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Anti-Inflammatory and General Glucocorticoid Physiology in Skeletal Muscles Affected by Duchenne Muscular Dystrophy: Exploration of Steroid-Sparing Agents

International journal of molecular sciences, 2020-06, Vol.21 (13), p.4596

2020

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Scanning for Therapeutic Targets within the Cytokine Network of Idiopathic Inflammatory Myopathies

International journal of molecular sciences, 2015-08, Vol.16 (8), p.18683-18713

2015

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Progressive Skeletal Muscle Atrophy in Muscular Dystrophies: A Role for Toll-like Receptor-Signaling in Disease Pathogenesis

International journal of molecular sciences, 2020-06, Vol.21 (12), p.4440

De Paepe, Boel

2020

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The Cytokine Growth Differentiation Factor-15 and Skeletal Muscle Health: Portrait of an Emerging Widely Applicable Disease Biomarker

International journal of molecular sciences, 2022-11, Vol.23 (21), p.13180

De Paepe, Boel

2022

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Biallelic Mutations in TMEM126B Cause Severe Complex I Deficiency with a Variable Clinical Phenotype

American journal of human genetics, 2016-07, Vol.99 (1), p.217-227

2016

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Nanoscopic X‐ray imaging and quantification of the iron cellular architecture within single fibroblasts of Friedreich's ataxia patients

Journal of synchrotron radiation, 2020-01, Vol.27 (1), p.185-198

2020

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How long noncoding RNAs enforce their will on mitochondrial activity: regulation of mitochondrial respiration, reactive oxygen species production, apoptosis, and metabolic reprogramming in cancer

Current genetics, 2018-02, Vol.64 (1), p.163-172

2018

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Sporadic Inclusion Body Myositis: An Acquired Mitochondrial Disease with Extras

Biomolecules (Basel, Switzerland), 2019-01, Vol.9 (1), p.15

De Paepe, Boel

2019

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What Nutraceuticals Can Do for Duchenne Muscular Dystrophy: Lessons Learned from Amino Acid Supplementation in Mouse Models

Biomedicines, 2023-07, Vol.11 (7), p.2033

De Paepe, Boel

2023

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The Role of Taurine in Skeletal Muscle Functioning and Its Potential as a Supportive Treatment for Duchenne Muscular Dystrophy

Metabolites, 2022-02, Vol.12 (2), p.193

2022

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How mitochondrial DNA-driven changes to chromosomal DNA methylation add a layer of complexity to mitochondrial disease

Epigenomics, 2019-12, Vol.11 (16), p.1749-1751

De Paepe, Boel

2019

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Incorporating circulating cytokines into the idiopathic inflammatory myopathy subclassification toolkit

Frontiers in medicine, 2023-03, Vol.10, p.1130614-1130614

De Paepe, Boel

2023

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Chemokines in idiopathic inflammatory myopathies

Frontiers in bioscience, 2008, Vol.13 (13), p.2548

Paepe, Boel De

2008

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Heat shock protein families 70 and 90 in Duchenne muscular dystrophy and inflammatory myopathy: Balancing muscle protection and destruction

Neuromuscular disorders : NMD, 2012-01, Vol.22 (1), p.26-33

2012

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Abnormal NFAT5 Physiology in Duchenne Muscular Dystrophy Fibroblasts as a Putative Explanation for the Permanent Fibrosis Formation in Duchenne Muscular Dystrophy

International journal of molecular sciences, 2020-10, Vol.21 (21), p.7888

2020

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Urine lactate concentration as a non-invasive screener for metabolic abnormalities: Findings in children with autism spectrum disorder and regression

PloS one, 2022-09, Vol.17 (9), p.e0274310-e0274310

2022

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Urine lactate concentration as a non-invasive screener for metabolic abnormalities: Findings in children with autism spectrum disorder and regression

PloS one, 2022-09, Vol.17 (9), p.e0274310

2022

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Cytokines and Chemokines as Regulators of Skeletal Muscle Inflammation: Presenting the Case of Duchenne Muscular Dystrophy

Mediators of Inflammation, 2013-01, Vol.2013 (2013), p.977-986-189

2013

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Possible Pathogenic Mechanism of Propofol Infusion Syndrome Involves Coenzyme Q

Anesthesiology (Philadelphia), 2015-02, Vol.122 (2), p.343-352

2015

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Relevance of solute carrier family 5 transporter defects to inherited and acquired human disease

