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1 chieved following transfection of cells by a retrovirus vector.
2 vo with the NOD/SCID mouse system using onco-retrovirus vector.
3 receptor (sFlt-1) on N202.1A cells, using a retrovirus vector.
4 ession of Gata4, Mef2c, and Tbx5 (GMT) using retrovirus vectors.
5 and in chickens using replication-competent retrovirus vectors.
6 mbryonic and postnatal cerebral cortex using retrovirus vectors.
7 etochore requires transfection of cells by a retrovirus vector, a step that is potentially mutagenic.
8 udy, using busulfan conditioning and an SFFV retrovirus vector, achieved more than 20% marking in 2 p
9 -globin capable of efficient expression in a retrovirus vector and form the basis for further refinem
11 nts was then investigated using MoMuLV-based retrovirus vectors and HIV-1-based lentivirus vectors.
12 Moloney murine leukemia virus (MoMLV)-based retrovirus vectors and that such vectors can transduce h
13 aimed at the preparation of tissue-targeted retrovirus vectors and will also aid in studies of nucle
14 oduced into normal bone marrow cells through retrovirus vectors, and neutrophils expressing this muta
17 genes were constructed and used to generate retrovirus vectors bearing corresponding Env proteins.
18 ared the binding and infectivity patterns of retrovirus vectors bearing either FeLV-B-90Z or FeLV-B-G
19 ty characteristics not only over amphotropic retrovirus vectors but also over genetically tropism-mod
20 opoietic stem cells (HSCs) transduced with a retrovirus vector carrying an activated ABL oncogene can
22 retroviral DNA upon arrested cells when the retrovirus vector contained the corresponding binding mo
25 eatment with a self-inactivating (SIN) gamma-retrovirus vector containing deletions in viral enhancer
26 4(+) cells from these patients using an MFGS retrovirus vector containing the gamma(c) gene IL2RG pse
27 owth factors and transduced with recombinant retrovirus vectors containing allogeneic (n=4) or syngen
29 le that this novel ecotropic-based conjugate retrovirus vector could also potentially provide enhance
30 old differences in levels of expression of a retrovirus vector depending on its site of insertion in
33 o fibroblasts to an excess of an amphotropic retrovirus vector encoding alkaline phosphatase results
34 ic neurons using diphtheria toxin (DT) and a retrovirus vector encoding DT receptor abolished the ben
35 (+) cells were transduced with an MFGS-based retrovirus vector encoding mCD24 using 4 daily transduct
36 eral blood-mobilized stem cells (PBSCs) with retrovirus vector encoding wild-type (wt) CXCR4 or WHIM-
37 ines displayed varying capacities to produce retrovirus vectors even at the same transduction efficie
39 a Moloney murine leukemia virus-based gamma-retrovirus vector expressing interleukin-2 receptor gamm
42 lls were transduced through infection with a retrovirus vector expressing the human telomerase cataly
46 th this system resulted in the production of retrovirus vectors for more than 1 week and the long-ter
48 enous feline or human CXCR4 expressed from a retrovirus vector, indicating that experiments investiga
50 jections with 10(8) CFU of the LHBc-NEO(6A3) retrovirus vector into rhesus monkeys induced HBc/eAg-sp
53 nclude that infection of mammary glands with retrovirus vectors is an efficient means to screen candi
54 Transduction by murine leukemia virus-based retrovirus vectors is limited in certain cell types, par
55 ells of the T cell line were inserted into a retrovirus vector linked by an oligonucleotide encoding
57 demonstrates that such modified pseudotyped retrovirus vectors may be useful reagents for studies of
59 as carried out by topical application of two retrovirus vectors, MFGlacZ (10(7) blue forming units pe
61 expression of HINT1 in these cells, using a retrovirus vector (pLNCX2) that encodes either wild-type
62 hed bone marrow stem cells transduced with a retrovirus vector preparation containing replication-com
63 on assay to directly compare GALV-pseudotype retrovirus vectors produced by either Phoenix-GALV or by
64 id amplicons to efficiently convert cells to retrovirus vector producer cells after single-step trans
66 o infection by a murine leukemia virus-based retrovirus vector pseudotyped with the MMTV envelope pro
67 xperiments in the presence of FN CH-296 with retrovirus vectors pseudotyped with the same or a differ
69 us, efficient transduction by an amphotropic retrovirus vector requires high-level expression of the
73 omatitis virus G protein (VSV-G) pseudotyped retrovirus vector that was concentrated to high titer.
74 e inserted the Ank/(A)gamma-globin gene into retrovirus vectors that could transfer one or two copies
75 in red blood cells, we could generate stable retrovirus vectors that would express globin at sufficie
78 1 infection, we used a murine leukemia virus retrovirus vector to transduce and overexpress the cDNA
80 orders has been hampered by the inability of retrovirus vectors to transfer globin genes and their ci
83 ssion of Fpg in bone marrow (BM) cells via a retrovirus vector was associated with demonstrable 8-oxo
85 Moloney murine leukemia virus (MoMuLV)-based retrovirus vectors was investigated in various settings.
86 udies amphotropic MFGS-gp91phox (murine onco-retrovirus vector) was used in a clinical trial of X-lin
87 ndividual myeloid colonies demonstrated that retrovirus vectors with FeLV-C and RD114 pseudotypes wer
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