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1  developed murine leukemia virus (MLV)-based self-inactivating and self-activating vectors to show th
2             We developed a novel conditional self-inactivating (C-SIN) vector, TL-SN, by replacement
3                         Substrate-initiated, self-inactivating, cell-penetrating poly(disulfide)s (si
4  To overcome this limitation, we developed a self-inactivating DeltaG-rabies virus (SiR) that transcr
5                                            A self-inactivating EIAV minimal lentiviral vector that ex
6 omegalovirus minimal promoter, the vector is self-inactivating, eliminating transcription from the lo
7 n H synthase (PGHS) is a self-activating and self-inactivating enzyme.
8                             Using a panel of self-inactivating gamma-retroviral vectors that express
9           We recently developed an insulated self-inactivating gammaretroviral vector, RMSinOFB, whic
10 Spleen Focus Forming Virus promoter within a self-inactivating HIV-based lentiviral vector.
11  use of cellular promoters in "enhancerless" self-inactivating integrating vectors.
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
16                                            A self-inactivating lentiviral vector harboring these targ
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
24                       Given the shift toward self-inactivating long terminal repeats with weaker prom
25 l vectors, including lentiviral vectors with self-inactivating long terminal repeats, have been shown
26 rom the chicken beta-globin locus within the self-inactivating long-terminal repeat.
27 ressed full-length type VII collagen using a self-inactivating minimal lentivirus-based vector.
28                          We have developed a self-inactivating PiggyBac transposon system for tamoxif
29                    A recent study employed a self-inactivating rabies (SiR) virus that enables record
30                                 We developed self-inactivating retroviral vectors that incorporate ge
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
33                         In addition, using a self-inactivating retrovirus luciferase reporter constru
34                                      Fifteen self- inactivating (SIN) lentiviral vectors using 4 eryt
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).
40 no LTR-directed transcription and are called self-inactivating (SIN) lentivectors.
41                                        Via a self-inactivating (SIN) lentiviral vector a 3' RNA trans
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
45 utside of its normal MLV genome context in a self-inactivating (SIN) lentiviral vector.
46                                              Self-inactivating (SIN) lentiviral vectors have been dem
47                                     Although self-inactivating (SIN) lentiviral vectors with or witho
48 othelial-specific, and doxycycline-inducible self-inactivating (SIN) lentiviral vectors.
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
51                The distinguishing feature of self-inactivating (SIN) retroviral vectors is the deleti
52                                            A self-inactivating (SIN) vector was constructed by deleti
53                                   The use of self-inactivating (SIN) vectors in which a deletion of t
54  added safety modification that renders them self-inactivating through the deletion of the 3' U3 enha
55          These effects were abrogated with a self-inactivating vector.
56 omoter and Deltagag(871-1612) were used in a self-inactivating-vector setting that has a further dele
57                                              Self-inactivating vectors devoid of viral long-terminal-
58                                              Self-inactivating vectors with internal heterologous reg
59                                The resulting self-inactivating viruses drive global and persistent ge

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