Francesco Chemello, Zhaoning Wang, Hui Li, John R McAnally, Ning Liu, Rhonda Bassel-Duby, Eric N Olson. Proc Natl Acad Sci U S A 2020
Times Cited: 36
Times Cited: 36
Times Cited
Times Co-cited
Similarity
Single-nucleus RNA-seq and FISH identify coordinated transcriptional activity in mammalian myofibers.
Matthieu Dos Santos, Stéphanie Backer, Benjamin Saintpierre, Brigitte Izac, Muriel Andrieu, Franck Letourneur, Frederic Relaix, Athanassia Sotiropoulos, Pascal Maire. Nat Commun 2020
Matthieu Dos Santos, Stéphanie Backer, Benjamin Saintpierre, Brigitte Izac, Muriel Andrieu, Franck Letourneur, Frederic Relaix, Athanassia Sotiropoulos, Pascal Maire. Nat Commun 2020
38
Single-nucleus transcriptomics reveals functional compartmentalization in syncytial skeletal muscle cells.
Minchul Kim, Vedran Franke, Bettina Brandt, Elijah D Lowenstein, Verena Schöwel, Simone Spuler, Altuna Akalin, Carmen Birchmeier. Nat Commun 2020
Minchul Kim, Vedran Franke, Bettina Brandt, Elijah D Lowenstein, Verena Schöwel, Simone Spuler, Altuna Akalin, Carmen Birchmeier. Nat Commun 2020
38
Single-nucleus RNA-seq identifies transcriptional heterogeneity in multinucleated skeletal myofibers.
Michael J Petrany, Casey O Swoboda, Chengyi Sun, Kashish Chetal, Xiaoting Chen, Matthew T Weirauch, Nathan Salomonis, Douglas P Millay. Nat Commun 2020
Michael J Petrany, Casey O Swoboda, Chengyi Sun, Kashish Chetal, Xiaoting Chen, Matthew T Weirauch, Nathan Salomonis, Douglas P Millay. Nat Commun 2020
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High-Dimensional Single-Cell Cartography Reveals Novel Skeletal Muscle-Resident Cell Populations.
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Dystrophin: the protein product of the Duchenne muscular dystrophy locus.
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Postnatal genome editing partially restores dystrophin expression in a mouse model of muscular dystrophy.
Chengzu Long, Leonela Amoasii, Alex A Mireault, John R McAnally, Hui Li, Efrain Sanchez-Ortiz, Samadrita Bhattacharyya, John M Shelton, Rhonda Bassel-Duby, Eric N Olson. Science 2016
Chengzu Long, Leonela Amoasii, Alex A Mireault, John R McAnally, Hui Li, Efrain Sanchez-Ortiz, Samadrita Bhattacharyya, John M Shelton, Rhonda Bassel-Duby, Eric N Olson. Science 2016
25
Single-Cell Analysis of the Muscle Stem Cell Hierarchy Identifies Heterotypic Communication Signals Involved in Skeletal Muscle Regeneration.
Andrea J De Micheli, Emily J Laurilliard, Charles L Heinke, Hiranmayi Ravichandran, Paula Fraczek, Sharon Soueid-Baumgarten, Iwijn De Vlaminck, Olivier Elemento, Benjamin D Cosgrove. Cell Rep 2020
Andrea J De Micheli, Emily J Laurilliard, Charles L Heinke, Hiranmayi Ravichandran, Paula Fraczek, Sharon Soueid-Baumgarten, Iwijn De Vlaminck, Olivier Elemento, Benjamin D Cosgrove. Cell Rep 2020
25
In vivo genome editing improves muscle function in a mouse model of Duchenne muscular dystrophy.
Christopher E Nelson, Chady H Hakim, David G Ousterout, Pratiksha I Thakore, Eirik A Moreb, Ruth M Castellanos Rivera, Sarina Madhavan, Xiufang Pan, F Ann Ran, Winston X Yan,[...]. Science 2016
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Gene editing restores dystrophin expression in a canine model of Duchenne muscular dystrophy.
Leonela Amoasii, John C W Hildyard, Hui Li, Efrain Sanchez-Ortiz, Alex Mireault, Daniel Caballero, Rachel Harron, Thaleia-Rengina Stathopoulou, Claire Massey, John M Shelton,[...]. Science 2018
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Single cell analysis of adult mouse skeletal muscle stem cells in homeostatic and regenerative conditions.
Stefania Dell'Orso, Aster H Juan, Kyung-Dae Ko, Faiza Naz, Jelena Perovanovic, Gustavo Gutierrez-Cruz, Xuesong Feng, Vittorio Sartorelli. Development 2019
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CRISPR-Cas9 corrects Duchenne muscular dystrophy exon 44 deletion mutations in mice and human cells.
