John N. Mariani, Ph.D.

Affiliations: 
2009-2016 Neuroscience, Neurology Icahn School of Medicine at Mount Sinai, New York, NY, United States 
 2016- Neurology, Center for Translational Neuromedicine University of Rochester, Rochester, NY 
Area:
Synaptogenesis, Synaptic Plasticity, Astrocytes, MS, Oligodendrocytes, Glia, Blood Brain Barrier, Endothelial Cells, Bioinformatics, Sequencing
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"John Mariani"
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Publications

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Mariani JN, Mansky B, Madsen PM, et al. (2024) Repression of developmental transcription factor networks triggers aging-associated gene expression in human glial progenitor cells. Nature Communications. 15: 3873
Takasugi M, Ohtani N, Takemura K, et al. (2023) CD44 correlates with longevity and enhances basal ATF6 activity and ER stress resistance. Cell Reports. 42: 113130
Vieira R, Mariani JN, Huynh NPT, et al. (2023) Young glial progenitor cells competitively replace aged and diseased human glia in the adult chimeric mouse brain. Nature Biotechnology
Osorio MJ, Mariani JN, Zou L, et al. (2022) Glial progenitor cells of the adult human white and grey matter are contextually distinct. Glia
Benraiss A, Mariani JN, Tate A, et al. (2022) A TCF7L2-responsive suppression of both homeostatic and compensatory remyelination in Huntington disease mice. Cell Reports. 40: 111291
Benraiss A, Mariani JN, Osipovitch M, et al. (2021) Cell-intrinsic glial pathology is conserved across human and murine models of Huntington's disease. Cell Reports. 36: 109308
Goldman SA, Mariani JN, Madsen PM. (2021) Glial progenitor cell-based repair of the dysmyelinated brain: Progression to the clinic. Seminars in Cell & Developmental Biology
Windrem MS, Schanz SJ, Zou L, et al. (2020) Human Glial Progenitor Cells Effectively Remyelinate the Demyelinated Adult Brain. Cell Reports. 31: 107658
Mariani JN, Zou L, Goldman SA. (2019) Human Glial Chimeric Mice to Define the Role of Glial Pathology in Human Disease. Methods in Molecular Biology (Clifton, N.J.). 1936: 311-331
Osipovitch M, Asenjo Martinez A, Mariani JN, et al. (2019) Human ESC-Derived Chimeric Mouse Models of Huntington's Disease Reveal Cell-Intrinsic Defects in Glial Progenitor Cell Differentiation. Cell Stem Cell. 24: 107-122.e7
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