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La ricerca find articoli where soggetti phrase all words 'nondividing cells' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 275 riferimenti
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    1. Pfeifer, A; Verma, IM
      Gene therapy: Promises and problems

      ANNUAL REVIEW OF GENOMICS AND HUMAN GENETICS
    2. Desmaris, N; Bosch, A; Salaun, C; Petit, C; Prevost, MC; Tordo, N; Perrin, P; Schwartz, O; de Rocquigny, H; Heard, JM
      Production and neurotropism of lentivirus vectors pseudotyped with lyssavirus envelope glycoproteins

      MOLECULAR THERAPY
    3. Yamada, K; Olsen, JC; Patel, M; Rao, KW; Walsh, CE
      Functional correction of Fanconi anemia group C hematopoietic cells by theuse of a novel lentiviral vector

      MOLECULAR THERAPY
    4. Pandya, S; Klimatcheva, E; Planelles, V
      Lentivirus and foamy virus vectors: novel gene therapy tools

      EXPERT OPINION ON BIOLOGICAL THERAPY
    5. Turelli, P; Doucas, V; Craig, E; Mangeat, B; Klages, N; Evans, R; Kalpana, G; Trono, D
      Cytoplasmic recruitment of INI1 and PML on incoming HIV preintegration complexes: Interference with early steps of viral replication

      MOLECULAR CELL
    6. Bouyac-Bertoia, M; Dvorin, JD; Fouchier, RAM; Jenkins, Y; Meyer, BE; Wu, LI; Emerman, M; Malim, MH
      HIV-1 infection requires a functional integrase NLS

      MOLECULAR CELL
    7. Choi, JK; Hoang, N; Vilardi, AM; Conrad, P; Emerson, SG; Gewirtz, AM
      Hybrid HIV/MSCV LTR enhances transgene expression of lentiviral vectors inhuman CD34(+) hematopoietic cells

      STEM CELLS
    8. Gatlin, J; Padgett, A; Melkus, MW; Kelly, PF; Garcia, JV
      Long-term engraftment of nonobese diabetic/severe combined immunodeficientmice with human CD34(+) cells transduced by a self-inactivating human immunodeficiency virus type 1 vector

      HUMAN GENE THERAPY
    9. Barry, SC; Harder, B; Brzezinski, M; Flint, LY; Seppen, J; Osborne, WRA
      Lentivirus vectors encoding both central polypurine tract and posttranscriptional regulatory element provide enhanced transduction and transgene expression

      HUMAN GENE THERAPY
    10. Farson, D; Witt, R; McGuinness, R; Dull, T; Kelly, M; Song, JP; Radeke, R; Bukovsky, A; Consiglio, A; Naldini, L
      A new-generation stable inducible packaging cell line for lentiviral vectors

      HUMAN GENE THERAPY
    11. Pandya, S; Boris-Lawrie, K; Leung, NJ; Akkina, R; Planelles, V
      Development of an rev-independent, minimal simian immunodeficiency virus-derived vector system

      HUMAN GENE THERAPY
    12. Douglas, JL; Lin, WY; Panis, ML; Veres, G
      Efficient human immunodeficiency virus-based vector transduction of unstimulated human mobilized peripheral blood CD34(+) cells in the SCID-hu Thy/Liv model of human T cell lymphopoiesis

      HUMAN GENE THERAPY
    13. Miyake, K; Iijima, O; Suzuki, N; Matsukura, M; Shimada, T
      Selective killing of human immunodeficiency virus-infected cells by targeted gene transfer and inducible gene expression using a recombinant human immunodeficiency virus vector

      HUMAN GENE THERAPY
    14. Loewen, N; Fautsch, MP; Peretz, M; Bahler, CK; Cameron, JD; Johnson, DH; Poeschla, EM
      Genetic modification of human trabecular meshwork with lentiviral vectors

      HUMAN GENE THERAPY
    15. Kumar, M; Keller, B; Makalou, N; Sutton, RE
      Systematic determination of the packaging limit of lentiviral vectors

      HUMAN GENE THERAPY
    16. Aitken, ML; Moss, RB; Waltz, DA; Dovey, ME; Tonelli, MR; McNamara, SC; Gibson, RL; Ramsey, BW; Carter, BJ; Reynolds, TC
      A phase I study of aerosolized administration of tgAAVCF to cystic fibrosis subjects with mild lung disease

