Mário André Saporta, PhD
Affiliations: | UFRJ, Rio de Janeiro, Rio de Janeiro, Brazil |
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Publications
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Rebelo AP, Abad C, Dohrn MF, et al. (2023) Sord deficient rats develop a motor-predominant peripheral neuropathy unveiling novel pathophysiological insights. Biorxiv : the Preprint Server For Biology |
Cutrupi AN, Narayanan RK, Perez-Siles G, et al. (2022) Novel gene-intergenic fusion involving ubiquitin E3 ligase UBE3C causes distal hereditary motor neuropathy. Brain : a Journal of Neurology |
Besser RR, Bowles AC, Alassaf A, et al. (2021) Correction to: A Chemically Defined Common Medium for Culture of C2C12 Skeletal Muscle and Human Induced Pluripotent Stem Cell Derived Spinal Spheroids. Cellular and Molecular Bioengineering. 14: 131 |
Besser RR, Bowles AC, Alassaf A, et al. (2020) A Chemically Defined Common Medium for Culture of C2C12 Skeletal Muscle and Human Induced Pluripotent Stem Cell Derived Spinal Spheroids. Cellular and Molecular Bioengineering. 13: 605-619 |
Besser RR, Bowles AC, Alassaf A, et al. (2019) Enzymatically crosslinked gelatin-laminin hydrogels for applications in neuromuscular tissue engineering. Biomaterials Science |
Maciel R, Correa R, Taniguchi JB, et al. (2019) Human tridimensional neuronal cultures for phenotypic drug screening in inherited peripheral neuropathies. Clinical Pharmacology and Therapeutics |
Maciel R, Bis DM, Rebelo AP, et al. (2018) The human motor neuron axonal transcriptome is enriched for transcripts related to mitochondrial function and microtubule-based axonal transport. Experimental Neurology. 307: 155-163 |
Saporta MA, Dang V, Volfson D, et al. (2015) Axonal Charcot-Marie-Tooth disease patient-derived motor neurons demonstrate disease-specific phenotypes including abnormal electrophysiological properties. Experimental Neurology. 263: 190-9 |
Saporta MA, Grskovic M, Dimos JT. (2011) Induced pluripotent stem cells in the study of neurological diseases. Stem Cell Research & Therapy. 2: 37 |