Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 104

1.

Optimization of feline immunodeficiency virus vectors for RNA interference.

Harper SQ, Staber PD, Beck CR, Fineberg SK, Stein C, Ochoa D, Davidson BL.

J Virol. 2006 Oct;80(19):9371-80.

2.

Efficient transduction of nondividing cells by optimized feline immunodeficiency virus vectors.

Curran MA, Kaiser SM, Achacoso PL, Nolan GP.

Mol Ther. 2000 Jan;1(1):31-8.

3.

Minimum requirements for efficient transduction of dividing and nondividing cells by feline immunodeficiency virus vectors.

Johnston JC, Gasmi M, Lim LE, Elder JH, Yee JK, Jolly DJ, Campbell KP, Davidson BL, Sauter SL.

J Virol. 1999 Jun;73(6):4991-5000.

4.

Inhibition of the replication of feline immunodeficiency virus by lentiviral vector-mediated RNA interference in feline cell lines.

Baba K, Goto-Koshino Y, Mizukoshi F, Setoguchi-Mukai A, Fujino Y, Ohno K, Tsujimoto H.

J Vet Med Sci. 2008 Aug;70(8):777-83.

5.

Expression from second-generation feline immunodeficiency virus vectors is impaired in human hematopoietic cells.

Price MA, Case SS, Carbonaro DA, Yu XJ, Petersen D, Sabo KM, Curran MA, Engel BC, Margarian H, Abkowitz JL, Nolan GP, Kohn DB, Crooks GM.

Mol Ther. 2002 Nov;6(5):645-52.

PMID:
12409263
6.

Efficient transduction of nondividing human cells by feline immunodeficiency virus lentiviral vectors.

Poeschla EM, Wong-Staal F, Looney DJ.

Nat Med. 1998 Mar;4(3):354-7.

PMID:
9500613
7.

Transduction of cell lines and primary cells by FIV-packaged HIV vectors.

Morris KV, Gilbert J, Wong-Staal F, Gasmi M, Looney DJ.

Mol Ther. 2004 Jul;10(1):181-90.

PMID:
15272479
8.

Streamlined design of a self-inactivating feline immunodeficiency virus vector for transducing ex vivo dendritic cells and T lymphocytes.

Pistello M, Vannucci L, Ravani A, Bonci F, Chiuppesi F, del Santo B, Freer G, Bendinelli M.

Genet Vaccines Ther. 2007 Sep 19;5:8.

9.

Persistent gene expression in mouse nasal epithelia following feline immunodeficiency virus-based vector gene transfer.

Sinn PL, Burnight ER, Hickey MA, Blissard GW, McCray PB Jr.

J Virol. 2005 Oct;79(20):12818-27.

10.

Comparison of wild-type and class I integrase mutant-FIV vectors in retina demonstrates sustained expression of integrated transgenes in retinal pigment epithelium.

Loewen N, Leske DA, Chen Y, Teo WL, Saenz DT, Peretz M, Holmes JM, Poeschla EM.

J Gene Med. 2003 Dec;5(12):1009-17.

PMID:
14661176
11.

FIV vector systems.

Sauter SL, Gasmi M.

Somat Cell Mol Genet. 2001 Nov;26(1-6):99-129. Review.

PMID:
12465464
13.

In vivo gene transfer using a nonprimate lentiviral vector pseudotyped with Ross River Virus glycoproteins.

Kang Y, Stein CS, Heth JA, Sinn PL, Penisten AK, Staber PD, Ratliff KL, Shen H, Barker CK, Martins I, Sharkey CM, Sanders DA, McCray PB Jr, Davidson BL.

J Virol. 2002 Sep;76(18):9378-88.

14.

Lentiviral vectors that carry anti-HIV shRNAs: problems and solutions.

ter Brake O, Berkhout B.

J Gene Med. 2007 Sep;9(9):743-50.

PMID:
17628029
15.

Comparative studies of various artificial microRNA expression vectors for RNAi in mammalian cells.

Hu T, Chen P, Fu Q, Liu Y, Ishaq M, Li J, Ma L, Guo D.

Mol Biotechnol. 2010 Sep;46(1):34-40. doi: 10.1007/s12033-010-9264-7.

PMID:
20300885
16.

pSM155 and pSM30 vectors for miRNA and shRNA expression.

Wu J, Bonsra AN, Du G.

Methods Mol Biol. 2009;487:205-19. doi: 10.1007/978-1-60327-547-7_10.

PMID:
19301649
17.

RNAi expression vectors in mammalian cells.

Miyagishi M, Taira K.

Methods Mol Biol. 2004;252:483-91.

PMID:
15017073
18.

Generation of hairpin-based RNAi vectors for biological and therapeutic application.

Boudreau RL, Davidson BL.

Methods Enzymol. 2012;507:275-96. doi: 10.1016/B978-0-12-386509-0.00014-4. Review.

PMID:
22365779
19.

Liver-directed gene therapy: quantitative evaluation of promoter elements by using in vivo retroviral transduction.

Rettinger SD, Kennedy SC, Wu X, Saylors RL, Hafenrichter DG, Flye MW, Ponder KP.

Proc Natl Acad Sci U S A. 1994 Feb 15;91(4):1460-4.

20.

Enhanced gene expression conferred by stepwise modification of a nonprimate lentiviral vector.

Sinn PL, Goreham-Voss JD, Arias AC, Hickey MA, Maury W, Chikkanna-Gowda CP, McCray PB Jr.

Hum Gene Ther. 2007 Dec;18(12):1244-52.

PMID:
18052720

Supplemental Content

Support Center