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Handbook of Clinical Neurology
|
February 27, 2018
Spinal muscular atrophy
Eveline S Arnold, Kenneth H Fischbeck
Neurobiology of Disease
|
January 22, 2016
CNS uptake of bortezomib is enhanced by P-glycoprotein inhibition: implications for spinal muscular atrophy
Emily Foran, Deborah Y Kwon, Jonathan H Nofziger, et al.
Cell Reports
|
May 12, 2021
A high-throughput genome-wide RNAi screen identifies modifiers of survival motor neuron protein
Nikki M McCormack, Mahlet B Abera, Eveline S Arnold, et al.
Acta Neuropathologica Communications
|
June 26, 2015
Wild type human TDP-43 potentiates ALS-linked mutant TDP-43 driven progressive motor and cortical neuron degeneration with pathological features of ALS
Jacqueline C Mitchell, Remy Constable, Eva So, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
February 6, 2013
ALS-linked TDP-43 mutations produce aberrant RNA splicing and adult-onset motor neuron disease without aggregation or loss of nuclear TDP-43
Eveline S Arnold, Shuo-Chien Ling, Stephanie C Huelga, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 5) with videos related to
Sort By:
Page
of 1
Handbook of Clinical Neurology
|
February 27, 2018
Spinal muscular atrophy
Eveline S Arnold, Kenneth H Fischbeck
Neurobiology of Disease
|
January 22, 2016
CNS uptake of bortezomib is enhanced by P-glycoprotein inhibition: implications for spinal muscular atrophy
Emily Foran, Deborah Y Kwon, Jonathan H Nofziger, et al.
Cell Reports
|
May 12, 2021
A high-throughput genome-wide RNAi screen identifies modifiers of survival motor neuron protein
Nikki M McCormack, Mahlet B Abera, Eveline S Arnold, et al.
Acta Neuropathologica Communications
|
June 26, 2015
Wild type human TDP-43 potentiates ALS-linked mutant TDP-43 driven progressive motor and cortical neuron degeneration with pathological features of ALS
Jacqueline C Mitchell, Remy Constable, Eva So, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
February 6, 2013
ALS-linked TDP-43 mutations produce aberrant RNA splicing and adult-onset motor neuron disease without aggregation or loss of nuclear TDP-43
Eveline S Arnold, Shuo-Chien Ling, Stephanie C Huelga, et al.
Page
of 1