Search research articles
Contact Us
Filters
Showing results (81-90 of 91) with videos related to
Page
of 10
Sort By:
American Journal of Human Genetics
|
May 22, 2012
Strikingly different clinicopathological phenotypes determined by progranulin-mutation dosage
Katherine R Smith, John Damiano, Silvana Franceschetti, et al.
Nature Communications
|
June 4, 2014
ER-mitochondria associations are regulated by the VAPB-PTPIP51 interaction and are disrupted by ALS/FTD-associated TDP-43
Radu Stoica, Kurt J De Vos, Sébastien Paillusson, et al.
Human Molecular Genetics
|
February 14, 2004
CHIP and Hsp70 regulate tau ubiquitination, degradation and aggregation
Leonard Petrucelli, Dennis Dickson, Kathryn Kehoe, et al.
Acta Neuropathologica
|
April 28, 2012
Neuronal sensitivity to TDP-43 overexpression is dependent on timing of induction
Ashley Cannon, Baoli Yang, Joshua Knight, et al.
Acta Neuropathologica
|
May 14, 2013
Robust cytoplasmic accumulation of phosphorylated TDP-43 in transgenic models of tauopathy
Amy K Clippinger, Simon D'Alton, Wen-Lang Lin, et al.
Neurobiology of Disease
|
June 20, 2026
Robust tauopathy and memory deficits in a mouse model constitutively overexpressing human P301L MAPT
Matthew J Hamm, Kevin McNaught, Christopher Janus, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
February 18, 2026
Progressive Supranuclear Palsy PERK haplotype B selectively translates DLX1 promoting tau toxicity
Christian B Lessard, Diego Rubio Rubio, Samantha Tolton, et al.
Biorxiv : the Preprint Server for Biology
|
July 9, 2025
Progressive Supranuclear Palsy PERK haplotype B selectively translates DLX1 promoting tau toxicity
Christian B Lessard, Diego Rubio-Rubio, Samantha Tolton, et al.
Human Molecular Genetics
|
February 9, 2013
Atp13a2-deficient mice exhibit neuronal ceroid lipofuscinosis, limited α-synuclein accumulation and age-dependent sensorimotor deficits
Patrick J Schultheis, Sheila M Fleming, Amy K Clippinger, et al.
Plos One
|
May 4, 2017
A KCNC3 mutation causes a neurodevelopmental, non-progressive SCA13 subtype associated with dominant negative effects and aberrant EGFR trafficking
Swati Khare, Jerelyn A Nick, Yalan Zhang, et al.
Page
of 10
Search research articles
Search
Showing results (81-90 of 91) with videos related to
Sort By:
Page
of 10
American Journal of Human Genetics
|
May 22, 2012
Strikingly different clinicopathological phenotypes determined by progranulin-mutation dosage
Katherine R Smith, John Damiano, Silvana Franceschetti, et al.
Nature Communications
|
June 4, 2014
ER-mitochondria associations are regulated by the VAPB-PTPIP51 interaction and are disrupted by ALS/FTD-associated TDP-43
Radu Stoica, Kurt J De Vos, Sébastien Paillusson, et al.
Human Molecular Genetics
|
February 14, 2004
CHIP and Hsp70 regulate tau ubiquitination, degradation and aggregation
Leonard Petrucelli, Dennis Dickson, Kathryn Kehoe, et al.
Acta Neuropathologica
|
April 28, 2012
Neuronal sensitivity to TDP-43 overexpression is dependent on timing of induction
Ashley Cannon, Baoli Yang, Joshua Knight, et al.
Acta Neuropathologica
|
May 14, 2013
Robust cytoplasmic accumulation of phosphorylated TDP-43 in transgenic models of tauopathy
Amy K Clippinger, Simon D'Alton, Wen-Lang Lin, et al.
Neurobiology of Disease
|
June 20, 2026
Robust tauopathy and memory deficits in a mouse model constitutively overexpressing human P301L MAPT
Matthew J Hamm, Kevin McNaught, Christopher Janus, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
February 18, 2026
Progressive Supranuclear Palsy PERK haplotype B selectively translates DLX1 promoting tau toxicity
Christian B Lessard, Diego Rubio Rubio, Samantha Tolton, et al.
Biorxiv : the Preprint Server for Biology
|
July 9, 2025
Progressive Supranuclear Palsy PERK haplotype B selectively translates DLX1 promoting tau toxicity
Christian B Lessard, Diego Rubio-Rubio, Samantha Tolton, et al.
Human Molecular Genetics
|
February 9, 2013
Atp13a2-deficient mice exhibit neuronal ceroid lipofuscinosis, limited α-synuclein accumulation and age-dependent sensorimotor deficits
Patrick J Schultheis, Sheila M Fleming, Amy K Clippinger, et al.
Plos One
|
May 4, 2017
A KCNC3 mutation causes a neurodevelopmental, non-progressive SCA13 subtype associated with dominant negative effects and aberrant EGFR trafficking
Swati Khare, Jerelyn A Nick, Yalan Zhang, et al.
Page
of 10