BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

150 related articles for article (PubMed ID: 25264173)

  • 1. 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]  

  • 2. Myofibrillar myopathies.
    Selcen D
    Curr Opin Neurol; 2010 Oct; 23(5):477-81. PubMed ID: 20664348
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Myofibrillar myopathies.
    Claeys KG; Fardeau M
    Handb Clin Neurol; 2013; 113():1337-42. PubMed ID: 23622358
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Chemical chaperone ameliorates pathological protein aggregation in plectin-deficient muscle.
    Winter L; Staszewska I; Mihailovska E; Fischer I; Goldmann WH; Schröder R; Wiche G
    J Clin Invest; 2014 Mar; 124(3):1144-57. PubMed ID: 24487589
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Progress in desmin-related myopathies.
    Goebel HH; Warlo IA
    J Child Neurol; 2000 Sep; 15(9):565-72. PubMed ID: 11019786
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Patient-specific protein aggregates in myofibrillar myopathies: laser microdissection and differential proteomics for identification of plaque components.
    Feldkirchner S; Schessl J; Müller S; Schoser B; Hanisch FG
    Proteomics; 2012 Dec; 12(23-24):3598-609. PubMed ID: 23044792
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Molecular pathology of myofibrillar myopathies.
    Ferrer I; Olivé M
    Expert Rev Mol Med; 2008 Sep; 10():e25. PubMed ID: 18764962
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. Biomechanical characterization of a desminopathy in primary human myoblasts.
    Bonakdar N; Luczak J; Lautscham L; Czonstke M; Koch TM; Mainka A; Jungbauer T; Goldmann WH; Schröder R; Fabry B
    Biochem Biophys Res Commun; 2012 Mar; 419(4):703-7. PubMed ID: 22386993
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Gene-related protein surplus myopathies.
    Goebel HH; Warlo I
    Mol Genet Metab; 2000; 71(1-2):267-75. PubMed ID: 11001821
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. Desminopathies: good stuff lost, garbage gained, or the trashman misdirected?
    Hoffman EP
    Muscle Nerve; 2003 Jun; 27(6):643-5. PubMed ID: 12766974
    [No Abstract]   [Full Text] [Related]  

  • 13. Cytoskeletal derangements in hereditary myopathy with a desmin L345P mutation.
    Carlsson L; Fischer C; Sjöberg G; Robson RM; Sejersen T; Thornell LE
    Acta Neuropathol; 2002 Nov; 104(5):493-504. PubMed ID: 12410397
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Myofibrillar myopathies.
    Selcen D; Engel AG
    Handb Clin Neurol; 2011; 101():143-54. PubMed ID: 21496631
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Myofibrillar myopathies].
    Olivé-Plana M
    Rev Neurol; 2003 Oct 16-31; 37(8):770-2. PubMed ID: 14593638
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Two desmin gene mutations associated with myofibrillar myopathies in Polish families.
    Fichna JP; Karolczak J; Potulska-Chromik A; Miszta P; Berdynski M; Sikorska A; Filipek S; Redowicz MJ; Kaminska A; Zekanowski C
    PLoS One; 2014; 9(12):e115470. PubMed ID: 25541946
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Desmin myopathy, a skeletal myopathy with cardiomyopathy caused by mutations in the desmin gene.
    Dalakas MC; Park KY; Semino-Mora C; Lee HS; Sivakumar K; Goldfarb LG
    N Engl J Med; 2000 Mar; 342(11):770-80. PubMed ID: 10717012
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Myofibrillar myopathies.
    Selcen D
    Neuromuscul Disord; 2011 Mar; 21(3):161-71. PubMed ID: 21256014
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Conspicuous involvement of desmin tail mutations in diverse cardiac and skeletal myopathies.
    Bär H; Goudeau B; Wälde S; Casteras-Simon M; Mücke N; Shatunov A; Goldberg YP; Clarke C; Holton JL; Eymard B; Katus HA; Fardeau M; Goldfarb L; Vicart P; Herrmann H
    Hum Mutat; 2007 Apr; 28(4):374-86. PubMed ID: 17221859
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Myofibrillar myopathy with congenital cataract and skeletal anomalies without mutations in the desmin, alphaB-crystallin, myotilin, LMNA or SEPN1 genes.
    Kostera-Pruszczyk A; Goudeau B; Ferreiro A; Richard P; Simon S; Vicart P; Fidzianska A
    Neuromuscul Disord; 2006 Nov; 16(11):759-62. PubMed ID: 17005401
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.