Значения термина therapeutic gene на английском

As a result, the treated patients continued to benefit from therapeutic gene transfer.

In this chapter, we recount our development of E1A as a therapeutic gene.

As such, this enhancer is a novel, attractive target for therapeutic gene editing.

Suicide gene therapy of malignant melanoma essentially requires efficient gene transfer and highly selective therapeutic gene expression.

We believe that insulated SB-derived vectors will become useful tools in transposon-based transgenesis and therapeutic gene transfer.

Somatic gene therapy involves the introduction of novel genetic material into somatic cells to express therapeutic gene products.

Nonviral integration systems are widely used genetic tools in transgenesis and play increasingly important roles in strategies for therapeutic gene transfer.

These reporter genes can be coupled with a therapeutic gene of interest to indirectly monitor the expression of the therapeutic gene.

Reporter genes are emerging as very powerful tools to monitor the delivery, magnitude, and time variation of therapeutic gene transfer in vivo.

To assess the potential for arginine peptide as an agent for therapeutic gene delivery, in vivo complexed DNA transduction studies were performed.

Intramuscular electroporation of the therapeutic gene is a simple, economic, and low toxic method compared with systemic administration of the purified proteins or peptides.

This response curtails the duration of mouse EPO expression in mice, presumably by destroying the cells that co-express transcription factors and the therapeutic gene.

Two tools essentially constitute such concepts, the vector for efficient transfer and expression of the transgene in the cancer cell, and the therapeutic gene.

These data suggest that a therapeutic gene, when expressed in xenogenic animals, can be a tumor antigen which is recognized by a host defense system.

Hematopoietic progenitor cells (HPCs) are an ideal therapeutic gene transfer target as they are used in therapy for a variety of hematologic and metabolic conditions.

Replication-competent adenoviruses could provide an efficient method for delivering therapeutic genes to tumors.