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Nature Medicine
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March 2, 2016
Major histocompatibility complex class I molecules protect motor neurons from astrocyte-induced toxicity in amyotrophic lateral sclerosis
SungWon Song, Carlos J Miranda, Lyndsey Braun, et al.
Human Molecular Genetics
|
July 20, 2010
Early heart failure in the SMNDelta7 model of spinal muscular atrophy and correction by postnatal scAAV9-SMN delivery
Adam K Bevan, Kirk R Hutchinson, Kevin D Foust, et al.
Nature Biotechnology
|
March 2, 2010
Rescue of the spinal muscular atrophy phenotype in a mouse model by early postnatal delivery of SMN
Kevin D Foust, Xueyong Wang, Vicki L McGovern, et al.
Nature Biotechnology
|
October 6, 2022
Retraction Note: Rescue of the spinal muscular atrophy phenotype in a mouse model by early postnatal delivery of SMN
Kevin D Foust, Xueyong Wang, Vicki L McGovern, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
November 1, 2014
Improving single injection CSF delivery of AAV9-mediated gene therapy for SMA: a dose-response study in mice and nonhuman primates
Kathrin Meyer, Laura Ferraiuolo, Leah Schmelzer, et al.
Human Molecular Genetics
|
April 11, 2015
SMN deficiency disrupts gastrointestinal and enteric nervous system function in mice
Sara E Gombash, Christopher J Cowley, Julie A Fitzgerald, et al.
Human Molecular Genetics
|
July 31, 2015
SMN deficiency disrupts gastrointestinal and enteric nervous system function in mice
Sara E Gombash, Christopher J Cowley, Julie A Fitzgerald, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
March 12, 2009
Nigrostriatal rAAV-mediated GDNF overexpression induces robust weight loss in a rat model of age-related obesity
Fredric P Manfredsson, Nihal Tumer, Benedek Erdos, et al.
Neuron
|
March 11, 2014
Microglia induce motor neuron death via the classical NF-κB pathway in amyotrophic lateral sclerosis
Ashley E Frakes, Laura Ferraiuolo, Amanda M Haidet-Phillips, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
July 23, 2023
Novel MECP2 gene therapy is effective in a multicenter study using two mouse models of Rett syndrome and is safe in non-human primates
Samantha Powers, Shibi Likhite, Kamal K Gadalla, et al.
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of 4
Search research articles
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Showing results (21-30 of 33) with videos related to
Sort By:
Page
of 4
Nature Medicine
|
March 2, 2016
Major histocompatibility complex class I molecules protect motor neurons from astrocyte-induced toxicity in amyotrophic lateral sclerosis
SungWon Song, Carlos J Miranda, Lyndsey Braun, et al.
Human Molecular Genetics
|
July 20, 2010
Early heart failure in the SMNDelta7 model of spinal muscular atrophy and correction by postnatal scAAV9-SMN delivery
Adam K Bevan, Kirk R Hutchinson, Kevin D Foust, et al.
Nature Biotechnology
|
March 2, 2010
Rescue of the spinal muscular atrophy phenotype in a mouse model by early postnatal delivery of SMN
Kevin D Foust, Xueyong Wang, Vicki L McGovern, et al.
Nature Biotechnology
|
October 6, 2022
Retraction Note: Rescue of the spinal muscular atrophy phenotype in a mouse model by early postnatal delivery of SMN
Kevin D Foust, Xueyong Wang, Vicki L McGovern, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
November 1, 2014
Improving single injection CSF delivery of AAV9-mediated gene therapy for SMA: a dose-response study in mice and nonhuman primates
Kathrin Meyer, Laura Ferraiuolo, Leah Schmelzer, et al.
Human Molecular Genetics
|
April 11, 2015
SMN deficiency disrupts gastrointestinal and enteric nervous system function in mice
Sara E Gombash, Christopher J Cowley, Julie A Fitzgerald, et al.
Human Molecular Genetics
|
July 31, 2015
SMN deficiency disrupts gastrointestinal and enteric nervous system function in mice
Sara E Gombash, Christopher J Cowley, Julie A Fitzgerald, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
March 12, 2009
Nigrostriatal rAAV-mediated GDNF overexpression induces robust weight loss in a rat model of age-related obesity
Fredric P Manfredsson, Nihal Tumer, Benedek Erdos, et al.
Neuron
|
March 11, 2014
Microglia induce motor neuron death via the classical NF-κB pathway in amyotrophic lateral sclerosis
Ashley E Frakes, Laura Ferraiuolo, Amanda M Haidet-Phillips, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
July 23, 2023
Novel MECP2 gene therapy is effective in a multicenter study using two mouse models of Rett syndrome and is safe in non-human primates
Samantha Powers, Shibi Likhite, Kamal K Gadalla, et al.
Page
of 4