Proteinopathy - OmicsDI

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KU Leuven - University of Leuven, Department of Neurosciences, Experimental Neurology and Leuven Research Institute for Neuroscience and Disease (LIND), B-3000 Leuven, Belgium; VIB, Center for Brain and Disease Research, Laboratory of Neurobiology, Leuven, Belgium; University Hospitals Leuven, Department of Neurology, Leuven, Belgium. (1)
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Neurodegeneration Pathobiology Laboratory, Queensland Brain Institute, The University of Queensland, Brisbane, QLD, Australia (1)
Proteomics Unit, Navarrabiomed-IDISNA Proteored-ISCIII Pamplona, Spain (1)
School of Biological Sciences Nanyang Technological University 60 Nanyang Drive, Singapore 637551 Tel: (65) 6514-1006; Fax: (65) 6791-3856 (1)
School of Biological Sciences, Seoul National University, 1 Gwanak-ro, Gwanak-gu, Seoul 08826, Korea (1)
Skotte Research Group Department for Drug Design and Pharmacology Molecular Neuroprotection Novo Nordisk Foundation Center for Protein Research Clinical Proteomics University of Copenhagen (1)
UNIL | University of Lausanne Faculty of Biology and Medicine Department of Biomedical Sciences Rue du Bugnon 7 CH-1005 Lausanne (1)
University of Pennsylvania Perelman School of Medicine 3600 Civic Center Blvd 17th floor, room 17-104 Philadelphia, PA 19104 Office: 215-573-4109 (1)
University of Toronto (1)

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Dynamics of gene expression changes in the spinal cord during FUS-mediated proteinopathy

PRJNA448573 | ENA

Bassoon proteinopathy drives neurodegeneration in multiple sclerosis

PRJNA414103 | ENA

TMEM106B C-terminal fragments aggregate and drive neurodegenerative proteinopathy.

Not available

S-EPMC11195232 | biostudies-literature

Neurotoxic microglia promote TDP-43 proteinopathy in progranulin deficiency.

Not available

S-EPMC7746606 | biostudies-literature

Dynamics of gene expression changes in the spinal cord during FUS-mediated proteinopathy

Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disorder leading to the eventual death of motor neurons. Described cases of familial ALS have emerged the significance of protein misfolding and aggregation of two functionally related proteins, FUS and TDP-43, implicated in RNA metabolism. ...

ORGANISM(S): Mus musculus

2018-04-04 | GSE112629 | GEO

Genetic associations with dementia-related proteinopathy: Application of item response theory.

Not available

S-EPMC11032554 | biostudies-literature

TDP-43 proteinopathy impairs mRNP granule mediated postsynaptic translation and mRNA metabolism.

Not available

S-EPMC7681104 | biostudies-literature

TDP-43 proteinopathy and motor neuron disease in chronic traumatic encephalopathy.

Not available

S-EPMC2951281 | biostudies-literature

Targeting autophagy and proteinopathy provides sweet relief for preeclampsia