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Author Details

Diego E Rincon-Limas
University of Florida
1990
55
20
PMIDPaper TitleJournal TitlePublished Year
36533811Identification of potential pathways and biomarkers linked to progression in ALS.Ann Clin Transl Neurol2023
37710351Amyloid fibril proteomics of AD brains reveals modifiers of aggregation and toxicity.Mol Neurodegener2023
37139514Insights from <i>Drosophila</i> on Aβ- and tau-induced mitochondrial dysfunction: mechanisms and tools.Front Neurosci2023
33398283Infection and chronic disease activate a brain-muscle signaling axis that regulates muscle performance.bioRxiv2022
35535891TDP-35, a truncated fragment of TDP-43, induces dose-dependent toxicity and apoptosis in flies.Neural Regen Res2022
36482422Nuclear import receptors are recruited by FG-nucleoporins to rescue hallmarks of TDP-43 proteinopathy.Mol Neurodegener2022
34013172Molecular, functional, and pathological aspects of TDP-43 fragmentation.iScience2021
34759799TDP-43 and ER Stress in Neurodegeneration: Friends or Foes?Front Mol Neurosci2021
32652492PhotoGal4: A Versatile Light-Dependent Switch for Spatiotemporal Control of Gene Expression in Drosophila Explants.iScience2020
32053595NCBP2 modulates neurodevelopmental defects of the 3q29 deletion in Drosophila and Xenopus laevis models.PLoS Genet2020
33069251Aÿ40 displays amyloidogenic properties in the non-transgenic mouse brain but does not exacerbate Aÿ42 toxicity in Drosophila.Alzheimers Res Ther2020
29208777Short Aβ peptides attenuate Aβ42 toxicity in vivo.J Exp Med2018
29967544Engineered Hsp70 chaperones prevent Aβ42-induced memory impairments in a Drosophila model of Alzheimer's disease.Sci Rep2018
30450113Bringing Light to Transcription: The Optogenetics Repertoire.Front Genet2018
29615466Lmx1a is required for the development of the ovarian stem cell niche in <i>Drosophila</i>.Development2018
28900185Anti-Aβ single-chain variable fragment antibodies restore memory acquisition in a Drosophila model of Alzheimer's disease.Sci Rep2017
28415023Drosophila models of prionopathies: insight into prion protein function, transmission, and neurotoxicity.Curr Opin Genet Dev2017
28165856secHsp70 as a tool to approach amyloid-β42 and other extracellular amyloids.Fly (Austin)2017
28467418A KCNC3 mutation causes a neurodevelopmental, non-progressive SCA13 subtype associated with dominant negative effects and aberrant EGFR trafficking.PLoS One2017
27012543Identification of proteins that are differentially expressed in brains with Alzheimer's disease using iTRAQ labeling and tandem mass spectrometry.J Proteomics2016
27531960Holdase activity of secreted Hsp70 masks amyloid-β42 neurotoxicity in Drosophila.Proc Natl Acad Sci U S A2016
27477054A single amino acid (Asp159) from the dog prion protein suppresses the toxicity of the mouse prion protein in Drosophila.Neurobiol Dis2016
27257613Data set of interactomes and metabolic pathways of proteins differentially expressed in brains with Alzheimer׳s disease.Data Brief2016
26024860Modeling the complex pathology of Alzheimer's disease in Drosophila.Exp Neurol2015
26253732Anti-Aβ single-chain variable fragment antibodies exert synergistic neuroprotective activities in Drosophila models of Alzheimer's disease.Hum Mol Genet2015
24523910Combined pharmacological induction of Hsp70 suppresses prion protein neurotoxicity in Drosophila.PLoS One2014
25152487KCNC3(R420H), a K(+) channel mutation causative in spinocerebellar ataxia 13 displays aberrant intracellular trafficking.Neurobiol Dis2014
24810400Launching Hsp70 neuroprotection: two drugs better than one.Cell Cycle2014
23524378Purification of transcripts and metabolites from Drosophila heads.J Vis Exp2013
23681549pâ¿¿TubHA4C, a new versatile vector for constitutive expression in Drosophila.Mol Biol Rep2013
23771030Polar substitutions in helix 3 of the prion protein produce transmembrane isoforms that disturb vesicle trafficking.Hum Mol Genet2013
22288402Drosophila models of proteinopathies: the little fly that could.Curr Pharm Des2012
22528838Differential activation of the ER stress factor XBP1 by oligomeric assemblies.Neurochem Res2012
