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Jack Humphrey

Showing results (31-40 of 67) with videos related to

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Medrxiv : the Preprint Server for Health Sciences|March 17, 2025
SingleBrain: A Meta-Analysis of Single-Nucleus eQTLs Linking Genetic Risk to Brain DisordersBeomjin Jang, Kailash Bp, Alex Tokolyi, et al.
Nature Neuroscience|August 5, 2025
Alzheimer's disease transcriptional landscape in ex vivo human microgliaRoman Kosoy, John F Fullard, Jaroslav Bendl, et al.
Nature Genetics|August 5, 2022
Genetics of the human microglia regulome refines Alzheimer's disease risk lociRoman Kosoy, John F Fullard, Biao Zeng, et al.
Brain : a Journal of Neurology|October 21, 2017
Humanized mutant FUS drives progressive motor neuron degeneration without aggregation in 'FUSDelta14' knockin miceAnny Devoy, Bernadett Kalmar, Michelle Stewart, et al.
Science Advances|July 22, 2021
FUS-ALS mutants alter FMRP phase separation equilibrium and impair protein translationNicol Birsa, Agnieszka M Ule, Maria Giovanna Garone, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 6, 2023
An Autopsy Series of Seven Cases of VPS13A Disease (Chorea-Acanthocytosis)Ricky M Ditzel, Ruth H Walker, Melissa J Nirenberg, et al.
Biorxiv : the Preprint Server for Biology|February 5, 2024
TDP-43 loss induces extensive cryptic polyadenylation in ALS/FTDSam Bryce-Smith, Anna-Leigh Brown, Puja R Mehta, et al.
Molecular Neurodegeneration|August 17, 2022
Transcriptome deregulation of peripheral monocytes and whole blood in GBA-related Parkinson's diseaseGiulietta Maria Riboldi, Ricardo A Vialle, Elisa Navarro, et al.
Nucleic Acids Research|June 2, 2020
FUS ALS-causative mutations impair FUS autoregulation and splicing factor networks through intron retentionJack Humphrey, Nicol Birsa, Carmelo Milioto, et al.
Biorxiv : the Preprint Server for Biology|June 10, 2024
<i>LRRK2</i> G2019S variant is associated with transcriptional changes in Parkinson's disease human myeloid cells under proinflammatory environmentElisa Navarro, Anastasia G Efthymiou, Madison Parks, et al.
Pageof 7

Showing results (31-40 of 67) with videos related to

Sort By:
Pageof 7
Medrxiv : the Preprint Server for Health Sciences|March 17, 2025
SingleBrain: A Meta-Analysis of Single-Nucleus eQTLs Linking Genetic Risk to Brain DisordersBeomjin Jang, Kailash Bp, Alex Tokolyi, et al.
Nature Neuroscience|August 5, 2025
Alzheimer's disease transcriptional landscape in ex vivo human microgliaRoman Kosoy, John F Fullard, Jaroslav Bendl, et al.
Nature Genetics|August 5, 2022
Genetics of the human microglia regulome refines Alzheimer's disease risk lociRoman Kosoy, John F Fullard, Biao Zeng, et al.
Brain : a Journal of Neurology|October 21, 2017
Humanized mutant FUS drives progressive motor neuron degeneration without aggregation in 'FUSDelta14' knockin miceAnny Devoy, Bernadett Kalmar, Michelle Stewart, et al.
Science Advances|July 22, 2021
FUS-ALS mutants alter FMRP phase separation equilibrium and impair protein translationNicol Birsa, Agnieszka M Ule, Maria Giovanna Garone, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 6, 2023
An Autopsy Series of Seven Cases of VPS13A Disease (Chorea-Acanthocytosis)Ricky M Ditzel, Ruth H Walker, Melissa J Nirenberg, et al.
Biorxiv : the Preprint Server for Biology|February 5, 2024
TDP-43 loss induces extensive cryptic polyadenylation in ALS/FTDSam Bryce-Smith, Anna-Leigh Brown, Puja R Mehta, et al.
Molecular Neurodegeneration|August 17, 2022
Transcriptome deregulation of peripheral monocytes and whole blood in GBA-related Parkinson's diseaseGiulietta Maria Riboldi, Ricardo A Vialle, Elisa Navarro, et al.
Nucleic Acids Research|June 2, 2020
FUS ALS-causative mutations impair FUS autoregulation and splicing factor networks through intron retentionJack Humphrey, Nicol Birsa, Carmelo Milioto, et al.
Biorxiv : the Preprint Server for Biology|June 10, 2024
<i>LRRK2</i> G2019S variant is associated with transcriptional changes in Parkinson's disease human myeloid cells under proinflammatory environmentElisa Navarro, Anastasia G Efthymiou, Madison Parks, et al.
Pageof 7