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Acta Neuropathologica Communications|July 20, 2021
The ESCRT-III protein VPS4, but not CHMP4B or CHMP2B, is pathologically increased in familial and sporadic ALS neuronal nucleiAlyssa N Coyne, Jeffrey D Rothstein
Acta Neuropathologica Communications|March 20, 2021
Nuclear lamina invaginations are not a pathological feature of C9orf72 ALS/FTDAlyssa N Coyne, Jeffrey D Rothstein
Journal of Visualized Experiments : Jove|September 27, 2021
Nuclei Isolation and Super-Resolution Structured Illumination Microscopy for Examining Nucleoporin Alterations in Human NeurodegenerationAlyssa N Coyne, Jeffrey D Rothstein
Nature Reviews. Neurology|April 29, 2022
Nuclear pore complexes - a doorway to neural injury in neurodegenerationAlyssa N Coyne, Jeffrey D Rothstein
Australian Dental Journal|December 1, 1995
A survey of the pattern of private general dental practice in Queensland, 1992M H Spratley, L N Coyne
Australian Dental Journal|October 1, 1989
A survey of the pattern of private general dental practice in QueenslandM H Spratley, L N Coyne
Biorxiv : the Preprint Server for Biology|January 3, 2024
Highly variable molecular signatures of TDP-43 loss of function are associated with nuclear pore complex injury in a population study of sporadic ALS patient iPSNsJeffrey D Rothstein, Caroline Warlick, Alyssa N Coyne
FEBS Letters|September 1, 2023
Nuclear pore complex and nucleocytoplasmic transport disruption in neurodegenerationAmérica Chandía Cristi, Sampath Rapuri, Alyssa N Coyne
Brain Research|May 13, 2018
Drosophila models of amyotrophic lateral sclerosis with defects in RNA metabolismKe Zhang, Alyssa N Coyne, Thomas E Lloyd
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