Similar articles for PMID: 1964096

Year	Number of Results
1986	2
1987	5
1988	1
1989	4
1990	7
1991	9
1992	3
1993	7
1994	6
1995	3
1996	4
1997	1
1998	2
1999	1
2000	3
2001	3
2003	3
2006	1
2007	1
2011	1
2012	1
2019	1
2022	1
2024	0

1

In vivo expression and survival of gene-modified T lymphocytes in rhesus monkeys.

Culver KW, Morgan RA, Osborne WR, Lee RT, Lenschow D, Able C, Cornetta K, Anderson WF, Blaese RM. Culver KW, et al. Hum Gene Ther. 1990 Winter;1(4):399-410. doi: 10.1089/hum.1990.1.4-399. Hum Gene Ther. 1990. PMID: 1964096

2

Retroviral-mediated gene transfer into mammalian cells.

Kohn DB, Kantoff PW, Eglitis MA, McLachlin JR, Moen RC, Karson E, Zwiebel JA, Nienhuis A, Karlsson S, O'Reilly R, et al. Kohn DB, et al. Blood Cells. 1987;13(1-2):285-98. Blood Cells. 1987. PMID: 3311223 Review.

3

Transduction of rIL-2 expanded CD4+ and CD8+ ovarian TIL-derived T cell lines with the G1Na (neor) replication-deficient retroviral vector.

Nash MA, Platsoucas CD, Wong BY, Wong PM, Cottler-Fox M, Otto E, Freedman RS. Nash MA, et al. Hum Gene Ther. 1995 Nov;6(11):1379-89. doi: 10.1089/hum.1995.6.11-1379. Hum Gene Ther. 1995. PMID: 8573611

4

L-histidinol provides effective selection of retrovirus-vector-transduced keratinocytes without impairing their proliferative potential.

Stockschlaeder MA, Storb R, Osborne WR, Miller AD. Stockschlaeder MA, et al. Hum Gene Ther. 1991 Spring;2(1):33-9. doi: 10.1089/hum.1991.2.1-33. Hum Gene Ther. 1991. PMID: 1650586

5

Recombinant gene expression in human umbilical vein endothelial cells transduced by retroviral vectors.

Zwiebel JA, Freeman SM, Cornetta K, Forough R, Maciag T, Anderson WF. Zwiebel JA, et al. Biochem Biophys Res Commun. 1990 Jul 16;170(1):209-13. doi: 10.1016/0006-291x(90)91261-p. Biochem Biophys Res Commun. 1990. PMID: 2164804 Free article.

6

Cryopreserved cord blood myeloid progenitor cells can serve as targets for retroviral-mediated gene transduction and gene-transduced progenitors can be cryopreserved and recovered.

Li ZH, Broxmeyer HE, Lu L. Li ZH, et al. Leukemia. 1995 Oct;9 Suppl 1:S12-6. Leukemia. 1995. PMID: 7475303

7

Gene-transferred oligoclonal T cells predominantly persist in peripheral blood from an adenosine deaminase-deficient patient during gene therapy.

Misaki Y, Ezaki I, Ariga T, Kawamura N, Sakiyama Y, Yamamoto K. Misaki Y, et al. Mol Ther. 2001 Jan;3(1):24-7. doi: 10.1006/mthe.2000.0232. Mol Ther. 2001. PMID: 11162307 Free article.

8

Lymphocytes as cellular vehicles for gene therapy in mouse and man.

Culver K, Cornetta K, Morgan R, Morecki S, Aebersold P, Kasid A, Lotze M, Rosenberg SA, Anderson WF, Blaese RM. Culver K, et al. Proc Natl Acad Sci U S A. 1991 Apr 15;88(8):3155-9. doi: 10.1073/pnas.88.8.3155. Proc Natl Acad Sci U S A. 1991. PMID: 2014235 Free PMC article.

9

An in vivo model of somatic cell gene therapy for human severe combined immunodeficiency.

Ferrari G, Rossini S, Giavazzi R, Maggioni D, Nobili N, Soldati M, Ungers G, Mavilio F, Gilboa E, Bordignon C. Ferrari G, et al. Science. 1991 Mar 15;251(4999):1363-6. doi: 10.1126/science.1848369. Science. 1991. PMID: 1848369

10

Expression of human adenosine deaminase in nonhuman primates after retrovirus-mediated gene transfer.

Kantoff PW, Gillio AP, McLachlin JR, Bordignon C, Eglitis MA, Kernan NA, Moen RC, Kohn DB, Yu SF, Karson E, et al. Kantoff PW, et al. J Exp Med. 1987 Jul 1;166(1):219-34. doi: 10.1084/jem.166.1.219. J Exp Med. 1987. PMID: 3298525 Free PMC article.

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