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Showing results (361-370 of 396) with videos related to

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Science Advances|May 5, 2023
Short tandem repeat expansions in sporadic amyotrophic lateral sclerosis and frontotemporal dementiaLyndal Henden, Liam G Fearnley, Natalie Grima, et al.
Science (New York, N.Y.)|March 3, 2009
Mutations in FUS, an RNA processing protein, cause familial amyotrophic lateral sclerosis type 6Caroline Vance, Boris Rogelj, Tibor Hortobágyi, et al.
Nature|January 27, 2022
Brahma safeguards canalization of cardiac mesoderm differentiationSwetansu K Hota, Kavitha S Rao, Andrew P Blair, et al.
Human Molecular Genetics|May 21, 2026
Ultra-rare variants in LAMA2 are risk factors for frontotemporal dementia and motor neuron diseaseHiu Chuen Lok, Carol Dobson-Stone, Marianne Hallupp, et al.
Cellular and Molecular Life Sciences : CMLS|August 31, 2017
Pathogenic mutation in the ALS/FTD gene, CCNF, causes elevated Lys48-linked ubiquitylation and defective autophagyAlbert Lee, Stephanie L Rayner, Serene S L Gwee, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 27, 2011
Loss of the retinoblastoma binding protein 2 (RBP2) histone demethylase suppresses tumorigenesis in mice lacking Rb1 or Men1Wenchu Lin, Jian Cao, Jiayun Liu, et al.
Molecular Neurodegeneration|September 10, 2020
Impaired NHEJ repair in amyotrophic lateral sclerosis is associated with TDP-43 mutationsAnna Konopka, Donna R Whelan, Md Shafi Jamali, et al.
Frontiers in Molecular Neuroscience|May 14, 2021
Unbiased Label-Free Quantitative Proteomics of Cells Expressing Amyotrophic Lateral Sclerosis (ALS) Mutations in <i>CCNF</i> Reveals Activation of the Apoptosis Pathway: A Workflow to Screen Pathogenic Gene MutationsFlora Cheng, Alana De Luca, Alison L Hogan, et al.
Brain : a Journal of Neurology|May 5, 2022
Altered SOD1 maturation and post-translational modification in amyotrophic lateral sclerosis spinal cordBenjamin G Trist, Sian Genoud, Stéphane Roudeau, et al.
European Journal of Human Genetics : EJHG|April 28, 2021
Polygenic risk score analysis for amyotrophic lateral sclerosis leveraging cognitive performance, educational attainment and schizophreniaRestuadi Restuadi, Fleur C Garton, Beben Benyamin, et al.
Pageof 40

Showing results (361-370 of 396) with videos related to

Sort By:
Pageof 40
Science Advances|May 5, 2023
Short tandem repeat expansions in sporadic amyotrophic lateral sclerosis and frontotemporal dementiaLyndal Henden, Liam G Fearnley, Natalie Grima, et al.
Science (New York, N.Y.)|March 3, 2009
Mutations in FUS, an RNA processing protein, cause familial amyotrophic lateral sclerosis type 6Caroline Vance, Boris Rogelj, Tibor Hortobágyi, et al.
Nature|January 27, 2022
Brahma safeguards canalization of cardiac mesoderm differentiationSwetansu K Hota, Kavitha S Rao, Andrew P Blair, et al.
Human Molecular Genetics|May 21, 2026
Ultra-rare variants in LAMA2 are risk factors for frontotemporal dementia and motor neuron diseaseHiu Chuen Lok, Carol Dobson-Stone, Marianne Hallupp, et al.
Cellular and Molecular Life Sciences : CMLS|August 31, 2017
Pathogenic mutation in the ALS/FTD gene, CCNF, causes elevated Lys48-linked ubiquitylation and defective autophagyAlbert Lee, Stephanie L Rayner, Serene S L Gwee, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 27, 2011
Loss of the retinoblastoma binding protein 2 (RBP2) histone demethylase suppresses tumorigenesis in mice lacking Rb1 or Men1Wenchu Lin, Jian Cao, Jiayun Liu, et al.
Molecular Neurodegeneration|September 10, 2020
Impaired NHEJ repair in amyotrophic lateral sclerosis is associated with TDP-43 mutationsAnna Konopka, Donna R Whelan, Md Shafi Jamali, et al.
Frontiers in Molecular Neuroscience|May 14, 2021
Unbiased Label-Free Quantitative Proteomics of Cells Expressing Amyotrophic Lateral Sclerosis (ALS) Mutations in <i>CCNF</i> Reveals Activation of the Apoptosis Pathway: A Workflow to Screen Pathogenic Gene MutationsFlora Cheng, Alana De Luca, Alison L Hogan, et al.
Brain : a Journal of Neurology|May 5, 2022
Altered SOD1 maturation and post-translational modification in amyotrophic lateral sclerosis spinal cordBenjamin G Trist, Sian Genoud, Stéphane Roudeau, et al.
European Journal of Human Genetics : EJHG|April 28, 2021
Polygenic risk score analysis for amyotrophic lateral sclerosis leveraging cognitive performance, educational attainment and schizophreniaRestuadi Restuadi, Fleur C Garton, Beben Benyamin, et al.
Pageof 40