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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-synuclein
Karishma 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 UNC13A
Anna-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 UNC13A
Anna-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 kinase
Emil 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 analyses
Emil 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 GBA1
Pilar Álvarez Jerez, Peter Wild Crea, Daniel M Ramos, et al.
Human Molecular Genetics
|
November 13, 2013
DNAJC13 mutations in Parkinson disease
Carles Vilariño-Güell, Alex Rajput, Austen J Milnerwood, et al.
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of 9
Search research articles
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Showing results (71-80 of 83) with videos related to
Sort By:
Page
of 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-synuclein
Karishma 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 UNC13A
Anna-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 UNC13A
Anna-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 kinase
Emil 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 analyses
Emil 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 GBA1
Pilar Álvarez Jerez, Peter Wild Crea, Daniel M Ramos, et al.
Human Molecular Genetics
|
November 13, 2013
DNAJC13 mutations in Parkinson disease
Carles Vilariño-Güell, Alex Rajput, Austen J Milnerwood, et al.
Page
of 9