𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Protocols cookbook for cancer gene therapy

✍ Scribed by Frank Marini


Publisher
John Wiley and Sons
Year
2000
Tongue
English
Weight
31 KB
Volume
23
Category
Article
ISSN
0265-9247

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πŸ“œ SIMILAR VOLUMES


Gene therapy for pancreatic cancer
✍ Shin Takeda; Akimasa Nakao; Koji Miyoshi; Hiroshi Takagi πŸ“‚ Article πŸ“… 1998 πŸ› John Wiley and Sons 🌐 English βš– 36 KB πŸ‘ 2 views

It has been approximately 7 years since the introduction of gene therapy. Since conventional procedures such as surgery, chemotherapy, and radiotherapy have had limited therapeutic value for cancer patients, the evolution of gene therapy seems a promising alternative to many researchers and clinicia

Gene therapy for hemophilia
✍ Marinee K. L. Chuah; Desire Collen; Thierry VandenDriessche πŸ“‚ Article πŸ“… 2001 πŸ› John Wiley and Sons 🌐 English βš– 185 KB
Gene therapy for colon cancer with the h
✍ Link, Charles J.; Levy, John P.; McCann, Leisa Z.; Moorman, Donald W. πŸ“‚ Article πŸ“… 1997 πŸ› John Wiley and Sons 🌐 English βš– 74 KB πŸ‘ 1 views

## Background: The suicide gene and prodrug, herpes simplex thymidine kinase (hstk) and ganciclovir (gcv), are now in clinical trials for recurrent malignancies. ## Methods: We evaluated in vitro and in vivo efficacy of hstk gene transfer and gcv treatment of colonic adenocarcinoma in a syngeneic

Prodrug activation enzymes in cancer gen
✍ Manish Aghi; Fred Hochberg; Xandra O. Breakefield πŸ“‚ Article πŸ“… 2000 πŸ› John Wiley and Sons 🌐 English βš– 202 KB πŸ‘ 2 views

Among the broad array of genes that have been evaluated for tumor therapy, those encoding prodrug activation enzymes are especially appealing as they directly complement ongoing clinical chemotherapeutic regimes. These enzymes can activate prodrugs that have low inherent toxicity using both bacteria

Progress in antiangiogenic gene therapy
✍ Andrew L. Feldman; Steven K. Libutti πŸ“‚ Article πŸ“… 2000 πŸ› John Wiley and Sons 🌐 English βš– 145 KB πŸ‘ 2 views

## BACKGROUND. Because tumors require angiogenesis for growth, inhibiting angiogenesis is a promising strategy for treating cancer patients. Although numerous endogenous angiogenesis inhibitors have been discovered, the clinical evaluation of these agents has been hindered by high dose requirement