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Frontiers in Cellular Neuroscience
|
February 4, 2020
Modeling Cell-Cell Interactions in Parkinson's Disease Using Human Stem Cell-Based Models
Katrin Simmnacher, Jonas Lanfer, Tania Rizo, et al.
Glia
|
July 23, 2015
NLRP3 inflammasome is expressed by astrocytes in the SOD1 mouse model of ALS and in human sporadic ALS patients
Sonja Johann, Marius Heitzer, Mithila Kanagaratnam, et al.
Brain : a Journal of Neurology
|
September 14, 2022
Store-operated calcium entry is reduced in spastin-linked hereditary spastic paraplegia
Tania Rizo, Lisa Gebhardt, Julia Riedlberger, et al.
The Journal of Cell Biology
|
April 9, 2017
Defects in ER-endosome contacts impact lysosome function in hereditary spastic paraplegia
Rachel Allison, James R Edgar, Guy Pearson, et al.
Brain : a Journal of Neurology
|
February 27, 2018
Mechanistic basis of an epistatic interaction reducing age at onset in hereditary spastic paraplegia
Timothy Newton, Rachel Allison, James R Edgar, et al.
Biorxiv : the Preprint Server for Biology
|
April 8, 2025
TNF-α disrupts the malate-aspartate shuttle, driving metabolic rewiring in iPSC-derived enteric neural lineages from Parkinson's Disease patients
Bruno Ghirotto, Luís Eduardo Gonçalves, Vivien Ruder, et al.
Nature Communications
|
April 1, 2026
TNF alpha unmasks enteric malate aspartate shuttle dysfunction bridging Parkinson disease and intestinal inflammation
Bruno Ghirotto, Luís Eduardo Gonçalves, Vivien Ruder, et al.
Autophagy
|
March 15, 2022
Recombinant pro-CTSD (cathepsin D) enhances SNCA/α-Synuclein degradation in α-Synucleinopathy models
Susy Prieto Huarcaya, Alice Drobny, André R A Marques, et al.
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of 1
Search research articles
Search
Showing results (1-10 of 8) with videos related to
Sort By:
Page
of 1
Frontiers in Cellular Neuroscience
|
February 4, 2020
Modeling Cell-Cell Interactions in Parkinson's Disease Using Human Stem Cell-Based Models
Katrin Simmnacher, Jonas Lanfer, Tania Rizo, et al.
Glia
|
July 23, 2015
NLRP3 inflammasome is expressed by astrocytes in the SOD1 mouse model of ALS and in human sporadic ALS patients
Sonja Johann, Marius Heitzer, Mithila Kanagaratnam, et al.
Brain : a Journal of Neurology
|
September 14, 2022
Store-operated calcium entry is reduced in spastin-linked hereditary spastic paraplegia
Tania Rizo, Lisa Gebhardt, Julia Riedlberger, et al.
The Journal of Cell Biology
|
April 9, 2017
Defects in ER-endosome contacts impact lysosome function in hereditary spastic paraplegia
Rachel Allison, James R Edgar, Guy Pearson, et al.
Brain : a Journal of Neurology
|
February 27, 2018
Mechanistic basis of an epistatic interaction reducing age at onset in hereditary spastic paraplegia
Timothy Newton, Rachel Allison, James R Edgar, et al.
Biorxiv : the Preprint Server for Biology
|
April 8, 2025
TNF-α disrupts the malate-aspartate shuttle, driving metabolic rewiring in iPSC-derived enteric neural lineages from Parkinson's Disease patients
Bruno Ghirotto, Luís Eduardo Gonçalves, Vivien Ruder, et al.
Nature Communications
|
April 1, 2026
TNF alpha unmasks enteric malate aspartate shuttle dysfunction bridging Parkinson disease and intestinal inflammation
Bruno Ghirotto, Luís Eduardo Gonçalves, Vivien Ruder, et al.
Autophagy
|
March 15, 2022
Recombinant pro-CTSD (cathepsin D) enhances SNCA/α-Synuclein degradation in α-Synucleinopathy models
Susy Prieto Huarcaya, Alice Drobny, André R A Marques, et al.
Page
of 1