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Connection

Alexis Demonbreun to Animals

This is a "connection" page, showing publications Alexis Demonbreun has written about Animals.
Connection Strength

0.773
  1. A conserved annexin A6-mediated membrane repair mechanism in muscle, heart, and nerve. JCI Insight. 2022 07 22; 7(14).
    View in: PubMed
    Score: 0.055
  2. Loss of dysferlin or myoferlin results in differential defects in excitation-contraction coupling in mouse skeletal muscle. Sci Rep. 2021 08 05; 11(1):15865.
    View in: PubMed
    Score: 0.052
  3. A gene-edited mouse model of limb-girdle muscular dystrophy 2C for testing exon skipping. Dis Model Mech. 2019 11 04; 13(2).
    View in: PubMed
    Score: 0.046
  4. Recombinant annexin A6 promotes membrane repair and protects against muscle injury. J Clin Invest. 2019 11 01; 129(11):4657-4670.
    View in: PubMed
    Score: 0.046
  5. Muscle cell communication in development and repair. Curr Opin Pharmacol. 2017 06; 34:7-14.
    View in: PubMed
    Score: 0.038
  6. An actin-dependent annexin complex mediates plasma membrane repair in muscle. J Cell Biol. 2016 06 20; 213(6):705-18.
    View in: PubMed
    Score: 0.036
  7. Enhanced Muscular Dystrophy from Loss of Dysferlin Is Accompanied by Impaired Annexin A6 Translocation after Sarcolemmal Disruption. Am J Pathol. 2016 06; 186(6):1610-22.
    View in: PubMed
    Score: 0.036
  8. DNA Electroporation, Isolation and Imaging of Myofibers. J Vis Exp. 2015 Dec 23; (106):e53551.
    View in: PubMed
    Score: 0.035
  9. Plasma Membrane Repair in Health and Disease. Curr Top Membr. 2016; 77:67-96.
    View in: PubMed
    Score: 0.035
  10. Membrane fusion in muscle development and repair. Semin Cell Dev Biol. 2015 Sep; 45:48-56.
    View in: PubMed
    Score: 0.035
  11. Eps 15 Homology Domain (EHD)-1 Remodels Transverse Tubules in Skeletal Muscle. PLoS One. 2015; 10(9):e0136679.
    View in: PubMed
    Score: 0.034
  12. Dynamin 2 the rescue for centronuclear myopathy. J Clin Invest. 2014 Mar; 124(3):976-8.
    View in: PubMed
    Score: 0.031
  13. EHD1 mediates vesicle trafficking required for normal muscle growth and transverse tubule development. Dev Biol. 2014 Mar 15; 387(2):179-90.
    View in: PubMed
    Score: 0.031
  14. Dysferlin and myoferlin regulate transverse tubule formation and glycerol sensitivity. Am J Pathol. 2014 Jan; 184(1):248-59.
    View in: PubMed
    Score: 0.030
  15. Impaired muscle growth and response to insulin-like growth factor 1 in dysferlin-mediated muscular dystrophy. Hum Mol Genet. 2011 Feb 15; 20(4):779-89.
    View in: PubMed
    Score: 0.025
  16. Myoferlin regulation by NFAT in muscle injury, regeneration and repair. J Cell Sci. 2010 Jul 15; 123(Pt 14):2413-22.
    View in: PubMed
    Score: 0.024
  17. Myoferlin is required for insulin-like growth factor response and muscle growth. FASEB J. 2010 Apr; 24(4):1284-95.
    View in: PubMed
    Score: 0.023
  18. Transcriptional programming of translation by BCL6 controls skeletal muscle proteostasis. Nat Metab. 2024 Feb; 6(2):304-322.
    View in: PubMed
    Score: 0.015
  19. The super-healing MRL strain promotes muscle growth in muscular dystrophy through a regenerative extracellular matrix. JCI Insight. 2024 Jan 04; 9(3).
    View in: PubMed
    Score: 0.015
  20. Effects of Glucocorticoids in Murine Models of Duchenne and Limb-Girdle Muscular Dystrophy. Methods Mol Biol. 2023; 2587:467-478.
    View in: PubMed
    Score: 0.014
  21. Circulating ACE2-expressing extracellular vesicles block broad strains of SARS-CoV-2. Nat Commun. 2022 01 20; 13(1):405.
    View in: PubMed
    Score: 0.013
  22. Pulsed glucocorticoids enhance dystrophic muscle performance through epigenetic-metabolic reprogramming. JCI Insight. 2019 12 19; 4(24).
    View in: PubMed
    Score: 0.012
  23. Dusp6 is a genetic modifier of growth through enhanced ERK activity. Hum Mol Genet. 2019 01 15; 28(2):279-289.
    View in: PubMed
    Score: 0.011
  24. "Of Mice and Measures": A Project to Improve How We Advance Duchenne Muscular Dystrophy Therapies to the Clinic. J Neuromuscul Dis. 2018; 5(4):407-417.
    View in: PubMed
    Score: 0.010
  25. Genetic modifiers of muscular dystrophy act on sarcolemmal resealing and recovery from injury. PLoS Genet. 2017 Oct; 13(10):e1007070.
    View in: PubMed
    Score: 0.010
  26. Intermittent Glucocorticoid Dosing Improves Muscle Repair and Function in Mice with Limb-Girdle Muscular Dystrophy. Am J Pathol. 2017 Nov; 187(11):2520-2535.
    View in: PubMed
    Score: 0.010
  27. Intermittent glucocorticoid steroid dosing enhances muscle repair without eliciting muscle atrophy. J Clin Invest. 2017 Jun 01; 127(6):2418-2432.
    View in: PubMed
    Score: 0.010
  28. Reengineering a transmembrane protein to treat muscular dystrophy using exon skipping. J Clin Invest. 2015 Nov 02; 125(11):4186-95.
    View in: PubMed
    Score: 0.009
  29. Annexin A6 modifies muscular dystrophy by mediating sarcolemmal repair. Proc Natl Acad Sci U S A. 2014 Apr 22; 111(16):6004-9.
    View in: PubMed
    Score: 0.008
  30. Ferlin proteins in myoblast fusion and muscle growth. Curr Top Dev Biol. 2011; 96:203-30.
    View in: PubMed
    Score: 0.006
  31. Endocytic recycling proteins EHD1 and EHD2 interact with fer-1-like-5 (Fer1L5) and mediate myoblast fusion. J Biol Chem. 2011 Mar 04; 286(9):7379-88.
    View in: PubMed
    Score: 0.006
  32. The endocytic recycling protein EHD2 interacts with myoferlin to regulate myoblast fusion. J Biol Chem. 2008 Jul 18; 283(29):20252-60.
    View in: PubMed
    Score: 0.005
  33. Nuclear sequestration of delta-sarcoglycan disrupts the nuclear localization of lamin A/C and emerin in cardiomyocytes. Hum Mol Genet. 2007 Feb 15; 16(4):355-63.
    View in: PubMed
    Score: 0.005
  34. Genetic background influences muscular dystrophy. Neuromuscul Disord. 2005 Oct; 15(9-10):601-9.
    View in: PubMed
    Score: 0.004
Connection Strength

The connection strength for concepts is the sum of the scores for each matching publication.

Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.