| Year |
Citation |
Score |
| 2024 |
Medina J, Rebelo A, Danzi MC, Jacobs EH, Xu IRL, Ahrens KP, Chen S, Raposo J, Yanick C, Zuchner S, Saporta MA. Customized antisense oligonucleotide-based therapy for neurofilament-associated Charcot-Marie-Tooth disease. Brain : a Journal of Neurology. PMID 39008620 DOI: 10.1093/brain/awae225 |
0.366 |
|
| 2024 |
Van Lent J, Prior R, Pérez Siles G, Cutrupi AN, Kennerson ML, Vangansewinkel T, Wolfs E, Mukherjee-Clavin B, Nevin Z, Judge L, Conklin B, Tyynismaa H, Clark AJ, Bennett DL, Van Den Bosch L, ... Saporta M, et al. Advances and challenges in modeling inherited peripheral neuropathies using iPSCs. Experimental & Molecular Medicine. PMID 38825644 DOI: 10.1038/s12276-024-01250-x |
0.32 |
|
| 2024 |
Yanick C, Maciel R, Jacobs E, Schatzman J, Shy M, Zuchner S, Saporta M. Generation of 3 patient induced Pluripotent stem cell lines containing SORD mutations linked to a recessive neuropathy. Stem Cell Research. 78: 103449. PMID 38796985 DOI: 10.1016/j.scr.2024.103449 |
0.625 |
|
| 2024 |
Rebelo AP, Abad C, Dohrn MF, Li JJ, Tieu EK, Medina J, Yanick C, Huang J, Zotter B, Young JI, Saporta M, Scherer SS, Walz K, Zuchner S. SORD-deficient rats develop a motor-predominant peripheral neuropathy unveiling novel pathophysiological insights. Brain : a Journal of Neurology. PMID 38538210 DOI: 10.1093/brain/awae079 |
0.304 |
|
| 2023 |
Rebelo AP, Abad C, Dohrn MF, Li JJ, Tieu E, Medina J, Yanick C, Huang J, Zotter B, Young JI, Saporta M, Scherer SS, Walz K, Zuchner S. Sord deficient rats develop a motor-predominant peripheral neuropathy unveiling novel pathophysiological insights. Biorxiv : the Preprint Server For Biology. PMID 38106042 DOI: 10.1101/2023.12.05.570001 |
0.311 |
|
| 2021 |
Feliciano CM, Wu K, Watry HL, Marley CBE, Ramadoss GN, Ghanim HY, Liu AZ, Zholudeva LV, McDevitt TC, Saporta MA, Conklin BR, Judge LM. Allele-Specific Gene Editing Rescues Pathology in a Human Model of Charcot-Marie-Tooth Disease Type 2E. Frontiers in Cell and Developmental Biology. 9: 723023. PMID 34485306 DOI: 10.3389/fcell.2021.723023 |
0.305 |
|
| 2021 |
Besser RR, Bowles AC, Alassaf A, Carbonero D, Maciel R, Saporta M, Agarwal A. 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. PMID 33643471 DOI: 10.1007/s12195-020-00662-9 |
0.658 |
|
| 2020 |
Besser RR, Bowles AC, Alassaf A, Carbonero D, Maciel R, Saporta M, Agarwal A. 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. PMID 33281990 DOI: 10.1007/S12195-020-00624-1 |
0.671 |
|
| 2019 |
Besser RR, Bowles AC, Alassaf A, Carbonero D, Claure I, Jones E, Reda J, Wubker L, Batchelor W, Ziebarth N, Silvera R, Khan A, Maciel R, Saporta M, Agarwal A. Enzymatically crosslinked gelatin-laminin hydrogels for applications in neuromuscular tissue engineering. Biomaterials Science. PMID 31859298 DOI: 10.1039/C9Bm01430F |
0.663 |
|
| 2019 |
Maciel R, Correa R, Taniguchi JB, Araujo IP, Saporta MA. Human tridimensional neuronal cultures for phenotypic drug screening in inherited peripheral neuropathies. Clinical Pharmacology and Therapeutics. PMID 31715019 DOI: 10.1002/cpt.1718 |
0.672 |
|
| 2018 |
Maciel R, Bis DM, Rebelo AP, Saghira C, Züchner S, Saporta MA. The human motor neuron axonal transcriptome is enriched for transcripts related to mitochondrial function and microtubule-based axonal transport. Experimental Neurology. 307: 155-163. PMID 29935168 DOI: 10.1016/J.Expneurol.2018.06.008 |
0.64 |
|
| 2015 |
Saporta MA, Dang V, Volfson D, Zou B, Xie XS, Adebola A, Liem RK, Shy M, Dimos JT. Axonal Charcot-Marie-Tooth disease patient-derived motor neurons demonstrate disease-specific phenotypes including abnormal electrophysiological properties. Experimental Neurology. 263: 190-9. PMID 25448007 DOI: 10.1016/J.Expneurol.2014.10.005 |
0.407 |
|
| 2011 |
Saporta MA, Grskovic M, Dimos JT. Induced pluripotent stem cells in the study of neurological diseases. Stem Cell Research & Therapy. 2: 37. PMID 21936964 DOI: 10.1186/scrt78 |
0.335 |
|
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