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	Amedeo Prize 2008 The 21 Finalists

Stem Cell Research

Free Subscription Articles published in Gene Ther Retrieve available abstracts of 34 articles: HTML format

Single Articles

April 2008
1. SPAETH E , Klopp A, Dembinski J, Andreeff M, et al
   Inflammation and tumor microenvironments: defining the migratory itinerary of mesenchymal stem cells.
   Gene Ther. 2008;.
   PubMed     Related articles    Abstract available
   
   
   March 2008
2. WESTWOOD JA , Murray WK, Trivett M, Shin A, et al
   Absence of retroviral vector-mediated transformation of gene-modified T cells after long-term engraftment in mice.
   Gene Ther. 2008;.
   PubMed     Related articles    Abstract available
   
   
   
3. TAHER TE , Tulone C, Fatah R, D'Acquisto F, et al
   Repopulation of B-lymphocytes with restricted gene expression using haematopoietic stem cells engineered with lentiviral vectors.
   Gene Ther. 2008;.
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4. KUMAR S , Chanda D, Ponnazhagan S
   Therapeutic potential of genetically modified mesenchymal stem cells.
   Gene Ther. 2008;.
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5. FLAGLER K , Alexeev V, Pierce EA, Igoucheva O, et al
   Site-specific gene modification by oligodeoxynucleotides in mouse bone marrow-derived mesenchymal stem cells.
   Gene Ther. 2008;.
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6. CHENG T
   Toward 'SMART' stem cells.
   Gene Ther. 2008;15:391.
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7. PALMER GD , Stoddart MJ, Gouze E, Gouze JN, et al
   A simple, lanthanide-based method to enhance the transduction efficiency of adenovirus vectors.
   Gene Ther. 2008;15:357-63.
   PubMed     Related articles    Abstract available
   
   
   February 2008
8. KAZUKI Y , Hoshiya H, Kai Y, Abe S, et al
   Correction of a genetic defect in multipotent germline stem cells using a human artificial chromosome.
   Gene Ther. 2008;.
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9. FERREIRA E , Potier E, Logeart-Avramoglou D, Salomskaite-Davalgiene S, et al
   Optimization of a gene electrotransfer method for mesenchymal stem cell transfection.
   Gene Ther. 2008;.
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   January 2008
10. FEHSE B , Roeder I
    Insertional mutagenesis and clonal dominance: biological and statistical considerations.
    Gene Ther. 2008;15:143-53.
    PubMed     Related articles    Abstract available
    
    
    December 2007
11. NIU Y , Epperly MW, Shen H, Smith T, et al
    Intraesophageal MnSOD-plasmid liposome enhances engraftment and self-renewal of bone marrow derived progenitors of esophageal squamous epithelium.
    Gene Ther. 2007;.
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12. BOUCHENTOUF M , Benabdallah BF, Bigey P, Yau TM, et al
    Vascular endothelial growth factor reduced hypoxia-induced death of human myoblasts and improved their engraftment in mouse muscles.
    Gene Ther. 2007;.
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    November 2007
13. CHENG T
    Toward 'SMART' stem cells.
    Gene Ther. 2007;.
    PubMed     Related articles    Abstract available
    
    
    
