用于全长人类抗肌萎缩蛋白cDNA基因转移的腺病毒载体。 - Suppr

Adenoviral vectors for gene transfer of full-length human dystrophin cDNAs.

Murphy S, Turner G, Piper T, Roberts B, Wadworth S, Smith A E, Wells D J, Dickson G

School of Biological Sciences, Royal Holloway College, University of London, Surrey, UK.

Biochem Soc Trans. 1996 May;24(2):277S. doi: 10.1042/bst024277s.

Abstract

摘要

Biochem Soc Trans. 1996 May;24(2):277S. doi: 10.1042/bst024277s.

Neuromuscul Disord. 1997 Jul;7(5):277-83. doi: 10.1016/s0960-8966(97)00052-7.

Biochem Soc Trans. 1996 May;24(2):275S. doi: 10.1042/bst024275s.

Hum Gene Ther. 1994 Feb;5(2):165-73. doi: 10.1089/hum.1994.5.2-165.

Hum Mol Genet. 1995 Aug;4(8):1251-8. doi: 10.1093/hmg/4.8.1251.

Hum Mol Genet. 1993 Jun;2(6):717-23. doi: 10.1093/hmg/2.6.717.

Hum Gene Ther. 2007 Jun;18(6):490-501. doi: 10.1089/hum.2006.155.

Biochem Soc Trans. 1996 May;24(2):279S. doi: 10.1042/bst024279s.

J Gene Med. 1999 Jul-Aug;1(4):280-9. doi: 10.1002/(SICI)1521-2254(199907/08)1:4<280::AID-JGM45>3.0.CO;2-L.

Mol Cell Biol Hum Dis Ser. 1993;3:283-302. doi: 10.1007/978-94-011-1528-5_11.

20分钟写一篇综述，助力文献阅读效率提升50倍。

大模型驱动的PubMed中文搜索引擎

学术文献翻译模型，支持多种主流文档格式。