      HUMAN GENE THERAPY
    17. Fleming, J; Ginn, SL; Weinberger, RP; Trahair, TN; Smythe, JA; Alexander, IE
      Adeno-associated virus and lentivirus vectors mediate efficient and sustained transduction of cultured mouse and human dorsal root ganglia sensory neurons

      HUMAN GENE THERAPY
    18. Dardalhon, V; Herpers, B; Noraz, N; Pflumio, F; Guetard, D; Leveau, C; Dubart-Kupperschmitt, A; Charneau, P; Taylor, N
      Lentivirus-mediated gene transfer in primary T cells is enhanced by a central DNA flap

      GENE THERAPY
    19. McCarty, DM; Monahan, PE; Samulski, RJ
      Self-complementary recombinant adeno-associated virus (scAAV) vectors promote efficient transduction independently of DNA synthesis

      GENE THERAPY
    20. Mazarakis, ND; Azzouz, M; Rohll, JB; Ellard, FM; Wilkes, FJ; Olsen, AL; Carter, EE; Barber, RD; Baban, DF; Kingsman, SM; Kingsman, AJ; O'Malley, K; Mitrophanous, KA
      Rabies virus glycoprotein pseudotyping of lentiviral vectors enables retrograde axonal transport and access to the nervous system after peripheral delivery

      HUMAN MOLECULAR GENETICS
    21. Woods, NB; Mikkola, H; Nilsson, E; Olsson, K; Trono, D; Karlsson, S
      Lentiviral-mediated gene transfer into haematopoietic stem cells

      JOURNAL OF INTERNAL MEDICINE
    22. Mokkapati, SK; de Henestrosa, ARF; Bhagwat, AS
      Escherichia coli DNA glycosylase Mug: a growth-regulated enzyme required for mutation avoidance in stationary-phase cells

      MOLECULAR MICROBIOLOGY
    23. Kanazawa, T; Urabe, M; Mizukami, H; Okada, T; Kume, A; Nishino, H; Monahan, J; Kitamura, K; Ichimura, K; Ozawa, K
      gamma-Rays enhance rAAV-mediated transgene expression and cytocidal effectof AAV-HSVtk/ganciclovir on cancer cells

      CANCER GENE THERAPY
    24. Teramoto, S; Ishii, T; Matsuse, T
      Variables pertinent to the efficiency of adeno-associated virus (AAV) vectors mediated gene transfer to human vascular endothelial cells

      Hypertension research
    25. Nomura, T; Yabe, T; Mochizuki, H; Reiser, J; Becerra, SP; Schwartz, JP
      Survival effects of pigment epithelium-derived factor expressed by a lentiviral vector in rat cerebellar granule cells

      DEVELOPMENTAL NEUROSCIENCE
    26. Metharom, P; Takyar, S; Xia, HQ; Ellem, KAO; Wilcox, GE; Wei, MQ
      Development of disabled, replication-defective gene transfer vectors from the Jembrana disease virus, a new infectious agent of cattle

      VETERINARY MICROBIOLOGY
    27. Murphy, EA; Waring, AJ; Murphy, JC; Willson, RC; Longmuir, KJ
      Development of an effective gene delivery system: a study of complexes composed of a peptide-based amphiphilic DNA compaction agent and phospholipid

      NUCLEIC ACIDS RESEARCH
    28. Unutmaz, D
      T cell signaling mechanisms that regulate HIV-1 infection

      IMMUNOLOGIC RESEARCH
    29. Pacchia, AL; Adelson, ME; Kaul, M; Ron, Y; Dougherty, JP
      An inducible packaging cell system for safe, efficient lentiviral vector production in the absence of HIV-1 accessory proteins

      VIROLOGY
    30. Kim, SS; Kothari, N; You, XJ; Robinson, WE; Schnell, T; Uberla, K; Fan, H
      Generation of replication-defective helper-free vectors based on simian immunodeficiency virus

      VIROLOGY
    31. Berkowitz, RD; Ilves, H; Plavec, I; Veres, G
      Gene transfer systems derived from visna virus: Analysis of virus production and infectivity

