Manzoor Bhat

Affiliations: 
 
Google:
"Manzoor Bhat"
BETA: Related publications

Publications

You can help our author matching system! If you notice any publications incorrectly attributed to this author, please sign in and mark matches as correct or incorrect.

Chang C, Sell LB, Shi Q, et al. (2023) Mouse models of human CNTNAP1-associated congenital hypomyelinating neuropathy and genetic restoration of murine neurological deficits. Cell Reports. 42: 113274
Kunisawa K, Hatanaka N, Shimizu T, et al. (2020) Focal loss of the paranodal domain protein Neurofascin155 in the internal capsule impairs cortically induced muscle activity in vivo. Molecular Brain. 13: 159
Saifetiarova J, Bhat MA. (2018) Ablation of cytoskeletal scaffolding proteins, Band 4.1B and Whirlin, leads to cerebellar purkinje axon pathology and motor dysfunction. Journal of Neuroscience Research
Shi Q, Saifetiarova J, Taylor AM, et al. (2018) mTORC1 Activation by Loss of in Myelinating Glia Causes Downregulation of Quaking and Neurofascin 155 Leading to Paranodal Domain Disorganization. Frontiers in Cellular Neuroscience. 12: 201
Kunisawa K, Shimizu T, Kushima I, et al. (2018) Dysregulation of schizophrenia-related aquaporin 3 through disruption of paranode influences neuronal viability. Journal of Neurochemistry
Taylor AM, Shi Q, Bhat MA. (2018) Simultaneous Ablation of Neuronal Neurofascin and Ankyrin G in Young and Adult Mice Reveals Age-Dependent Increase in Nodal Stability in Myelinated Axons and Differential Effects on the Lifespan. Eneuro. 5
Saifetiarova J, Shi Q, Paukert M, et al. (2018) Reorganization of Destabilized Nodes of Ranvier in Mutants Uncovers Critical Timelines for Nodal Restoration and Prevention of Motor Paresis. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience
Barron T, Saifetiarova J, Bhat MA, et al. (2018) Myelination of Purkinje axons is critical for resilient synaptic transmission in the deep cerebellar nucleus. Scientific Reports. 8: 1022
Banerjee S, Mino E, Fisher ES, et al. (2017) A Versatile Genetic Tool to Study Midline Glia Function in the Drosophila CNS. Developmental Biology
Saifetiarova J, Liu X, Taylor AM, et al. (2017) Axonal domain disorganization in Caspr1 and Caspr2 mutant myelinated axons affects neuromuscular junction integrity, leading to muscle atrophy. Journal of Neuroscience Research
See more...