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John E Landers

Showing results (1-10 of 100) with videos related to

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Methods in Molecular Biology (Clifton, N.J.)|April 22, 2009
High-throughput mutation screening using a single amplification conditionLijia Shi, John E Landers
Neurogenetics|March 30, 2010
RNA processing pathways in amyotrophic lateral sclerosisMarka van Blitterswijk, John E Landers
CNS & Neurological Disorders Drug Targets|October 15, 2010
Genetic determinants of amyotrophic lateral sclerosis as therapeutic targetsDaryl A Bosco, John E Landers
Iscience|June 1, 2026
Global transcriptional changes across multiple isogenic <i>C9orf72</i> patient iPSC-derived neuronsAparna Sreeram, Desiree M Baron, Alberto Brusati, et al.
Nucleic Acids Research|January 8, 2005
A simple, bead-based approach for multi-SNP molecular haplotypingJames D Hurley, Linda J Engle, Jesse T Davis, et al.
Human Molecular Genetics|April 6, 2017
A Drosophila model of ALS reveals a partial loss of function of causative human PFN1 mutantsChi-Hong Wu, Anthony Giampetruzzi, Helene Tran, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 30, 2016
Mutant PFN1 causes ALS phenotypes and progressive motor neuron degeneration in mice by a gain of toxicityChunxing Yang, Eric W Danielson, Tao Qiao, et al.
Nature Reviews. Genetics|April 6, 2023
Amyotrophic lateral sclerosis: translating genetic discoveries into therapiesFulya Akçimen, Elia R Lopez, John E Landers, et al.
Biochimica Et Biophysica Acta. Gene Regulatory Mechanisms|August 6, 2019
TDP-43 and NOVA-1 RNA-binding proteins as competitive splicing regulators of the schizophrenia-associated TNIK geneValentina Gumina, Claudia Colombrita, Claudia Fallini, et al.
The Journal of Biological Chemistry|May 17, 2019
The RNA-binding protein FUS/TLS undergoes calcium-mediated nuclear egress during excitotoxic stress and is required for <i>GRIA2</i> mRNA processingMaeve Tischbein, Desiree M Baron, Yen-Chen Lin, et al.
Pageof 10

Showing results (1-10 of 100) with videos related to

Sort By:
Pageof 10
Methods in Molecular Biology (Clifton, N.J.)|April 22, 2009
High-throughput mutation screening using a single amplification conditionLijia Shi, John E Landers
Neurogenetics|March 30, 2010
RNA processing pathways in amyotrophic lateral sclerosisMarka van Blitterswijk, John E Landers
CNS & Neurological Disorders Drug Targets|October 15, 2010
Genetic determinants of amyotrophic lateral sclerosis as therapeutic targetsDaryl A Bosco, John E Landers
Iscience|June 1, 2026
Global transcriptional changes across multiple isogenic <i>C9orf72</i> patient iPSC-derived neuronsAparna Sreeram, Desiree M Baron, Alberto Brusati, et al.
Nucleic Acids Research|January 8, 2005
A simple, bead-based approach for multi-SNP molecular haplotypingJames D Hurley, Linda J Engle, Jesse T Davis, et al.
Human Molecular Genetics|April 6, 2017
A Drosophila model of ALS reveals a partial loss of function of causative human PFN1 mutantsChi-Hong Wu, Anthony Giampetruzzi, Helene Tran, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 30, 2016
Mutant PFN1 causes ALS phenotypes and progressive motor neuron degeneration in mice by a gain of toxicityChunxing Yang, Eric W Danielson, Tao Qiao, et al.
Nature Reviews. Genetics|April 6, 2023
Amyotrophic lateral sclerosis: translating genetic discoveries into therapiesFulya Akçimen, Elia R Lopez, John E Landers, et al.
Biochimica Et Biophysica Acta. Gene Regulatory Mechanisms|August 6, 2019
TDP-43 and NOVA-1 RNA-binding proteins as competitive splicing regulators of the schizophrenia-associated TNIK geneValentina Gumina, Claudia Colombrita, Claudia Fallini, et al.
The Journal of Biological Chemistry|May 17, 2019
The RNA-binding protein FUS/TLS undergoes calcium-mediated nuclear egress during excitotoxic stress and is required for <i>GRIA2</i> mRNA processingMaeve Tischbein, Desiree M Baron, Yen-Chen Lin, et al.
Pageof 10