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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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發(fā)表于 2025-3-28 16:06:12 | 只看該作者
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發(fā)表于 2025-3-28 20:04:17 | 只看該作者
MIDGE Technology for the Production of a Fourfold Gene-Modified, Allogenic Cell-Based Vaccine for Carposes, like gene correction or production of therapeutics. Here, we describe the generation of a cell-based tumor vaccine via fourfold transient gene modification of a human renal cell carcinoma (RCC) cell line for high expression of CD80, CD154, GM-CSF, and IL-7 by use of MIDGE. vectors. The two c
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發(fā)表于 2025-3-28 23:26:08 | 只看該作者
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發(fā)表于 2025-3-29 03:26:00 | 只看該作者
Oncoleaking: Use of the Pore-Forming , Enterotoxin (CPE) for Suicide Gene Therapyheir therapeutic potential in clinical trials. Apart from this, still growing efforts are made to generate more targeted and more effective suicide gene systems for cancer gene therapy. In this regard bacterial toxins are an alternative, which add to the broad spectrum of different suicide strategie
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發(fā)表于 2025-3-29 10:40:23 | 只看該作者
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發(fā)表于 2025-3-29 14:52:31 | 只看該作者
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發(fā)表于 2025-3-29 19:14:15 | 只看該作者
A qRT-PCR Method for Determining the Biodistribution Profile of a miR-34a Mimicivo, a quantitation method is needed that exhibits high precision, accuracy, and robustness. While most clinical applications for oligonucleotide therapeutics involve methods based on hybridization assays and liquid chromatography-tandem mass spectrometry, quantitative PCR (qPCR) is a less well-desc
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發(fā)表于 2025-3-29 21:56:52 | 只看該作者
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發(fā)表于 2025-3-30 00:28:58 | 只看該作者
RNA Interference for Antimetastatic Therapyancer disease. Efficient delivery of interfering molecules and their sustained presence in tumor cells are required for therapeutic success. This chapter describes a method of systemic application of shRNA expression plasmid via tail vein injection in xenograft mice, causing the sustained reduction
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發(fā)表于 2025-3-30 04:58:13 | 只看該作者
STAT3 Decoy ODN Therapy for Cancerentiation, proliferation, and survival, and is associated with angiogenesis and immune dysfunction during tumorigenesis. Double-stranded decoy oligodeoxynucleotide (ODN) targeting over-activated STAT3 in tumor cells have shown significant antitumor efficiency. Here, we describe the materials and met
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