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Mina Ryten

Showing results (131-140 of 176) with videos related to

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Cell Reports|June 9, 2021
An integrated genomic approach to dissect the genetic landscape regulating the cell-to-cell transfer of α-synucleinEleanna Kara, Alessandro Crimi, Anne Wiedmer, et al.
American Journal of Human Genetics|December 3, 2014
Mutations in SNX14 cause a distinctive autosomal-recessive cerebellar ataxia and intellectual disability syndromeAnna C Thomas, Hywel Williams, Núria Setó-Salvia, et al.
Science Advances|April 11, 2025
Astrocytic RNA editing regulates the host immune response to alpha-synucleinKarishma D'Sa, Minee L Choi, Aaron Z Wagen, et al.
Biorxiv : the Preprint Server for Biology|April 29, 2026
The complete genome of the KOLF2.1J reference iPSC linePilar Alvarez Jerez, Arang Rhie, Juhyun Kim, et al.
Brain : a Journal of Neurology|September 11, 2019
Biallelic mutations in neurofascin cause neurodevelopmental impairment and peripheral demyelinationStephanie Efthymiou, Vincenzo Salpietro, Nancy Malintan, et al.
Genome Biology|February 1, 2017
Discovery and functional prioritization of Parkinson's disease candidate genes from large-scale whole exome sequencingIris E Jansen, Hui Ye, Sasja Heetveld, et al.
Annals of Clinical and Translational Neurology|August 11, 2020
Neuronal intranuclear inclusion disease is genetically heterogeneousZhongbo Chen, Wai Yan Yau, Zane Jaunmuktane, et al.
Brain Communications|November 19, 2020
Analysis of brain atrophy and local gene expression in genetic frontotemporal dementiaAndre Altmann, David M Cash, Martina Bocchetta, et al.
Science Advances|June 26, 2024
The annotation of <i>GBA1</i> has been concealed by its protein-coding pseudogene <i>GBAP1</i>Emil K Gustavsson, Siddharth Sethi, Yujing Gao, et al.
American Journal of Human Genetics|May 19, 2015
A missense mutation in KCTD17 causes autosomal dominant myoclonus-dystoniaNiccolo E Mencacci, Ignacio Rubio-Agusti, Anselm Zdebik, et al.
Pageof 18

Showing results (131-140 of 176) with videos related to

Sort By:
Pageof 18
Cell Reports|June 9, 2021
An integrated genomic approach to dissect the genetic landscape regulating the cell-to-cell transfer of α-synucleinEleanna Kara, Alessandro Crimi, Anne Wiedmer, et al.
American Journal of Human Genetics|December 3, 2014
Mutations in SNX14 cause a distinctive autosomal-recessive cerebellar ataxia and intellectual disability syndromeAnna C Thomas, Hywel Williams, Núria Setó-Salvia, et al.
Science Advances|April 11, 2025
Astrocytic RNA editing regulates the host immune response to alpha-synucleinKarishma D'Sa, Minee L Choi, Aaron Z Wagen, et al.
Biorxiv : the Preprint Server for Biology|April 29, 2026
The complete genome of the KOLF2.1J reference iPSC linePilar Alvarez Jerez, Arang Rhie, Juhyun Kim, et al.
Brain : a Journal of Neurology|September 11, 2019
Biallelic mutations in neurofascin cause neurodevelopmental impairment and peripheral demyelinationStephanie Efthymiou, Vincenzo Salpietro, Nancy Malintan, et al.
Genome Biology|February 1, 2017
Discovery and functional prioritization of Parkinson's disease candidate genes from large-scale whole exome sequencingIris E Jansen, Hui Ye, Sasja Heetveld, et al.
Annals of Clinical and Translational Neurology|August 11, 2020
Neuronal intranuclear inclusion disease is genetically heterogeneousZhongbo Chen, Wai Yan Yau, Zane Jaunmuktane, et al.
Brain Communications|November 19, 2020
Analysis of brain atrophy and local gene expression in genetic frontotemporal dementiaAndre Altmann, David M Cash, Martina Bocchetta, et al.
Science Advances|June 26, 2024
The annotation of <i>GBA1</i> has been concealed by its protein-coding pseudogene <i>GBAP1</i>Emil K Gustavsson, Siddharth Sethi, Yujing Gao, et al.
American Journal of Human Genetics|May 19, 2015
A missense mutation in KCTD17 causes autosomal dominant myoclonus-dystoniaNiccolo E Mencacci, Ignacio Rubio-Agusti, Anselm Zdebik, et al.
Pageof 18