, STO
Citation: Vr. Arruda et al., beta-thalassemia trait might increase the severity of hemochromatosis in subjects with the C282Y mutation in the HFE gene, AM J HEMAT, 63(4), 2000, pp. 230-230
Absence of circulating factor IX antigen in hemophilia B dogs of the UNC-Chapel Hill colony
Authors: Herzog, RW Arruda, VR Fisher, TH Read, MS Nichols, TC High, KA
Citation: Rw. Herzog et al., Absence of circulating factor IX antigen in hemophilia B dogs of the UNC-Chapel Hill colony, THROMB HAEM, 84(2), 2000, pp. 352-354
The human platelet alloantigen 5 polymorphism as a risk for the development of acute idiopathic thrombocytopenia purpura
Authors: Castro, V Oliveira, GB Origa, AF Annichino-Bizzacchi, JM Arruda, VR
Citation: V. Castro et al., The human platelet alloantigen 5 polymorphism as a risk for the development of acute idiopathic thrombocytopenia purpura, THROMB HAEM, 84(2), 2000, pp. 360-361
Inherited thrombophilia as a risk factor for the development of ischemic stroke in young adults
Authors: Voetsch, B Damasceno, BP Camargo, ECS Massaro, A Bacheschi, LA Scaff, M Annichino-Bizzacchi, JM Arruda, VR
Citation: B. Voetsch et al., Inherited thrombophilia as a risk factor for the development of ischemic stroke in young adults, THROMB HAEM, 83(2), 2000, pp. 229-233
Improved muscle-derived expression of human coagulation factor IX from a skeletal actin/CMV hybrid enhancer/promoter
Authors: Hagstrom, JN Couto, LB Scallan, C Burton, M McCleland, ML Fields, PA Arruda, VR Herzog, RW High, KA
Citation: Jn. Hagstrom et al., Improved muscle-derived expression of human coagulation factor IX from a skeletal actin/CMV hybrid enhancer/promoter, BLOOD, 95(8), 2000, pp. 2536-2542
Possible association between cytomegalovirus infection and gastrointestinal bleeding in hemophiliac patients
Authors: Nogueira, E Arruda, VR Bizzacchi, JMA Costa, FF Ozelo, MC Rossi, CL Costa, SCB
Citation: E. Nogueira et al., Possible association between cytomegalovirus infection and gastrointestinal bleeding in hemophiliac patients, ACT HAEMAT, 103(2), 2000, pp. 73-77
Mutation analysis of the HFE gene in Brazilian populations
Authors: Agostinho, MF Arruda, VR Basseres, DS Bordin, S Soares, MCP Menezes, RC Costa, FF Saad, STO
Citation: Mf. Agostinho et al., Mutation analysis of the HFE gene in Brazilian populations, BL CELL M D, 25(21), 1999, pp. 324-327
Frequencies of platelet-specific alloantigen systems 1-5 in three distinctethnic groups in Brazil
Authors: Castro, V Origa, AF Annichino-Bizzacchi, JM Soares, M Menezes, RC Goncalves, MS Costa, FF Arruda, VR
Citation: V. Castro et al., Frequencies of platelet-specific alloantigen systems 1-5 in three distinctethnic groups in Brazil, EUR J IMM, 26(5), 1999, pp. 355-360
Hb Rio Claro [beta 34(B16)Val -> Met]: a novel electrophoretically silent variant found in association with Hb Hasharon [alpha 47(CE5)Asp -> His] andalpha-thalassemia-2 (-alpha(3.7))
Authors: Grignoli, CRE Wenning, MRSC Sonati, MF Kimura, EM Arruda, VR Saad, STO Costa, FF
Citation: Cre. Grignoli et al., Hb Rio Claro [beta 34(B16)Val -> Met]: a novel electrophoretically silent variant found in association with Hb Hasharon [alpha 47(CE5)Asp -> His] andalpha-thalassemia-2 (-alpha(3.7)), HEMOGLOBIN, 23(2), 1999, pp. 177-182
Spontaneous erythroid colony formation in Brazilian patients with sickle cell disease
Authors: Perlingeiro, RCR Costa, FF Saad, STO Arruda, VR Queiroz, MLS
Citation: Rcr. Perlingeiro et al., Spontaneous erythroid colony formation in Brazilian patients with sickle cell disease, AM J HEMAT, 61(1), 1999, pp. 40-45
Inherited risk factors for thrombophilia among children with Legg-Calve-Perthes disease
Authors: Arruda, VR Belangero, WD Ozelo, MC Oliveira, GB Pagnano, RG Volpon, JB Annichino-Bizzacchi, JM
Citation: Vr. Arruda et al., Inherited risk factors for thrombophilia among children with Legg-Calve-Perthes disease, J PED ORTH, 19(1), 1999, pp. 84-87
Hereditary hemorrhagic telangiectasia response to aminocaproic acid treatment
Authors: Annichino-Bizzacchi, JM Facchini, RM Torresan, MZ Arruda, VR
Citation: Jm. Annichino-bizzacchi et al., Hereditary hemorrhagic telangiectasia response to aminocaproic acid treatment, THROMB RES, 96(1), 1999, pp. 73-76
Risultati: 1-25 | 26-28