Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Evan Reid

Showing results (21-30 of 47) with videos related to

Pageof 5
Sort By:
Journal of Cell Science|October 7, 2010
The cargo-selective retromer complex is a recruiting hub for protein complexes that regulate endosomal tubule dynamicsMichael E Harbour, Sophia Y A Breusegem, Robin Antrobus, et al.
Neurobiology of Disease|June 8, 2024
Atlastin-1 regulates endosomal tubulation and lysosomal proteolysis in human cortical neuronsEliska Zlamalova, Catherine Rodger, Francesca Greco, et al.
Neurobiology of Disease|December 22, 2025
Protrudin acts at ER-endosome contacts to promote KIF5-mediated endosomal tubule fissionJulia Kleniuk, Aishwarya G Nadadhur, Catherine Rodger, et al.
The Biochemical Journal|July 8, 2009
Endogenous spartin (SPG20) is recruited to endosomes and lipid droplets and interacts with the ubiquitin E3 ligases AIP4 and AIP5Thomas L Edwards, Virginia E Clowes, Hilda T H Tsang, et al.
The Journal of Cell Biology|July 31, 2013
An ESCRT-spastin interaction promotes fission of recycling tubules from the endosomeRachel Allison, Jennifer H Lumb, Coralie Fassier, et al.
Human Molecular Genetics|December 13, 2005
Spastin and atlastin, two proteins mutated in autosomal-dominant hereditary spastic paraplegia, are binding partnersChristopher M Sanderson, James W Connell, Thomas L Edwards, et al.
Development (Cambridge, England)|August 8, 2018
BMP- and neuropilin 1-mediated motor axon navigation relies on spastin alternative translationNicolas Jardin, François Giudicelli, Daniel Ten Martín, et al.
Brain Communications|February 26, 2021
Evidence that autosomal recessive spastic cerebral palsy-1 (CPSQ1) is caused by a missense variant in <i>HPDL</i>Neil V Morgan, Bryndis Yngvadottir, Mary O'Driscoll, et al.
American Journal of Human Genetics|December 13, 2006
Mutations in the KIAA0196 gene at the SPG8 locus cause hereditary spastic paraplegiaPaul N Valdmanis, Inge A Meijer, Annie Reynolds, et al.
Human Molecular Genetics|July 22, 2009
The hereditary spastic paraplegia proteins NIPA1, spastin and spartin are inhibitors of mammalian BMP signallingHilda T H Tsang, Thomas L Edwards, Xinnan Wang, et al.
Pageof 5

Showing results (21-30 of 47) with videos related to

Sort By:
Pageof 5
Journal of Cell Science|October 7, 2010
The cargo-selective retromer complex is a recruiting hub for protein complexes that regulate endosomal tubule dynamicsMichael E Harbour, Sophia Y A Breusegem, Robin Antrobus, et al.
Neurobiology of Disease|June 8, 2024
Atlastin-1 regulates endosomal tubulation and lysosomal proteolysis in human cortical neuronsEliska Zlamalova, Catherine Rodger, Francesca Greco, et al.
Neurobiology of Disease|December 22, 2025
Protrudin acts at ER-endosome contacts to promote KIF5-mediated endosomal tubule fissionJulia Kleniuk, Aishwarya G Nadadhur, Catherine Rodger, et al.
The Biochemical Journal|July 8, 2009
Endogenous spartin (SPG20) is recruited to endosomes and lipid droplets and interacts with the ubiquitin E3 ligases AIP4 and AIP5Thomas L Edwards, Virginia E Clowes, Hilda T H Tsang, et al.
The Journal of Cell Biology|July 31, 2013
An ESCRT-spastin interaction promotes fission of recycling tubules from the endosomeRachel Allison, Jennifer H Lumb, Coralie Fassier, et al.
Human Molecular Genetics|December 13, 2005
Spastin and atlastin, two proteins mutated in autosomal-dominant hereditary spastic paraplegia, are binding partnersChristopher M Sanderson, James W Connell, Thomas L Edwards, et al.
Development (Cambridge, England)|August 8, 2018
BMP- and neuropilin 1-mediated motor axon navigation relies on spastin alternative translationNicolas Jardin, François Giudicelli, Daniel Ten Martín, et al.
Brain Communications|February 26, 2021
Evidence that autosomal recessive spastic cerebral palsy-1 (CPSQ1) is caused by a missense variant in <i>HPDL</i>Neil V Morgan, Bryndis Yngvadottir, Mary O'Driscoll, et al.
American Journal of Human Genetics|December 13, 2006
Mutations in the KIAA0196 gene at the SPG8 locus cause hereditary spastic paraplegiaPaul N Valdmanis, Inge A Meijer, Annie Reynolds, et al.
Human Molecular Genetics|July 22, 2009
The hereditary spastic paraplegia proteins NIPA1, spastin and spartin are inhibitors of mammalian BMP signallingHilda T H Tsang, Thomas L Edwards, Xinnan Wang, et al.
Pageof 5