Examples of 'gene therapy vector' in a sentence
Meaning of "gene therapy vector"
gene therapy vector: A carrier used to deliver genes into cells for therapeutic purposes. This can be a virus or other vehicle that is modified to carry the desired genetic material into target cells in gene therapy treatments
How to use "gene therapy vector" in a sentence
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gene therapy vector
A gene therapy vector may be used.
Baculovirus system for the expression of a gene therapy vector.
The gene therapy vector includes one or more promoters.
Preferably the vector is a secretion vector or a gene therapy vector.
The cell or gene therapy vector includes one or more promoters.
It is preferred to deliver them by means of any suitable gene therapy vector.
A pharmaceutical preparation of the gene therapy vector may also be administered to a subject.
A nucleic acid construct according to the invention is a viral gene therapy vector.
Specific examples of viral gene therapy vector systems are briefly described below.
AAV has a number of features that make it particularly attractive as a gene therapy vector.
Portions of the retroviral gene therapy vector may be derived from different retroviruses.
These properties of AAV also recommend it as a potentially useful human gene therapy vector.
Portions of the retroviral gene therapy vector maybe derived from different retroviruses.
This finding paves the way for the use of OAV as a human gene therapy vector.
A preferred viral gene therapy vector is an AAV or Lentiviral vector.
See also
As such, it has been patented as a potential gene therapy vector.
In one case, a gene therapy vector is used.
In another embodiment, the vector is a gene therapy vector.
The gene therapy vector is formulated to contain common salts, buffer and excipients.
In one embodiment, a gene therapy vector is used.
In another particular embodiment, said medicament is a gene therapy vector.
Within the brain, gene therapy vector may be administered to the parenchyma or the ventricles.
In another embodiment, the invention provides a gene therapy vector.
A gene therapy vector comprising the cDNA according to Claim 7.
In a further preferred embodiment, the vector is a gene therapy vector.
A gene therapy vector comprised the cDNA according to Claim 6.
In one embodiment, the expression vector is a gene therapy vector.
A gene therapy vector expressing a nucleotide sequence, which encodes the sdAb according to claims 1 to 3.
Preferably, the recombinant nucleic acid is a gene therapy vector.
A preferred viral gene therapy vector is an adeno-associated virus ( AAV ).
In some circumstances, it is desirable to regulate expression of a transgene in a gene therapy vector.
In one embodiment of the present invention, the gene therapy vector is an adenovirus-derived vector.
In this respect, the recombinant lentivirus produced will be usable as a gene therapy vector.
Therefore, the invention relates to a gene therapy vector comprising an IBDV CVLP-pVP2 *.
Because of these properties, HSV is very promising as a gene therapy vector.
The gene therapy vector may for example be an adeno-associated vector ( AAV ).
Thus, in a preferred aspect of the present disclosure, the gene therapy vector is a viral vector.
Preferably, the gene therapy vector of the invention comprises the sequence SEQ ID No. 1.
In a particular embodiment, the background gene therapy vector is an AAV.
A particularly suitable gene therapy vector includes an Adenoviral and Adeno-associated virus ( AAV ) vector.
In this respect, the recombinant AAV produced will be usable as a gene therapy vector.
Another virus-based gene therapy vector comprises the gene sequences of US3 and US6, respectively.
In certain further embodiments, the gene therapy vector will be HSV.
The gene therapy vector may be, e.g., a viral vector such as adenovirus and adeno-associated virus.
Use according to claim 13, wherein said medicament is a gene therapy vector.
The use according to claim 6, whereby said medicament is a gene therapy vector.
The expression vector of claim 7, wherein said vector is a gene therapy vector.
An implantable matrix material, capable of rapid off-loading of AAV gene therapy vector e . g.
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