about
Disrupted axo-glial junctions result in accumulation of abnormal mitochondria at nodes of ranvierGenetic aspects of autism spectrum disorders: insights from animal modelsDrosophila Crumbs is a positional cue in photoreceptor adherens junctions and rhabdomeresWhirlin, a cytoskeletal scaffolding protein, stabilizes the paranodal region and axonal cytoskeleton in myelinated axonsPostnatal Loss of Neuronal and Glial Neurofascins Differentially Affects Node of Ranvier Maintenance and Myelinated Axon Function.Axonal ensheathment and intercellular barrier formation in Drosophila.Novel forms of neurofascin 155 in the central nervous system: alterations in paranodal disruption models and multiple sclerosisNo effect of genetic deletion of contactin-associated protein (CASPR) on axonal orientation and synaptic plasticity.Neuron-glial interactions in blood-brain barrier formation.Spatiotemporal ablation of myelinating glia-specific neurofascin (Nfasc NF155) in mice reveals gradual loss of paranodal axoglial junctions and concomitant disorganization of axonal domains.Drosophila neurexin IV interacts with Roundabout and is required for repulsive midline axon guidanceA Laminin G-EGF-Laminin G module in Neurexin IV is essential for the apico-lateral localization of Contactin and organization of septate junctions.The relationship of nerve fibre pathology to sensory function in entrapment neuropathy.Nodes of Ranvier act as barriers to restrict invasion of flanking paranodal domains in myelinated axons.The cytoskeletal adaptor protein band 4.1B is required for the maintenance of paranodal axoglial septate junctions in myelinated axons.Molecular organization of axo-glial junctions.Drosophila Varicose, a member of a new subgroup of basolateral MAGUKs, is required for septate junctions and tracheal morphogenesisSeptate junctions are required for ommatidial integrity and blood-eye barrier function in Drosophila.Altered potassium channel distribution and composition in myelinated axons suppresses hyperexcitability following injury.The septate junction protein caspr is required for structural support and retention of KCNQ4 at calyceal synapses of vestibular hair cells.Neurexin IV and Wrapper interactions mediate Drosophila midline glial migration and axonal ensheathment.A versatile genetic tool to study midline glia function in the Drosophila CNS.Axonal domain disorganization in Caspr1 and Caspr2 mutant myelinated axons affects neuromuscular junction integrity, leading to muscle atrophy.Drosophila Ringmaker regulates microtubule stabilization and axonal extension during embryonic developmentROP, the Drosophila Sec1 homolog, interacts with syntaxin and regulates neurotransmitter release in a dosage-dependent manner.Early and Late Loss of the Cytoskeletal Scaffolding Protein, Ankyrin G Reveals Its Role in Maturation and Maintenance of Nodes of Ranvier in Myelinated Axons.Neurexin, Neuroligin and Wishful Thinking coordinate synaptic cytoarchitecture and growth at neuromuscular junctions.Axonal ensheathment and septate junction formation in the peripheral nervous system of Drosophila.In vivo inactivation of pRb, p107 and p130 in murine neuroprogenitor cells leads to major CNS developmental defects and high seizure rates.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.Microfluorimetry defines early axonal damage in a rat model of optic neuritis: a novel method targeting early CNS autoimmunityReorganization of Destabilized Nodes of Ranvier in βIV Spectrin Mutants Uncovers Critical Timelines for Nodal Restoration and Prevention of Motor ParesisAblation of cytoskeletal scaffolding proteins, Band 4.1B and Whirlin, leads to cerebellar purkinje axon pathology and motor dysfunction
P50
Q24681410-EE9641CC-59B4-449E-84B5-34EB525A5F4AQ27687011-EC037F81-6B1D-4911-880C-B40F9DCEC111Q28202043-B8A0364D-F726-4261-B523-67CE45082070Q28506822-9B2A580D-E82D-4F0F-A4D7-01E03F2FD87FQ30837291-62ADCC3D-99DB-4EBB-A4BE-84F2CD740C3EQ33608874-01DA6438-9477-4A4B-B52D-DA13CF75B32DQ33656323-5EA512E9-C671-47B6-8F2F-AD6573C3FBEDQ33666268-EF7B21F8-97A1-4CFE-82BD-DE49DB9804A0Q33670796-E103B99F-0544-412F-82F0-23DB9611C537Q33722493-64B8F591-817E-4A72-B96E-44190014FBBAQ33847359-F08797C8-17EF-4F80-A745-06969DF71475Q34055809-A948D0B2-0374-40F1-97F1-1F25C15FC74DQ34555983-682DDBFF-9EFF-4EFB-A406-69CBA827AE29Q34558317-B1F15E3F-8DFD-4708-AF37-25C2B4632B63Q35063962-261671E8-EEA4-4BE0-A567-452917475D7CQ35589888-31CF3295-09B0-4F3C-B36B-32D727F2FBD4Q35956016-CDA8C394-9B77-418B-98C1-DE2F4D737F45Q36711549-955218B9-5864-4DAC-A735-53DFE4866C03Q36827564-7AD8BC9F-1D06-400A-A5B5-987FB08E6564Q37158009-0E12AF4E-524C-4507-9B41-4AA2F33680C2Q38356082-F3A22639-4D4A-469C-B7EA-991BC2CCB275Q38672261-231FD87B-951F-4108-874B-BB3B0381C892Q38859584-1324653E-0DED-4A44-8BD4-31EDA93E13E3Q39597230-046C651A-AE0A-4BCE-BA41-3EDD9CB284DAQ41831887-B7F870F2-BD52-4116-A0FC-4D4FCFF8F422Q42010808-76FAE3DA-66B0-4AA1-B082-BAD995E9B047Q46460659-832FF8DE-DB6F-41ED-AAA3-44B3710FC22DQ47071364-F16A62B5-CACE-4760-8E8E-C437D4C8AB2EQ48419482-E4D9E4A4-EADA-4FEB-971A-F92D10B739C8Q55360507-353928AC-7C7E-4560-833D-30A58EB299A1Q80844191-9D73699A-A88F-4EBC-82AD-EB118E85D99AQ89120913-20B32485-8AA2-42B0-B767-7EFBC04725E0Q93185930-5C440CC7-7A4E-4DDF-AB58-1EABF1F3F93D
P50
description
onderzoeker
@nl
researcher ORCID ID = 0000-0003-0989-1498
@en
name
Manzoor A Bhat
@ast
Manzoor A Bhat
@en
Manzoor A Bhat
@es
Manzoor A Bhat
@nl
type
label
Manzoor A Bhat
@ast
Manzoor A Bhat
@en
Manzoor A Bhat
@es
Manzoor A Bhat
@nl
prefLabel
Manzoor A Bhat
@ast
Manzoor A Bhat
@en
Manzoor A Bhat
@es
Manzoor A Bhat
@nl
P106
P1153
7102578680
P31
P496
0000-0003-0989-1498