Peter Pytel to Muscle, Skeletal
This is a "connection" page, showing publications Peter Pytel has written about Muscle, Skeletal.
Connection Strength
1.556
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A pattern-based approach to the interpretation of skeletal muscle biopsies. Mod Pathol. 2019 04; 32(4):462-483.
Score: 0.531
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Myopathy associated BAG3 mutations lead to protein aggregation by stalling Hsp70 networks. Nat Commun. 2018 12 17; 9(1):5342.
Score: 0.134
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Eps 15 Homology Domain (EHD)-1 Remodels Transverse Tubules in Skeletal Muscle. PLoS One. 2015; 10(9):e0136679.
Score: 0.107
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Muscle hypertrophy induced by myostatin inhibition accelerates degeneration in dysferlinopathy. Hum Mol Genet. 2015 Oct 15; 24(20):5711-9.
Score: 0.106
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Dysferlin and myoferlin regulate transverse tubule formation and glycerol sensitivity. Am J Pathol. 2014 Jan; 184(1):248-59.
Score: 0.094
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Selective inhibition of caspases in skeletal muscle reverses the apoptotic synaptic degeneration in slow-channel myasthenic syndrome. Hum Mol Genet. 2014 Jan 01; 23(1):69-77.
Score: 0.092
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Animal models of antimuscle-specific kinase myasthenia. Ann N Y Acad Sci. 2012 Dec; 1274:140-7.
Score: 0.088
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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.
Score: 0.077
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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.
Score: 0.077
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Myoferlin regulation by NFAT in muscle injury, regeneration and repair. J Cell Sci. 2010 Jul 15; 123(Pt 14):2413-22.
Score: 0.074
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Myoferlin is required for insulin-like growth factor response and muscle growth. FASEB J. 2010 Apr; 24(4):1284-95.
Score: 0.072
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Impaired exercise tolerance and skeletal muscle myopathy in sulfonylurea receptor-2 mutant mice. Am J Physiol Regul Integr Comp Physiol. 2009 Oct; 297(4):R1144-53.
Score: 0.070
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Disseminated intravascular large-cell lymphoma with initial presentation mimicking Guillain-Barré syndrome. Muscle Nerve. 2010 Jul; 42(1):133-6.
Score: 0.019
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Disruption of nesprin-1 produces an Emery Dreifuss muscular dystrophy-like phenotype in mice. Hum Mol Genet. 2009 Feb 15; 18(4):607-20.
Score: 0.017