ERBB3 and NGFR mark a distinct skeletal muscle progenitor cell in human development and hPSCs
暂无分享,去创建一个
Ben Van Handel | Denis Evseenko | Michael R Hicks | April D Pyle | Stanley F Nelson | S. Nelson | A. Pyle | A. Eskin | D. Evseenko | Haibin Xi | Melissa J Spencer | M. Spencer | Michael R. Hicks | Julia Hiserodt | Katrina I Paras | W. Fujiwara | M. Jan | C. Young | B. V. Handel | Ascia Eskin | Julia Hiserodt | Katrina Paras | Wakana Fujiwara | Majib Jan | Haibin Xi | Courtney S Young | Julia Hiserodt
[1] K. Schenke-Layland,et al. In Vivo Human Somitogenesis Guides Somite Development from hPSCs. , 2017, Cell reports.
[2] A. Pyle,et al. Creation of a Novel Humanized Dystrophic Mouse Model of Duchenne Muscular Dystrophy and Application of a CRISPR/Cas9 Gene Editing Therapy. , 2017, Journal of neuromuscular diseases.
[3] J. Spinazzola,et al. CD82 Is a Marker for Prospective Isolation of Human Muscle Satellite Cells and Is Linked to Muscular Dystrophies. , 2016, Cell stem cell.
[4] Olivier Pourquié,et al. Generation of human muscle fibers and satellite-like cells from human pluripotent stem cells in vitro , 2016, Nature Protocols.
[5] C. Birchmeier,et al. Muscle contraction is required to maintain the pool of muscle progenitors via YAP and NOTCH during fetal myogenesis , 2016, eLife.
[6] Pang Wei Koh,et al. Mapping the Pairwise Choices Leading from Pluripotency to Human Bone, Heart, and Other Mesoderm Cell Types , 2016, Cell.
[7] G. Coppola,et al. A Novel Protocol for Directed Differentiation of C9orf72-Associated Human Induced Pluripotent Stem Cells Into Contractile Skeletal Myotubes , 2016, Stem cells translational medicine.
[8] M. Oshimura,et al. Concordant but Varied Phenotypes among Duchenne Muscular Dystrophy Patient-Specific Myoblasts Derived using a Human iPSC-Based Model. , 2016, Cell reports.
[9] A. Sacco,et al. Satellite Cell Heterogeneity in Skeletal Muscle Homeostasis. , 2016, Trends in cell biology.
[10] J. Shrager,et al. A bioengineered niche preserves the quiescence of muscle stem cells and enhances their therapeutic efficacy , 2016, Nature Biotechnology.
[11] Atsushi Nakano,et al. A Single CRISPR-Cas9 Deletion Strategy that Targets the Majority of DMD Patients Restores Dystrophin Function in hiPSC-Derived Muscle Cells. , 2016, Cell stem cell.
[12] A. Sacco,et al. Autonomous Extracellular Matrix Remodeling Controls a Progressive Adaptation in Muscle Stem Cell Regenerative Capacity during Development , 2016, Cell reports.
[13] J. Pomerantz,et al. Human Satellite Cell Transplantation and Regeneration from Diverse Skeletal Muscles , 2015, Stem cell reports.
[14] Olivier Tassy,et al. Differentiation of pluripotent stem cells to muscle fiber to model Duchenne muscular dystrophy , 2015, Nature Biotechnology.
[15] Carlo Reggiani,et al. Developmental myosins: expression patterns and functional significance , 2015, Skeletal Muscle.
[16] S. Hammond,et al. How much dystrophin is enough: the physiological consequences of different levels of dystrophin in the mdx mouse. , 2015, Human molecular genetics.
[17] P. Rosenfeld,et al. Human embryonic stem cell-derived retinal pigment epithelium in patients with age-related macular degeneration and Stargardt's macular dystrophy: follow-up of two open-label phase 1/2 studies , 2015, The Lancet.
