These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

311 related articles for article (PubMed ID: 28436394)

  • 21. KBTBD13 is an actin-binding protein that modulates muscle kinetics.
    de Winter JM; Molenaar JP; Yuen M; van der Pijl R; Shen S; Conijn S; van de Locht M; Willigenburg M; Bogaards SJ; van Kleef ES; Lassche S; Persson M; Rassier DE; Sztal TE; Ruparelia AA; Oorschot V; Ramm G; Hall TE; Xiong Z; Johnson CN; Li F; Kiss B; Lozano-Vidal N; Boon RA; Marabita M; Nogara L; Blaauw B; Rodenburg RJ; Küsters B; Doorduin J; Beggs AH; Granzier H; Campbell K; Ma W; Irving T; Malfatti E; Romero NB; Bryson-Richardson RJ; van Engelen BG; Voermans NC; Ottenheijm CA
    J Clin Invest; 2020 Feb; 130(2):754-767. PubMed ID: 31671076
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Troponin activator augments muscle force in nemaline myopathy patients with nebulin mutations.
    de Winter JM; Buck D; Hidalgo C; Jasper JR; Malik FI; Clarke NF; Stienen GJ; Lawlor MW; Beggs AH; Ottenheijm CA; Granzier H
    J Med Genet; 2013 Jun; 50(6):383-92. PubMed ID: 23572184
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Nemaline myopathies: a current view.
    Sewry CA; Laitila JM; Wallgren-Pettersson C
    J Muscle Res Cell Motil; 2019 Jun; 40(2):111-126. PubMed ID: 31228046
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Nemaline myopathies: State of the art.
    Malfatti E; Romero NB
    Rev Neurol (Paris); 2016 Oct; 172(10):614-619. PubMed ID: 27659899
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Triggering typical nemaline myopathy with compound heterozygous nebulin mutations reveals myofilament structural changes as pathomechanism.
    Lindqvist J; Ma W; Li F; Hernandez Y; Kolb J; Kiss B; Tonino P; van der Pijl R; Karimi E; Gong H; Strom J; Hourani Z; Smith JE; Ottenheijm C; Irving T; Granzier H
    Nat Commun; 2020 Jun; 11(1):2699. PubMed ID: 32483185
    [TBL] [Abstract][Full Text] [Related]  

  • 26. [Nemaline myopathy as a cause of neonatal hypotonia - with emphasis on personal experiences. Report of a family with two brothers affected].
    Bojdo A; Obersztyn E; Wallgren-Pettersson C; Lehtokari V; Laing N; Davis M; Kułakowska Z
    Med Wieku Rozwoj; 2009; 13(1):5-10. PubMed ID: 19648653
    [TBL] [Abstract][Full Text] [Related]  

