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Comment on: The reliability of immunoassays to detect autoantibodies in patients with myositis is dependent on autoantibody specificity
Mahler M, Malyavantham K, Fritzler MJ, et al.
Rheumatology (Oxford, England), 2021, 60, 1, e35
Comment on: The reliability of immunoassays to detect autoantibodies in patients with myositis is dependent on autoantibody specificity: reply
Tansley SL, McHugh NJ
Rheumatology (Oxford, England), 2021, 60, 1, e38
Comment on: The reliability of immunoassays to detect autoantibodies in patients with myositis is dependent on autoantibody specificity
Sabour S
Rheumatology (Oxford, England), 2020
Comment on: The reliability of immunoassays to detect autoantibodies in patients with myositis is dependent on autoantibody specificity: reply
Tansley SL, McHugh NJ
Rheumatology (Oxford, England), 2020
Ubiquitin ligase LRSAM1 suppresses neurodegenerative diseases linked aberrant proteins induced cell death
Mishra R, Amanullah A, Upadhyay A, et al.
The International Journal of Biochemistry & Cell Biology, 2020, 120
Modulators of calpain activity: inhibitors and activators as potential drugs
Dokus LE, Yousef M, Banoczi Z
Expert opinion on drug discovery, 2020
Spinal muscular atrophy diagnosis and carrier screening from genome sequencing data
Chen X, Sanchis-Juan A, French CE, et al.
Genetics in medicine : official journal of the American College of Medical Genetics, 2020
Antibodies against nodo-paranodal proteins are not present in genetic neuropathies
Martin-Aguilar L, Pascual-Goni E, Lleixà C, et al.
Neurology, 2020
The reliability of immunoassays to detect autoantibodies in patients with myositis is dependent on autoantibody specificity
Tansley SL, Li D, Betteridge ZE, et al.
Rheumatology (Oxford, England), 2020
Dissecting the Extracellular Complexity of Neuromuscular Junction Organizers
Guarino SR, Canciani A, Forneris F
Frontiers in molecular biosciences, 2020, 6, p 156
Fast Assays to Detect Interruptions in CTG.CAG Repeat Expansions
Tomé S, Gourdon G
Methods in molecular biology (Clifton, N.J.), 2020, 2056, p 11
Crystal structures of fukutin-related protein (FKRP), a ribitol-phosphate transferase related to muscular dystrophy
Kuwabara N, Imae R, Manya H, et al.
Nature communications, 2020, 11, 1, p 303
Dysfunctional polycomb transcriptional repression contributes to Lamin A/C dependent muscular dystrophy
Bianchi A, Mozzetta C, Pegoli G, et al.
The Journal of clinical investigation, 2020
Control of Muscle Fibro-Adipogenic Progenitors by Myogenic Lineage is Altered in Aging and Duchenne Muscular Dystrophy
Moratal C, Arrighi N, Dechesne CA, et al.
Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology, 2019, 53, 6, p 1029
Pulsed glucocorticoids enhance dystrophic muscle performance through epigenetic-metabolic reprogramming
Quattrocelli M, Zelikovich AS, Jiang Z, et al.
JCI insight, 2019, 4, 24
[JAK inhibitors: Perspectives in internal medicine] : Les inhibiteurs de JAK : perspectives pour la médecine interne
El Jammal T, Gerfaud-Valentin M, Seve P, et al.
La Revue de medecine interne, 2019, 40, 12, p 816
Identification of the hyaluronic acid pathway as a therapeutic target for facioscapulohumeral muscular dystrophy
DeSimone AM, Leszyk J, Wagner K, et al.
Science advances, 2019, 5, 12
Chemical Proteomics and Phenotypic Profiling Identifies the Aryl Hydrocarbon Receptor as a Molecular Target of the Utrophin Modulator Ezutromid
Wilkinson IVL, Perkins KJ, Dugdale H, et al.
Angewandte Chemie (International ed. in English), 2019
Targeting the programmed axon degeneration pathway as a potential therapeutic for Charcot-Marie-Tooth disease
Moss KR, Höke A
Brain research, 2019
Force Generation by Myosin Motors: A Structural Perspective
Robert-Paganin J, Pylypenko O, Kikuti C, et al.
Chemical reviews, 2019
Characterizing the interplay between gene nucleotide composition bias and splicing
Lemaire S, Fontrodona N, Aube F, et al.
Genome biology, 2019, 20, 1, p 259
MicroRNA-Based Therapeutic Perspectives in Myotonic Dystrophy
Lopez Castel A, Overby SJ, Artero R
International Journal of molecular sciences, 2019, 20, 22
How the central domain of dystrophin acts to bridge F-actin to sarcolemmal lipids
Mias-Lucquin D, Dos Santos Morais R, Chéron A, et al.
Journal of structural biology, 2019
Transcriptional dysregulation by a nucleus-localized aminoacyl-tRNA synthetase associated with Charcot-Marie-Tooth neuropathy
Bervoets S, Wei N, Erfurth ML, et al.
Nature communications, 2019, 10, 1
Mitochondrial impairment activates the Wallerian pathway through depletion of NMNAT2 leading to SARM1-dependent axon degeneration
Loreto A, Hill CS, Hewitt VL, et al.
Neurobiology of disease, 2019, 134
