Umrao Monani, Phd
Affiliations: | Columbia University, New York, NY |
Area:
Pediatric Neurology, Neurobiology of Disease, Motor Neuron Disease, Synapses and CircuitsGoogle:
"Umrao Monani"Mean distance: 106866
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Publications
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| Jha NN, Kim JK, Her YR, et al. (2023) Muscle: an independent contributor to the neuromuscular spinal muscular atrophy disease phenotype. Jci Insight. 8 |
| Kim JK, Jha NN, Awano T, et al. (2023) A spinal muscular atrophy modifier implicates the SMN protein in SNARE complex assembly at neuromuscular synapses. Neuron |
| Gollapalli K, Kim JK, Monani UR. (2021) Emerging concepts underlying selective neuromuscular dysfunction in infantile-onset spinal muscular atrophy. Neural Regeneration Research. 16: 1978-1984 |
| Kim JK, Jha NN, Feng Z, et al. (2020) Muscle-specific SMN reduction reveals motor neuron-independent disease in spinal muscular atrophy models. The Journal of Clinical Investigation |
| Jha NN, Kim JK, Monani UR. (2018) Motor neuron biology and disease: A current perspective on infantile-onset spinal muscular atrophy. Future Neurology. 13: 161-172 |
| Majumder S, Varadharaj S, Ghoshal K, et al. (2018) Identification of a novel cyclic AMP-response element (CRE-II) and the role of CREB-1 in the cAMP-induced expression of the survival motor neuron () gene. The Journal of Biological Chemistry. 293: 12946 |
| Pappas SS, Li J, LeWitt TM, et al. (2018) A cell autonomous torsinA requirement for cholinergic neuron survival and motor control. Elife. 7 |
| Kim JK, Caine C, Awano T, et al. (2017) Motor neuronal repletion of the NMJ organizer, Agrin, modulates the severity of the spinal muscular atrophy disease phenotype in model mice. Human Molecular Genetics |
| Harding BN, Kariya S, Monani UR, et al. (2015) Spectrum of neuropathophysiology in spinal muscular atrophy type I. Journal of Neuropathology and Experimental Neurology. 74: 15-24 |
| Kye MJ, Niederst ED, Wertz MH, et al. (2014) SMN regulates axonal local translation via miR-183/mTOR pathway. Human Molecular Genetics. 23: 6318-31 |