Immune response to enzyme replacement therapy in lysosomal storage disorder patients and animal models.
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[1] C. Bond,et al. Immune response to enzyme replacement therapy: 4-sulfatase epitope reactivity of plasma antibodies from MPS VI cats. , 1999, Molecular genetics and metabolism.
[2] M. Rosenberg,et al. Immunosurveillance of alglucerase enzyme therapy for Gaucher patients: induction of humoral tolerance in seroconverted patients after repeat administration. , 1999, Blood.
[3] P. Meikle,et al. Prevalence of lysosomal storage disorders. , 1999, JAMA.
[4] D. Brooks,et al. Immune response to enzyme replacement therapy: clinical signs of hypersensitivity reactions and altered enzyme distribution in a high titre rat model. , 1998, Biochimica et biophysica acta.
[5] T. Stockley,et al. Suppression of immunological response against a transgene product delivered from microencapsulated cells. , 1998, Human gene therapy.
[6] E. Beutler. 8 Enzyme replacement therapy for Gaucher's disease , 1997 .
[7] R. Brady. 1 Gaucher's disease: past, present and future , 1997 .
[8] R. Brady,et al. Management of neutralizing antibody to Ceredase in a patient with type 3 Gaucher disease. , 1997, Pediatrics.
[9] I. Mellman,et al. Delivery of B Cell Receptor–internalized Antigen to Endosomes and Class II Vesicles , 1997, The Journal of experimental medicine.
[10] D. Brooks,et al. Enzyme replacement therapy in Mucopolysaccharidosis VI: evidence for immune responses and altered efficacy of treatment in animal models. , 1997, Biochimica et biophysica acta.
[11] G. Grabowski,et al. Enzyme therapy in Gaucher disease type 1: effect of neutralizing antibodies to acid beta-glucosidase. , 1997, Blood.
[12] W. Sly,et al. Murine mucopolysaccharidosis type VII: long term therapeutic effects of enzyme replacement and enzyme replacement followed by bone marrow transplantation. , 1997, The Journal of clinical investigation.
[13] F. Jirik,et al. Murine mucopolysaccharidosis type I: targeted disruption of the murine alpha-L-iduronidase gene. , 1997, Human molecular genetics.
[14] J. Hopwood,et al. Enzyme replacement therapy from birth in a feline model of mucopolysaccharidosis type VI. , 1997, The Journal of clinical investigation.
[15] A. Schmidtchen,et al. Long-term and high-dose trials of enzyme replacement therapy in the canine model of mucopolysaccharidosis I. , 1996, Biochemical and molecular medicine.
[16] D. Brooks,et al. Enzyme replacement therapy in a feline model of Maroteaux-Lamy syndrome. , 1996, The Journal of clinical investigation.
[17] J. Dambrosia,et al. Enzyme replacement therapy for Gaucher disease: skeletal responses to macrophage-targeted glucocerebrosidase. , 1995, Pediatrics.
[18] M. Kay,et al. Immunomodulation to enhance gene therapy , 1995, Nature Network Boston.
[19] M. Mcentee,et al. Enzyme replacement in a canine model of Hurler syndrome. , 1994, Proceedings of the National Academy of Sciences of the United States of America.
[20] W. Sly,et al. Enzyme replacement therapy for murine mucopolysaccharidosis type VII. , 1994, The Journal of clinical investigation.
[21] I. Mellman,et al. Transient accumulation of new class II MHC molecules in a novel endocytic compartment in B lymphocytes , 1994, Nature.
[22] G. Grabowski,et al. Enzyme therapy in Gaucher disease type 1: dosage efficacy and adverse effects in 33 patients treated for 6 to 24 months. , 1993, Blood.
[23] J. Dambrosia,et al. Dose-dependent responses to macrophage-targeted glucocerebrosidase in a child with Gaucher disease. , 1992, The Journal of pediatrics.
[24] J. Dambrosia,et al. Replacement therapy for inherited enzyme deficiency--macrophage-targeted glucocerebrosidase for Gaucher's disease. , 1991, The New England journal of medicine.
[25] H. Hers. INBORN LYSOSOMAL DISEASES. , 1965, Gastroenterology.
[26] Charles R.scriver,et al. The Metabolic basis of inherited disease , 1989 .
[27] Hers Hg,et al. The genetic pathology of lysosomes. , 1970 .
[28] C. Duve,et al. Functions of lysosomes. , 1966, Annual review of physiology.
[29] C. Deduve. FROM CYTASES TO LYSOSOMES. , 1964, Federation proceedings.
[30] H. Hers. α-Glucosidase deficiency in generalized glycogen-storage disease (Pompe's disease) , 1963 .