21393248Amyloid-beta42 interacts mainly with insoluble prion protein in the Alzheimer brain.J Biol Chem2011
21980555Pulling rabbits to reveal the secrets of the prion protein.Commun Integr Biol2011
21389082The ER stress factor XBP1s prevents amyloid-beta neurotoxicity.Hum Mol Genet2011
20083902Exploring prion protein biology in flies: genetics and beyond.Prion2010
20817727Sequence-dependent prion protein misfolding and neurotoxicity.J Biol Chem2010
19503596In vivo generation of neurotoxic prion protein: role for hsp70 in accumulation of misfolded isoforms.PLoS Genet2009
17984172Comparative analysis of genetic modifiers in Drosophila points to common and distinct mechanisms of pathogenesis among polyglutamine diseases.Hum Mol Genet2008
12537575Assessing the impact of comparative genomic sequence data on the functional annotation of the Drosophila genome.Genome Biol2002
11091089Conserved overlapping and reciprocal expression of msh/Msx1 and apterous/Lhx2 in Drosophila and mice.Mech Dev2000
10835358The level of DLDB/CHIP controls the activity of the LIM homeodomain protein apterous: evidence for a functional tetramer complex in vivo.EMBO J2000
10051612Conservation of the expression and function of apterous orthologs in Drosophila and mammals.Proc Natl Acad Sci U S A1999
9735354Lhx2, a vertebrate homologue of apterous, regulates vertebrate limb outgrowth.Development1998
9843490The relative expression amounts of apterous and its co-factor dLdb/Chip are critical for dorso-ventral compartmentalization in the Drosophila wing.EMBO J1998
9697309Protein complex formation between Msx1 and Lhx2 homeoproteins is incompatible with DNA binding activity.Differentiation1998
8524221Ubiquitous and neuronal DNA-binding proteins interact with a negative regulatory element of the human hypoxanthine phosphoribosyltransferase gene.Mol Cell Biol1995
75236865'-flanking sequences of the human HPRT gene direct neuronal expression in the brain of transgenic mice.J Neurosci Res1994
8094629Association between genetic variation at the porphobilinogen deaminase gene and schizophrenia.Schizophr Res1993
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Collaborators

Baylor College of Medicine
Co-authored papers 8
Emory Center for Neurodegenerative Disease
Co-authored papers 6
Emory University School of Medicine
Co-authored papers 4
College of Medicine, University of Florida
Co-authored papers 2
Baylor College of Medicine
Co-authored papers 2
Inc., Salk Institute for Biological Studies
Co-authored papers 2
College of Medicine, University of Florida
Co-authored papers 2
Center for Translational Research in Neurodegenerative Disease, University of Florida
Co-authored papers 2
College of Medicine, University of Florida
Co-authored papers 1
Co-authored papers 1
Center for Psychiatric Genetics, NorthShore University HealthSystem
Co-authored papers 1
Lawrence Berkeley National Laboratory
Co-authored papers 1
The Huck Institutes of Life Sciences, University Park, Pennsylvania State University
Co-authored papers 1
University of California berkeley
Co-authored papers 1
Co-authored papers 1
Howard Hughes Medical Institute
Co-authored papers 1
Center for Genetics, Children's Hospital Oakland Research Institute
Co-authored papers 1
Lawrence Berkeley National Laboratory
Co-authored papers 1
Howard Hughes Medical Institute
Co-authored papers 1
University of Georgia
Co-authored papers 1
Lawrence Berkeley National Laboratory
Co-authored papers 1
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International Society for Biocuration, Lawrence Berkeley National Laboratory, University of Edinburgh, University of Edinburgh School of Biological Sciences
Co-authored papers 1
The University of Florida
Co-authored papers 1
Center for Quantitative Life Sciences, Oregon State University
Co-authored papers 1
University of California berkeley
Co-authored papers 1
Lawrence Berkeley National Laboratory
Co-authored papers 1
The Center for Genome Architecture, Baylor College of Medicine
Co-authored papers 1
Perelman School of Medicine at the University of Pennsylvania
Co-authored papers 1
University of Texas McGovern Medical School at Houston
Co-authored papers 1