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Molecular Therapy. Nucleic Acids
|
February 12, 2021
Targeting the 5' untranslated region of <i>SMN2</i> as a therapeutic strategy for spinal muscular atrophy
Audrey M Winkelsas, Christopher Grunseich, George G Harmison, et al.
Human Molecular Genetics
|
August 14, 2010
SMN deficiency disrupts brain development in a mouse model of severe spinal muscular atrophy
Thomas M Wishart, Jack P-W Huang, Lyndsay M Murray, et al.
Ebiomedicine
|
August 13, 2022
Targeting phosphoglycerate kinase 1 with terazosin improves motor neuron phenotypes in multiple models of amyotrophic lateral sclerosis
Helena Chaytow, Emily Carroll, David Gordon, et al.
EMBO Molecular Medicine
|
September 19, 2023
PRMT inhibitor promotes SMN2 exon 7 inclusion and synergizes with nusinersen to rescue SMA mice
Anna J Kordala, Jessica Stoodley, Nina Ahlskog, et al.
Plos Genetics
|
December 7, 2011
Charcot-Marie-Tooth-linked mutant GARS is toxic to peripheral neurons independent of wild-type GARS levels
William W Motley, Kevin L Seburn, Mir Hussain Nawaz, et al.
Human Brain Mapping
|
January 4, 2008
Investigation of white matter pathology in ALS and PLS using tract-based spatial statistics
Olga Ciccarelli, Timothy E Behrens, Heidi Johansen-Berg, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
September 14, 2016
Systemic peptide-mediated oligonucleotide therapy improves long-term survival in spinal muscular atrophy
Suzan M Hammond, Gareth Hazell, Fazel Shabanpoor, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration
|
July 25, 2022
Measuring disability in amyotrophic lateral sclerosis/motor neuron disease: the WHODAS 2.0-36, WHODAS 2.0-32, and WHODAS 2.0-12
Carolyn A Young, John Ealing, Christopher J McDermott, et al.
Human Molecular Genetics
|
August 16, 2011
Reversible molecular pathology of skeletal muscle in spinal muscular atrophy
Chantal A Mutsaers, Thomas M Wishart, Douglas J Lamont, et al.
Annals of Clinical and Translational Neurology
|
April 25, 2015
Identification of distinct circulating exosomes in Parkinson's disease
Paul R Tomlinson, Ying Zheng, Roman Fischer, et al.
Page
of 26
Search research articles
Search
Showing results (181-190 of 255) with videos related to
Sort By:
Page
of 26
Molecular Therapy. Nucleic Acids
|
February 12, 2021
Targeting the 5' untranslated region of <i>SMN2</i> as a therapeutic strategy for spinal muscular atrophy
Audrey M Winkelsas, Christopher Grunseich, George G Harmison, et al.
Human Molecular Genetics
|
August 14, 2010
SMN deficiency disrupts brain development in a mouse model of severe spinal muscular atrophy
Thomas M Wishart, Jack P-W Huang, Lyndsay M Murray, et al.
Ebiomedicine
|
August 13, 2022
Targeting phosphoglycerate kinase 1 with terazosin improves motor neuron phenotypes in multiple models of amyotrophic lateral sclerosis
Helena Chaytow, Emily Carroll, David Gordon, et al.
EMBO Molecular Medicine
|
September 19, 2023
PRMT inhibitor promotes SMN2 exon 7 inclusion and synergizes with nusinersen to rescue SMA mice
Anna J Kordala, Jessica Stoodley, Nina Ahlskog, et al.
Plos Genetics
|
December 7, 2011
Charcot-Marie-Tooth-linked mutant GARS is toxic to peripheral neurons independent of wild-type GARS levels
William W Motley, Kevin L Seburn, Mir Hussain Nawaz, et al.
Human Brain Mapping
|
January 4, 2008
Investigation of white matter pathology in ALS and PLS using tract-based spatial statistics
Olga Ciccarelli, Timothy E Behrens, Heidi Johansen-Berg, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
September 14, 2016
Systemic peptide-mediated oligonucleotide therapy improves long-term survival in spinal muscular atrophy
Suzan M Hammond, Gareth Hazell, Fazel Shabanpoor, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration
|
July 25, 2022
Measuring disability in amyotrophic lateral sclerosis/motor neuron disease: the WHODAS 2.0-36, WHODAS 2.0-32, and WHODAS 2.0-12
Carolyn A Young, John Ealing, Christopher J McDermott, et al.
Human Molecular Genetics
|
August 16, 2011
Reversible molecular pathology of skeletal muscle in spinal muscular atrophy
Chantal A Mutsaers, Thomas M Wishart, Douglas J Lamont, et al.
Annals of Clinical and Translational Neurology
|
April 25, 2015
Identification of distinct circulating exosomes in Parkinson's disease
Paul R Tomlinson, Ying Zheng, Roman Fischer, et al.
Page
of 26