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Retroviral vectors for use in human gene therapy for cancer, Gaucher disease, and arthritis.

作者信息

Robbins P D, Tahara H, Mueller G, Hung G, Bahnson A, Zitvogel L, Galea-Lauri J, Ohashi T, Patrene K, Boggs S S

机构信息

Department of Molecular Genetics and Biochemistry, University of Pittsburgh School of Medicine, Pennsylvania 15261.

出版信息

Ann N Y Acad Sci. 1994 May 31;716:72-88; discussion 88-9. doi: 10.1111/j.1749-6632.1994.tb21704.x.

DOI:10.1111/j.1749-6632.1994.tb21704.x
PMID:7912915
Abstract
摘要

相似文献

1
Retroviral vectors for use in human gene therapy for cancer, Gaucher disease, and arthritis.用于人类癌症、戈谢病和关节炎基因治疗的逆转录病毒载体。
Ann N Y Acad Sci. 1994 May 31;716:72-88; discussion 88-9. doi: 10.1111/j.1749-6632.1994.tb21704.x.
2
The molecular biology of Gaucher disease and the potential for gene therapy.戈谢病的分子生物学及基因治疗潜力
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Expression levels by retroviral vectors based upon the N2 and the MFG backbones.基于N2和MFG骨架的逆转录病毒载体的表达水平。
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Gaucher disease: retrovirus-mediated correction of the enzymatic defect in cultured cells.戈谢病:逆转录病毒介导的培养细胞中酶缺陷的纠正。
Cold Spring Harb Symp Quant Biol. 1986;51 Pt 2:1041-6. doi: 10.1101/sqb.1986.051.01.120.
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[Gene therapy for arthritis--past and future].[关节炎的基因治疗——过去与未来]
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Retroviral-mediated transfer of the human glucocerebrosidase gene into cultured Gaucher bone marrow.逆转录病毒介导的人葡萄糖脑苷脂酶基因转移至培养的戈谢病患者骨髓细胞中。
J Clin Invest. 1992 Aug;90(2):342-8. doi: 10.1172/JCI115868.
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Toward gene therapy for Gaucher disease.迈向戈谢病的基因治疗
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Retroviral transfer of the glucocerebrosidase gene into CD34+ cells from patients with Gaucher disease: in vivo detection of transduced cells without myeloablation.将葡糖脑苷脂酶基因通过逆转录病毒转移至戈谢病患者的CD34+细胞:无需骨髓消融即可在体内检测转导细胞
Hum Gene Ther. 1998 Nov 20;9(17):2629-40. doi: 10.1089/hum.1998.9.17-2629.
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Retrovirus-mediated transfer of the cDNA for human glucocerebrosidase into peripheral blood repopulating cells of patients with Gaucher's disease.逆转录病毒介导的人葡萄糖脑苷脂酶cDNA转移至戈谢病患者的外周血重建细胞中。
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Gene Therapy in Orthopaedics: Progress and Challenges in Pre-Clinical Development and Translation.骨科中的基因治疗:临床前开发与转化中的进展与挑战
Front Bioeng Biotechnol. 2022 Jun 28;10:901317. doi: 10.3389/fbioe.2022.901317. eCollection 2022.
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Gene delivery into primary T cells: overview and characterization of a transgenic model for efficient adenoviral transduction.将基因导入原代T细胞:高效腺病毒转导转基因模型的概述与表征
Immunol Res. 2002;26(1-3):131-41. doi: 10.1385/ir:26:1-3:131.
3
Effects of cytokine gene therapy on particulate-induced inflammation in the murine air pouch.
Inflammation. 2001 Dec;25(6):361-72. doi: 10.1023/a:1012898513512.
4
Gene therapy for rheumatoid arthritis.
Springer Semin Immunopathol. 1998;20(1-2):197-209. doi: 10.1007/BF00832007.
5
Gene therapy in sports medicine.
Sports Med. 1998 Feb;25(2):73-7. doi: 10.2165/00007256-199825020-00001.
6
Gene therapy vectors as drug delivery systems.作为药物递送系统的基因治疗载体。
Clin Pharmacokinet. 1995 Mar;28(3):181-9. doi: 10.2165/00003088-199528030-00001.
7
Amplified and tissue-directed expression of retroviral vectors using ping-pong techniques.利用乒乓技术实现逆转录病毒载体的扩增及组织定向表达。
J Mol Med (Berl). 1995 Mar;73(3):113-20. doi: 10.1007/BF00198238.