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Neuro-Degenerative Diseases
|
June 20, 2016
Novel Compound Heterozygous Spatacsin Mutations in a Greek Kindred with Hereditary Spastic Paraplegia SPG11 and Dementia
Matthew J Fraidakis, Maura Brunetti, Craig Blackstone, et al.
The Journal of Clinical Investigation
|
March 5, 2010
Hereditary spastic paraplegia proteins REEP1, spastin, and atlastin-1 coordinate microtubule interactions with the tubular ER network
Seong H Park, Peng-Peng Zhu, Rell L Parker, et al.
The Journal of Biological Chemistry
|
August 24, 2005
Release of OPA1 during apoptosis participates in the rapid and complete release of cytochrome c and subsequent mitochondrial fragmentation
Damien Arnoult, Alain Grodet, Yang-Ja Lee, et al.
Neurobiology of Disease
|
July 8, 2026
Mutation-specific cellular mechanisms in Drosophila models of ATL1-associated hereditary spastic paraplegia
Emma Cadoria, Anood Sohail, Breandan N Kennedy, et al.
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia
|
May 13, 2014
Ataxia with oculomotor apraxia type 2 fibroblasts exhibit increased susceptibility to oxidative DNA damage
Ricardo H Roda, Carlo Rinaldi, Rajat Singh, et al.
Molecular Biology of the Cell
|
September 28, 2012
MITD1 is recruited to midbodies by ESCRT-III and participates in cytokinesis
Seongju Lee, Jaerak Chang, Benoît Renvoisé, et al.
Archives of Neurology
|
April 17, 2008
Lack of spartin protein in Troyer syndrome: a loss-of-function disease mechanism?
Joanna C Bakowska, Heng Wang, Baozhong Xin, et al.
Annals of Clinical and Translational Neurology
|
September 9, 2016
Neurologic syndrome associated with homozygous mutation at MAG sialic acid binding site
Ricardo H Roda, Edmond J FitzGibbon, Houda Boucekkine, et al.
Neurogenetics
|
July 28, 2010
Targeted disruption of the Mast syndrome gene SPG21 in mice impairs hind limb function and alters axon branching in cultured cortical neurons
Cynthia Soderblom, Julia Stadler, Henri Jupille, et al.
Human Molecular Genetics
|
March 16, 2006
SPG3A protein atlastin-1 is enriched in growth cones and promotes axon elongation during neuronal development
Peng-Peng Zhu, Cynthia Soderblom, Jung-Hwa Tao-Cheng, et al.
Page
of 13
Search research articles
Search
Showing results (51-60 of 125) with videos related to
Sort By:
Page
of 13
Neuro-Degenerative Diseases
|
June 20, 2016
Novel Compound Heterozygous Spatacsin Mutations in a Greek Kindred with Hereditary Spastic Paraplegia SPG11 and Dementia
Matthew J Fraidakis, Maura Brunetti, Craig Blackstone, et al.
The Journal of Clinical Investigation
|
March 5, 2010
Hereditary spastic paraplegia proteins REEP1, spastin, and atlastin-1 coordinate microtubule interactions with the tubular ER network
Seong H Park, Peng-Peng Zhu, Rell L Parker, et al.
The Journal of Biological Chemistry
|
August 24, 2005
Release of OPA1 during apoptosis participates in the rapid and complete release of cytochrome c and subsequent mitochondrial fragmentation
Damien Arnoult, Alain Grodet, Yang-Ja Lee, et al.
Neurobiology of Disease
|
July 8, 2026
Mutation-specific cellular mechanisms in Drosophila models of ATL1-associated hereditary spastic paraplegia
Emma Cadoria, Anood Sohail, Breandan N Kennedy, et al.
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia
|
May 13, 2014
Ataxia with oculomotor apraxia type 2 fibroblasts exhibit increased susceptibility to oxidative DNA damage
Ricardo H Roda, Carlo Rinaldi, Rajat Singh, et al.
Molecular Biology of the Cell
|
September 28, 2012
MITD1 is recruited to midbodies by ESCRT-III and participates in cytokinesis
Seongju Lee, Jaerak Chang, Benoît Renvoisé, et al.
Archives of Neurology
|
April 17, 2008
Lack of spartin protein in Troyer syndrome: a loss-of-function disease mechanism?
Joanna C Bakowska, Heng Wang, Baozhong Xin, et al.
Annals of Clinical and Translational Neurology
|
September 9, 2016
Neurologic syndrome associated with homozygous mutation at MAG sialic acid binding site
Ricardo H Roda, Edmond J FitzGibbon, Houda Boucekkine, et al.
Neurogenetics
|
July 28, 2010
Targeted disruption of the Mast syndrome gene SPG21 in mice impairs hind limb function and alters axon branching in cultured cortical neurons
Cynthia Soderblom, Julia Stadler, Henri Jupille, et al.
Human Molecular Genetics
|
March 16, 2006
SPG3A protein atlastin-1 is enriched in growth cones and promotes axon elongation during neuronal development
Peng-Peng Zhu, Cynthia Soderblom, Jung-Hwa Tao-Cheng, et al.
Page
of 13