      VIROLOGY
    32. de Noronha, CMC; Sherman, MP; Lin, HW; Cavrois, MV; Moir, RD; Goldman, RD; Greene, WC
      Dynamic disruptions in nuclear envelope architecture and integrity inducedby HIV-1 Vpr

      SCIENCE
    33. Ha, HC; Juluri, K; Zhou, Y; Leung, S; Hermankova, M; Snyder, SH
      Poly(ADP-ribose) polymerase-1 is required for efficient HIV-1 integration

      PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
    34. Hansen, J; Qing, K; Srivastava, A
      Adeno-associated virus type 2-mediated gene transfer: Altered endocytic processing enhances transduction efficiency in murine fibroblasts

      JOURNAL OF VIROLOGY
    35. Christodoulopoulos, I; Cannon, PM
      Sequences in the cytoplasmic tail of the gibbon ape leukemia virus envelope protein that prevent its incorporation into lentivirus vectors

      JOURNAL OF VIROLOGY
    36. Mautino, MR; Keiser, N; Morgan, RA
      Inhibition of human immunodeficiency virus type 1 (HIV-1) replication by HIV-1-based lentivirus vectors expressing transdominant Rev

      JOURNAL OF VIROLOGY
    37. Fassati, A; Goff, SP
      Characterization of intracellular reverse transcription complexes of humanimmunodeficiency virus type 1

      JOURNAL OF VIROLOGY
    38. Berkowitz, R; Ilves, H; Lin, WY; Eckert, K; Coward, A; Tamaki, S; Veres, G; Plavec, I
      Construction and molecular analysis of gene transfer systems derived from bovine immunodeficiency virus

      JOURNAL OF VIROLOGY
    39. Kobayashi, T; Kamitani, W; Zhang, GQ; Watanabe, M; Tomonaga, K; Ikuta, K
      Borna disease virus nucleoprotein requires both nuclear localization and export activities for viral nucleocytoplasmic shuttling

      JOURNAL OF VIROLOGY
    40. Sherman, MP; de Noronha, CMC; Heusch, MI; Greene, S; Greene, WC
      Nucleocytoplasmic shuttling by human immunodeficiency virus type 1 Vpr

      JOURNAL OF VIROLOGY
    41. Borok, Z; Harboe-Schmidt, JE; Brody, SL; You, YJ; Zhou, BY; Li, X; Cannon, PM; Kim, KJ; Crandall, ED; Kasahara, N
      Vesicular stomatitis virus G-pseudotyped lentivirus vectors mediate efficient apical transduction of polarized quiescent primary alveolar epithelial cells

      JOURNAL OF VIROLOGY
    42. Lewis, BC; Chinnasamy, N; Morgan, RA; Varmus, HE
      Development of an avian leukosis-sarcoma virus subgroup A pseudotyped lentiviral vector

      JOURNAL OF VIROLOGY
    43. Neil, S; Martin, F; Ikeda, Y; Collins, M
      Postentry restriction to human immunodeficiency virus-based vector transduction in human monocytes

      JOURNAL OF VIROLOGY
    44. Browning, MT; Schmidt, RD; Lew, KA; Rizvi, TA
      Primate and feline lentivirus vector RNA packaging and propagation by heterologous lentivirus virions

      JOURNAL OF VIROLOGY
    45. Kowolik, CM; Hu, J; Yee, JK
      Locus control region of the human CD2 gene in a lentivirus vector confers position-independent transgene expression

      JOURNAL OF VIROLOGY
    46. D'Costa, J; Brown, HM; Kundra, P; Davis-Warren, A; Arya, SK
      Human immunodeficiency virus type 2 lentiviral vectors: packaging signal and splice donor in expression and encapsidation

      JOURNAL OF GENERAL VIROLOGY
    47. Depienne, C; Mousnier, A; Leh, H; Le Rouzic, E; Dormont, D; Benichou, S; Dargemont, C
      Characterization of the nuclear import pathway for HIV-1 integrase

      JOURNAL OF BIOLOGICAL CHEMISTRY
    48. Moreau-Gaudry, F; Xia, P; Jiang, G; Perelman, NP; Bauer, G; Ellis, J; Surinya, KH; Mavilio, F; Shen, CK; Malik, P
      High-level erythroid-specific gene expression in primary human and murine hematopoietic cells with self-inactivating lentiviral vectors

