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Citation: I. Bahner et al., INFECTION OF HUMAN MARROW STROMA BY HIV-1 IS BOTH REQUIRED AND SUFFICIENT FOR HIV-1-INDUCED HEMATOPOIETIC SUPPRESSION IN-VITRO - DEMONSTRATION BY GENE-MODIFICATION OF PRIMARY HUMAN STROMA, Blood, 88(10), 1996, pp. 1979-1979
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Citation: Em. Gordon et al., CHARACTERIZATION OF A MONOCLONAL ANTIBODY-PURIFIED RECOMBINANT FACTOR-IX PRODUCED IN HUMAN HEPATOMA (HEPG2) CELL-CULTURES AFTER RETROVIRAL VECTOR-MEDIATED TRANSFER, International journal of pediatric hematology/oncology, 2(3), 1995, pp. 185-191
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Citation: R. Parkman et al., ANALYSIS OF T-LYMPHOCYTES FROM PATIENTS WITH ADENOSINE-DEAMINASE (ADA) DEFICIENCY TRANSPLANTED WITH ADA TRANSDUCED CORD-BLOOD CELLS, Journal of cellular biochemistry, 1995, pp. 369-369
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Citation: Cie. Smith et al., RETROVIRAL GENE-TRANSFER TO XID BONE-MARROW CELLS - AN EXPERIMENTAL-MODEL FOR GENE-THERAPY IN X-LINKED AGAMMAGLOBULINEMIA, Journal of cellular biochemistry, 1995, pp. 372-372
Citation: Pb. Robbins et Db. Kohn, RETROVIRAL VECTORS FOR ENHANCED GENE-EXPRESSION IN-VIVO AND IN-VITRO, Journal of cellular biochemistry, 1995, pp. 383-383
Citation: K. Kearns et al., INHIBITION OF HIV-1JR-FL REPLICATION IN HUMAN LONG-TERM BONE-MARROW CULTURES EXPRESSING ANTI-HIV-1 GENES, Journal of cellular biochemistry, 1995, pp. 395-395
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Citation: C. Zhou et al., EXPRESSION OF FUSION PROTEINS BETWEEN CD4 AND LYSOSOME TARGETING DOMAINS INHIBITS HIV-1 REPLICATION IN HUMAN T-LYMPHOCYTES, Journal of cellular biochemistry, 1995, pp. 402-402
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Citation: E. Hara et al., THERAPEUTIC CTL FROM MOUSE SPLEEN IMMUNIZED WITH IRRADIATED TNF-ALPHAGENE-MODIFIED TUMOR-CELLS, Journal of cellular biochemistry, 1995, pp. 422-422
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Citation: Ja. Nolta et al., TRANSDUCTION OF PLURIPOTENT HUMAN HEMATOPOIETIC STEM-CELLS DEMONSTRATED BY CLONAL ANALYSIS IN IMMUNE-DEFICIENT MICE, Experimental hematology, 23(8), 1995, pp. 892-892
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Citation: M. Kido et al., USE OF A RETROVIRAL VECTOR WITH AN INTERNAL OPSIN PROMOTER TO DIRECT GENE-EXPRESSION TO RETINAL PHOTORECEPTOR CELLS, Investigative ophthalmology & visual science, 36(4), 1995, pp. 846-846
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Citation: Db. Kohn et al., GENE-THERAPY FOR NEONATES WITH ADA DEFICIENCY BY TRANSFER OF THE HUMAN ADA CDNA INTO UMBILICAL-CORD CD34-YEAR FOLLOW-UP( CELLS 2), Pediatric research, 37(4), 1995, pp. 9-9
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Citation: Pm. Challita et al., MULTIPLE MODIFICATIONS IN CIS-ELEMENTS OF THE LONG TERMINAL REPEAT OFRETROVIRAL VECTORS LEAD TO INCREASED EXPRESSION AND DECREASED DNA METHYLATION IN EMBRYONIC CARCINOMA-CELLS, Journal of virology, 69(2), 1995, pp. 748-755