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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

335 related items for PubMed ID: 32242220

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  • 22. Muscle xenografts reproduce key molecular features of facioscapulohumeral muscular dystrophy.
    Mueller AL, O'Neill A, Jones TI, Llach A, Rojas LA, Sakellariou P, Stadler G, Wright WE, Eyerman D, Jones PL, Bloch RJ.
    Exp Neurol; 2019 Oct; 320():113011. PubMed ID: 31306642
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  • 28. Single-cell spatial transcriptomics reveals a dystrophic trajectory following a developmental bifurcation of myoblast cell fates in facioscapulohumeral muscular dystrophy.
    Chen L, Kong X, Johnston KG, Mortazavi A, Holmes TC, Tan Z, Yokomori K, Xu X.
    Genome Res; 2024 Jun 25; 34(5):665-679. PubMed ID: 38777608
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  • 30. Expression patterns of FSHD-causing DUX4 and myogenic transcription factors PAX3 and PAX7 are spatially distinct in differentiating human stem cell cultures.
    Haynes P, Kernan K, Zhou SL, Miller DG.
    Skelet Muscle; 2017 Jun 21; 7(1):13. PubMed ID: 28637492
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  • 34. DUX4 expression in FSHD muscle cells: how could such a rare protein cause a myopathy?
    Tassin A, Laoudj-Chenivesse D, Vanderplanck C, Barro M, Charron S, Ansseau E, Chen YW, Mercier J, Coppée F, Belayew A.
    J Cell Mol Med; 2013 Jan 21; 17(1):76-89. PubMed ID: 23206257
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  • 35. Protein kinase A activation inhibits DUX4 gene expression in myotubes from patients with facioscapulohumeral muscular dystrophy.
    Cruz JM, Hupper N, Wilson LS, Concannon JB, Wang Y, Oberhauser B, Patora-Komisarska K, Zhang Y, Glass DJ, Trendelenburg AU, Clarke BA.
    J Biol Chem; 2018 Jul 27; 293(30):11837-11849. PubMed ID: 29899111
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  • 40. The FSHD atrophic myotube phenotype is caused by DUX4 expression.
    Vanderplanck C, Ansseau E, Charron S, Stricwant N, Tassin A, Laoudj-Chenivesse D, Wilton SD, Coppée F, Belayew A.
    PLoS One; 2011 Jul 27; 6(10):e26820. PubMed ID: 22053214
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