      BLOOD
    49. Seppen, J; Barry, SC; Harder, B; Osborne, WRA
      Lentivirus administration to rat muscle provides efficient sustained expression of erythropoietin

      BLOOD
    50. Sondhi, D; Hackett, NR; Apblett, RL; Kaminsky, SM; Pergolizzi, RG; Crystal, RG
      Feasibility of gene therapy for late neuronal ceroid lipofuscinosis

      ARCHIVES OF NEUROLOGY
    51. Hengge, UR; Mirmohammadsadegh, A
      Adeno-associated virus expresses transgenes in hair follicles and epidermis

      MOLECULAR THERAPY
    52. DePolo, NJ; Reed, JD; Sheridan, PL; Townsend, K; Sauter, SL; Jolly, DJ; Dubensky, TW
      VSV-G pseudotyped lentiviral vector particles produced in human cells are inactivated by human serum

      MOLECULAR THERAPY
    53. Klages, N; Zufferey, R; Trono, D
      A stable system for the high-titer production of multiply attenuated lentiviral vectors

      MOLECULAR THERAPY
    54. Guenechea, G; Gan, OI; Inamitsu, T; Dorrell, C; Pereira, DS; Kelly, M; Naldini, L; Dick, JE
      Transduction of human CD34(+)CD38(-) bone marrow and cord blood-derived SCID-repopulating cells with third-generation lentiviral vectors

      MOLECULAR THERAPY
    55. Somia, N; Verma, IM
      Gene therapy: Trials and tribulations

      NATURE REVIEWS GENETICS
    56. Ott, M; Schmidt, HHJ; Cichon, G; Manns, MP
      Emerging therapies in hepatology: Liver-directed gene transfer and hepatocyte transplantation

      CELLS TISSUES ORGANS
    57. Vigna, E; Naldini, L
      Lentiviral vectors: excellent tools for experimental gene transfer and promising candidates for gene therapy

      JOURNAL OF GENE MEDICINE
    58. Metharom, P; Takyar, S; Xia, HH; Ellem, KAO; Macmillan, J; Shepherd, RW; Wilcox, GE; Wei, MQ
      Novel bovine lentiviral vectors based on Jembrana disease virus

      JOURNAL OF GENE MEDICINE
    59. Zahler, MH; Irani, A; Malhi, H; Reutens, AT; Albanese, C; Bouzahzah, B; Joyce, D; Gupta, S; Pestell, RG
      The application of a lentiviral vector for gene transfer in fetal human hepatocytes

      JOURNAL OF GENE MEDICINE
    60. Parveen, Z; Krupetsky, A; Engelstadter, M; Cichutek, K; Pomerantz, RJ; Dornburg, R
      Spleen necrosis virus-derived C-type retroviral vectors for gene transfer to quiescent cells

      NATURE BIOTECHNOLOGY
    61. Stevenson, M
      HIV nuclear import: What's the flap

      NATURE MEDICINE
    62. Follenzi, A; Ailles, LE; Bakovic, S; Geuna, M; Naldini, L
      Gene transfer by lentiviral vectors is limited by nuclear translocation and rescued by HIV-1 pol sequences

      NATURE GENETICS
    63. Bosch, A; Perret, E; Desmaris, N; Trono, D; Heard, JM
      Reversal of pathology in the entire brain of mucopolysaccharidosis type VII mice after lentivirus-mediated gene transfer

      HUMAN GENE THERAPY
    64. Mautino, MR; Ramsey, WJ; Reiser, J; Morgan, RA
      Modified human immunodeficiency virus-based lentiviral vectors display decreased sensitivity to trans-dominant rev

      HUMAN GENE THERAPY
    65. Pruchnic, R; Cao, BH; Peterson, ZQQ; Xiao, X; Li, J; Samulski, RJ; Epperly, M; Huard, J
      The use of adeno-associated virus to circumvent the maturation-dependent viral transduction of muscle fibers

      HUMAN GENE THERAPY
    66. Turnbull, AE; Skulimowski, A; Smythe, JA; Alexander, IE
      Adeno-associated virus vectors show variable dependence on divalent cations for thermostability: Implications for purification and handling

      HUMAN GENE THERAPY
    67. Schnell, T; Foley, P; Wirth, M; Munch, J; Uberla, K
      Development of a self-inactivating, minimal lentivirus vector based on simian immunodeficiency virus

