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Journal Abstract Search

154 related items for PubMed ID: 29474540

  • 1. SPEG-deficient skeletal muscles exhibit abnormal triad and defective calcium handling.
    Huntoon V, Widrick JJ, Sanchez C, Rosen SM, Kutchukian C, Cao S, Pierson CR, Liu X, Perrella MA, Beggs AH, Jacquemond V, Agrawal PB.
    Hum Mol Genet; 2018 May 01; 27(9):1608-1617. PubMed ID: 29474540
    [Abstract] [Full Text] [Related]

  • 2. Striated Preferentially Expressed Protein Kinase (SPEG)-Deficient Skeletal Muscles Display Fewer Satellite Cells with Reduced Proliferation and Delayed Differentiation.
    Li Q, Lin J, Rosen SM, Zhang T, Kazerounian S, Luo S, Agrawal PB.
    Am J Pathol; 2020 Dec 01; 190(12):2453-2463. PubMed ID: 32919980
    [Abstract] [Full Text] [Related]

  • 3. SPEG binds with desmin and its deficiency causes defects in triad and focal adhesion proteins.
    Luo S, Li Q, Lin J, Murphy Q, Marty I, Zhang Y, Kazerounian S, Agrawal PB.
    Hum Mol Genet; 2021 Feb 25; 29(24):3882-3891. PubMed ID: 33355670
    [Abstract] [Full Text] [Related]

  • 4. Dynamin-2 reduction rescues the skeletal myopathy of a SPEG-deficient mouse model.
    Li Q, Lin J, Widrick JJ, Luo S, Li G, Zhang Y, Laporte J, Perrella MA, Liu X, Agrawal PB.
    JCI Insight; 2022 Aug 08; 7(15):. PubMed ID: 35763354
    [Abstract] [Full Text] [Related]

  • 5. Characterization of a novel zebrafish model of SPEG-related centronuclear myopathy.
    Espinosa KG, Geissah S, Groom L, Volpatti J, Scott IC, Dirksen RT, Zhao M, Dowling JJ.
    Dis Model Mech; 2022 May 01; 15(5):. PubMed ID: 35293586
    [Abstract] [Full Text] [Related]

  • 6. Integrated multi-omics approach reveals the role of striated muscle preferentially expressed protein kinase in skeletal muscle including its relationship with myospryn complex.
    Li Q, Lin J, Luo S, Schmitz-Abe K, Agrawal R, Meng M, Moghadaszadeh B, Beggs AH, Liu X, Perrella MA, Agrawal PB.
    J Cachexia Sarcopenia Muscle; 2024 Jun 01; 15(3):1003-1015. PubMed ID: 38725372
    [Abstract] [Full Text] [Related]

  • 7. SPEG interacts with myotubularin, and its deficiency causes centronuclear myopathy with dilated cardiomyopathy.
    Agrawal PB, Pierson CR, Joshi M, Liu X, Ravenscroft G, Moghadaszadeh B, Talabere T, Viola M, Swanson LC, Haliloğlu G, Talim B, Yau KS, Allcock RJ, Laing NG, Perrella MA, Beggs AH.
    Am J Hum Genet; 2014 Aug 07; 95(2):218-26. PubMed ID: 25087613
    [Abstract] [Full Text] [Related]

  • 8. Novel SPEG mutations in congenital myopathies: Genotype-phenotype correlations.
    Qualls AE, Donkervoort S, Herkert JC, D'gama AM, Bharucha-Goebel D, Collins J, Chao KR, Foley AR, Schoots MH, Jongbloed JDH, Bönnemann CG, Agrawal PB.
    Muscle Nerve; 2019 Mar 07; 59(3):357-362. PubMed ID: 30412272
    [Abstract] [Full Text] [Related]

  • 9. Striated Preferentially Expressed Protein Kinase (SPEG) in Muscle Development, Function, and Disease.
    Luo S, Rosen SM, Li Q, Agrawal PB.
    Int J Mol Sci; 2021 May 27; 22(11):. PubMed ID: 34072258
    [Abstract] [Full Text] [Related]

  • 10. Novel SPEG Mutations in Congenital Myopathy without Centralized Nuclei.
    Lornage X, Sabouraud P, Lannes B, Gaillard D, Schneider R, Deleuze JF, Boland A, Thompson J, Böhm J, Biancalana V, Laporte J.
    J Neuromuscul Dis; 2018 May 27; 5(2):257-260. PubMed ID: 29614691
    [Abstract] [Full Text] [Related]

  • 11. Speg interactions that regulate the stability of excitation-contraction coupling protein complexes in triads and dyads.
    Lee CS, Jung SY, Yee RSZ, Agha NH, Hong J, Chang T, Babcock LW, Fleischman JD, Clayton B, Hanna AD, Ward CS, Lanza D, Hurley AE, Zhang P, Wehrens XHT, Lagor WR, Rodney GG, Hamilton SL.
    Commun Biol; 2023 Sep 14; 6(1):942. PubMed ID: 37709832
    [Abstract] [Full Text] [Related]

  • 12. Integrated multi-omics approach reveals the role of SPEG in skeletal muscle biology including its relationship with myospryn complex.
    Li Q, Lin J, Luo S, Schmitz-Abe K, Agrawal R, Meng M, Moghadaszadeh B, Beggs AH, Liu X, Perrella MA, Agrawal PB.
    bioRxiv; 2023 Apr 24. PubMed ID: 37162921
    [Abstract] [Full Text] [Related]

  • 13. SPEG (Striated Muscle Preferentially Expressed Protein Kinase) Is Essential for Cardiac Function by Regulating Junctional Membrane Complex Activity.
    Quick AP, Wang Q, Philippen LE, Barreto-Torres G, Chiang DY, Beavers D, Wang G, Khalid M, Reynolds JO, Campbell HM, Showell J, McCauley MD, Scholten A, Wehrens XH.
    Circ Res; 2017 Jan 06; 120(1):110-119. PubMed ID: 27729468
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  • 17. Clinical and genetic analysis of a case with centronuclear myopathy caused by SPEG gene mutation: a case report and literature review.
    Zhang G, Xu M, Huang T, Lin W, Chen J, Chen W, Chang X.
    BMC Pediatr; 2021 Apr 29; 21(1):209. PubMed ID: 33926407
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  • 19. Striated preferentially expressed gene deficiency leads to mitochondrial dysfunction in developing cardiomyocytes.
    Li G, Huang H, Wu Y, Shu C, Hwang N, Li Q, Zhao R, Lam HC, Oldham WM, Ei-Chemaly S, Agrawal PB, Tian J, Liu X, Perrella MA.
    Basic Res Cardiol; 2024 Feb 29; 119(1):151-168. PubMed ID: 38145999
    [Abstract] [Full Text] [Related]

  • 20. A Novel SPEG mutation causing congenital myopathy with fiber size disproportion and dilated cardiomyopathy with heart transplantation.
    Gurgel-Giannetti J, Souza LS, Messina de Pádua Andrade GF, Derlene MF, Meira ZMA, Azevedo BVM, Jr WC, Diniz SSL, Carvalhais MB, Oliveira JRS, Uliana L, Bráulio R, Costa PHN, Filho GB, Vainzof M.
    Neuromuscul Disord; 2021 Nov 29; 31(11):1199-1206. PubMed ID: 34742623
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