  • 27. NRAP reduction rescues sarcomere defects in nebulin-related nemaline myopathy.
    Casey JG; Kim ES; Joseph R; Li F; Granzier H; Gupta VA
    Hum Mol Genet; 2023 May; 32(10):1711-1721. PubMed ID: 36661122
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Nemaline myopathies.
    Wallgren-Pettersson C; Sewry CA; Nowak KJ; Laing NG
    Semin Pediatr Neurol; 2011 Dec; 18(4):230-8. PubMed ID: 22172418
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Loss of Tropomodulin4 in the zebrafish mutant träge causes cytoplasmic rod formation and muscle weakness reminiscent of nemaline myopathy.
    Berger J; Tarakci H; Berger S; Li M; Hall TE; Arner A; Currie PD
    Dis Model Mech; 2014 Dec; 7(12):1407-15. PubMed ID: 25288681
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Troponin T is essential for sarcomere assembly in zebrafish skeletal muscle.
    Ferrante MI; Kiff RM; Goulding DA; Stemple DL
    J Cell Sci; 2011 Feb; 124(Pt 4):565-77. PubMed ID: 21245197
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Muscle weakness in respiratory and peripheral skeletal muscles in a mouse model for nebulin-based nemaline myopathy.
    Joureau B; de Winter JM; Stam K; Granzier H; Ottenheijm CA
    Neuromuscul Disord; 2017 Jan; 27(1):83-89. PubMed ID: 27890461
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Expressing a Z-disk nebulin fragment in nebulin-deficient mouse muscle: effects on muscle structure and function.
    Li F; Kolb J; Crudele J; Tonino P; Hourani Z; Smith JE; Chamberlain JS; Granzier H
    Skelet Muscle; 2020 Jan; 10(1):2. PubMed ID: 31992366
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Muscle histopathology in nebulin-related nemaline myopathy: ultrastrastructural findings correlated to disease severity and genotype.
    Malfatti E; Lehtokari VL; Böhm J; De Winter JM; Schäffer U; Estournet B; Quijano-Roy S; Monges S; Lubieniecki F; Bellance R; Viou MT; Madelaine A; Wu B; Taratuto AL; Eymard B; Pelin K; Fardeau M; Ottenheijm CA; Wallgren-Pettersson C; Laporte J; Romero NB
    Acta Neuropathol Commun; 2014 Apr; 2():44. PubMed ID: 24725366
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Mutation-specific effects on thin filament length in thin filament myopathy.
    Winter JM; Joureau B; Lee EJ; Kiss B; Yuen M; Gupta VA; Pappas CT; Gregorio CC; Stienen GJ; Edvardson S; Wallgren-Pettersson C; Lehtokari VL; Pelin K; Malfatti E; Romero NB; Engelen BG; Voermans NC; Donkervoort S; Bönnemann CG; Clarke NF; Beggs AH; Granzier H; Ottenheijm CA
    Ann Neurol; 2016 Jun; 79(6):959-69. PubMed ID: 27074222
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Removal of MuRF1 Increases Muscle Mass in Nemaline Myopathy Models, but Does Not Provide Functional Benefits.
    Lindqvist J; Kolb J; de Winter J; Tonino P; Hourani Z; Labeit S; Ottenheijm C; Granzier H
    Int J Mol Sci; 2022 Jul; 23(15):. PubMed ID: 35897687
    [TBL] [Abstract][Full Text] [Related]  

  • 36. An alphaTropomyosin mutation alters dimer preference in nemaline myopathy.
    Corbett MA; Akkari PA; Domazetovska A; Cooper ST; North KN; Laing NG; Gunning PW; Hardeman EC
    Ann Neurol; 2005 Jan; 57(1):42-9. PubMed ID: 15562513
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Novel large deletion in the ACTA1 gene in a child with autosomal recessive nemaline myopathy.
    Friedman B; Simpson K; Tesi-Rocha C; Zhou D; Palmer CA; Suchy SF
    Neuromuscul Disord; 2014 Apr; 24(4):331-4. PubMed ID: 24447884
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Leiomodin-3-deficient mice display nemaline myopathy with fast-myofiber atrophy.
    Tian L; Ding S; You Y; Li TR; Liu Y; Wu X; Sun L; Xu T
    Dis Model Mech; 2015 Jun; 8(6):635-41. PubMed ID: 26035871
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Nemaline myopathy with minicores caused by mutation of the CFL2 gene encoding the skeletal muscle actin-binding protein, cofilin-2.
    Agrawal PB; Greenleaf RS; Tomczak KK; Lehtokari VL; Wallgren-Pettersson C; Wallefeld W; Laing NG; Darras BT; Maciver SK; Dormitzer PR; Beggs AH
    Am J Hum Genet; 2007 Jan; 80(1):162-7. PubMed ID: 17160903
    [TBL] [Abstract][Full Text] [Related]  

  • 40. A nemaline myopathy mutation in alpha-tropomyosin causes defective regulation of striated muscle force production.
    Michele DE; Albayya FP; Metzger JM
    J Clin Invest; 1999 Dec; 104(11):1575-81. PubMed ID: 10587521
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 16.