| P50 | author | Thibaut Larcher | Q37373430 |
| | Charles Pineau | Q37382984 |
| | Mélanie Lagarrigue | Q87896690 |
| P2093 | author name string | Laurence Dubreil | |
| | Karl Rouger | |
| | Mireille Ledevin | |
| | Aurélie Lardenois | |
| | Blandine Guével | |
| | Laëtitia Guével | |
| | Sabrina Jagot | |
| P2860 | cites work | Analysis of the myosin-II-responsive focal adhesion proteome reveals a role for β-Pix in negative regulation of focal adhesion maturation | Q24297812 |
| | Proteomic profiling of the dystrophin-deficient mdx phenocopy of dystrophinopathy-associated cardiomyopathy | Q27006945 |
| | Differential Gene Expression Profiling of Dystrophic Dog Muscle after MuStem Cell Transplantation | Q27309883 |
| | Muscle-specific SIRT1 gain-of-function increases slow-twitch fibers and ameliorates pathophysiology in a mouse model of duchenne muscular dystrophy | Q27314850 |
| | Fiji: an open-source platform for biological-image analysis | Q27860912 |
| | Cellular iron uptake, trafficking and metabolism: Key molecules and mechanisms and their roles in disease | Q28087521 |
| | The complete sequence of the human beta-myosin heavy chain gene and a comparative analysis of its product | Q28118956 |
| | Cellular and molecular regulation of muscle regeneration | Q28238078 |
| | Mesoangioblast stem cells ameliorate muscle function in dystrophic dogs | Q28274324 |
| | Troponin T isoforms and posttranscriptional modifications: Evolution, regulation and function | Q28296309 |
| | Quantitative analysis of 2,3,7,8-tetrachlorodibenzo-p-dioxin-induced proteome alterations in 5L rat hepatoma cells using isotope-coded protein labels | Q28571697 |
| | The ferritins: molecular properties, iron storage function and cellular regulation | Q28609366 |
| | Murine and human myogenic cells identified by elevated aldehyde dehydrogenase activity: implications for muscle regeneration and repair | Q28741359 |
| | ProteomeXchange provides globally coordinated proteomics data submission and dissemination | Q29614806 |
| | Membrane organization of the dystrophin-glycoprotein complex | Q29615149 |
| | Dystrophin: the protein product of the Duchenne muscular dystrophy locus | Q29618077 |
| | Large-scale analysis of differential gene expression in the hindlimb muscles and diaphragm of mdx mouse | Q30813768 |
| | The Annotation, Mapping, Expression and Network (AMEN) suite of tools for molecular systems biology | Q33318567 |
| | Human skeletal muscle-derived CD133(+) cells form functional satellite cells after intramuscular transplantation in immunodeficient host mice | Q33562298 |
| | Porcine skeletal muscle-derived multipotent PW1pos/Pax7neg interstitial cells: isolation, characterization, and long-term culture. | Q33690004 |
| | Haptoglobin is required to prevent oxidative stress and muscle atrophy | Q33800519 |
| | Predictive markers of clinical outcome in the GRMD dog model of Duchenne muscular dystrophy | Q34424160 |
| | IGF-1, inflammation and stem cells: interactions during muscle regeneration. | Q34444122 |
| | Motor physical therapy affects muscle collagen type I and decreases gait speed in dystrophin-deficient dogs. | Q35142741 |
| | A calcineurin-dependent transcriptional pathway controls skeletal muscle fiber type | Q35207780 |
| | Systemic delivery of allogenic muscle stem cells induces long-term muscle repair and clinical efficacy in duchenne muscular dystrophy dogs | Q35475301 |
| | Duchenne's muscular dystrophy: animal models used to investigate pathogenesis and develop therapeutic strategies | Q35591025 |
| | Labile iron pool: the main determinant of cellular response to oxidative stress | Q35592855 |
| | Human muscle-derived cell populations isolated by differential adhesion rates: phenotype and contribution to skeletal muscle regeneration in Mdx/SCID mice | Q35706322 |
| | Expression profiling in the muscular dystrophies: identification of novel aspects of molecular pathophysiology | Q36360412 |
| | Identification of disease specific pathways using in vivo SILAC proteomics in dystrophin deficient mdx mouse. | Q36832437 |
| | Isolation of muscle-derived stem/progenitor cells based on adhesion characteristics to collagen-coated surfaces | Q37065904 |
| | Newborn bloodspot screening for Duchenne muscular dystrophy: 21 years experience in Wales (UK). | Q37185971 |
| | Muscular dystrophy therapy by nonautologous mesenchymal stem cells: muscle regeneration without immunosuppression and inflammation | Q37352442 |
| | Canine models of Duchenne muscular dystrophy and their use in therapeutic strategies | Q37548291 |
| | Proteomic profiling of x-linked muscular dystrophy | Q37676955 |
| | Cytosolic and mitochondrial ferritins in the regulation of cellular iron homeostasis and oxidative damage | Q37696653 |
| | Annexin A1: novel roles in skeletal muscle biology | Q37972834 |
| | Invited review: Stem cells and muscle diseases: advances in cell therapy strategies | Q38269131 |
| | Mesenchymal-stem-cell-derived exosomes accelerate skeletal muscle regeneration | Q38888737 |
| | Pericytes of human skeletal muscle are myogenic precursors distinct from satellite cells | Q40243228 |
| | Training-induced morphological and functional changes in skeletal muscle | Q40328007 |
| | Global/temporal gene expression in diaphragm and hindlimb muscles of dystrophin-deficient (mdx) mice | Q40639635 |
| | Muscle genome-wide expression profiling during disease evolution in mdx mice. | Q44471658 |
| | Fast muscle fibers are preferentially affected in Duchenne muscular dystrophy. | Q45966003 |
| | Apolipoprotein E-/- mice have delayed skeletal muscle healing after hind limb ischemia-reperfusion | Q46524635 |
| | Cytoplasmic gelsolin in pheochromocytoma-12 cells forms a complex with amyloid beta-protein | Q46743519 |
| | Temporal gene expression profiling of dystrophin-deficient (mdx) mouse diaphragm identifies conserved and muscle group-specific mechanisms in the pathogenesis of muscular dystrophy | Q47314000 |
| | Dissection of temporal gene expression signatures of affected and spared muscle groups in dystrophin-deficient (mdx) mice | Q47745483 |
| | Gene expression profiling of Duchenne muscular dystrophy skeletal muscle | Q47970351 |
| | Quantitative proteomic Isotope-Coded Protein Label (ICPL) analysis reveals alteration of several functional processes in the glioblastoma | Q48520367 |
| | Canine X-linked muscular dystrophy. An animal model of Duchenne muscular dystrophy: clinical studies. | Q50892927 |
| | Quantitative proteomic analysis of dystrophic dog muscle. | Q54382935 |
| | Gene expression profiling in the early phases of DMD: a constant molecular signature characterizes DMD muscle from early postnatal life throughout disease progression | Q57588305 |
| | The homologue of the Duchenne locus is defective in X-linked muscular dystrophy of dogs | Q59051983 |
| P433 | issue | 14 | |
| P304 | page(s) | 2028-2042 | |
| P577 | publication date | 2016-07-01 | |
| P1433 | published in | Proteomics | Q15614164 |
| P1476 | title | Quantitative proteome profiling of dystrophic dog skeletal muscle reveals a stabilized muscular architecture and protection against oxidative stress after systemic delivery of MuStem cells | |
| P478 | volume | 16 | |