Search Results - "Winter, Christa"
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Cross-sectional study into age-related pathology of mouse models for limb girdle muscular dystrophy types 2D and 2F
Published in PloS one (20-08-2019)“…Limb girdle muscular dystrophy (LGMD) types 2D and 2F are caused by mutations in the genes encoding for α- and δ-sarcoglycan, respectively, leading to…”
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Voluntary exercise improves muscle function and does not exacerbate muscle and heart pathology in aged Duchenne muscular dystrophy mice
Published in Journal of molecular and cellular cardiology (01-12-2018)“…Duchenne muscular dystrophy is a severe muscle wasting disease, characterized by a severely reduced lifespan in which cardiomyopathy is one of the leading…”
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Cyclic Peptides to Improve Delivery and Exon Skipping of Antisense Oligonucleotides in a Mouse Model for Duchenne Muscular Dystrophy
Published in Molecular therapy (03-01-2018)“…Duchenne muscular dystrophy (DMD) is a severe, progressive muscle wasting disorder caused by reading frame disrupting mutations in the DMD gene. Exon skipping…”
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In vivo comparison of 2′-O-methyl phosphorothioate and morpholino antisense oligonucleotides for Duchenne muscular dystrophy exon skipping
Published in The journal of gene medicine (01-03-2009)“…Background Antisense‐mediated exon skipping is a putative treatment for Duchenne muscular dystrophy (DMD). Using antisense oligonucleotides (AONs), the…”
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Music alters heart rate and psychological responses but not muscle activation during light-intensity isometric exercise
Published in Sports medicine and health science (01-12-2024)“…Listening to music manipulates attention to be more externally focused, which has the potential to improve muscular efficiency. This study aimed to determine…”
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Guidelines for Antisense Oligonucleotide Design and Insight Into Splice-modulating Mechanisms
Published in Molecular therapy (01-03-2009)“…Antisense oligonucleotides (AONs) can interfere with mRNA processing through RNase H–mediated degradation, translational arrest, or modulation of splicing. The…”
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Assessment of the feasibility of exon 45-55 multiexon skipping for Duchenne muscular dystrophy
Published in BMC medical genetics (01-12-2008)“…The specific skipping of an exon, induced by antisense oligonucleotides (AON) during splicing, has shown to be a promising therapeutic approach for Duchenne…”
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Peptide conjugation of 2'-O-methyl phosphorothioate antisense oligonucleotides enhances cardiac uptake and exon skipping in mdx mice
Published in Nucleic acid therapeutics (01-02-2014)“…Antisense oligonucleotide (AON)-mediated exon skipping is a promising therapeutic approach for Duchenne muscular dystrophy that is currently being tested in…”
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Comparing the Changes in Blood Pressure After Acute Exposure to Tai Chi and Walking
Published in International journal of exercise science (2019)“…Hypertension is a major health concern throughout the United States and is a major cause of cardiovascular disease. The purpose of this study was to compare…”
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The Effects of Mental Imagery with Video-Modeling on Self-Efficacy and Maximal Front Squat Ability
Published in Sports (Basel) (14-04-2016)“…This study was designed to assess the effectiveness of mental imagery supplemented with video-modeling on self-efficacy and front squat strength (three…”
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Evaluation of 2’-Deoxy-2’-fluoro Antisense Oligonucleotides for Exon Skipping in Duchenne Muscular Dystrophy
Published in Molecular therapy. Nucleic acids (01-12-2015)“…Duchenne muscular dystrophy (DMD) is a severe muscle wasting disorder typically caused by frame-shifting mutations in the DMD gene. Restoration of the reading…”
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Long-term Exon Skipping Studies With 2′-O-Methyl Phosphorothioate Antisense Oligonucleotides in Dystrophic Mouse Models
Published in Molecular therapy. Nucleic acids (01-09-2012)“…Antisense-mediated exon skipping for Duchenne muscular dystrophy (DMD) is currently tested in phase 3 clinical trials. The aim of this approach is to modulate…”
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Development of Antisense-Mediated Exon Skipping as a Treatment for Duchenne Muscular Dystrophy
Published in Annals of the New York Academy of Sciences (01-09-2009)“…Duchenne muscular dystrophy (DMD) is a severe muscle‐wasting disease caused by frame shifting and nonsense mutations in the dystrophin gene. Through skipping…”
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Comparative analysis of antisense oligonucleotide sequences targeting exon 53 of the human DMD gene: Implications for future clinical trials
Published in Neuromuscular disorders : NMD (01-02-2010)“…Abstract Duchenne muscular dystrophy (DMD) is caused by the lack of functional dystrophin protein, most commonly as a result of a range of out-of-frame…”
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Preclinical PK and PD Studies on 2′-O-Methyl-phosphorothioate RNA Antisense Oligonucleotides in the mdx Mouse Model
Published in Molecular therapy (01-06-2010)“…Antisense oligonucleotides (AONs) are being developed as RNA therapeutic molecules for Duchenne muscular dystrophy. For oligonucleotides with the…”
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Dose-dependent pharmacokinetic profiles of 2'-O-methyl phosphorothioate antisense oligonucleotidesin mdx mice
Published in Nucleic acid therapeutics (01-06-2013)“…Antisense-mediated exon skipping is a promising therapeutic approach for Duchenne muscular dystrophy. It aims to restore the dystrophin open reading frame by…”
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Effects of physioball and conventional floor exercises on early phase adaptations in back and abdominal core stability and balance in women
Published in Journal of strength and conditioning research (01-11-2003)“…The purpose of this study was to compare the effects of 5 weeks of physioball core stability and balance exercises with conventional floor exercises in women…”
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Dystrophin deficiency leads to dysfunctional glutamate clearance in iPSC derived astrocytes
Published in Translational psychiatry (21-08-2019)“…Duchenne muscular dystrophy (DMD) results, beside muscle degeneration in cognitive defects. As neuronal function is supported by astrocytes, which express…”
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