BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

448 related articles for article (PubMed ID: 23206279)

  • 1. Perspectives of stem cell therapy in Duchenne muscular dystrophy.
    Meregalli M; Farini A; Belicchi M; Parolini D; Cassinelli L; Razini P; Sitzia C; Torrente Y
    FEBS J; 2013 Sep; 280(17):4251-62. PubMed ID: 23206279
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Cell therapy for Duchenne muscular dystrophy].
    Zhou C; Zhang C
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2006 Dec; 23(6):659-61. PubMed ID: 17160947
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Cell based therapy for Duchenne muscular dystrophy.
    Farini A; Razini P; Erratico S; Torrente Y; Meregalli M
    J Cell Physiol; 2009 Dec; 221(3):526-34. PubMed ID: 19688776
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Stem cell therapies to treat muscular dystrophy: progress to date.
    Meregalli M; Farini A; Parolini D; Maciotta S; Torrente Y
    BioDrugs; 2010 Aug; 24(4):237-47. PubMed ID: 20623990
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Duchenne muscular dystrophy: perspectives of treatment].
    Palmieri B; Sblendorio V
    Recenti Prog Med; 2006 Sep; 97(9):448-58. PubMed ID: 17017294
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Human mesenchymal stem cells ectopically expressing full-length dystrophin can complement Duchenne muscular dystrophy myotubes by cell fusion.
    Gonçalves MA; de Vries AA; Holkers M; van de Watering MJ; van der Velde I; van Nierop GP; Valerio D; Knaän-Shanzer S
    Hum Mol Genet; 2006 Jan; 15(2):213-21. PubMed ID: 16321987
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Human Skeletal Muscle Cells Derived from the Orbicularis Oculi Have Regenerative Capacity for Duchenne Muscular Dystrophy.
    Yamanaka Y; Takenaka N; Sakurai H; Ueno M; Kinoshita S; Sotozono C; Sato T
    Int J Mol Sci; 2019 Jul; 20(14):. PubMed ID: 31337111
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Muscle-derived stem cells: potential for muscle regeneration.
    Huard J; Cao B; Qu-Petersen Z
    Birth Defects Res C Embryo Today; 2003 Aug; 69(3):230-7. PubMed ID: 14671776
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A highly functional mini-dystrophin/GFP fusion gene for cell and gene therapy studies of Duchenne muscular dystrophy.
    Li S; Kimura E; Ng R; Fall BM; Meuse L; Reyes M; Faulkner JA; Chamberlain JS
    Hum Mol Genet; 2006 May; 15(10):1610-22. PubMed ID: 16595609
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Therapy of Duchenne muscular dystrophy with umbilical cord blood stem cell transplantation].
    Zhang C; Feng HY; Huang SL; Fang JP; Xiao LL; Yao XL; Chen C; Ye X; Zeng Y; Lu XL; Wen JM; Zhang WX; Li Z; Feng SW; Xu HG; Huang K; Zhou DH; Chen W; Xie YM; Xi J; Zhang M; Li Y; Liu Y
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2005 Aug; 22(4):399-405. PubMed ID: 16086277
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Advance in therapy for Duchenne/Becker muscular dystrophy].
    Xu TT; Lan D
    Zhongguo Dang Dai Er Ke Za Zhi; 2015 Mar; 17(3):294-8. PubMed ID: 25815505
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Myogenic stem cells: regeneration and cell therapy in human skeletal muscle.
    Negroni E; Butler-Browne GS; Mouly V
    Pathol Biol (Paris); 2006 Mar; 54(2):100-8. PubMed ID: 16246502
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Development of therapy for Duchenne muscular dystrophy.
    Zhang S; Xie H; Zhou G; Yang Z
    Zhongguo Xiu Fu Chong Jian Wai Ke Za Zhi; 2007 Feb; 21(2):194-203. PubMed ID: 17357471
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Systemic delivery of allogenic muscle stem cells induces long-term muscle repair and clinical efficacy in duchenne muscular dystrophy dogs.
    Rouger K; Larcher T; Dubreil L; Deschamps JY; Le Guiner C; Jouvion G; Delorme B; Lieubeau B; Carlus M; Fornasari B; Theret M; Orlando P; Ledevin M; Zuber C; Leroux I; Deleau S; Guigand L; Testault I; Le Rumeur E; Fiszman M; Chérel Y
    Am J Pathol; 2011 Nov; 179(5):2501-18. PubMed ID: 21924229
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Cell therapies for muscular dystrophy.
    Blau HM
    N Engl J Med; 2008 Sep; 359(13):1403-5. PubMed ID: 18815403
    [No Abstract]   [Full Text] [Related]  

  • 16. Repair or replace? Exploiting novel gene and cell therapy strategies for muscular dystrophies.
    Benedetti S; Hoshiya H; Tedesco FS
    FEBS J; 2013 Sep; 280(17):4263-80. PubMed ID: 23387802
    [TBL] [Abstract][Full Text] [Related]  

  • 17. The allure of stem cell therapy for muscular dystrophy.
    Grounds MD; Davies KE
    Neuromuscul Disord; 2007 Mar; 17(3):206-8. PubMed ID: 17306535
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Exon-skipping therapy for Duchenne muscular dystrophy.
    Nakamura A; Takeda S
    Neuropathology; 2009 Aug; 29(4):494-501. PubMed ID: 19486303
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Therapeutic Strategies for Duchenne Muscular Dystrophy: An Update.
    Sun C; Shen L; Zhang Z; Xie X
    Genes (Basel); 2020 Jul; 11(8):. PubMed ID: 32717791
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Stable transduction of myogenic cells with lentiviral vectors expressing a minidystrophin.
    Li S; Kimura E; Fall BM; Reyes M; Angello JC; Welikson R; Hauschka SD; Chamberlain JS
    Gene Ther; 2005 Jul; 12(14):1099-108. PubMed ID: 15759015
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 23.