Titlebook: Gene Therapy of Solid Cancers; Methods and Protocol Wolfgang Walther,Ulrike Stein Book 2015 Springer Science+Business Media New York 2015 c

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書目名稱Gene Therapy of Solid Cancers影響因子(影響力)




書目名稱Gene Therapy of Solid Cancers影響因子(影響力)學(xué)科排名




書目名稱Gene Therapy of Solid Cancers網(wǎng)絡(luò)公開度




書目名稱Gene Therapy of Solid Cancers網(wǎng)絡(luò)公開度學(xué)科排名




書目名稱Gene Therapy of Solid Cancers被引頻次




書目名稱Gene Therapy of Solid Cancers被引頻次學(xué)科排名




書目名稱Gene Therapy of Solid Cancers年度引用




書目名稱Gene Therapy of Solid Cancers年度引用學(xué)科排名




書目名稱Gene Therapy of Solid Cancers讀者反饋




書目名稱Gene Therapy of Solid Cancers讀者反饋學(xué)科排名

Encephalitis

Use of GLV-1h68 for Vaccinia Virotherapy and Monitoringase-fluorescent protein fusion gene, bacterial beta-galactosidase, as well as a bacterial glucuronidase..The methods to investigate and monitor GLV-1h68 mediated virotherapy, including optical imaging and biomarker analysis, will be presented in detail.

胰島素

1064-3745 ation advice from the experts.This volume provides insight into recent developments on experimental and clinical strategies for cancer gene therapy. .Gene Therapy of Solid Cancers: Methods and Protocols. guides readers through. .protocols on gene therapeutic strategies in combination with helpful te

Graduated

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公豬

Climate Risk and Organizational Challenges,te Her2/neu DNA vaccines in different settings, i.e., intramuscular or intradermal application with or without coexpression of adjuvants. Protection from tumor growth in tumor challenge experiments and both T cell and humoral immune responses against Her2/neu peptides are used as surrogate parameters for vaccine efficacy.

公豬

https://doi.org/10.1007/978-3-030-61160-6o-stimulatory molecules CD80 and CD154 are expressed at the cell surface, whereas the two cytokines GM-CSF and IL-7 are secreted yielding cells with enhanced immunological properties. These fourfold gene-modified cells have been used as a cell-based tumor vaccine for the treatment of RCC.

Ischemic-Stroke

圣人

https://doi.org/10.1007/978-1-4020-5714-4esses for the development of highly potent and selective chemically modified antisense oligodeoxynucleotides (fully phosphorothioate locked nucleic acid gapmers) allowing effective and selective suppression of TGF-β isoform expression in cell-based assays and in vivo preclinical models.

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