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Scientific Reports
|
July 5, 2019
FGF family members differentially regulate maturation and proliferation of stem cell-derived astrocytes
Ekaterina Savchenko, Gabriel N Teku, Antonio Boza-Serrano, et al.
The Journal of Experimental Medicine
|
February 20, 2008
Glutamate mediates platelet activation through the AMPA receptor
Craig N Morrell, Henry Sun, Masahiro Ikeda, et al.
Muscle & Nerve
|
June 6, 2025
Efficacy and Safety of Once Daily Dosing vs. Approved On/Off Dosing of Edaravone Oral Suspension Up to 48 Weeks in Patients With Amyotrophic Lateral Sclerosis (Study MT-1186-A02)
Jeffrey Rothstein, Angela Genge, Shari De Silva, et al.
Muscle & Nerve
|
December 23, 2025
Phase 3b Extension Study MT-1186-A04 to Evaluate the Continued Efficacy and Safety of Edaravone Oral Suspension for Up to an Additional 48 Weeks in Patients With Amyotrophic Lateral Sclerosis
Angela Genge, Jeffrey Rothstein, Shari De Silva, et al.
Science Translational Medicine
|
October 2, 2015
Human endogenous retrovirus-K contributes to motor neuron disease
Wenxue Li, Myoung-Hwa Lee, Lisa Henderson, et al.
Cell Reports
|
May 31, 2016
Concordant but Varied Phenotypes among Duchenne Muscular Dystrophy Patient-Specific Myoblasts Derived using a Human iPSC-Based Model
In Young Choi, HoTae Lim, Kenneth Estrellas, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration
|
May 18, 2013
Deciphering amyotrophic lateral sclerosis: what phenotype, neuropathology and genetics are telling us about pathogenesis
John Ravits, Stanley Appel, Robert H Baloh, et al.
Scientific Data
|
January 11, 2023
NeuroLINCS Proteomics: Defining human-derived iPSC proteomes and protein signatures of pluripotency
Andrea D Matlock, Vineet Vaibhav, Ronald Holewinski, et al.
The Lancet. Neurology
|
March 17, 2007
Genome-wide genotyping in amyotrophic lateral sclerosis and neurologically normal controls: first stage analysis and public release of data
Jennifer C Schymick, Sonja W Scholz, Hon-Chung Fung, et al.
The Lancet. Neurology
|
April 2, 2013
An antisense oligonucleotide against SOD1 delivered intrathecally for patients with SOD1 familial amyotrophic lateral sclerosis: a phase 1, randomised, first-in-man study
Timothy M Miller, Alan Pestronk, William David, et al.
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Search research articles
Search
Showing results (11-20 of 28) with videos related to
Sort By:
Page
of 3
Scientific Reports
|
July 5, 2019
FGF family members differentially regulate maturation and proliferation of stem cell-derived astrocytes
Ekaterina Savchenko, Gabriel N Teku, Antonio Boza-Serrano, et al.
The Journal of Experimental Medicine
|
February 20, 2008
Glutamate mediates platelet activation through the AMPA receptor
Craig N Morrell, Henry Sun, Masahiro Ikeda, et al.
Muscle & Nerve
|
June 6, 2025
Efficacy and Safety of Once Daily Dosing vs. Approved On/Off Dosing of Edaravone Oral Suspension Up to 48 Weeks in Patients With Amyotrophic Lateral Sclerosis (Study MT-1186-A02)
Jeffrey Rothstein, Angela Genge, Shari De Silva, et al.
Muscle & Nerve
|
December 23, 2025
Phase 3b Extension Study MT-1186-A04 to Evaluate the Continued Efficacy and Safety of Edaravone Oral Suspension for Up to an Additional 48 Weeks in Patients With Amyotrophic Lateral Sclerosis
Angela Genge, Jeffrey Rothstein, Shari De Silva, et al.
Science Translational Medicine
|
October 2, 2015
Human endogenous retrovirus-K contributes to motor neuron disease
Wenxue Li, Myoung-Hwa Lee, Lisa Henderson, et al.
Cell Reports
|
May 31, 2016
Concordant but Varied Phenotypes among Duchenne Muscular Dystrophy Patient-Specific Myoblasts Derived using a Human iPSC-Based Model
In Young Choi, HoTae Lim, Kenneth Estrellas, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration
|
May 18, 2013
Deciphering amyotrophic lateral sclerosis: what phenotype, neuropathology and genetics are telling us about pathogenesis
John Ravits, Stanley Appel, Robert H Baloh, et al.
Scientific Data
|
January 11, 2023
NeuroLINCS Proteomics: Defining human-derived iPSC proteomes and protein signatures of pluripotency
Andrea D Matlock, Vineet Vaibhav, Ronald Holewinski, et al.
The Lancet. Neurology
|
March 17, 2007
Genome-wide genotyping in amyotrophic lateral sclerosis and neurologically normal controls: first stage analysis and public release of data
Jennifer C Schymick, Sonja W Scholz, Hon-Chung Fung, et al.
The Lancet. Neurology
|
April 2, 2013
An antisense oligonucleotide against SOD1 delivered intrathecally for patients with SOD1 familial amyotrophic lateral sclerosis: a phase 1, randomised, first-in-man study
Timothy M Miller, Alan Pestronk, William David, et al.
Page
of 3