Gene therapy.
作者信息
Weatherall D J
机构信息
MRC Molecular Haematology Unit, Nuffield Department of Clinical Medicine, John Radcliffe Hospital, Oxford.
出版信息
BMJ. 1989 Mar 18;298(6675):691-3. doi: 10.1136/bmj.298.6675.691.
Abstract
摘要
相似文献
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Gene therapy.基因治疗。
BMJ. 1989 Mar 18;298(6675):691-3. doi: 10.1136/bmj.298.6675.691.
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本文引用的文献
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2
Prospects for human gene therapy.人类基因治疗的前景。
Science. 1984 Oct 26;226(4673):401-9. doi: 10.1126/science.6093246.
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Position-independent, high-level expression of the human beta-globin gene in transgenic mice.人β-珠蛋白基因在转基因小鼠中与位置无关的高水平表达。
Cell. 1987 Dec 24;51(6):975-85. doi: 10.1016/0092-8674(87)90584-8.
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Towards gene therapy for hemophilia B.
Mol Biol Med. 1987 Feb;4(1):11-20.
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Retroviral gene transfer into primary hepatocytes: implications for genetic therapy of liver-specific functions.逆转录病毒基因导入原代肝细胞：对肝脏特异性功能基因治疗的意义。
Proc Natl Acad Sci U S A. 1987 Aug;84(15):5335-9. doi: 10.1073/pnas.84.15.5335.
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Targeted modification of human chromosomal genes.人类染色体基因的靶向修饰
Cold Spring Harb Symp Quant Biol. 1986;51 Pt 2:1093-9. doi: 10.1101/sqb.1986.051.01.127.
7
Retrovirus-mediated transfer of human adenosine deaminase gene sequences into cells in culture and into murine hematopoietic cells in vivo.逆转录病毒介导的人腺苷脱氨酶基因序列向培养细胞及体内小鼠造血细胞的转移。
Proc Natl Acad Sci U S A. 1986 Apr;83(8):2566-70. doi: 10.1073/pnas.83.8.2566.
8
An alternative approach to somatic cell gene therapy.体细胞基因治疗的另一种方法。
Proc Natl Acad Sci U S A. 1988 May;85(9):3150-4. doi: 10.1073/pnas.85.9.3150.
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Disruption of the proto-oncogene int-2 in mouse embryo-derived stem cells: a general strategy for targeting mutations to non-selectable genes.小鼠胚胎衍生干细胞中原癌基因int-2的破坏：一种将突变靶向非选择基因的通用策略。
Nature. 1988 Nov 24;336(6197):348-52. doi: 10.1038/336348a0.
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