[18] Karl Deisseroth,et al. Optogenetics enables functional analysis of human embryonic stem cell–derived grafts in a Parkinson's disease model , 2015, Nature Biotechnology.
[19] G. Crooks,et al. GPI-80 defines self-renewal ability in hematopoietic stem cells during human development. , 2015, Cell stem cell.
[20] D. Melton,et al. Generation of Functional Human Pancreatic β Cells In Vitro , 2014, Cell.
[21] John K. Hall,et al. Adeno-associated viral vectors do not efficiently target muscle satellite cells , 2014, Molecular therapy. Methods & clinical development.
[22] W. Stanford,et al. Derivation and Expansion of PAX7-Positive Muscle Progenitors from Human and Mouse Embryonic Stem Cells , 2014, Stem cell reports.
[23] S. Kattman,et al. The generation of the epicardial lineage from human pluripotent stem cells , 2014, Nature Biotechnology.
[24] Charles E. Murry,et al. Human Embryonic Stem Cell-Derived Cardiomyocytes Regenerate Non-Human Primate Hearts , 2014, Nature.
[25] D. Gifford,et al. Differentiated human stem cells resemble fetal, not adult, β cells , 2014, Proceedings of the National Academy of Sciences.
[26] C. Marcelle,et al. ErbB3 binding protein-1 (Ebp1) controls proliferation and myogenic differentiation of muscle stem cells. , 2014, Developmental biology.
[27] Bahram Valamehr,et al. Myogenic Differentiation of Muscular Dystrophy‐Specific Induced Pluripotent Stem Cells for Use in Drug Discovery , 2014, Stem cells translational medicine.
[28] Lil Pabon,et al. Engineering Adolescence: Maturation of Human Pluripotent Stem Cell–Derived Cardiomyocytes , 2014, Circulation research.
[29] A. Wagers,et al. Isolation of Progenitors that Exhibit Myogenic/Osteogenic Bipotency In Vitro by Fluorescence-Activated Cell Sorting from Human Fetal Muscle , 2014, Stem cell reports.
[30] Joseph Chen,et al. Derivation and FACS-Mediated Purification of PAX3+/PAX7+ Skeletal Muscle Precursors from Human Pluripotent Stem Cells , 2013, Stem cell reports.
[31] L. Zon,et al. A Zebrafish Embryo Culture System Defines Factors that Promote Vertebrate Myogenesis across Species , 2013, Cell.
[32] C. Keller,et al. Myf5 expression during fetal myogenesis defines the developmental progenitors of adult satellite cells. , 2013, Developmental biology.
[33] P. Cahan,et al. Origins and implications of pluripotent stem cell variability and heterogeneity , 2013, Nature Reviews Molecular Cell Biology.
[34] S. Anderson,et al. Directed differentiation and functional maturation of cortical interneurons from human embryonic stem cells. , 2013, Cell stem cell.
[35] Feodor Price,et al. Satellite cells and the muscle stem cell niche. , 2013, Physiological reviews.
[36] A. Rozkalne,et al. Human fetal skeletal muscle contains a myogenic side population that expresses the melanoma cell-adhesion molecule. , 2012, Human molecular genetics.
[37] M. Kyba,et al. Human ES- and iPS-derived myogenic progenitors restore DYSTROPHIN and improve contractility upon transplantation in dystrophic mice. , 2012, Cell stem cell.
[38] Gary R. Mirams,et al. Application of human stem cell-derived cardiomyocytes in safety pharmacology requires caution beyond hERG. , 2012, Journal of molecular and cellular cardiology.
[39] F. Relaix,et al. Neural crest cell lineage restricts skeletal muscle progenitor cell differentiation through Neuregulin1-ErbB3 signaling. , 2011, Developmental cell.
[40] H. Bye-A-Jee,et al. Physiological characterization of muscle strength with variable levels of dystrophin restoration in mdx mice following local antisense therapy. , 2011, Molecular therapy : the journal of the American Society of Gene Therapy.
