ライフサイエンスコーパス: recombinant retrovirus

1 od that allows for precise quantification of recombinant retrovirus.

2 occurs pairwise, resembling the formation of recombinant retroviruses.

3 ression and structure of randomly integrated recombinant retroviruses.

4 nt PCR-based rescue procedure for integrated recombinant retroviruses.

5 human and mouse fibroblasts using high-titer recombinant retroviruses, allowing analysis of E1A in ge

6 Replication-incompetent recombinant retroviruses are currently used for gene del

7 r retroviruses using a replication-defective recombinant retrovirus as a model retrovirus.

8 These phenomena hamper the use of recombinant retroviruses as stable gene delivery vectors

9 When using recombinant retroviruses as vectors for gene transfer an

10 ted vesicular stomatitis virus-G-pseudotyped recombinant retrovirus by transfection into 293GPG cells

11 at hepatocytes using a replication-defective recombinant retrovirus capable of transferring a gene en

12 a 50-day-old female rat and infected with a recombinant retrovirus carrying a v-src gene after 2, 7,

13 tor necessary for transformation we passaged recombinant retroviruses carrying the axl cDNA in NIH3T3

14 t produces a high titer (>10(6) i.p. per ml) recombinant retrovirus constructed to transduce and corr

15 atopoietic stem cells (HSCs) transduced with recombinant retroviruses containing B domain-deleted por

16 e and human B lymphocytes were infected with recombinant retroviruses containing Smu and S gamma 2b s

17 Ectopic expression of Id2 with recombinant retroviruses converted ectodermal cells to a

18 genously or expressed by keratinocytes via a recombinant retrovirus encoding KGF.

19 SCs) that had been transduced ex vivo with a recombinant retrovirus encoding normal p47(phox).

20 BLCL were transduced with a recombinant retrovirus encoding pp65, the immunodominant

21 nt with this mutation were immortalized by a recombinant retrovirus encoding the E6 and E7 genes of h

22 Using a model recombinant retrovirus encoding the Escherichia coli lac

23 rom the resected liver and transduced with a recombinant retrovirus encoding the gene for the human l

24 and one normal FLS lines were infected with recombinant retrovirus encoding the neomycin resistance

25 genes to various cell lines, we constructed recombinant retroviruses encoding gB, gH, gL, and gO.

26 These recombinant retroviruses establish infection of immunode

27 addition, PalF cells acutely infected with a recombinant retrovirus expressing E5 were also examined.

28 tes from multiple sources were infected with recombinant retrovirus expressing HPV 16 E6 and E7 or co

29 In this study, we have used a recombinant retrovirus expressing noggin to inhibit the

30 ient cell line (3T6-C26) was infected with a recombinant retrovirus expressing the human MDR1 gene.

31 and dermal fibroblasts were transduced with recombinant retroviruses expressing a reporter gene (lac

32 A comparison between animals exposed to recombinant retroviruses expressing cEPOR and cEPORYF sh

33 Recombinant retroviruses expressing high-risk E6 alone,

34 of primary human foreskin keratinocytes with recombinant retroviruses expressing HPV-16 E7 resulted i

35 IH 3T3 cells were stably transduced by using recombinant retroviruses expressing these genes or the k

36 Recombinant retroviruses expressing three chick lens con

37 We have constructed a high-titer recombinant retrovirus for expression of gp91-phox, defi

38 Autologous BMC were transduced ex vivo with recombinant retroviruses for allogeneic DRB followed by

39 signaling pathway by screening a library of recombinant retroviruses for clones that inhibit the exp

40 SMC lines were isolated after infection with recombinant retroviruses harboring OPN sense and antisen

41 To overcome this, a bicistronic recombinant retrovirus has been generated that delivers

42 Recombinant retroviruses have been shown to bind to fibr

43 Ectopic expression of p16ink4a with a recombinant retrovirus in this cell line also induced a

44 ction of constitutively active Ras or Raf by recombinant retroviruses induced FucT-VII expression onl

45 tumor cells as vaccine, cells transduced via recombinant retrovirus (MC38/R-B7) and recombinant vacci

46 The recombinant retrovirus, MoFe2-MuLV (MoFe2), was construc

47 ocultivation directly on producer cells; (2) recombinant retrovirus particles directly adhere to FN 3

48 The recombinant retrovirus pMXIG, which was designed to coex

49 Recombinant retroviruses provide highly efficient gene d

50 This goal is achieved by using recombinant retroviruses pseudotyped with either the gib

51 Recombinant retrovirus (R-B7) and the recombinant vaccin

52 h normal kinetics in cells coinfected with a recombinant retrovirus, retroUL69, which expresses UL69

53 in the transformation process, we generated recombinant retrovirus selectively encoding epitope-tagg

54 BM cells were infected with a recombinant retrovirus, SF91, containing the Fpg gene an

55 of STAT-1 levels in HPV-positive cells using recombinant retroviruses significantly impaired viral am

56 Infecting glial progenitors with Cre-recombinant retrovirus simultaneously activates expressi

57 he findings demonstrate the utility of novel recombinant retroviruses such as MoFe2 to contribute new

58 Introduction of Fes into these lines with a recombinant retrovirus suppressed their growth in soft a

59 A recombinant retrovirus, termed MoFe2-MuLV, was construct

60 on is markedly increased by the emergence of recombinant retroviruses that repeatedly infect host cel

61 llular domain (N2ICD) is expressed from this recombinant retrovirus through internal ribosome entry.

62 Saos-2 cells were infected with recombinant retrovirus to establish a proliferating pool

63 In this study, we used recombinant retroviruses to express M33 in wild-type and

64 oblems prevent the application of MuLV-based recombinant retroviruses to lung gene therapy: (i) the l

65 Recombinant retrovirus vectors are widely used for gene

66 oned with growth factors and transduced with recombinant retrovirus vectors containing allogeneic (n=

67 A panel of recombinant retrovirus vectors expressing different form

68 The potent ability of recombinant retrovirus vectors to induce HBcAg- and eAg-

69 ol retrovirus, LXSN, or HPV16 2E5-expressing recombinant retrovirus was quantitated.

70 cells that bear a single copy of integrated recombinant retroviruses was generated without using dru

71 Using recombinant retroviruses, we acutely transduced neonatal

72 Here, recombinant retroviruses were used to deliver six differ

73 Recombinant retroviruses were used to transduce 9L glios