Quantitative magnetic resonance imaging assessment of muscle composition in myotonic dystrophy mice
暂无分享,去创建一个
[1] G. Cutter,et al. Muscle magnetic resonance imaging in myotonic dystrophy type 1 (DM1): Refining muscle involvement and implications for clinical trials , 2021, European journal of neurology.
[2] A. Bargiela,et al. Musashi-2 contributes to myotonic dystrophy muscle dysfunction by promoting excessive autophagy through miR-7 biogenesis repression , 2021, Molecular therapy. Nucleic acids.
[3] C. Zimmer,et al. Regional variation of thigh muscle fat infiltration in patients with neuromuscular diseases compared to healthy controls. , 2021, Quantitative imaging in medicine and surgery.
[4] R. Artero,et al. Myotonic dystrophy type 1 drug development: A pipeline toward the market , 2021, Drug discovery today.
[5] R. Weiss,et al. Population-Based Prevalence of Myotonic Dystrophy Type 1 Using Genetic Analysis of Statewide Blood Screening Program , 2021, Neurology.
[6] P. Nopoulos,et al. Quantitative muscle MRI as a sensitive marker of early muscle pathology in myotonic dystrophy type 1 , 2021, Muscle & nerve.
[7] H. Andersen,et al. Isokinetic strength and degeneration of lower extremity muscles in patients with myotonic dystrophy; an MRI study , 2020, Neuromuscular Disorders.
[8] A. Bargiela,et al. The hallmarks of myotonic dystrophy type 1 muscle dysfunction , 2020, Biological reviews of the Cambridge Philosophical Society.
[9] G. García-Martí,et al. The Role of Imaging Biomarkers in the Assessment of Sarcopenia , 2020, Diagnostics.
[10] Christine Péladeau,et al. Overexpression of Staufen1 in DM1 mouse skeletal muscle exacerbates dystrophic and atrophic features. , 2020, Human molecular genetics.
[11] H. Reyngoudt,et al. The expanding role of MRI in neuromuscular disorders , 2020, Nature Reviews Neurology.
[12] M. Swanson,et al. HNRNPA1-induced spliceopathy in a transgenic mouse model of myotonic dystrophy , 2020, Proceedings of the National Academy of Sciences.
[13] D. Furling,et al. miR-7 Restores Phenotypes in Myotonic Dystrophy Muscle Cells by Repressing Hyperactivated Autophagy , 2019, Molecular therapy. Nucleic acids.
[14] Guillaume Bassez,et al. Lower extremity muscle pathology in myotonic dystrophy type 1 assessed by quantitative MRI , 2019, Neurology.
[15] G. Della Marca,et al. Prevalence and predictor factors of respiratory impairment in a large cohort of patients with Myotonic Dystrophy type 1 (DM1): A retrospective, cross sectional study , 2019, Journal of the Neurological Sciences.
[16] T. Khoo,et al. Respiratory dysfunction in myotonic dystrophy type 1: A systematic review , 2019, Neuromuscular Disorders.
[17] M. Nakamori,et al. Furamidine Rescues Myotonic Dystrophy Type I Associated Mis-Splicing through Multiple Mechanisms. , 2018, ACS chemical biology.
[18] T. Cooper,et al. Mechanisms of skeletal muscle wasting in a mouse model for myotonic dystrophy type 1 , 2018, Human molecular genetics.
[19] Jin-Hong Shin,et al. Lower limb muscle magnetic resonance imaging in myotonic dystrophy type 1 correlates with the six-minute walk test and CTG repeats , 2018, Neuromuscular Disorders.
[20] V. Rakocevic-Stojanovic,et al. Magnetic resonance imaging of leg muscles in patients with myotonic dystrophies , 2017, Journal of Neurology.
[21] C. Angelini,et al. Targeting deregulated AMPK/mTORC1 pathways improves muscle function in myotonic dystrophy type I , 2017, The Journal of clinical investigation.
[22] L. Gutmann,et al. Myotonic Dystrophy Type 1 Management and Therapeutics , 2016, Current Treatment Options in Neurology.
[23] G. Sergi,et al. Imaging of sarcopenia. , 2016, European journal of radiology.
[24] P. Carlier,et al. Skeletal Muscle Quantitative Nuclear Magnetic Resonance Imaging and Spectroscopy as an Outcome Measure for Clinical Trials , 2016, Journal of neuromuscular diseases.
[25] I. Illa,et al. Muscle MRI in muscular dystrophies , 2015, Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology.
[26] G. Carter,et al. Therapeutic impact of systemic AAV-mediated RNA interference in a mouse model of myotonic dystrophy. , 2015, Human molecular genetics.
[27] T. Jensen,et al. Molecular mechanisms in DM1 — a focus on foci , 2015, Nucleic acids research.
[28] J. Woodgett,et al. GSK3β mediates muscle pathology in myotonic dystrophy. , 2012, The Journal of clinical investigation.
[29] F. Metzger,et al. Molecular, Physiological, and Motor Performance Defects in DMSXL Mice Carrying >1,000 CTG Repeats from the Human DM1 Locus , 2012, PLoS genetics.
[30] M. Narici,et al. Sarcopenia, Dynapenia, and the Impact of Advancing Age on Human Skeletal Muscle Size and Strength; a Quantitative Review , 2012, Front. Physio..
[31] E. Mohammadi,et al. Barriers and facilitators related to the implementation of a physiological track and trigger system: A systematic review of the qualitative evidence , 2017, International journal for quality in health care : journal of the International Society for Quality in Health Care.
[32] C. Angelini,et al. Normal myogenesis and increased apoptosis in myotonic dystrophy type-1 muscle cells , 2010, Cell Death and Differentiation.
[33] Guido Gerig,et al. User-guided 3D active contour segmentation of anatomical structures: Significantly improved efficiency and reliability , 2006, NeuroImage.
[34] P. Scifo,et al. Postabsorptive and insulin-stimulated energy and protein metabolism in patients with myotonic dystrophy type 1. , 2004, The American journal of clinical nutrition.
[35] A. Paetau,et al. Histopathological differences of myotonic dystrophy type 1 (DM1) and PROMM/DM2 , 2003, Neurology.
[36] S. Cannon,et al. Expanded CUG repeats trigger aberrant splicing of ClC-1 chloride channel pre-mRNA and hyperexcitability of skeletal muscle in myotonic dystrophy. , 2002, Molecular cell.
[37] R. J. White,et al. Myotonic dystrophy in transgenic mice expressing an expanded CUG repeat. , 2000, Science.
[38] N. Otsu. A threshold selection method from gray level histograms , 1979 .