Gene therapy for a lethal genetic blistering disease: a status report.
作者信息
Bauer E A, Herron G S, Marinkovich M P, Khavari P A, Lane A T
机构信息
Department of Dermatology, Stanford University School of Medicine, CA 94305, USA.
出版信息
Trans Am Clin Climatol Assoc. 1999;110:86-92.
Abstract
摘要
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本文引用的文献
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Hemidesmosomal variants of epidermolysis bullosa. Mutations in the alpha6beta4 integrin and the 180-kD bullous pemphigoid antigen/type XVII collagen genes.大疱性表皮松解症的半桥粒变体。α6β4整合素和180-kD类天疱疮抗原/ XVII型胶原蛋白基因中的突变。
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Gene therapy: progress, problems, prospects.基因治疗：进展、问题与前景。
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Premature termination codons in the type VII collagen gene (COL7A1) underlie severe, mutilating recessive dystrophic epidermolysis bullosa.VII型胶原蛋白基因（COL7A1）中的提前终止密码子是严重致残性隐性营养不良型大疱性表皮松解症的病因。
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Gamma 2 chain of laminin-5 is recognized by monoclonal antibody GB3.层粘连蛋白-5的γ2链可被单克隆抗体GB3识别。
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The assembly of laminin-5 subunits.层粘连蛋白-5亚基的组装。
J Biol Chem. 1995 Oct 6;270(40):23496-503. doi: 10.1074/jbc.270.40.23496.
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Epidermolysis bullosa simplex: evidence in two families for keratin gene abnormalities.单纯性大疱性表皮松解症：两个家族中角蛋白基因异常的证据。
Science. 1991 Nov 22;254(5035):1202-5. doi: 10.1126/science.1720261.
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Point mutations in human keratin 14 genes of epidermolysis bullosa simplex patients: genetic and functional analyses.单纯性大疱性表皮松解症患者人类角蛋白14基因的点突变：遗传与功能分析
Cell. 1991 Sep 20;66(6):1301-11. doi: 10.1016/0092-8674(91)90051-y.
8
Recessive dystrophic epidermolysis bullosa phenotype is preserved in xenografts using SCID mice: development of an experimental in vivo model.使用SCID小鼠的异种移植保留了隐性营养不良性大疱性表皮松解症表型：一种实验性体内模型的建立。
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