about
Neurodegeneration and microtubule dynamics: death by a thousand cutsThe vesicle protein SAM-4 regulates the processivity of synaptic vesicle transportColored polydimethylsiloxane micropillar arrays for high throughput measurements of forces applied by genetic model organisms.The Caenorhabditis elegans Kinesin-3 motor UNC-104/KIF1A is degraded upon loss of specific binding to cargoThe kinesin-3 family motor KLP-4 regulates anterograde trafficking of GLR-1 glutamate receptors in the ventral nerve cord of Caenorhabditis elegans.In vivo nanosecond laser axotomy: cavitation dynamics and vesicle transport.Differential and inefficient splicing of a broadly expressed Drosophila erect wing transcript results in tissue-specific enrichment of the vital EWG protein isoform.The neuron-enriched splicing pattern of Drosophila erect wing is dependent on the presence of ELAV proteinThe Caenorhabditis elegans JIP3 protein UNC-16 functions as an adaptor to link kinesin-1 with cytoplasmic dynein.Simple microfluidic devices for in vivo imaging of C. elegans, Drosophila and zebrafish."JIP"ing along the axon: the complex roles of JIPs in axonal transport.Distinct DNA binding sites contribute to the TCF transcriptional switch in C. elegans and Drosophila.RAB-6.1 and RAB-6.2 Promote Retrograde Transport in C. eleganslet-7 miRNA controls CED-7 homotypic adhesion and EFF-1-mediated axonal self-fusion to restore touch sensation following injury.UNC-16/JIP3 regulates early events in synaptic vesicle protein trafficking via LRK-1/LRRK2 and AP complexes.Cargo crowding at actin-rich regions along axons causes local traffic jams.Mutations in Caenorhabditis elegans cytoplasmic dynein components reveal specificity of neuronal retrograde cargo.Loss of the putative RNA-directed RNA polymerase RRF-3 makes C. elegans hypersensitive to RNAi.Imaging in vivo neuronal transport in genetic model organisms using microfluidic devices.Inhibition of tau aggregation in a novel Caenorhabditis elegans model of tauopathy mitigates proteotoxicity.In vivo imaging of retrogradely transported synaptic vesicle proteins in Caenorhabditis elegans neurons.Microfluidic devices for imaging trafficking events in vivo using genetic model organisms.ELAV, a Drosophila neuron-specific protein, mediates the generation of an alternatively spliced neural protein isoform.The C-terminal of CASY-1/Calsyntenin regulates GABAergic synaptic transmission at the Caenorhabditis elegans neuromuscular junction.UNC-16/JIP3 and UNC-76/FEZ1 limit the density of mitochondria in C. elegans neurons by maintaining the balance of anterograde and retrograde mitochondrial transport.An autonomous DNA nanomachine maps spatiotemporal pH changes in a multicellular living organismTied up: Does altering phosphoinositide-mediated membrane trafficking influence neurodegenerative disease phenotypes?Crowd Control: Effects of Physical Crowding on Cargo Movement in Healthy and Diseased NeuronsRole of actin in organelle trafficking in neurons
P50
Q26781649-34D9A726-4391-41BF-BCA7-B2B837C6FA76Q27313266-F71AA5D6-C232-4320-877D-BF5D7B029071Q27332129-E3FEEDC1-159A-4536-9B72-445D6B5BD0BDQ27345244-252EB6ED-DA02-4DA8-A29F-69F8C20562B7Q30524916-123467B5-830F-4FEE-BC64-3CB68A2675A5Q33346174-D308AC79-C217-426C-ACDE-76EFF661E898Q33651635-24D7016D-E594-4CAD-B010-ABBEB465B85BQ33962315-930E688E-FBE7-4415-9F6C-2D7FD3E935C5Q34163603-EE010429-83BB-474D-AFBC-3410A33C403FQ34439273-C33162BA-A55B-42D3-A9DB-29F5FB52CA22Q34725658-0829C42B-CE8F-475A-85C4-08980831B810Q35091279-15FD555D-B403-4F5D-96C5-3F016F6D8CA8Q35927492-6DE6EDF1-5DEA-4AC4-A419-23C3F979B88DQ47103765-E26DC6F1-6940-4DC4-BDBF-77B5EECEAC1BQ47169436-B6F42BA5-6FFA-46B6-80D6-A69035921B56Q47596063-7558C98B-2038-48D0-B1B4-D930D5763C17Q47717805-181D1D43-2AEA-4B87-9AB2-D7EC5F6EA2F5Q47884643-9D37E694-B06E-4409-8837-2974F64007D8Q48298651-AFB0D7E9-00F3-4757-BF8E-EA8FEC72EF31Q48501542-6D3D7A16-521B-4CF3-BBFC-57430F924F3AQ50537042-C0CE1306-0BA3-4EFD-920D-BFC5D1BEA45FQ50654285-095A8A05-D554-4528-A2F8-F86FEC730958Q52552034-F5E1C90A-3F21-41E6-B11A-4734DB21979DQ53436292-D47D642A-91B3-4A43-9747-E01B7526DCA3Q55383005-F564820A-8E40-4EB7-968D-26BBFECEE288Q61198343-72469B34-70C1-4BC9-87B7-DD3D25860C71Q90359253-6D38F6D8-1A5B-48E9-B528-5238662706D6Q91217419-BB9C46AA-DA59-44B3-B9C0-B2DB92944BE4Q91280711-F968B831-3002-4CD9-A113-24549AFC09A8
P50
description
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Sandhya P Koushika
@ast
Sandhya P Koushika
@en
Sandhya P Koushika
@es
Sandhya P Koushika
@nl
type
label
Sandhya P Koushika
@ast
Sandhya P Koushika
@en
Sandhya P Koushika
@es
Sandhya P Koushika
@nl
prefLabel
Sandhya P Koushika
@ast
Sandhya P Koushika
@en
Sandhya P Koushika
@es
Sandhya P Koushika
@nl
P108
P106
P108
P31
P496
0000-0002-1742-7356