14. GALLO P , Grimaldi S, Latronico MV, Bonci D, et al
    A lentiviral vector with a short troponin-I promoter for tracking cardiomyocyte differentiation of human embryonic stem cells.
    Gene Ther. 2007;.
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15. ADAMS GB , Scadden DT
    A niche opportunity for stem cell therapeutics.
    Gene Ther. 2007;.
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16. SCHUGAR RC , Robbins PD, Deasy BM
    Small molecules in stem cell self-renewal and differentiation.
    Gene Ther. 2007;.
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17. BOYER MJ , Cheng T
    The CDK inhibitors: potential targets for therapeutic stem cell manipulations?
    Gene Ther. 2007;.
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18. OHTSUKA S , Dalton S
    Molecular and biological properties of pluripotent embryonic stem cells.
    Gene Ther. 2007;.
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19. ABDALLAH BM , Kassem M
    Human mesenchymal stem cells: from basic biology to clinical applications.
    Gene Ther. 2007;.
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20. LAGASSE E
    Cancer stem cells with genetic instability: the best vehicle with the best engine for cancer.
    Gene Ther. 2007;.
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21. MURAKAMI S , Sakurai F, Kawabata K, Okada N, et al
    Interaction of penton base Arg-Gly-Asp motifs with integrins is crucial for adenovirus serotype 35 vector transduction in human hematopoietic cells.
    Gene Ther. 2007;14:1525-33.
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22. NAUMANN N , De Ravin SS, Choi U, Moayeri M, et al
    Simian immunodeficiency virus lentivector corrects human X-linked chronic granulomatous disease in the NOD/SCID mouse xenograft.
    Gene Ther. 2007;14:1513-24.
    PubMed     Related articles    Abstract available
    
    
    September 2007
23. ANDERSON J , Akkina R
    Complete knockdown of CCR5 by lentiviral vector-expressed siRNAs and protection of transgenic macrophages against HIV-1 infection.
    Gene Ther. 2007;14:1287-97.
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    August 2007
24. GREENBERGER JS
    Gene therapy approaches for stem cell protection.
    Gene Ther. 2007;.
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25. BAI H , Wang ZZ
    Directing human embryonic stem cells to generate vascular progenitor cells.
    Gene Ther. 2007;.
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26. YAN C , Lian X, Dai Y, Wang X, et al
    Gene delivery by the hSP-B promoter to lung alveolar type II epithelial cells in LAL-knockout mice through bone marrow mesenchymal stem cells.
    Gene Ther. 2007;.
    PubMed     Related articles    Abstract available
    
    
    July 2007
27. CHUANG CK , Sung LY, Hwang SM, Lo WH, et al
    Baculovirus as a new gene delivery vector for stem cell engineering and bone tissue engineering.
    Gene Ther. 2007;.
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28. OEHMIG A , Cortes ML, Perry KF, Sena-Esteves M, et al
    Integration of active human beta-galactosidase gene (100 kb) into genome using HSV/AAV amplicon vector.
    Gene Ther. 2007;14:1078-91.
    PubMed     Related articles    Abstract available
    
    
    June 2007
29. RABIE AB , Dai J, Xu R
    Recombinant AAV-mediated VEGF gene therapy induces mandibular condylar growth.
    Gene Ther. 2007;14:972-80.
    PubMed     Related articles    Abstract available
    
    
    May 2007
30. SHIMATO S , Natsume A, Takeuchi H, Wakabayashi T, et al
    Human neural stem cells target and deliver therapeutic gene to experimental leptomeningeal medulloblastoma.
    Gene Ther. 2007;.
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31. PAGNOTTO MR , Wang Z, Karpie JC, Ferretti M, et al
    Adeno-associated viral gene transfer of transforming growth factor-beta1 to human mesenchymal stem cells improves cartilage repair.
    Gene Ther. 2007;14:804-13.
    PubMed     Related articles    Abstract available
    
    
    March 2007
32. CHARRIER S , Dupre L, Scaramuzza S, Jeanson-Leh L, et al
    Lentiviral vectors targeting WASp expression to hematopoietic cells, efficiently transduce and correct cells from WAS patients.
    Gene Ther. 2007;14:415-28.
    PubMed     Related articles    Abstract available
    
    
    February 2007
33. MURPHY BR , Moayedpardazi HS, Gewirtz AM, Diamond SL, et al
    Delivery and mechanistic considerations for the production of knock-in mice by single-stranded oligonucleotide gene targeting.
    Gene Ther. 2007;14:304-15.
    PubMed     Related articles    Abstract available
    
    
    
34. YOSHIMITSU M , Higuchi K, Ramsubir S, Nonaka T, et al
    Efficient correction of Fabry mice and patient cells mediated by lentiviral transduction of hematopoietic stem/progenitor cells.
    Gene Ther. 2007;14:256-65.
    PubMed     Related articles    Abstract available
    
    

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