BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

168 related articles for article (PubMed ID: 19181098)

  • 21. Myofibrillar myopathy with limb-girdle phenotype in a Thai patient.
    Liewluck T; Kintarak J; Sangruchi T; Selcen D; Kulkantrakorn K
    J Med Assoc Thai; 2009 Feb; 92(2):290-5. PubMed ID: 19253808
    [TBL] [Abstract][Full Text] [Related]  

  • 22. The Role of Z-disc Proteins in Myopathy and Cardiomyopathy.
    Wadmore K; Azad AJ; Gehmlich K
    Int J Mol Sci; 2021 Mar; 22(6):. PubMed ID: 33802723
    [TBL] [Abstract][Full Text] [Related]  

  • 23. 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]  

  • 24. [Myofibrillar myopathies].
    Nakano S
    Rinsho Shinkeigaku; 2012; 52(11):1151-3. PubMed ID: 23196546
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Myofibrillar myopathies: State of the art, present and future challenges.
    Béhin A; Salort-Campana E; Wahbi K; Richard P; Carlier RY; Carlier P; Laforêt P; Stojkovic T; Maisonobe T; Verschueren A; Franques J; Attarian S; Maues de Paula A; Figarella-Branger D; Bécane HM; Nelson I; Duboc D; Bonne G; Vicart P; Udd B; Romero N; Pouget J; Eymard B
    Rev Neurol (Paris); 2015 Oct; 171(10):715-29. PubMed ID: 26342832
    [TBL] [Abstract][Full Text] [Related]  

  • 26. 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]  

  • 27. Myopathies resulting from mutations in sarcomeric proteins.
    Bönnemann CG; Laing NG
    Curr Opin Neurol; 2004 Oct; 17(5):529-37. PubMed ID: 15367857
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Myotilinopathy: refining the clinical and myopathological phenotype.
    Olivé M; Goldfarb LG; Shatunov A; Fischer D; Ferrer I
    Brain; 2005 Oct; 128(Pt 10):2315-26. PubMed ID: 15947064
    [TBL] [Abstract][Full Text] [Related]  

  • 29. A novel mutation in the PDZ-like motif of ZASP causes distal ZASP-related myofibrillar myopathy.
    Zheng J; Chen S; Chen Y; Zhu M; Hong D
    Neuropathology; 2017 Feb; 37(1):45-51. PubMed ID: 27546599
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Clinical and myopathological evaluation of early- and late-onset subtypes of myofibrillar myopathy.
    Olivé M; Odgerel Z; Martínez A; Poza JJ; Bragado FG; Zabalza RJ; Jericó I; Gonzalez-Mera L; Shatunov A; Lee HS; Armstrong J; Maraví E; Arroyo MR; Pascual-Calvet J; Navarro C; Paradas C; Huerta M; Marquez F; Rivas EG; Pou A; Ferrer I; Goldfarb LG
    Neuromuscul Disord; 2011 Aug; 21(8):533-42. PubMed ID: 21676617
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Expression of the intermediate filament protein synemin in myofibrillar myopathies and other muscle diseases.
    Olivé M; Goldfarb L; Dagvadorj A; Sambuughin N; Paulin D; Li Z; Goudeau B; Vicart P; Ferrer I
    Acta Neuropathol; 2003 Jul; 106(1):1-7. PubMed ID: 12669240
    [TBL] [Abstract][Full Text] [Related]  

  • 32. 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]  

  • 33. Myofibrillar instability exacerbated by acute exercise in filaminopathy.
    Chevessier F; Schuld J; Orfanos Z; Plank AC; Wolf L; Maerkens A; Unger A; Schlötzer-Schrehardt U; Kley RA; Von Hörsten S; Marcus K; Linke WA; Vorgerd M; van der Ven PF; Fürst DO; Schröder R
    Hum Mol Genet; 2015 Dec; 24(25):7207-20. PubMed ID: 26472074
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Mouse models for thin filament disease.
    Nguyen MA; Hardeman EC
    Adv Exp Med Biol; 2008; 642():66-77. PubMed ID: 19181094
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Investigations into the pathobiology of thin-filament myopathies.
    Ilkovski B
    Adv Exp Med Biol; 2008; 642():55-65. PubMed ID: 19181093
    [TBL] [Abstract][Full Text] [Related]  

  • 36. 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]  

  • 37. Dominant-negative effects of a novel mutation in the filamin myopathy.
    Kono S; Nishio T; Takahashi Y; Goto-Inoue N; Kinoshita M; Zaima N; Suzuki H; Fukutoku-Otsuji A; Setou M; Miyajima H
    Neurology; 2010 Aug; 75(6):547-54. PubMed ID: 20697107
    [TBL] [Abstract][Full Text] [Related]  

  • 38. A case report: a heterozygous deletion (2791_2805 del) in exon 18 of the filamin C gene causing filamin C-related myofibrillar myopathies in a Chinese family.
    Miao J; Su FF; Liu XM; Wei XJ; Yuan Y; Yu XF
    BMC Neurol; 2018 Jun; 18(1):79. PubMed ID: 29866061
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Transgenic mice expressing the myotilin T57I mutation unite the pathology associated with LGMD1A and MFM.
    Garvey SM; Miller SE; Claflin DR; Faulkner JA; Hauser MA
    Hum Mol Genet; 2006 Aug; 15(15):2348-62. PubMed ID: 16801328
    [TBL] [Abstract][Full Text] [Related]  

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

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