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K Gustavsson

Showing results (71-80 of 83) with videos related to

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Acta Neuropathologica Communications|January 3, 2024
Letter to the editor on: Hornerin deposits in neuronal intranuclear inclusion disease: direct identification of proteins with compositionally biased regions in inclusions by Park et al. (2022)Huihui Luo, Emil K Gustavsson, Hannah Macpherson, 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.
Nature|February 24, 2022
TDP-43 loss and ALS-risk SNPs drive mis-splicing and depletion of UNC13AAnna-Leigh Brown, Oscar G Wilkins, Matthew J Keuss, et al.
Nature|June 18, 2024
Author Correction: TDP-43 loss and ALS-risk SNPs drive mis-splicing and depletion of UNC13AAnna-Leigh Brown, Oscar G Wilkins, Matthew J Keuss, 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.
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.
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.
Nature Structural & Molecular Biology|December 12, 2024
African ancestry neurodegeneration risk variant disrupts an intronic branchpoint in GBA1Pilar Álvarez Jerez, Peter Wild Crea, Daniel M Ramos, et al.
Human Molecular Genetics|November 13, 2013
DNAJC13 mutations in Parkinson diseaseCarles Vilariño-Güell, Alex Rajput, Austen J Milnerwood, et al.
Pageof 9

Showing results (71-80 of 83) with videos related to

Sort By:
Pageof 9
Acta Neuropathologica Communications|January 3, 2024
Letter to the editor on: Hornerin deposits in neuronal intranuclear inclusion disease: direct identification of proteins with compositionally biased regions in inclusions by Park et al. (2022)Huihui Luo, Emil K Gustavsson, Hannah Macpherson, 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.
Nature|February 24, 2022
TDP-43 loss and ALS-risk SNPs drive mis-splicing and depletion of UNC13AAnna-Leigh Brown, Oscar G Wilkins, Matthew J Keuss, et al.
Nature|June 18, 2024
Author Correction: TDP-43 loss and ALS-risk SNPs drive mis-splicing and depletion of UNC13AAnna-Leigh Brown, Oscar G Wilkins, Matthew J Keuss, 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.
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.
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.
Nature Structural & Molecular Biology|December 12, 2024
African ancestry neurodegeneration risk variant disrupts an intronic branchpoint in GBA1Pilar Álvarez Jerez, Peter Wild Crea, Daniel M Ramos, et al.
Human Molecular Genetics|November 13, 2013
DNAJC13 mutations in Parkinson diseaseCarles Vilariño-Güell, Alex Rajput, Austen J Milnerwood, et al.
Pageof 9