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Mina Ryten

Showing results (81-90 of 176) with videos related to

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Annals of Neurology|February 21, 2013
Mutations in the autoregulatory domain of β-tubulin 4a cause hereditary dystoniaJoshua Hersheson, Niccolo E Mencacci, Mary Davis, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|November 8, 2013
Novel C12orf65 mutations in patients with axonal neuropathy and optic atrophyArianna Tucci, Yo-Tsen Liu, Elisabeth Preza, et al.
Medrxiv : the Preprint Server for Health Sciences|July 10, 2023
Genetic meta-analysis of levodopa induced dyskinesia in Parkinson's diseaseAlejandro Martinez-Carrasco, Raquel Real, Michael Lawton, et al.
NPJ Parkinson'S Disease|August 31, 2023
Genetic meta-analysis of levodopa induced dyskinesia in Parkinson's diseaseAlejandro Martinez-Carrasco, Raquel Real, Michael Lawton, et al.
NPJ Genomic Medicine|September 6, 2022
Huntington's disease age at motor onset is modified by the tandem hexamer repeat in TCERG1Sergey V Lobanov, Branduff McAllister, Mia McDade-Kumar, et al.
Human Mutation|March 1, 2020
Pathogenic PTPN11 variants involving the poly-glutamine Gln<sup>255</sup> -Gln<sup>256</sup> -Gln<sup>257</sup> stretch highlight the relevance of helix B in SHP2's functional regulationSimone Martinelli, Luca Pannone, Christina Lissewski, et al.
Science Advances|February 1, 2021
Genetic analysis of amyotrophic lateral sclerosis identifies contributing pathways and cell typesSara Saez-Atienzar, Sara Bandres-Ciga, Rebekah G Langston, et al.
Human Molecular Genetics|June 23, 2012
MAPT expression and splicing is differentially regulated by brain region: relation to genotype and implication for tauopathiesDaniah Trabzuni, Selina Wray, Jana Vandrovcova, et al.
Biorxiv : the Preprint Server for Biology|November 19, 2025
Long-Read epigenetic clocks identify improved brain aging predictionsSpencer M Grant, Mary B Makarious, Melissa Meredith, et al.
Brain Communications|April 11, 2020
Genetic variability in response to amyloid beta deposition influences Alzheimer's disease riskDervis A Salih, Sevinc Bayram, Sebastian Guelfi, et al.
Pageof 18

Showing results (81-90 of 176) with videos related to

Sort By:
Pageof 18
Annals of Neurology|February 21, 2013
Mutations in the autoregulatory domain of β-tubulin 4a cause hereditary dystoniaJoshua Hersheson, Niccolo E Mencacci, Mary Davis, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|November 8, 2013
Novel C12orf65 mutations in patients with axonal neuropathy and optic atrophyArianna Tucci, Yo-Tsen Liu, Elisabeth Preza, et al.
Medrxiv : the Preprint Server for Health Sciences|July 10, 2023
Genetic meta-analysis of levodopa induced dyskinesia in Parkinson's diseaseAlejandro Martinez-Carrasco, Raquel Real, Michael Lawton, et al.
NPJ Parkinson'S Disease|August 31, 2023
Genetic meta-analysis of levodopa induced dyskinesia in Parkinson's diseaseAlejandro Martinez-Carrasco, Raquel Real, Michael Lawton, et al.
NPJ Genomic Medicine|September 6, 2022
Huntington's disease age at motor onset is modified by the tandem hexamer repeat in TCERG1Sergey V Lobanov, Branduff McAllister, Mia McDade-Kumar, et al.
Human Mutation|March 1, 2020
Pathogenic PTPN11 variants involving the poly-glutamine Gln<sup>255</sup> -Gln<sup>256</sup> -Gln<sup>257</sup> stretch highlight the relevance of helix B in SHP2's functional regulationSimone Martinelli, Luca Pannone, Christina Lissewski, et al.
Science Advances|February 1, 2021
Genetic analysis of amyotrophic lateral sclerosis identifies contributing pathways and cell typesSara Saez-Atienzar, Sara Bandres-Ciga, Rebekah G Langston, et al.
Human Molecular Genetics|June 23, 2012
MAPT expression and splicing is differentially regulated by brain region: relation to genotype and implication for tauopathiesDaniah Trabzuni, Selina Wray, Jana Vandrovcova, et al.
Biorxiv : the Preprint Server for Biology|November 19, 2025
Long-Read epigenetic clocks identify improved brain aging predictionsSpencer M Grant, Mary B Makarious, Melissa Meredith, et al.
Brain Communications|April 11, 2020
Genetic variability in response to amyloid beta deposition influences Alzheimer's disease riskDervis A Salih, Sevinc Bayram, Sebastian Guelfi, et al.
Pageof 18