Examples of 'vectors for gene' in a sentence
Meaning of "vectors for gene"
vectors for gene ~ Organisms, typically insects or bacteria, that transmit genetic material from one organism to another. This phrase is commonly used in genetics and biotechnology to describe carriers of genes used for genetic engineering
How to use "vectors for gene" in a sentence
Basic
Advanced
vectors for gene
Therapeutic retroviral vectors for gene therapy.
Suitable vectors for gene therapy are known in the art.
This makes lentiviruses attractive vectors for gene therapy.
Manufacturing viral vectors for gene therapy, current difficulties and challenges.
Retroviruses and adenoviruses have been used as vectors for gene therapy.
Adenoviruses have been used as vectors for gene therapy and for expression of heterologous genes.
Adenoviral vectors may also be suitable viral vectors for gene transfer.
Examples of vectors for gene therapy are retrovirus vector, adenovirus vector or adeno-related virus vector.
The disclosure provides replication comptent retroviral vectors for gene delivery.
Stem cells as vectors for Gene Therapy.
The present invention is useful for production of virus vectors for gene therapy.
For a review of viral vectors for gene delivery to the CNS, see Davidson et al.
Adenoviral vectors also can be suitable viral vectors for gene transfer.
MOFs as non viral vectors for gene therapy.
These sequences are available for transfer into appropriate mammalian vectors for gene transfer.
See also
Recombinant DNA vectors for gene therapy.
Retroviral based vectors are the most commonly used integrating vectors for gene therapy.
Methods for using retroviral vectors for gene therapy are described in U. S.
The targeted vectors provided herein are intended for use as vectors for gene therapy.
Viruses offer a great potential as source of vectors for gene therapy and for gene vaccination.
Toxicology, biology, medicine ( purification of monoclonal antibodies, plasmids, enzymes, vaccines, viral vectors for gene delivery ).
Design of non-viral vectors for gene therapy.
Viruses from several different families have been modified to generate viral vectors for gene delivery.
BRAINCAV, Nonhuman adenovirus vectors for gene transfer to the brain.
The present invention provides recombinant replication competent retroviral vectors for gene delivery.
Adenoviruses have been used to generate a series of vectors for gene transfer cellular engineering.
These features make AAV a very attractive candidate for creating viral vectors for gene therapy.
These viruses have been used to generate a series of vectors for gene transfer cellular engineering.
More particularly, the present invention relates to recombinant adenoviruses as vectors for gene therapy.
The development of non-viral vectors for gene therapy.
Extended antegrade epicardial coronary infusion of adeno-associated viral vectors for gene therapy.
Modified factor VIII and factor IX genes and vectors for gene therapy.
Consequently, the polypeptide can be expressed in vivo by integrated into vectors for gene therapy.
Modified soluble VEGF receptor-1 genes and vectors for gene therapy.
Antigens or therapeutic agents, recombinant viruses for vaccines and viral vectors for gene therapy.
Thus, a need exists for additional and improved vectors for gene transfer.
The major difficulties arise due to a lack of safe and specific vectors for gene targeting.
AAVs have been extensively described in the art as suitable vectors for gene delivery.
To date, a number of viruses have been engineered as vectors for gene therapy.
Thus far, viruses have been extensively used as vectors for gene therapy.
Level 2 laboratory for producing recombinant proteins and vectors for gene therapy.
They facilitate the production of high-titer lentivirus vectors for gene therapy.
The following features of the characterized AAVs have made them attractive vectors for gene transfer ( 16 ).
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