      HUMAN GENE THERAPY
    68. Wagner, R; Graf, M; Bieler, K; Wolf, H; Grunwald, T; Foley, P; Uberla, K
      Rev-independent expression of synthetic gag-pol genes of human immunodeficiency virus type 1 and simian immunodeficiency virus: Implications for the safety of lentiviral vectors

      HUMAN GENE THERAPY
    69. Mautino, MR; Morgan, RA
      Potent inhibition of human immunodeficiency virus type 1 replication by conditionally replicating human immunodeficiency virus-based lentiviral vectors expressing envelope antisense mRNA

      HUMAN GENE THERAPY
    70. Nakajima, T; Nakamaru, K; Ido, E; Terao, K; Hayami, M; Hasegawa, M
      Development of novel simian immunodeficiency virus vectors carrying a dualgene expression system

      HUMAN GENE THERAPY
    71. Chinnasamy, N; Chinnasamy, D; Toso, JF; Lapointe, R; Candotti, F; Morgan, RA; Hwu, P
      Efficient gene transfer to human peripheral blood monocyte-derived dendritic cells using human immunodeficiency virus type 1-based lentiviral vectors

      HUMAN GENE THERAPY
    72. Herrlinger, U; Jacobs, A; Quinones, A; Woiciechowsky, C; Sena-Esteves, M; Rainov, NG; Fraefel, C; Breakefield, XO
      Helper virus-free herpes simplex virus type 1 amplicon vectors for granulocyte-macrophage colony-stimulating factor-enhanced vaccination therapy for experimental glioma

      HUMAN GENE THERAPY
    73. Deglon, N; Tseng, JL; Bensadoun, JC; Zurn, AD; Arsenijevic, Y; De Almeida, LP; Zufferey, R; Trono, D; Aebischer, P
      Self-inactivating lentiviral vectors with enhanced transgene expression aspotential gene transfer system in Parkinson's disease

      HUMAN GENE THERAPY
    74. Wang, X; Appukuttan, B; Ott, S; Patel, R; Irvine, J; Song, J; Park, JHC; Smith, R; Stout, JT
      Efficient and sustained transgene expression in human corneal cells mediated by a lentiviral vector

      GENE THERAPY
    75. Negre, D; Mangeot, PE; Duisit, G; Blanchard, S; Vidalain, PO; Leissner, P; Winter, AJ; Rabourdin-Combe, C; Mehtali, M; Moullier, P; Darlix, JL; Cosset, FL
      Characterization of novel safe lentiviral vectors derived from simian immunodeficiency virus (SIVmac251) that efficiently transduce mature human dendritic cells

      GENE THERAPY
    76. Reiser, J
      Production and concentration of pseudotyped HIV-1-based gene transfer vectors

      GENE THERAPY
    77. Trono, D
      Lentiviral vectors: turning a deadly foe into a therapeutic agent

      GENE THERAPY
    78. Alisky, JM; Hughes, SM; Sauter, SL; Jolly, D; Dubensky, TW; Staber, PD; Chiorini, JA; Davidson, BL
      Transduction of murine cerebellar neurons with recombinant FIV and AAV5 vectors

      NEUROREPORT
    79. Cherepanov, P; Pluymers, W; Claeys, A; Proost, P; De Clercq, E; Debyser, Z
      High-level expression of active HIV-1 integrase from a synthetic gene in human cells

      FASEB JOURNAL
    80. Goater, J; Muller, R; Kollias, G; Firestein, GS; Sanz, I; O'Keefe, RJ; Schwarz, EM
      Empirical advantages of adeno associated viral vectors for in vivo gene therapy for arthritis

      JOURNAL OF RHEUMATOLOGY
    81. Dang, VD; Levin, HL
      Nuclear import of the retrotransposon Tf1 is governed by a nuclear localization signal that possesses a unique requirement for the FXFG nuclear pore factor Nup124p

      MOLECULAR AND CELLULAR BIOLOGY
    82. Shimpo, M; Ikeda, U; Maeda, Y; Ueno, S; Ikeda, M; Minota, S; Takizawa, T; Urabe, M; Kume, A; Monahan, J; Ozawa, K; Shimada, K
      Gene transfer into rat renal cells using adeno-associated virus vectors

