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1 developed murine leukemia virus (MLV)-based self-inactivating and self-activating vectors to show th
4 To overcome this limitation, we developed a self-inactivating DeltaG-rabies virus (SiR) that transcr
6 omegalovirus minimal promoter, the vector is self-inactivating, eliminating transcription from the lo
12 alovirus (CMV) immediate-early promoter in a self-inactivating lentiviral vector (CSCG) is 4- to 15-f
13 reatment of children with a state-of-the-art self-inactivating lentiviral vector (LV-w1.6 WASp) has r
14 vitro fertilized ova were transduced with a self-inactivating lentiviral vector and transferred into
15 c progenitor cells transduced ex vivo with a self-inactivating lentiviral vector encoding a full-leng
17 e when inserted into the first intron, but a self-inactivating lentiviral vector with an internal cel
18 odeficiency (SCID-X1), we have evaluated new self-inactivating lentiviral vectors based on the HIV vi
19 such an approach using a therapeutic grade, self-inactivating-lentiviral vector, encoding codon opti
20 such an approach using a therapeutic grade, self-inactivating-lentiviral vector, encoding codon-opti
21 row and peripheral blood CD34+ cells using a self-inactivating lentivirus vector (CS-Rh-MLV-E) bearin
22 to 10-fold greater than that utilizing a non-self-inactivating lentivirus vector bearing the cytomega
23 ly integrated reporter system derived from a self-inactivating lentivirus vector, we showed in a BRG1
25 l vectors, including lentiviral vectors with self-inactivating long terminal repeats, have been shown
31 eveloped a reporter assay system employing a self-inactivating retrovirus and analyzed the cystatin C
32 We assessed the efficacy and safety of a self-inactivating retrovirus for the treatment of SCID-X
35 nsduce hematopoietic repopulating cells, and self-inactivating (SIN) designs can be produced at high
36 e United States to evaluate treatment with a self-inactivating (SIN) gamma-retrovirus vector containi
37 terestingly, the polyadenylation signal of a self-inactivating (SIN) HIV-1 vector was as leaky as tha
38 by use of a high-throughput screen involving self-inactivating (SIN) human immunodeficiency virus typ
39 ted using VSV-G-pseudotyped, 3rd-generation, self-inactivating (SIN) lentivector encoding gp91(phox).
42 oth separately and together into a series of self-inactivating (SIN) lentiviral vector backbones.
43 ells are transduced with a minimum amount of self-inactivating (SIN) lentiviral vector containing a p
44 globulin promoter and enhancer elements in a self-inactivating (SIN) lentiviral vector should lead to
49 roviral/lentiviral vectors (gammaRV/LV) with self-inactivating (SIN) long terminal repeats (LTRs) and
50 nternal promoters, chromatin insulators, and self-inactivating (SIN) long terminal repeats (LTRs) may
54 added safety modification that renders them self-inactivating through the deletion of the 3' U3 enha
56 omoter and Deltagag(871-1612) were used in a self-inactivating-vector setting that has a further dele
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