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 *

870 related articles for article (PubMed ID: 26941360)

  • 21. Vascular endothelial growth factor reduced hypoxia-induced death of human myoblasts and improved their engraftment in mouse muscles.
    Bouchentouf M; Benabdallah BF; Bigey P; Yau TM; Scherman D; Tremblay JP
    Gene Ther; 2008 Mar; 15(6):404-14. PubMed ID: 18079754
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Exercise improves the success of myoblast transplantation in mdx mice.
    Bouchentouf M; Benabdallah BF; Mills P; Tremblay JP
    Neuromuscul Disord; 2006 Aug; 16(8):518-29. PubMed ID: 16919954
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Recent progress in satellite cell/myoblast engraftment -- relevance for therapy.
    Briggs D; Morgan JE
    FEBS J; 2013 Sep; 280(17):4281-93. PubMed ID: 23560812
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Skeletal Muscle Differentiation on a Chip Shows Human Donor Mesoangioblasts' Efficiency in Restoring Dystrophin in a Duchenne Muscular Dystrophy Model.
    Serena E; Zatti S; Zoso A; Lo Verso F; Tedesco FS; Cossu G; Elvassore N
    Stem Cells Transl Med; 2016 Dec; 5(12):1676-1683. PubMed ID: 27502519
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Improved success of myoblast transplantation in mdx mice by blocking the myostatin signal.
    Benabdallah BF; Bouchentouf M; Tremblay JP
    Transplantation; 2005 Jun; 79(12):1696-702. PubMed ID: 15973171
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Pluripotent stem cell-induced skeletal muscle progenitor cells with givinostat promote myoangiogenesis and restore dystrophin in injured Duchenne dystrophic muscle.
    Xuan W; Khan M; Ashraf M
    Stem Cell Res Ther; 2021 Feb; 12(1):131. PubMed ID: 33579366
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Human multipotent adipose-derived stem cells restore dystrophin expression of Duchenne skeletal-muscle cells in vitro.
    Vieira NM; Brandalise V; Zucconi E; Jazedje T; Secco M; Nunes VA; Strauss BE; Vainzof M; Zatz M
    Biol Cell; 2008 Apr; 100(4):231-41. PubMed ID: 17997718
    [TBL] [Abstract][Full Text] [Related]  

  • 28. MMP1 gene expression enhances myoblast migration and engraftment following implanting into mdx/SCID mice.
    Pan H; Vojnits K; Liu TT; Meng F; Yang L; Wang Y; Huard J; Cox CS; Lally KP; Li Y
    Cell Adh Migr; 2015; 9(4):283-92. PubMed ID: 26223276
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Transforming growth factor type-β inhibits Mas receptor expression in fibroblasts but not in myoblasts or differentiated myotubes; Relevance to fibrosis associated to muscular dystrophies.
    Cofre C; Acuña MJ; Contreras O; Morales MG; Riquelme C; Cabello-Verrugio C; Brandan E
    Biofactors; 2015; 41(2):111-20. PubMed ID: 25809912
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Inhibiting myostatin with follistatin improves the success of myoblast transplantation in dystrophic mice.
    Benabdallah BF; Bouchentouf M; Rousseau J; Bigey P; Michaud A; Chapdelaine P; Scherman D; Tremblay JP
    Cell Transplant; 2008; 17(3):337-50. PubMed ID: 18522236
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Restoration of Functional Full-Length Dystrophin After Intramuscular Transplantation of Foamy Virus-Transduced Myoblasts.
    Meng J; Sweeney NP; Doreste B; Muntoni F; McClure M; Morgan J
    Hum Gene Ther; 2020 Feb; 31(3-4):241-252. PubMed ID: 31801386
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Dystrophin Expressing Chimeric (DEC) Human Cells Provide a Potential Therapy for Duchenne Muscular Dystrophy.
    Siemionow M; Cwykiel J; Heydemann A; Garcia J; Marchese E; Siemionow K; Szilagyi E
    Stem Cell Rev Rep; 2018 Jun; 14(3):370-384. PubMed ID: 29546607
    [TBL] [Abstract][Full Text] [Related]  

  • 33. 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]  

  • 34. Cardiac Protection after Systemic Transplant of Dystrophin Expressing Chimeric (DEC) Cells to the mdx Mouse Model of Duchenne Muscular Dystrophy.
    Siemionow M; Malik M; Langa P; Cwykiel J; Brodowska S; Heydemann A
    Stem Cell Rev Rep; 2019 Dec; 15(6):827-841. PubMed ID: 31612351
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Alterations in Notch signalling in skeletal muscles from mdx and dko dystrophic mice and patients with Duchenne muscular dystrophy.
    Church JE; Trieu J; Chee A; Naim T; Gehrig SM; Lamon S; Angelini C; Russell AP; Lynch GS
    Exp Physiol; 2014 Apr; 99(4):675-87. PubMed ID: 24443351
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Expression of CCAAT/Enhancer Binding Protein Beta in Muscle Satellite Cells Inhibits Myogenesis in Cancer Cachexia.
    Marchildon F; Lamarche É; Lala-Tabbert N; St-Louis C; Wiper-Bergeron N
    PLoS One; 2015; 10(12):e0145583. PubMed ID: 26709824
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Fetal skeletal muscle progenitors have regenerative capacity after intramuscular engraftment in dystrophin deficient mice.
    Sakai H; Sato T; Sakurai H; Yamamoto T; Hanaoka K; Montarras D; Sehara-Fujisawa A
    PLoS One; 2013; 8(5):e63016. PubMed ID: 23671652
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Cell-lineage regulated myogenesis for dystrophin replacement: a novel therapeutic approach for treatment of muscular dystrophy.
    Kimura E; Han JJ; Li S; Fall B; Ra J; Haraguchi M; Tapscott SJ; Chamberlain JS
    Hum Mol Genet; 2008 Aug; 17(16):2507-17. PubMed ID: 18511457
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Induced Fetal Human Muscle Stem Cells with High Therapeutic Potential in a Mouse Muscular Dystrophy Model.
    Zhao M; Tazumi A; Takayama S; Takenaka-Ninagawa N; Nalbandian M; Nagai M; Nakamura Y; Nakasa M; Watanabe A; Ikeya M; Hotta A; Ito Y; Sato T; Sakurai H
    Stem Cell Reports; 2020 Jul; 15(1):80-94. PubMed ID: 32619494
    [TBL] [Abstract][Full Text] [Related]  

  • 40. CRISPR/Cas9 editing of directly reprogrammed myogenic progenitors restores dystrophin expression in a mouse model of muscular dystrophy.
    Domenig SA; Bundschuh N; Lenardič A; Ghosh A; Kim I; Qabrati X; D'Hulst G; Bar-Nur O
    Stem Cell Reports; 2022 Feb; 17(2):321-336. PubMed ID: 34995499
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 44.