240th ENMC workshop: The involvement of skeletal muscle stem cells in the pathology of muscular dystrophies 25–27 January 2019, Hoofddorp, The Netherlands
暂无分享,去创建一个
K. Patel | F. Muntoni | C. Bönnemann | C. Birchmeier | G. Butler-Browne | P. Muñoz-Cánoves | P. Bonaldo | D. Furling | M. Grounds | M. Rüegg | C. Paradas | T. Partridge | A. Ferreiro | H. Jungbluth | J. Morgan | P. Zammit | F. Relaix | G. Padberg | M. Putten | H. Amthor | A. Wood | Dhananjay Chaturvedi | L. Giordani | Alison Stevenson | G. B. Browne | R. Davenport | P. Mishra | Lorenzo Giordani
[1] Annemieke Aartsma-Rus,et al. Natural disease history of the D2-mdx mouse model for Duchenne muscular dystrophy , 2019, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.
[2] A. Postigo,et al. ZEB1 protects skeletal muscle from damage and is required for its regeneration , 2019, Nature Communications.
[3] C. Banerji,et al. PAX7 target gene repression is a superior FSHD biomarker than DUX4 target gene activation, associating with pathological severity and identifying FSHD at the single-cell level , 2019, Human molecular genetics.
[4] S. Preibisch,et al. Oscillations of MyoD and Hes1 proteins regulate the maintenance of activated muscle stem cells , 2019, Genes & development.
[5] P. Currie,et al. RGD inhibition of itgb1 ameliorates laminin-&agr;2-deficient zebrafish fibre pathology , 2018, Human molecular genetics.
[6] Tom H. Cheung,et al. High-dimensional single-cell cartography reveals novel skeletal muscle resident cell populations , 2018, bioRxiv.
[7] M. Grounds. Obstacles and challenges for tissue engineering and regenerative medicine: Australian nuances , 2018, Clinical and experimental pharmacology & physiology.
[8] Simone Severini,et al. PAX7 target genes are globally repressed in facioscapulohumeral muscular dystrophy skeletal muscle , 2017, Nature Communications.
[9] Annemieke Aartsma-Rus,et al. Natural disease history of mouse models for limb girdle muscular dystrophy types 2D and 2F , 2017, PloS one.
[10] Janice S. Lee,et al. A defect in myoblast fusion underlies Carey-Fineman-Ziter syndrome , 2017, Nature Communications.
[11] Shuo Lin,et al. Linker proteins restore basement membrane and correct LAMA2-related muscular dystrophy in mice , 2017, Science Translational Medicine.
[12] M. Rüegg,et al. Chimeric protein repair of laminin polymerization ameliorates muscular dystrophy phenotype , 2017, The Journal of clinical investigation.
[13] G. Pita,et al. A POGLUT1 mutation causes a muscular dystrophy with reduced Notch signaling and satellite cell loss , 2016, EMBO molecular medicine.
[14] Ashley L. Siegel,et al. Asymmetric division of clonal muscle stem cells coordinates muscle regeneration in vivo , 2016, Science.
[15] E. Ballestar,et al. Autophagy maintains stemness by preventing senescence , 2016, Nature.
[16] Yu Xin Wang,et al. Dystrophin expression in muscle stem cells regulates their polarity and asymmetric division , 2015, Nature Medicine.
[17] J. Morgan,et al. Satellite cells from dystrophic muscle retain regenerative capacity , 2015, Stem cell research.
[18] M. Grounds. The need to more precisely define aspects of skeletal muscle regeneration. , 2014, The international journal of biochemistry & cell biology.
[19] E. Ballestar,et al. Geriatric muscle stem cells switch reversible quiescence into senescence , 2014, Nature.
[20] M. Goddeeris,et al. LARGE glycans on dystroglycan function as a tunable matrix scaffold to prevent dystrophy , 2013, Nature.
[21] Marco Quarta,et al. Collagen VI regulates satellite cell self-renewal and muscle regeneration , 2013, Nature Communications.
[22] P. Currie,et al. Epistatic dissection of laminin-receptor interactions in dystrophic zebrafish muscle. , 2012, Human molecular genetics.
[23] Susan C. Brown,et al. Defects in Glycosylation Impair Satellite Stem Cell Function and Niche Composition in the Muscles of the Dystrophic Largemyd Mouse , 2012, Stem cells.
[24] H. Rahn,et al. Colonization of the satellite cell niche by skeletal muscle progenitor cells depends on Notch signals. , 2012, Developmental cell.
[25] Ping Huang,et al. Myotubularin-deficient myoblasts display increased apoptosis, delayed proliferation, and poor cell engraftment. , 2012, The American journal of pathology.
[26] F. Muntoni,et al. Donor Satellite Cell Engraftment is Significantly Augmented When the Host Niche is Preserved and Endogenous Satellite Cells are Incapacitated , 2012, Stem cells.
[27] L. Kunkel,et al. Mutations in the satellite cell gene MEGF10 cause a recessive congenital myopathy with minicores , 2012, neurogenetics.
[28] D. Castel,et al. A Critical Requirement for Notch Signaling in Maintenance of the Quiescent Skeletal Muscle Stem Cell State , 2012, Stem cells.
[29] Tom H. Cheung,et al. Notch Signaling Is Necessary to Maintain Quiescence in Adult Muscle Stem Cells , 2012, Stem cells.
[30] Colin A. Johnson,et al. Mutations in MEGF10, a regulator of satellite cell myogenesis, cause early onset myopathy, areflexia, respiratory distress and dysphagia (EMARDD) , 2011, Nature Genetics.
[31] A. Krol,et al. Satellite cell loss and impaired muscle regeneration in selenoprotein N deficiency. , 2011, Human Molecular Genetics.
[32] N. Maraldi,et al. Autophagy is defective in collagen VI muscular dystrophies, and its reactivation rescues myofiber degeneration , 2010, Nature Medicine.
[33] J. Morgan,et al. Direct effects of the pathogenic mutation on satellite cell function in muscular dystrophy. , 2010, Experimental cell research.
[34] Daniel G. Miller,et al. A Unifying Genetic Model for Facioscapulohumeral Muscular Dystrophy , 2010, Science.
[35] Hiroshi Yamamoto,et al. Genetic background affects properties of satellite cells and mdx phenotypes. , 2010, The American journal of pathology.
[36] A. Palmer,et al. Latent TGF-beta-binding protein 4 modifies muscular dystrophy in mice. , 2009, The Journal of clinical investigation.
[37] A. Bigot,et al. Large CTG repeats trigger p16-dependent premature senescence in myotonic dystrophy type 1 muscle precursor cells. , 2009, The American journal of pathology.
[38] H. Qian,et al. DUX4, a candidate gene of facioscapulohumeral muscular dystrophy, encodes a transcriptional activator of PITX1 , 2007, Proceedings of the National Academy of Sciences.
[39] C. Reggiani,et al. Mitochondrial dysfunction and apoptosis in myopathic mice with collagen VI deficiency , 2003, Nature Genetics.
[40] J. Rommens,et al. Short GCG expansions in the PABP2 gene cause oculopharyngeal muscular dystrophy , 1998, Nature Genetics.