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 *

270 related articles for article (PubMed ID: 11157795)

  • 21. Actin nemaline myopathy mouse reproduces disease, suggests other actin disease phenotypes and provides cautionary note on muscle transgene expression.
    Ravenscroft G; Jackaman C; Sewry CA; McNamara E; Squire SE; Potter AC; Papadimitriou J; Griffiths LM; Bakker AJ; Davies KE; Laing NG; Nowak KJ
    PLoS One; 2011; 6(12):e28699. PubMed ID: 22174871
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Distinct underlying mechanisms of limb and respiratory muscle fiber weaknesses in nemaline myopathy.
    Lindqvist J; Cheng AJ; Renaud G; Hardeman EC; Ochala J
    J Neuropathol Exp Neurol; 2013 Jun; 72(6):472-81. PubMed ID: 23656990
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Changes in cross-bridge cycling underlie muscle weakness in patients with tropomyosin 3-based myopathy.
    Ottenheijm CA; Lawlor MW; Stienen GJ; Granzier H; Beggs AH
    Hum Mol Genet; 2011 May; 20(10):2015-25. PubMed ID: 21357678
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Congenital myopathy with nemaline rods and cap structures caused by a mutation in the beta-tropomyosin gene (TPM2).
    Tajsharghi H; Ohlsson M; Lindberg C; Oldfors A
    Arch Neurol; 2007 Sep; 64(9):1334-8. PubMed ID: 17846275
    [TBL] [Abstract][Full Text] [Related]  

  • 25. 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]  

  • 26. Skeletal muscle sarcoplasmic reticulum phenotype in myotonic dystrophy.
    Damiani E; Angelini C; Pelosi M; Sacchetto R; Bortoloso E; Margreth A
    Neuromuscul Disord; 1996 Jan; 6(1):33-47. PubMed ID: 8845717
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Autosomal dominant nemaline myopathy with intranuclear rods due to mutation of the skeletal muscle ACTA1 gene: clinical and pathological variability within a kindred.
    Hutchinson DO; Charlton A; Laing NG; Ilkovski B; North KN
    Neuromuscul Disord; 2006 Feb; 16(2):113-21. PubMed ID: 16427282
    [TBL] [Abstract][Full Text] [Related]  

  • 28. TNNT1 nemaline myopathy: natural history and therapeutic frontier.
    Fox MD; Carson VJ; Feng HZ; Lawlor MW; Gray JT; Brigatti KW; Jin JP; Strauss KA
    Hum Mol Genet; 2018 Sep; 27(18):3272-3282. PubMed ID: 29931346
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Combined cap disease and nemaline myopathy in the same patient caused by an autosomal dominant mutation in the TPM3 gene.
    Malfatti E; Schaeffer U; Chapon F; Yang Y; Eymard B; Xu R; Laporte J; Romero NB
    Neuromuscul Disord; 2013 Dec; 23(12):992-7. PubMed ID: 24095155
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Mild phenotype of nemaline myopathy with sleep hypoventilation due to a mutation in the skeletal muscle alpha-actin (ACTA1) gene.
    Jungbluth H; Sewry CA; Brown SC; Nowak KJ; Laing NG; Wallgren-Pettersson C; Pelin K; Manzur AY; Mercuri E; Dubowitz V; Muntoni F
    Neuromuscul Disord; 2001 Jan; 11(1):35-40. PubMed ID: 11166164
    [TBL] [Abstract][Full Text] [Related]  

  • 31. A second pedigree with autosomal dominant nemaline myopathy caused by TPM3 mutation: a clinical and pathological study.
    Pénisson-Besnier I; Monnier N; Toutain A; Dubas F; Laing N
    Neuromuscul Disord; 2007 Apr; 17(4):330-7. PubMed ID: 17376686
    [TBL] [Abstract][Full Text] [Related]  

  • 32. The molecular basis of skeletal muscle weakness in a mouse model of inflammatory myopathy.
    Coley W; Rayavarapu S; Pandey GS; Sabina RL; Van der Meulen JH; Ampong B; Wortmann RL; Rawat R; Nagaraju K
    Arthritis Rheum; 2012 Nov; 64(11):3750-9. PubMed ID: 22806328
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Deleting nebulin's C-terminus reveals its importance to sarcomeric structure and function and is sufficient to invoke nemaline myopathy.
    Li F; Barton ER; Granzier H
    Hum Mol Genet; 2019 May; 28(10):1709-1725. PubMed ID: 30689900
    [TBL] [Abstract][Full Text] [Related]  

  • 34. A novel ACTA1 mutation causing progressive facioscapuloperoneal myopathy in an adult.
    Kao JC; Liewluck T; Milone M
    J Clin Neurosci; 2018 Jul; 53():261-262. PubMed ID: 29731279
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Deleting exon 55 from the nebulin gene induces severe muscle weakness in a mouse model for nemaline myopathy.
    Ottenheijm CA; Buck D; de Winter JM; Ferrara C; Piroddi N; Tesi C; Jasper JR; Malik FI; Meng H; Stienen GJ; Beggs AH; Labeit S; Poggesi C; Lawlor MW; Granzier H
    Brain; 2013 Jun; 136(Pt 6):1718-31. PubMed ID: 23715096
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Adult nemaline myopathy with trabecular muscle fibers.
    Irodenko VS; Lee HS; de Armond SJ; Layzer RB
    Muscle Nerve; 2009 Jun; 39(6):871-5. PubMed ID: 19229965
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Nemaline myopathy-related skeletal muscle α-actin (ACTA1) mutation, Asp286Gly, prevents proper strong myosin binding and triggers muscle weakness.
    Ochala J; Ravenscroft G; Laing NG; Nowak KJ
    PLoS One; 2012; 7(9):e45923. PubMed ID: 23029319
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Skeletal muscle repair in a mouse model of nemaline myopathy.
    Sanoudou D; Corbett MA; Han M; Ghoddusi M; Nguyen MA; Vlahovich N; Hardeman EC; Beggs AH
    Hum Mol Genet; 2006 Sep; 15(17):2603-12. PubMed ID: 16877500
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Co-existence of nemaline and cytoplasmic bodies in muscle of an infant with nemaline myopathy.
    Suwa K; Mizuguchi M; Momoi MY; Nakamura M; Arima K; Komaki H; Nonaka I
    Neuropathology; 2002 Dec; 22(4):294-8. PubMed ID: 12564770
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Functional over-load saves motor units in the SOD1-G93A transgenic mouse model of amyotrophic lateral sclerosis.
    Gordon T; Tyreman N; Li S; Putman CT; Hegedus J
    Neurobiol Dis; 2010 Feb; 37(2):412-22. PubMed ID: 19879358
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 14.