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1 ecreted alkaline phosphatase (SEAP) reporter gene vector.
2 ex DNA and, thus, to potentially function as gene vectors.
3 prove transfection efficiencies of synthetic gene vectors.
4 ds on nonautonomous transposable elements as gene vectors.
5 trinsic tropism for liver, and are efficient gene vectors.
6 nd endoscopic ultrasound-guided injection of gene vectors.
7 he similarity between the pathway vector and gene vectors.
8 sirable inflammatory responses to adenoviral gene vectors.
9 ing factor to transfection by cationic lipid gene vectors.
10 rotects against immune responses directed at gene vectors.
11  infection with avian leukosis virus-derived gene vectors.
12 lular barriers which necessitates the use of gene vectors.
13 could be a powerful, novel way of optimizing gene vector activity.
14                            AdiNOS or control gene vector (AdLacZ) was delivered to the liver by donor
15    We describe an analytical method (Geneva: Gene Vector Analysis) to relate genes to biological prop
16 s in D. melanogaster and may be an effective gene vector and gene-tagging agent in this species and d
17 the link between limitations to dispersal in gene vectors and SGS is of key interest to biologists an
18 xplanations of complex data sets, identified gene vectors and their corresponding images that disting
19 emodynamics and thus improving oxygen, drug, gene vector, and effector cell delivery to solid tumors.
20 ation of therapeutic agents, growth factors, gene vectors, and cardioactive and vasoactive agents to
21                                    Non-viral gene vectors are commonly used for gene therapy owing to
22 excellent in vitro model reliably predicting gene vector behaviors in vivo.
23                                       Single-gene vectors, bicistronic vectors, and multigene vectors
24         We synthesized the 3 components of a gene vector binding complex: (1) A polyallylamine bispho
25 patient monitoring for RCR, and the National Gene Vector Biorepository is an NIH resource that has as
26                                          Two-gene vectors can be used to introduce the therapeutic ge
27 tionic liposomes (CLs) are used worldwide as gene vectors (carriers) in nonviral clinical application
28                          Reporter luciferase gene vectors containing the human gamma 3 ECS were used
29 problem in the development of novel TR split gene vectors currently being considered for genes too la
30 phosphonate binding can enable site-specific gene vector delivery from metal surfaces.
31               It is concluded that effective gene vector delivery from metallic stent surfaces can be
32 herapy to treat in-stent restenosis by using gene vector delivery from the metallic stent surfaces ha
33                   These finding suggest that gene vector delivery of soluble CD8 may have therapeutic
34  from An. gambiae have not been exploited as gene vectors/drivers because none have been isolated.
35 arkov chain whose state space is composed of gene vectors, each state of the Markov chain correspondi
36                                    The viral gene vectors explored to date cannot selectively transdu
37 or suppressor activity with that of a single gene vector for p53 (Adp53).
38 d out by inserting it into the pGL3 reporter gene vector for transfection into NIH3T3 cells.
39               The development of plant virus gene vectors for expression of foreign genes in plants p
40 -positive cancer cells, would make excellent gene vectors for GDEPT therapy of hepatocellular carcino
41 re effective than is a combination of single gene vectors for p14 and p53.
42 ellular barriers typically prevent non-viral gene vectors from having an effective transfection effic
43                                     This new gene vector has a great potential in clinical gene thera
44  Incorporation of drug resistance genes into gene vectors has 2 important roles in stem cell gene the
45  addition, the expression from intact globin gene vectors has been variable in red blood cells due to
46 e of the similarity measure between pairs of gene vectors impacts the properties of networks and of g
47 ch a biomaterial-guided delivery of a potent gene vector in an orthotopic large animal model of carti
48  throughout the heart and may be useful as a gene vector in organ transplantation.
49 ontrolled and minimally invasive delivery of gene vectors in a spatiotemporally precise manner, reduc
50 ation is a prerequisite for the transport of gene vectors in living cells.
51 Hilbert space to decompose the nonidentified gene vector into two components that are correlated and
52      Advanced biomaterial-guided delivery of gene vectors is an emerging and highly attractive therap
53 apy with various viral vectors and non-viral gene vectors is well tolerated by patients, and continue
54 se fibroblasts transduced with this ribozyme gene vector library were selected in a focus formation a
55  produced gadolinium/blue dye and gadolinium/gene-vector media by mixing Magnevist with a trypan-blue
56 itive PBN is composed of a pair, the current gene vector occupied by the network and the current cons
57 l protein translation, a luciferase reporter gene vector, pCMV/T7-NCRCdelta-luc, was constructed cont
58 loned into the mammalian luciferase reporter gene vector pGL3-Basic.
59 nto a T-vector constructed from the reporter gene vector pGL3.
60 action and cloned into a luciferase reporter gene vector, pGL3-basic.
61  of 3D models for screening newly engineered gene vectors prior to their in vivo evaluation.
62                                         Many gene vectors require large particle numbers for even ear
63 owever, the site-specific delivery of common gene vectors such as adeno-associated viruses (AAVs) is
64                                  To engineer gene vectors that target striated muscles after systemic
65                    When cloned into reporter gene vectors, the genomic fragment showed significant pr
66 hor considers the plausibility of developing gene vector therapies that use conditional expression sy
67 oretically have many desirable properties as gene vectors, there are several practical barriers to su
68  either a gamma-retroviral or lentiviral ADA gene vector to assess transgene mutational profiles.
69  attributed to the inability of conventional gene vectors to achieve gene transfer throughout highly
70 ate due in part to inability of conventional gene vectors to achieve widespread gene transfer through
71 ed origin could be used practically in human gene vectors to improve their efficiency in therapy and
72 ent, tunable method for sustained release of gene vectors to the vasculature.
73                                     Reporter gene vector transfection and CRISPR-Cas9 editing were us
74 ute, gene expression, and time course of AAV gene vector transfer to LG.
75 at a pool of eight African swine fever virus genes vectored using an adenovirus prime and modified va
76                                   A reporter gene vector was constructed so that expression of an ins
77 f this methodology produced a TBSV DNA-based gene vector which yielded readily detectable levels of l
78  a panel of 13 inducible luciferase reporter gene vectors which expression is driven by enhancer elem
79 m) protoplast system and a modified reporter gene vector with an internal transformation control, 25
80 thesis of new 3D "Single Cyclized" polymeric gene vectors with well-defined compositions and function