Livio Pellizzoni, Phd
Affiliations: | Columbia University, New York, NY |
Area:
Neural Degeneration and Repair, Neurobiology of Disease, Synapses and Circuits, Stem Cell Biology, Cellular/Molecular/Developmental NeuroscienceGoogle:
"Livio Pellizzoni"Mean distance: 53433
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Publications
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| Hassan A, di Vito R, Nuzzo T, et al. (2024) Dysregulated balance of D- and L-amino acids modulating glutamatergic neurotransmission in severe spinal muscular atrophy. Biorxiv : the Preprint Server For Biology |
| Fletcher EV, Chalif JI, Rotterman TM, et al. (2024) Synaptic imbalance and increased inhibition impair motor function in SMA. Biorxiv : the Preprint Server For Biology |
| Carlini MJ, Van Alstyne M, Yang H, et al. (2024) Stasimon/Tmem41b is required for cell proliferation and adult mouse survival. Biochemical and Biophysical Research Communications. 149923 |
| Lumpkin CJ, Harris AW, Connell AJ, et al. (2023) Evaluation of the orally bioavailable 4-phenylbutyrate-tethered trichostatin A analogue AR42 in models of spinal muscular atrophy. Scientific Reports. 13: 10374 |
| Tisdale S, Van Alstyne M, Simon CM, et al. (2022) SMN controls neuromuscular junction integrity through U7 snRNP. Cell Reports. 40: 111393 |
| Chen L, Roake CM, Maccallini P, et al. (2022) TGS1 impacts snRNA 3'-end processing, ameliorates survival motor neuron-dependent neurological phenotypes in vivo and prevents neurodegeneration. Nucleic Acids Research |
| Carlini MJ, Triplett MK, Pellizzoni L. (2022) Neuromuscular denervation and deafferentation but not motor neuron death are disease features in the Smn2B/- mouse model of SMA. Plos One. 17: e0267990 |
| Van Alstyne M, Tattoli I, Delestrée N, et al. (2021) Gain of toxic function by long-term AAV9-mediated SMN overexpression in the sensorimotor circuit. Nature Neuroscience |
| Osman EY, Van Alstyne M, Yen PF, et al. (2020) Minor snRNA gene delivery improves the loss of proprioceptive synapses on SMA motor neurons. Jci Insight |
| Simon CM, Van Alstyne M, Lotti F, et al. (2019) Stasimon Contributes to the Loss of Sensory Synapses and Motor Neuron Death in a Mouse Model of Spinal Muscular Atrophy. Cell Reports. 29: 3885-3901.e5 |