BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

164 related articles for article (PubMed ID: 23196546)

  • 21. Mitochondrial dysfunction in myofibrillar myopathy.
    Vincent AE; Grady JP; Rocha MC; Alston CL; Rygiel KA; Barresi R; Taylor RW; Turnbull DM
    Neuromuscul Disord; 2016 Oct; 26(10):691-701. PubMed ID: 27618136
    [TBL] [Abstract][Full Text] [Related]  

  • 22. BAG3
    Robertson R; Conte TC; Dicaire MJ; Rymar VV; Sadikot AF; Bryson-Richardson RJ; Lavoie JN; O'Ferrall E; Young JC; Brais B
    Am J Pathol; 2020 Mar; 190(3):554-562. PubMed ID: 31953038
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Myofibrillar myopathy in the genomic context.
    Fichna JP; Maruszak A; Żekanowski C
    J Appl Genet; 2018 Nov; 59(4):431-439. PubMed ID: 30203143
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Biomechanical characterization of myofibrillar myopathies.
    Winter L; Goldmann WH
    Cell Biol Int; 2015 Apr; 39(4):361-3. PubMed ID: 25264173
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Human Mutated
    Cannone E; Guglielmi V; Marchetto G; Tobia C; Gnutti B; Cisterna B; Tonin P; Barbon A; Vattemi G; Schiavone M
    Int J Mol Sci; 2023 Jul; 24(14):. PubMed ID: 37511242
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Myofibrillar and distal myopathies.
    Palmio J; Udd B
    Rev Neurol (Paris); 2016 Oct; 172(10):587-593. PubMed ID: 27638134
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Mutations in myotilin cause myofibrillar myopathy.
    Selcen D; Engel AG
    Neurology; 2004 Apr; 62(8):1363-71. PubMed ID: 15111675
    [TBL] [Abstract][Full Text] [Related]  

  • 28. The Z-disk diseases.
    Selcen D; Carpén O
    Adv Exp Med Biol; 2008; 642():116-30. PubMed ID: 19181098
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Mutations in ZASP define a novel form of muscular dystrophy in humans.
    Selcen D; Engel AG
    Ann Neurol; 2005 Feb; 57(2):269-76. PubMed ID: 15668942
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Myofibrillar myopathies: a clinical and myopathological guide.
    Schröder R; Schoser B
    Brain Pathol; 2009 Jul; 19(3):483-92. PubMed ID: 19563540
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Unusual multisystemic involvement and a novel BAG3 mutation revealed by NGS screening in a large cohort of myofibrillar myopathies.
    Semmler AL; Sacconi S; Bach JE; Liebe C; Bürmann J; Kley RA; Ferbert A; Anderheiden R; Van den Bergh P; Martin JJ; De Jonghe P; Neuen-Jacob E; Müller O; Deschauer M; Bergmann M; Schröder JM; Vorgerd M; Schulz JB; Weis J; Kress W; Claeys KG
    Orphanet J Rare Dis; 2014 Aug; 9():121. PubMed ID: 25208129
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Zebrafish models of BAG3 myofibrillar myopathy suggest a toxic gain of function leading to BAG3 insufficiency.
    Ruparelia AA; Oorschot V; Vaz R; Ramm G; Bryson-Richardson RJ
    Acta Neuropathol; 2014 Dec; 128(6):821-33. PubMed ID: 25273835
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Metformin rescues muscle function in BAG3 myofibrillar myopathy models.
    Ruparelia AA; McKaige EA; Williams C; Schulze KE; Fuchs M; Oorschot V; Lacene E; Meregalli M; Lee C; Serrano RJ; Baxter EC; Monro K; Torrente Y; Ramm G; Stojkovic T; Lavoie JN; Bryson-Richardson RJ
    Autophagy; 2021 Sep; 17(9):2494-2510. PubMed ID: 33030392
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Immunoblot as a potential diagnostic tool for myofibrillar myopathies.
    Marini M; Guglielmi V; Faulkner G; Piffer S; Tomelleri G; Vattemi G
    Electrophoresis; 2015 Dec; 36(24):3097-100. PubMed ID: 26383991
    [TBL] [Abstract][Full Text] [Related]  

  • 35. New aspects of myofibrillar myopathies.
    Kley RA; Olivé M; Schröder R
    Curr Opin Neurol; 2016 Oct; 29(5):628-34. PubMed ID: 27389816
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Clinical and histopathological features of myofibrillar myopathy in Warmblood horses.
    Valberg SJ; Nicholson AM; Lewis SS; Reardon RA; Finno CJ
    Equine Vet J; 2017 Nov; 49(6):739-745. PubMed ID: 28543538
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Myofibrillar myopathy with abnormal foci of desmin positivity. I. Light and electron microscopy analysis of 10 cases.
    Nakano S; Engel AG; Waclawik AJ; Emslie-Smith AM; Busis NA
    J Neuropathol Exp Neurol; 1996 May; 55(5):549-62. PubMed ID: 8627346
    [TBL] [Abstract][Full Text] [Related]  

  • 38. FLNC myofibrillar myopathy results from impaired autophagy and protein insufficiency.
    Ruparelia AA; Oorschot V; Ramm G; Bryson-Richardson RJ
    Hum Mol Genet; 2016 Jun; 25(11):2131-2142. PubMed ID: 26969713
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Electron microscopy in myofibrillar myopathies reveals clues to the mutated gene.
    Claeys KG; Fardeau M; Schröder R; Suominen T; Tolksdorf K; Behin A; Dubourg O; Eymard B; Maisonobe T; Stojkovic T; Faulkner G; Richard P; Vicart P; Udd B; Voit T; Stoltenburg G
    Neuromuscul Disord; 2008 Aug; 18(8):656-66. PubMed ID: 18653338
    [TBL] [Abstract][Full Text] [Related]  

  • 40.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.