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Muscle & Nerve
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May 10, 2005
Gait analysis detects early changes in transgenic SOD1(G93A) mice
Christine M Wooley, Roger B Sher, Ajit Kale, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology
|
September 11, 2008
The deacetylase HDAC4 controls myocyte enhancing factor-2-dependent structural gene expression in response to neural activity
Todd J Cohen, Tomasa Barrientos, Zachary C Hartman, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society
|
March 7, 2006
Grey, a novel mutation in the murine Lyst gene, causes the beige phenotype by skipping of exon 25
Fabian Runkel, Heinrich Büssow, Kevin L Seburn, et al.
Development (Cambridge, England)
|
June 2, 2016
Development-on-chip: in vitro neural tube patterning with a microfluidic device
Christopher J Demers, Prabakaran Soundararajan, Phaneendra Chennampally, et al.
Scientific Reports
|
September 14, 2021
A microfluidic approach to rescue ALS motor neuron degeneration using rapamycin
Phaneendra Chennampally, Ambreen Sayed-Zahid, Prabakaran Soundararajan, et al.
Human Molecular Genetics
|
August 11, 2024
Clinically relevant mouse models of severe spinal muscular atrophy with respiratory distress type 1
Sarah E Holbrook, Amy N Hicks, Paige B Martin, et al.
Nature Neuroscience
|
February 23, 2016
Hyperactive somatostatin interneurons contribute to excitotoxicity in neurodegenerative disorders
Wen Zhang, Lifeng Zhang, Bo Liang, et al.
Amino Acids
|
June 17, 2017
Analysis of BMAA enantiomers in cycads, cyanobacteria, and mammals: in vivo formation and toxicity of D-BMAA
J S Metcalf, Doug Lobner, Sandra Anne Banack, et al.
Cancer Genetics
|
June 12, 2012
Dystrophin and dysferlin double mutant mice: a novel model for rhabdomyosarcoma
Vishnu Hosur, Anoop Kavirayani, Jennifer Riefler, et al.
Human Molecular Genetics
|
June 20, 2019
Functional rescue in a mouse model of congenital muscular dystrophy with megaconial myopathy
Ambreen A Sayed-Zahid, Roger B Sher, Stacey J Sukoff Rizzo, et al.
Page
of 6
Search research articles
Search
Showing results (21-30 of 60) with videos related to
Sort By:
Page
of 6
Muscle & Nerve
|
May 10, 2005
Gait analysis detects early changes in transgenic SOD1(G93A) mice
Christine M Wooley, Roger B Sher, Ajit Kale, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology
|
September 11, 2008
The deacetylase HDAC4 controls myocyte enhancing factor-2-dependent structural gene expression in response to neural activity
Todd J Cohen, Tomasa Barrientos, Zachary C Hartman, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society
|
March 7, 2006
Grey, a novel mutation in the murine Lyst gene, causes the beige phenotype by skipping of exon 25
Fabian Runkel, Heinrich Büssow, Kevin L Seburn, et al.
Development (Cambridge, England)
|
June 2, 2016
Development-on-chip: in vitro neural tube patterning with a microfluidic device
Christopher J Demers, Prabakaran Soundararajan, Phaneendra Chennampally, et al.
Scientific Reports
|
September 14, 2021
A microfluidic approach to rescue ALS motor neuron degeneration using rapamycin
Phaneendra Chennampally, Ambreen Sayed-Zahid, Prabakaran Soundararajan, et al.
Human Molecular Genetics
|
August 11, 2024
Clinically relevant mouse models of severe spinal muscular atrophy with respiratory distress type 1
Sarah E Holbrook, Amy N Hicks, Paige B Martin, et al.
Nature Neuroscience
|
February 23, 2016
Hyperactive somatostatin interneurons contribute to excitotoxicity in neurodegenerative disorders
Wen Zhang, Lifeng Zhang, Bo Liang, et al.
Amino Acids
|
June 17, 2017
Analysis of BMAA enantiomers in cycads, cyanobacteria, and mammals: in vivo formation and toxicity of D-BMAA
J S Metcalf, Doug Lobner, Sandra Anne Banack, et al.
Cancer Genetics
|
June 12, 2012
Dystrophin and dysferlin double mutant mice: a novel model for rhabdomyosarcoma
Vishnu Hosur, Anoop Kavirayani, Jennifer Riefler, et al.
Human Molecular Genetics
|
June 20, 2019
Functional rescue in a mouse model of congenital muscular dystrophy with megaconial myopathy
Ambreen A Sayed-Zahid, Roger B Sher, Stacey J Sukoff Rizzo, et al.
Page
of 6