Yi-Li Min, Hui Li, Cristina Rodriguez-Caycedo, Alex A Mireault, Jian Huang, John M Shelton, John R McAnally, Leonela Amoasii, Pradeep P A Mammen, Rhonda Bassel-Duby,[...]. Sci Adv 2019
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Temporal Dynamics and Heterogeneity of Cell Populations during Skeletal Muscle Regeneration.
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Dynamics of cellular states of fibro-adipogenic progenitors during myogenesis and muscular dystrophy.
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CRISPR Correction of Duchenne Muscular Dystrophy.
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Muscle-specific CRISPR/Cas9 dystrophin gene editing ameliorates pathophysiology in a mouse model for Duchenne muscular dystrophy.
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Stem Cell-Derived Cardiomyocytes and Beta-Adrenergic Receptor Blockade in Duchenne Muscular Dystrophy Cardiomyopathy.
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Aging Disrupts Muscle Stem Cell Function by Impairing Matricellular WISP1 Secretion from Fibro-Adipogenic Progenitors.
Laura Lukjanenko, Sonia Karaz, Pascal Stuelsatz, Uxia Gurriaran-Rodriguez, Joris Michaud, Gabriele Dammone, Federico Sizzano, Omid Mashinchian, Sara Ancel, Eugenia Migliavacca,[...]. Cell Stem Cell 2019
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13
AMPK Activation Regulates LTBP4-Dependent TGF-β1 Secretion by Pro-inflammatory Macrophages and Controls Fibrosis in Duchenne Muscular Dystrophy.
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13
Nilotinib reduces muscle fibrosis in chronic muscle injury by promoting TNF-mediated apoptosis of fibro/adipogenic progenitors.
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13
Single-cut genome editing restores dystrophin expression in a new mouse model of muscular dystrophy.
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13
Somatic gene editing ameliorates skeletal and cardiac muscle failure in pig and human models of Duchenne muscular dystrophy.
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13
Adenine base editing in mouse embryos and an adult mouse model of Duchenne muscular dystrophy.
Seuk-Min Ryu, Taeyoung Koo, Kyoungmi Kim, Kayeong Lim, Gayoung Baek, Sang-Tae Kim, Heon Seok Kim, Da-Eun Kim, Hyunji Lee, Eugene Chung,[...]. Nat Biotechnol 2018
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13
Correction of Three Prominent Mutations in Mouse and Human Models of Duchenne Muscular Dystrophy by Single-Cut Genome Editing.
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16
Therapeutic developments for Duchenne muscular dystrophy.
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Enhanced CRISPR-Cas9 correction of Duchenne muscular dystrophy in mice by a self-complementary AAV delivery system.
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13
In vivo gene editing in dystrophic mouse muscle and muscle stem cells.
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A reference single-cell transcriptomic atlas of human skeletal muscle tissue reveals bifurcated muscle stem cell populations.
Andrea J De Micheli, Jason A Spector, Olivier Elemento, Benjamin D Cosgrove. Skelet Muscle 2020
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Muscle injury activates resident fibro/adipogenic progenitors that facilitate myogenesis.
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Regulation of muscle growth and regeneration by the immune system.
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PAX3 Confers Functional Heterogeneity in Skeletal Muscle Stem Cell Responses to Environmental Stress.
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Muscle Satellite Cell Cross-Talk with a Vascular Niche Maintains Quiescence via VEGF and Notch Signaling.
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Single-cell sequencing reveals dissociation-induced gene expression in tissue subpopulations.
Susanne C van den Brink, Fanny Sage, Ábel Vértesy, Bastiaan Spanjaard, Josi Peterson-Maduro, Chloé S Baron, Catherine Robin, Alexander van Oudenaarden. Nat Methods 2017
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In Situ Fixation Redefines Quiescence and Early Activation of Skeletal Muscle Stem Cells.
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11
Coupling between Myogenesis and Angiogenesis during Skeletal Muscle Regeneration Is Stimulated by Restorative Macrophages.
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11
Pax3 and Pax7 have distinct and overlapping functions in adult muscle progenitor cells.
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Hic1 Defines Quiescent Mesenchymal Progenitor Subpopulations with Distinct Functions and Fates in Skeletal Muscle Regeneration.
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Inflammatory monocytes recruited after skeletal muscle injury switch into antiinflammatory macrophages to support myogenesis.
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Mesenchymal Stromal Cells Are Required for Regeneration and Homeostatic Maintenance of Skeletal Muscle.
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The TREAT-NMD DMD Global Database: analysis of more than 7,000 Duchenne muscular dystrophy mutations.
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Correction of muscular dystrophies by CRISPR gene editing.
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AAV CRISPR editing rescues cardiac and muscle function for 18 months in dystrophic mice.
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Engineered CRISPR-Cas9 nuclease with expanded targeting space.
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Integrating single-cell transcriptomic data across different conditions, technologies, and species.
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CRISPR-Cpf1 correction of muscular dystrophy mutations in human cardiomyocytes and mice.
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Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.