      AMERICAN JOURNAL OF NEPHROLOGY
    83. Rossi, JJ
      Ribozyme therapy for HIV infection

      ADVANCED DRUG DELIVERY REVIEWS
    84. Peng, DC; Qian, C; Sun, YL; Barajas, MA; Prieto, J
      Transduction of hepatocellular carcinoma (HCC) using recombinant adeno-associated virus (rAAV): in vitro and in vivo effects of genotoxic agents

      JOURNAL OF HEPATOLOGY
    85. Maeda, Y; Ikeda, U; Shimpo, M; Shibuya, M; Monahan, J; Urabe, M; Ozawa, K; Shimada, K
      Adeno-associated virus-mediated vascular endothelial growth factor gene transfer into cardiac myocytes

      JOURNAL OF CARDIOVASCULAR PHARMACOLOGY
    86. Wang, CT; Yang, AH; Chiang, CC
      Analysis of a human immunodeficiency virus type 1 gag mutant with an engineered 110-amino-acid insertion in the matrix protein domain

      JOURNAL OF MEDICAL VIROLOGY
    87. Zennou, V; Petit, C; Guetard, D; Nerhbass, U; Montagnier, L; Charneau, P
      HIV-1 genome nuclear import is mediated by a central DNA flap

      CELL
    88. Kim, SH; Kim, SY; Robbins, PD
      Retroviral vectors

      ADVANCES IN VIRUS RESEARCH, VOL 55
    89. Naldini, L; Verma, IM
      Lentiviral vectors

      ADVANCES IN VIRUS RESEARCH, VOL 55
    90. Seamon, JA; Adams, M; Sengupta, S; Roth, MJ
      Differential effects of C-terminal molecular tagged integrase on replication competent Moloney murine leukemia virus

      VIROLOGY
    91. Sanlioglu, S; Benson, P; Engelhardt, JF
      Loss of ATM function enhances recombinant adeno-associated virus transduction and integration through pathways similar to UV irradiation

      VIROLOGY
    92. Hu, WS; Pathak, VK
      Design of retroviral vectors and helper cells for gene therapy

      PHARMACOLOGICAL REVIEWS
    93. Candotti, F
      The potential for therapy of immune disorders with gene therapy

      PEDIATRIC CLINICS OF NORTH AMERICA
    94. Pfeifer, A; Kessler, T; Silletti, S; Cheresh, DA; Verma, IM
      Suppression of angiogenesis by lentiviral delivery of PEX, a noncatalytic fragment of matrix metalloproteinase 2

      PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
    95. Lai, ZN; Han, I; Zirzow, G; Brady, RO; Reiser, J
      Intercellular delivery of a herpes simplex virus VP22 fusion protein from cells infected with lentiviral vectors

      PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
    96. Kung, SKP; An, DS; Chen, ISY
      A murine leukemia virus (MuLV) long terminal repeat derived from rhesus macaques in the context of a lentivirus vector and MuLV gag sequence results in high-level gene expression in human T lymphocytes

      JOURNAL OF VIROLOGY
    97. Kootstra, NA; Zwart, BM; Schuitemaker, H
      Diminished human immunodeficiency virus type 1 reverse transcription and nuclear transport in primary macrophages arrested in early G(1) phase of thecell cycle

      JOURNAL OF VIROLOGY
    98. An, DS; Wersto, RP; Agricola, BA; Metzger, ME; Lu, S; Amado, RG; Chen, ISY; Donahue, RE
      Marking and gene expression by a lentivirus vector in transplanted human and nonhuman primate CD34(+) cells

      JOURNAL OF VIROLOGY
    99. Gupta, K; Ott, D; Hope, TJ; Siliciano, RF; Boeke, JD
      A human nuclear shuttling protein that interacts with human immunodeficiency virus type 1 matrix is packaged into virions

      JOURNAL OF VIROLOGY
    100. Mikkola, H; Woods, NB; Sjogren, M; Helgadottir, H; Hamaguchi, I; Jacobsen, SE; Trono, D; Karlsson, S
      Lentivirus gene transfer in murine hematopoietic progenitor cells is compromised by a delay in proviral integration and results in transduction mosaicism and heterogeneous gene expression in progeny cells

      JOURNAL OF VIROLOGY


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Documento generato il 02/06/20 alle ore 04:21:05