These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

181 related articles for article (PubMed ID: 12436963)

  • 41. Highly efficient gene transfer into baboon marrow repopulating cells using GALV-pseudotype oncoretroviral vectors produced by human packaging cells.
    Horn PA; Topp MS; Morris JC; Riddell SR; Kiem HP
    Blood; 2002 Dec; 100(12):3960-7. PubMed ID: 12393453
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Concentrated RD114-pseudotyped MFGS-gp91phox vector achieves high levels of functional correction of the chronic granulomatous disease oxidase defect in NOD/SCID/beta -microglobulin-/- repopulating mobilized human peripheral blood CD34+ cells.
    Brenner S; Whiting-Theobald NL; Linton GF; Holmes KL; Anderson-Cohen M; Kelly PF; Vanin EF; Pilon AM; Bodine DM; Horwitz ME; Malech HL
    Blood; 2003 Oct; 102(8):2789-97. PubMed ID: 12829597
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Efficient transcriptional targeting of human hematopoietic stem cells and blood cell lineages by lentiviral vectors containing the regulatory element of the Wiskott-Aldrich syndrome gene.
    Leuci V; Gammaitoni L; Capellero S; Sangiolo D; Mesuraca M; Bond HM; Migliardi G; Cammarata C; Aglietta M; Morrone G; Piacibello W
    Stem Cells; 2009 Nov; 27(11):2815-23. PubMed ID: 19785032
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Short-term culture of human CD34+ cells for lentiviral gene transfer.
    Santoni de Sio F; Naldini L
    Methods Mol Biol; 2009; 506():59-70. PubMed ID: 19110619
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Lentiviral vectors for enhanced gene expression in human hematopoietic cells.
    Ramezani A; Hawley TS; Hawley RG
    Mol Ther; 2000 Nov; 2(5):458-69. PubMed ID: 11082319
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Improving Gene Therapy Efficiency through the Enrichment of Human Hematopoietic Stem Cells.
    Masiuk KE; Brown D; Laborada J; Hollis RP; Urbinati F; Kohn DB
    Mol Ther; 2017 Sep; 25(9):2163-2175. PubMed ID: 28663101
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Simplified retroviral vector gcsap with murine stem cell virus long terminal repeat allows high and continued expression of enhanced green fluorescent protein by human hematopoietic progenitors engrafted in nonobese diabetic/severe combined immunodeficient mice.
    Kaneko S; Onodera M; Fujiki Y; Nagasawa T; Nakauchi H
    Hum Gene Ther; 2001 Jan; 12(1):35-44. PubMed ID: 11177540
    [TBL] [Abstract][Full Text] [Related]  

  • 48. High-level transgene expression in human hematopoietic progenitors and differentiated blood lineages after transduction with improved lentiviral vectors.
    Salmon P; Kindler V; Ducrey O; Chapuis B; Zubler RH; Trono D
    Blood; 2000 Nov; 96(10):3392-8. PubMed ID: 11071633
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Stable transduction with lentiviral vectors and amplification of immature hematopoietic progenitors from cord blood of preterm human fetuses.
    Luther-Wyrsch A; Costello E; Thali M; Buetti E; Nissen C; Surbek D; Holzgreve W; Gratwohl A; Tichelli A; Wodnar-Filipowicz A
    Hum Gene Ther; 2001 Mar; 12(4):377-89. PubMed ID: 11242530
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Lentivirus-mediated gene transfer into hematopoietic repopulating cells in baboons.
    Horn PA; Morris JC; Bukovsky AA; Andrews RG; Naldini L; Kurre P; Kiem HP
    Gene Ther; 2002 Nov; 9(21):1464-71. PubMed ID: 12378409
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Efficient oncoretroviral transduction of extended long-term culture-initiating cells and NOD/SCID repopulating cells: enhanced reconstitution with gene-marked cells through an ex vivo expansion approach.
    Björgvinsdóttir H; Bryder D; Sitnicka E; Ramsfjell V; De Jong I; Olsson K; Rusterholz C; Karlsson S; Jacobsen SE
    Hum Gene Ther; 2002 Jun; 13(9):1061-73. PubMed ID: 12067439
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Transcriptional targeting of lentiviral vectors by long terminal repeat enhancer replacement.
    Lotti F; Menguzzato E; Rossi C; Naldini L; Ailles L; Mavilio F; Ferrari G
    J Virol; 2002 Apr; 76(8):3996-4007. PubMed ID: 11907239
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Differential transduction efficiency of SCID-repopulating cells derived from umbilical cord blood and granulocyte colony-stimulating factor-mobilized peripheral blood.
    Pollok KE; van Der Loo JC; Cooper RJ; Hartwell JR; Miles KR; Breese R; Williams EP; Montel A; Seshadri R; Hanenberg H; Williams DA
    Hum Gene Ther; 2001 Nov; 12(17):2095-108. PubMed ID: 11747599
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Prospectively Isolated Human Bone Marrow Cell-Derived MSCs Support Primitive Human CD34-Negative Hematopoietic Stem Cells.
    Matsuoka Y; Nakatsuka R; Sumide K; Kawamura H; Takahashi M; Fujioka T; Uemura Y; Asano H; Sasaki Y; Inoue M; Ogawa H; Takahashi T; Hino M; Sonoda Y
    Stem Cells; 2015 May; 33(5):1554-65. PubMed ID: 25537923
    [TBL] [Abstract][Full Text] [Related]  

  • 55. High-level sustained transgene expression in human embryonic stem cells using lentiviral vectors.
    Ma Y; Ramezani A; Lewis R; Hawley RG; Thomson JA
    Stem Cells; 2003; 21(1):111-7. PubMed ID: 12529558
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Competitive repopulation assay of two gene-marked cord blood units in NOD/SCID/gammac(null) mice.
    Yahata T; Ando K; Miyatake H; Uno T; Sato T; Ito M; Kato S; Hotta T
    Mol Ther; 2004 Nov; 10(5):882-91. PubMed ID: 15509506
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Enrichment of human hematopoietic stem/progenitor cells facilitates transduction for stem cell gene therapy.
    Baldwin K; Urbinati F; Romero Z; Campo-Fernandez B; Kaufman ML; Cooper AR; Masiuk K; Hollis RP; Kohn DB
    Stem Cells; 2015 May; 33(5):1532-42. PubMed ID: 25588820
    [TBL] [Abstract][Full Text] [Related]  

  • 58. In vivo selection of MGMT(P140K) lentivirus-transduced human NOD/SCID repopulating cells without pretransplant irradiation conditioning.
    Zielske SP; Reese JS; Lingas KT; Donze JR; Gerson SL
    J Clin Invest; 2003 Nov; 112(10):1561-70. PubMed ID: 14617757
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Inhibition of simian/human immunodeficiency virus replication in CD4+ T cells derived from lentiviral-transduced CD34+ hematopoietic cells.
    Braun SE; Wong FE; Connole M; Qiu G; Lee L; Gillis J; Lu X; Humeau L; Slepushkin V; Binder GK; Dropulic B; Johnson RP
    Mol Ther; 2005 Dec; 12(6):1157-67. PubMed ID: 16168713
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Targeted gene therapy to antigen-presenting cells in the central nervous system using hematopoietic stem cells.
    Lesniak MS; Kelleher E; Pardoll D; Cui Y
    Neurol Res; 2005 Dec; 27(8):820-6. PubMed ID: 16354542
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 10.