BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

399 related articles for article (PubMed ID: 24789910)

  • 1. MicroRNA-486-dependent modulation of DOCK3/PTEN/AKT signaling pathways improves muscular dystrophy-associated symptoms.
    Alexander MS; Casar JC; Motohashi N; Vieira NM; Eisenberg I; Marshall JL; Gasperini MJ; Lek A; Myers JA; Estrella EA; Kang PB; Shapiro F; Rahimov F; Kawahara G; Widrick JJ; Kunkel LM
    J Clin Invest; 2014 Jun; 124(6):2651-67. PubMed ID: 24789910
    [TBL] [Abstract][Full Text] [Related]  

  • 2. miR-146a deficiency does not aggravate muscular dystrophy in mdx mice.
    Bronisz-Budzyńska I; Chwalenia K; Mucha O; Podkalicka P; Karolina-Bukowska-Strakova ; Józkowicz A; Łoboda A; Kozakowska M; Dulak J
    Skelet Muscle; 2019 Aug; 9(1):22. PubMed ID: 31412923
    [TBL] [Abstract][Full Text] [Related]  

  • 3. MicroRNA-199a is induced in dystrophic muscle and affects WNT signaling, cell proliferation, and myogenic differentiation.
    Alexander MS; Kawahara G; Motohashi N; Casar JC; Eisenberg I; Myers JA; Gasperini MJ; Estrella EA; Kho AT; Mitsuhashi S; Shapiro F; Kang PB; Kunkel LM
    Cell Death Differ; 2013 Sep; 20(9):1194-208. PubMed ID: 23764775
    [TBL] [Abstract][Full Text] [Related]  

  • 4. PTEN contributes to profound PI3K/Akt signaling pathway deregulation in dystrophin-deficient dog muscle.
    Feron M; Guevel L; Rouger K; Dubreil L; Arnaud MC; Ledevin M; Megeney LA; Cherel Y; Sakanyan V
    Am J Pathol; 2009 Apr; 174(4):1459-70. PubMed ID: 19264909
    [TBL] [Abstract][Full Text] [Related]  

  • 5. DOCK3 is a dosage-sensitive regulator of skeletal muscle and Duchenne muscular dystrophy-associated pathologies.
    Reid AL; Wang Y; Samani A; Hightower RM; Lopez MA; Gilbert SR; Ianov L; Crossman DK; Dell'Italia LJ; Millay DP; van Groen T; Halade GV; Alexander MS
    Hum Mol Genet; 2020 Oct; 29(17):2855-2871. PubMed ID: 32766788
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Repression of phosphatidylinositol transfer protein α ameliorates the pathology of Duchenne muscular dystrophy.
    Vieira NM; Spinazzola JM; Alexander MS; Moreira YB; Kawahara G; Gibbs DE; Mead LC; Verjovski-Almeida S; Zatz M; Kunkel LM
    Proc Natl Acad Sci U S A; 2017 Jun; 114(23):6080-6085. PubMed ID: 28533404
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Levels of α7 integrin and laminin-α2 are increased following prednisone treatment in the mdx mouse and GRMD dog models of Duchenne muscular dystrophy.
    Wuebbles RD; Sarathy A; Kornegay JN; Burkin DJ
    Dis Model Mech; 2013 Sep; 6(5):1175-84. PubMed ID: 23846963
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Perturbation of PI3K/Akt signaling affected autophagy modulation in dystrophin-deficient myoblasts.
    Yazid MD; Hung-Chih C
    Cell Commun Signal; 2021 Oct; 19(1):105. PubMed ID: 34706731
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Pannexin 1 dysregulation in Duchenne muscular dystrophy and its exacerbation of dystrophic features in mdx mice.
    Freeman E; Langlois S; Leyba MF; Ammar T; Léger Z; McMillan HJ; Renaud JM; Jasmin BJ; Cowan KN
    Skelet Muscle; 2024 Apr; 14(1):8. PubMed ID: 38671506
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. MicroRNA-206 is highly expressed in newly formed muscle fibers: implications regarding potential for muscle regeneration and maturation in muscular dystrophy.
    Yuasa K; Hagiwara Y; Ando M; Nakamura A; Takeda S; Hijikata T
    Cell Struct Funct; 2008; 33(2):163-9. PubMed ID: 18827405
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Elevated p21 mRNA level in skeletal muscle of DMD patients and mdx mice indicates either an exhausted satellite cell pool or a higher p21 expression in dystrophin-deficient cells per se.
    Endesfelder S; Krahn A; Kreuzer KA; Lass U; Schmidt CA; Jahrmarkt C; von Moers A; Speer A
    J Mol Med (Berl); 2000; 78(10):569-74. PubMed ID: 11199330
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Protein-Anchoring Therapy of Biglycan for Mdx Mouse Model of Duchenne Muscular Dystrophy.
    Ito M; Ehara Y; Li J; Inada K; Ohno K
    Hum Gene Ther; 2017 May; 28(5):428-436. PubMed ID: 27485975
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. Myogenic Akt signaling attenuates muscular degeneration, promotes myofiber regeneration and improves muscle function in dystrophin-deficient mdx mice.
    Kim MH; Kay DI; Rudra RT; Chen BM; Hsu N; Izumiya Y; Martinez L; Spencer MJ; Walsh K; Grinnell AD; Crosbie RH
    Hum Mol Genet; 2011 Apr; 20(7):1324-38. PubMed ID: 21245083
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A comparative study of N-glycolylneuraminic acid (Neu5Gc) and cytotoxic T cell (CT) carbohydrate expression in normal and dystrophin-deficient dog and human skeletal muscle.
    Martin PT; Golden B; Okerblom J; Camboni M; Chandrasekharan K; Xu R; Varki A; Flanigan KM; Kornegay JN
    PLoS One; 2014; 9(2):e88226. PubMed ID: 24505439
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Sparing of the dystrophin-deficient cranial sartorius muscle is associated with classical and novel hypertrophy pathways in GRMD dogs.
    Nghiem PP; Hoffman EP; Mittal P; Brown KJ; Schatzberg SJ; Ghimbovschi S; Wang Z; Kornegay JN
    Am J Pathol; 2013 Nov; 183(5):1411-24. PubMed ID: 24160322
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Inositol 1,4,5-trisphosphate (IP3)-dependent Ca2+ signaling mediates delayed myogenesis in Duchenne muscular dystrophy fetal muscle.
    Farini A; Sitzia C; Cassinelli L; Colleoni F; Parolini D; Giovanella U; Maciotta S; Colombo A; Meregalli M; Torrente Y
    Development; 2016 Feb; 143(4):658-69. PubMed ID: 26884398
    [TBL] [Abstract][Full Text] [Related]  

  • 19. DOCK3 regulates normal skeletal muscle regeneration and glucose metabolism.
    Samani A; Karuppasamy M; English KG; Siler CA; Wang Y; Widrick JJ; Alexander MS
    FASEB J; 2023 Oct; 37(10):e23198. PubMed ID: 37742307
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Mdx mice inducibly expressing dystrophin provide insights into the potential of gene therapy for duchenne muscular dystrophy.
    Ahmad A; Brinson M; Hodges BL; Chamberlain JS; Amalfitano A
    Hum Mol Genet; 2000 Oct; 9(17):2507-15. PubMed ID: 11030755
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 20.