Journal of applied genetics, 2019-11, Vol.60 (3-4), p.305-317

2019

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The long non-coding RNA SAMMSON is essential for uveal melanoma cell survival

Oncogene, 2022-01, Vol.41 (1), p.15-25

2022

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Description of a Novel Mechanism Possibly Explaining the Antiproliferative Properties of Glucocorticoids in Duchenne Muscular Dystrophy Fibroblasts Based on Glucocorticoid Receptor GR and NFAT5

International journal of molecular sciences, 2020-12, Vol.21 (23), p.9225

2020

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205th ENMC International Workshop: Pathology diagnosis of idiopathic inflammatory myopathies Part II 28–30 March 2014, Naarden, The Netherlands

Neuromuscular disorders : NMD, 2015-03, Vol.25 (3), p.268-272

2015

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Description of Osmolyte Pathways in Maturing Mdx Mice Reveals Altered Levels of Taurine and Sodium/Myo-Inositol Co-Transporters

International journal of molecular sciences, 2022-03, Vol.23 (6), p.3251

2022

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Anti-Inflammatory and General Glucocorticoid Physiology in Skeletal Muscles Affected by Duchenne Muscular Dystrophy: Exploration of Steroid-Sparing Agents

Scanning for Therapeutic Targets within the Cytokine Network of Idiopathic Inflammatory Myopathies

Progressive Skeletal Muscle Atrophy in Muscular Dystrophies: A Role for Toll-like Receptor-Signaling in Disease Pathogenesis

The Cytokine Growth Differentiation Factor-15 and Skeletal Muscle Health: Portrait of an Emerging Widely Applicable Disease Biomarker

Biallelic Mutations in TMEM126B Cause Severe Complex I Deficiency with a Variable Clinical Phenotype

Nanoscopic X‐ray imaging and quantification of the iron cellular architecture within single fibroblasts of Friedreich's ataxia patients

How long noncoding RNAs enforce their will on mitochondrial activity: regulation of mitochondrial respiration, reactive oxygen species production, apoptosis, and metabolic reprogramming in cancer

Sporadic Inclusion Body Myositis: An Acquired Mitochondrial Disease with Extras

What Nutraceuticals Can Do for Duchenne Muscular Dystrophy: Lessons Learned from Amino Acid Supplementation in Mouse Models

The Role of Taurine in Skeletal Muscle Functioning and Its Potential as a Supportive Treatment for Duchenne Muscular Dystrophy

How mitochondrial DNA-driven changes to chromosomal DNA methylation add a layer of complexity to mitochondrial disease

Incorporating circulating cytokines into the idiopathic inflammatory myopathy subclassification toolkit

Chemokines in idiopathic inflammatory myopathies

Heat shock protein families 70 and 90 in Duchenne muscular dystrophy and inflammatory myopathy: Balancing muscle protection and destruction

Abnormal NFAT5 Physiology in Duchenne Muscular Dystrophy Fibroblasts as a Putative Explanation for the Permanent Fibrosis Formation in Duchenne Muscular Dystrophy

Urine lactate concentration as a non-invasive screener for metabolic abnormalities: Findings in children with autism spectrum disorder and regression

Urine lactate concentration as a non-invasive screener for metabolic abnormalities: Findings in children with autism spectrum disorder and regression

Cytokines and Chemokines as Regulators of Skeletal Muscle Inflammation: Presenting the Case of Duchenne Muscular Dystrophy

Possible Pathogenic Mechanism of Propofol Infusion Syndrome Involves Coenzyme Q

Relevance of solute carrier family 5 transporter defects to inherited and acquired human disease

The long non-coding RNA SAMMSON is essential for uveal melanoma cell survival

Description of a Novel Mechanism Possibly Explaining the Antiproliferative Properties of Glucocorticoids in Duchenne Muscular Dystrophy Fibroblasts Based on Glucocorticoid Receptor GR and NFAT5

205th ENMC International Workshop: Pathology diagnosis of idiopathic inflammatory myopathies Part II 28–30 March 2014, Naarden, The Netherlands

Low copy numbers of complement C4 and C4A deficiency are risk factors for myositis, its subgroups and autoantibodies

Description of Osmolyte Pathways in Maturing Mdx Mice Reveals Altered Levels of Taurine and Sodium/Myo-Inositol Co-Transporters

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