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Methods in Molecular Biology (Clifton, N.J.)
|
April 22, 2009
High-throughput mutation screening using a single amplification condition
Lijia Shi, John E Landers
Neurogenetics
|
March 30, 2010
RNA processing pathways in amyotrophic lateral sclerosis
Marka van Blitterswijk, John E Landers
CNS & Neurological Disorders Drug Targets
|
October 15, 2010
Genetic determinants of amyotrophic lateral sclerosis as therapeutic targets
Daryl A Bosco, John E Landers
Iscience
|
June 1, 2026
Global transcriptional changes across multiple isogenic <i>C9orf72</i> patient iPSC-derived neurons
Aparna Sreeram, Desiree M Baron, Alberto Brusati, et al.
Nucleic Acids Research
|
January 8, 2005
A simple, bead-based approach for multi-SNP molecular haplotyping
James 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 mutants
Chi-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 toxicity
Chunxing Yang, Eric W Danielson, Tao Qiao, et al.
Nature Reviews. Genetics
|
April 6, 2023
Amyotrophic lateral sclerosis: translating genetic discoveries into therapies
Fulya 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 gene
Valentina 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 processing
Maeve Tischbein, Desiree M Baron, Yen-Chen Lin, et al.
Page
of 10
Search research articles
Search
Showing results (1-10 of 100) with videos related to
Sort By:
Page
of 10
Methods in Molecular Biology (Clifton, N.J.)
|
April 22, 2009
High-throughput mutation screening using a single amplification condition
Lijia Shi, John E Landers
Neurogenetics
|
March 30, 2010
RNA processing pathways in amyotrophic lateral sclerosis
Marka van Blitterswijk, John E Landers
CNS & Neurological Disorders Drug Targets
|
October 15, 2010
Genetic determinants of amyotrophic lateral sclerosis as therapeutic targets
Daryl A Bosco, John E Landers
Iscience
|
June 1, 2026
Global transcriptional changes across multiple isogenic <i>C9orf72</i> patient iPSC-derived neurons
Aparna Sreeram, Desiree M Baron, Alberto Brusati, et al.
Nucleic Acids Research
|
January 8, 2005
A simple, bead-based approach for multi-SNP molecular haplotyping
James 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 mutants
Chi-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 toxicity
Chunxing Yang, Eric W Danielson, Tao Qiao, et al.
Nature Reviews. Genetics
|
April 6, 2023
Amyotrophic lateral sclerosis: translating genetic discoveries into therapies
Fulya 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 gene
Valentina 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 processing
Maeve Tischbein, Desiree M Baron, Yen-Chen Lin, et al.
Page
of 10