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Mina Ryten

Showing results (141-150 of 176) with videos related to

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Nature Biomedical Engineering|October 1, 2025
Large-scale visualization of α-synuclein oligomers in Parkinson's disease brain tissueRebecca Andrews, Bin Fu, Christina E Toomey, et al.
Nature|May 20, 2021
MIR-NATs repress MAPT translation and aid proteostasis in neurodegenerationRoberto Simone, Faiza Javad, Warren Emmett, et al.
The Lancet. Neurology|April 13, 2024
RAB32 Ser71Arg in autosomal dominant Parkinson's disease: linkage, association, and functional analysesEmil K Gustavsson, Jordan Follett, Joanne Trinh, et al.
Annals of Neurology|June 13, 2019
PDXK mutations cause polyneuropathy responsive to pyridoxal 5'-phosphate supplementationViorica Chelban, Matthew P Wilson, Jodi Warman Chardon, et al.
Medrxiv : the Preprint Server for Health Sciences|January 13, 2025
African ancestry neurodegeneration risk variant disrupts an intronic branchpoint in <i>GBA1</i>Pilar Álvarez Jerez, Peter A Wild Crea, Daniel M Ramos, et al.
Medrxiv : the Preprint Server for Health Sciences|January 31, 2024
A pathogenic variant in RAB32 causes autosomal dominant Parkinson's disease and activates LRRK2 kinaseEmil K Gustavsson, Jordan Follett, Joanne Trinh, et al.
Brain : a Journal of Neurology|June 22, 2023
Large-scale rare variant burden testing in Parkinson's diseaseMary B Makarious, Julie Lake, Vanessa Pitz, et al.
American Journal of Human Genetics|March 26, 2025
Consensus guidelines for assessing eligibility of pathogenic DNA variants for antisense oligonucleotide treatmentsDavid Cheerie, Margaret M Meserve, Danique Beijer, et al.
Science (New York, N.Y.)|September 4, 2025
Lewy body dementia promotion by air pollutantsXiaodi Zhang, Haiqing Liu, Xiao Wu, et al.
Neurobiology of Aging|June 13, 2017
NeuroChip, an updated version of the NeuroX genotyping platform to rapidly screen for variants associated with neurological diseasesCornelis Blauwendraat, Faraz Faghri, Lasse Pihlstrom, et al.
Pageof 18

Showing results (141-150 of 176) with videos related to

Sort By:
Pageof 18
Nature Biomedical Engineering|October 1, 2025
Large-scale visualization of α-synuclein oligomers in Parkinson's disease brain tissueRebecca Andrews, Bin Fu, Christina E Toomey, et al.
Nature|May 20, 2021
MIR-NATs repress MAPT translation and aid proteostasis in neurodegenerationRoberto Simone, Faiza Javad, Warren Emmett, et al.
The Lancet. Neurology|April 13, 2024
RAB32 Ser71Arg in autosomal dominant Parkinson's disease: linkage, association, and functional analysesEmil K Gustavsson, Jordan Follett, Joanne Trinh, et al.
Annals of Neurology|June 13, 2019
PDXK mutations cause polyneuropathy responsive to pyridoxal 5'-phosphate supplementationViorica Chelban, Matthew P Wilson, Jodi Warman Chardon, et al.
Medrxiv : the Preprint Server for Health Sciences|January 13, 2025
African ancestry neurodegeneration risk variant disrupts an intronic branchpoint in <i>GBA1</i>Pilar Álvarez Jerez, Peter A Wild Crea, Daniel M Ramos, et al.
Medrxiv : the Preprint Server for Health Sciences|January 31, 2024
A pathogenic variant in RAB32 causes autosomal dominant Parkinson's disease and activates LRRK2 kinaseEmil K Gustavsson, Jordan Follett, Joanne Trinh, et al.
Brain : a Journal of Neurology|June 22, 2023
Large-scale rare variant burden testing in Parkinson's diseaseMary B Makarious, Julie Lake, Vanessa Pitz, et al.
American Journal of Human Genetics|March 26, 2025
Consensus guidelines for assessing eligibility of pathogenic DNA variants for antisense oligonucleotide treatmentsDavid Cheerie, Margaret M Meserve, Danique Beijer, et al.
Science (New York, N.Y.)|September 4, 2025
Lewy body dementia promotion by air pollutantsXiaodi Zhang, Haiqing Liu, Xiao Wu, et al.
Neurobiology of Aging|June 13, 2017
NeuroChip, an updated version of the NeuroX genotyping platform to rapidly screen for variants associated with neurological diseasesCornelis Blauwendraat, Faraz Faghri, Lasse Pihlstrom, et al.
Pageof 18