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Plos One
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February 18, 2010
ENU mutagenesis reveals a novel phenotype of reduced limb strength in mice lacking fibrillin 2
Gaynor Miller, Monica Neilan, Ruth Chia, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association
|
December 24, 2025
Basic Science and Pathogenesis
Danielle M Picarello, Devynn A Adams, Tulsi Patel, et al.
Neurology. Genetics
|
September 9, 2024
Genome-Wide and Transcriptome-Wide Association Studies on Northern New England and Ohio Amyotrophic Lateral Sclerosis Cohorts
Siting Li, Jiang Gui, Michael N Passarelli, et al.
Brain Research
|
June 16, 2025
Regulation of LRRK2 activity by metabolic stress and heavy metal exposure
Michalis Kentros, Jordan Follett, Nitya Subrahmanian, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
July 27, 2022
Systematic evaluation of genetic mutations in ALS: a population-based study
Maurizio Grassano, Andrea Calvo, Cristina Moglia, et al.
Biorxiv : the Preprint Server for Biology
|
February 6, 2026
Inflammatory signaling differentially changes chromatin accessibility and gene expression of the PD- associated kinase LRRK2 between human and mice
Alexandra Beilina, Jae-Hyeon Park, Natalie Landeck, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
January 25, 2022
Identification of genetic risk loci and prioritization of genes and pathways for myasthenia gravis: a genome-wide association study
Ruth Chia, Sara Saez-Atienzar, Natalie Murphy, et al.
Neurology
|
November 19, 2020
Mutational Analysis of Known ALS Genes in an Italian Population-Based Cohort
Maurizio Grassano, Andrea Calvo, Cristina Moglia, et al.
Science Advances
|
February 1, 2021
Genetic analysis of amyotrophic lateral sclerosis identifies contributing pathways and cell types
Sara Saez-Atienzar, Sara Bandres-Ciga, Rebekah G Langston, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
August 25, 2022
Exploring the phenotype of Italian patients with ALS with intermediate <i>ATXN2</i> polyQ repeats
Adriano Chio, Cristina Moglia, Antonio Canosa, et al.
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of 7
Search research articles
Search
Showing results (31-40 of 69) with videos related to
Sort By:
Page
of 7
Plos One
|
February 18, 2010
ENU mutagenesis reveals a novel phenotype of reduced limb strength in mice lacking fibrillin 2
Gaynor Miller, Monica Neilan, Ruth Chia, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association
|
December 24, 2025
Basic Science and Pathogenesis
Danielle M Picarello, Devynn A Adams, Tulsi Patel, et al.
Neurology. Genetics
|
September 9, 2024
Genome-Wide and Transcriptome-Wide Association Studies on Northern New England and Ohio Amyotrophic Lateral Sclerosis Cohorts
Siting Li, Jiang Gui, Michael N Passarelli, et al.
Brain Research
|
June 16, 2025
Regulation of LRRK2 activity by metabolic stress and heavy metal exposure
Michalis Kentros, Jordan Follett, Nitya Subrahmanian, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
July 27, 2022
Systematic evaluation of genetic mutations in ALS: a population-based study
Maurizio Grassano, Andrea Calvo, Cristina Moglia, et al.
Biorxiv : the Preprint Server for Biology
|
February 6, 2026
Inflammatory signaling differentially changes chromatin accessibility and gene expression of the PD- associated kinase LRRK2 between human and mice
Alexandra Beilina, Jae-Hyeon Park, Natalie Landeck, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
January 25, 2022
Identification of genetic risk loci and prioritization of genes and pathways for myasthenia gravis: a genome-wide association study
Ruth Chia, Sara Saez-Atienzar, Natalie Murphy, et al.
Neurology
|
November 19, 2020
Mutational Analysis of Known ALS Genes in an Italian Population-Based Cohort
Maurizio Grassano, Andrea Calvo, Cristina Moglia, et al.
Science Advances
|
February 1, 2021
Genetic analysis of amyotrophic lateral sclerosis identifies contributing pathways and cell types
Sara Saez-Atienzar, Sara Bandres-Ciga, Rebekah G Langston, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
August 25, 2022
Exploring the phenotype of Italian patients with ALS with intermediate <i>ATXN2</i> polyQ repeats
Adriano Chio, Cristina Moglia, Antonio Canosa, et al.
Page
of 7