[41] K. Schenke-Layland,et al. Mapping the first stages of mesoderm commitment during differentiation of human embryonic stem cells , 2010, Proceedings of the National Academy of Sciences.
[42] Cole Trapnell,et al. Transcript assembly and quantification by RNA-Seq reveals unannotated transcripts and isoform switching during cell differentiation. , 2010, Nature biotechnology.
[43] N. Bresolin,et al. The low-affinity receptor for neurotrophins p75NTR plays a key role for satellite cell function in muscle repair acting via RhoA. , 2009, Molecular biology of the cell.
[44] Lior Pachter,et al. Sequence Analysis , 2020, Definitions.
[45] Brad T. Sherman,et al. Bioinformatics enrichment tools: paths toward the comprehensive functional analysis of large gene lists , 2008, Nucleic acids research.
[46] H. Blau,et al. Self-renewal and expansion of single transplanted muscle stem cells , 2008, Nature.
[47] S. Tapscott,et al. Cell-lineage regulated myogenesis for dystrophin replacement: a novel therapeutic approach for treatment of muscular dystrophy. , 2008, Human molecular genetics.
[48] A. Wagers,et al. Highly Efficient, Functional Engraftment of Skeletal Muscle Stem Cells in Dystrophic Muscles , 2008, Cell.
[49] Christophe Marcelle,et al. Myostatin promotes the terminal differentiation of embryonic muscle progenitors. , 2008, Genes & development.
[50] Chad A. Cowan,et al. Marked differences in differentiation propensity among human embryonic stem cell lines , 2008, Nature Biotechnology.
[51] Michael Kyba,et al. Functional skeletal muscle regeneration from differentiating embryonic stem cells , 2008, Nature Medicine.
[52] Brad T. Sherman,et al. Systematic and integrative analysis of large gene lists using DAVID bioinformatics resources , 2008, Nature Protocols.
[53] R. Sambasivan,et al. Skeletal muscle stem cell birth and properties. , 2007, Seminars in cell & developmental biology.
[54] T. Partridge,et al. Skeletal muscle stem cells express anti-apoptotic ErbB receptors during activation from quiescence. , 2007, Experimental cell research.
[55] Takeshi Imamura,et al. The ALK‐5 inhibitor A‐83‐01 inhibits Smad signaling and epithelial‐to‐mesenchymal transition by transforming growth factor‐β , 2005, Cancer science.
[56] Pablo Tamayo,et al. Gene set enrichment analysis: A knowledge-based approach for interpreting genome-wide expression profiles , 2005, Proceedings of the National Academy of Sciences of the United States of America.
[57] Charlotte Collins,et al. Direct Isolation of Satellite Cells for Skeletal Muscle Regeneration , 2005, Science.
[58] A. Reith,et al. SB-431542 is a potent and specific inhibitor of transforming growth factor-beta superfamily type I activin receptor-like kinase (ALK) receptors ALK4, ALK5, and ALK7. , 2002, Molecular pharmacology.
[59] C. Rommel,et al. Mediation of IGF-1-induced skeletal myotube hypertrophy by PI(3)K/Akt/mTOR and PI(3)K/Akt/GSK3 pathways , 2001, Nature Cell Biology.
[60] Y. Chan,et al. Learning and understanding the Kruskal-Wallis one-way analysis-of-variance-by-ranks test for differences among three or more independent groups. , 1997, Physical therapy.
[61] S. Ferrari,et al. Differential response of embryonic and fetal myoblasts to TGF beta: a possible regulatory mechanism of skeletal muscle histogenesis. , 1994, Development.
[62] T. M. Nguyen,et al. Use of epitope libraries to identify exon-specific monoclonal antibodies for characterization of altered dystrophins in muscular dystrophy. , 1993, American journal of human genetics.