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Author Details
Full Name
Smita Patel
Affiliation
Institute for Neurodegenerative Diseases, University of California san francisco
ORCID
Career Start Year
2000
Papers
26
H Index
18
Expertise
CM4AI Collaborator
Andrej Sali (CM4AI)
PMID
Paper Title
Journal Title
Published Year
32017806
Kinetics of α-synuclein prions preceding neuropathological inclusions in multiple system atrophy.
PLoS Pathog
2020
28849371
MSA prions exhibit remarkable stability and resistance to inactivation.
Acta Neuropathol
2018
29279394
Familial Parkinson's point mutation abolishes multiple system atrophy prion replication.
Proc Natl Acad Sci U S A
2018
29059326
Kinetics of Human Mutant Tau Prion Formation in the Brains of 2 Transgenic Mouse Lines.
JAMA Neurol
2017
27440899
Guinea Pig Prion Protein Supports Rapid Propagation of Bovine Spongiform Encephalopathy and Variant Creutzfeldt-Jakob Disease Prions.
J Virol
2016
27911827
Tau prions from Alzheimer's disease and chronic traumatic encephalopathy patients propagate in cultured cells.
Proc Natl Acad Sci U S A
2016
27350609
Towards authentic transgenic mouse models of heritable PrP prion diseases.
Acta Neuropathol
2016
26224882
Different 2-Aminothiazole Therapeutics Produce Distinct Patterns of Scrapie Prion Neuropathology in Mouse Brains.
J Pharmacol Exp Ther
2015
26324905
Evidence for α-synuclein prions causing multiple system atrophy in humans with parkinsonism.
Proc Natl Acad Sci U S A
2015
26286986
Propagation of prions causing synucleinopathies in cultured cells.
Proc Natl Acad Sci U S A
2015
26094969
Modulation of Creutzfeldt-Jakob disease prion propagation by the A224V mutation.
Ann Neurol
2015
24699458
Evidence that bank vole PrP is a universal acceptor for prions.
PLoS Pathog
2014
22331873
Spontaneous generation of rapidly transmissible prions in transgenic mice expressing wild-type bank vole prion protein.
Proc Natl Acad Sci U S A
2012
22438549
Identification of I137M and other mutations that modulate incubation periods for two human prion strains.
J Virol
2012
21727894
Conserved properties of human and bovine prion strains on transmission to guinea pigs.
Lab Invest
2011
20695008
Human prion strain selection in transgenic mice.
Ann Neurol
2010
16316656
Lack of direct role of parkin in the steady-state level and aggregation of alpha-synuclein and the clearance of pre-formed aggregates.
Exp Neurol
2006
15976091
Intravesicular localization and exocytosis of alpha-synuclein and its aggregates.
J Neurosci
2005
15850587
Distribution of brain atrophy in behavioral variant frontotemporal dementia.
J Neurol Sci
2005
15045511
Survival advantage of cultured human vascular endothelial cells that lost chromosome 13.
Chromosoma
2004
14985429
Clearance of alpha-synuclein oligomeric intermediates via the lysosomal degradation pathway.
J Neurosci
2004
11904757
Neuron loss from the hippocampus of Alzheimer's disease exceeds extracellular neurofibrillary tangle formation.
Acta Neuropathol
2002
12351643
Golgi fragmentation occurs in the cells with prefibrillar alpha-synuclein aggregates and precedes the formation of fibrillar inclusion.
J Biol Chem
2002
12468581
Loss of chromosome 16 from renal epithelial cells in humans.
Hypertension
2002
12023418
Patients with vascular dementia due to microvascular pathology have significant hippocampal neuronal loss.
J Neurol Neurosurg Psychiatry
2002
11035931
Loss of chromosome 13 in cultured human vascular endothelial cells.
Exp Cell Res
2000
1 - 26 of 26
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row(s) 1 - 30 of 30
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Daniel J Saltzberg
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Andrej Sali (CM4AI)
University of California San Francisco
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Carlo Condello
UCSF Weill Institute for Neurosciences, University of California san francisco
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1
Robert J Cotter
Co-authored papers
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University of California los angeles
Co-authored papers
1
Bruce L Miller
UCSF Weill Institute for Neurosciences, University of California san francisco
Co-authored papers
1
Brittany N Dugger
University of California davis
Co-authored papers
1
Adam R Renslo
Department of Pharmaceutical Chemistry, University of California san francisco
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1 - 18