| 36533811 | Identification of potential pathways and biomarkers linked to progression in ALS. | Ann Clin Transl Neurol | 2023 |
| 37710351 | Amyloid fibril proteomics of AD brains reveals modifiers of aggregation and toxicity. | Mol Neurodegener | 2023 |
| 37139514 | Insights from <i>Drosophila</i> on Aβ- and tau-induced mitochondrial dysfunction: mechanisms and tools. | Front Neurosci | 2023 |
| 33398283 | Infection and chronic disease activate a brain-muscle signaling axis that regulates muscle performance. | bioRxiv | 2022 |
| 35535891 | TDP-35, a truncated fragment of TDP-43, induces dose-dependent toxicity and apoptosis in flies. | Neural Regen Res | 2022 |
| 36482422 | Nuclear import receptors are recruited by FG-nucleoporins to rescue hallmarks of TDP-43 proteinopathy. | Mol Neurodegener | 2022 |
| 34013172 | Molecular, functional, and pathological aspects of TDP-43 fragmentation. | iScience | 2021 |
| 34759799 | TDP-43 and ER Stress in Neurodegeneration: Friends or Foes? | Front Mol Neurosci | 2021 |
| 32652492 | PhotoGal4: A Versatile Light-Dependent Switch for Spatiotemporal Control of Gene Expression in Drosophila Explants. | iScience | 2020 |
| 32053595 | NCBP2 modulates neurodevelopmental defects of the 3q29 deletion in Drosophila and Xenopus laevis models. | PLoS Genet | 2020 |
| 33069251 | Aÿ40 displays amyloidogenic properties in the non-transgenic mouse brain but does not exacerbate Aÿ42 toxicity in Drosophila. | Alzheimers Res Ther | 2020 |
| 29208777 | Short Aβ peptides attenuate Aβ42 toxicity in vivo. | J Exp Med | 2018 |
| 29967544 | Engineered Hsp70 chaperones prevent Aβ42-induced memory impairments in a Drosophila model of Alzheimer's disease. | Sci Rep | 2018 |
| 30450113 | Bringing Light to Transcription: The Optogenetics Repertoire. | Front Genet | 2018 |
| 29615466 | Lmx1a is required for the development of the ovarian stem cell niche in <i>Drosophila</i>. | Development | 2018 |
| 28900185 | Anti-Aβ single-chain variable fragment antibodies restore memory acquisition in a Drosophila model of Alzheimer's disease. | Sci Rep | 2017 |
| 28415023 | Drosophila models of prionopathies: insight into prion protein function, transmission, and neurotoxicity. | Curr Opin Genet Dev | 2017 |
| 28165856 | secHsp70 as a tool to approach amyloid-β42 and other extracellular amyloids. | Fly (Austin) | 2017 |
| 28467418 | A KCNC3 mutation causes a neurodevelopmental, non-progressive SCA13 subtype associated with dominant negative effects and aberrant EGFR trafficking. | PLoS One | 2017 |
| 27012543 | Identification of proteins that are differentially expressed in brains with Alzheimer's disease using iTRAQ labeling and tandem mass spectrometry. | J Proteomics | 2016 |
| 27531960 | Holdase activity of secreted Hsp70 masks amyloid-β42 neurotoxicity in Drosophila. | Proc Natl Acad Sci U S A | 2016 |
| 27477054 | A single amino acid (Asp159) from the dog prion protein suppresses the toxicity of the mouse prion protein in Drosophila. | Neurobiol Dis | 2016 |
| 27257613 | Data set of interactomes and metabolic pathways of proteins differentially expressed in brains with Alzheimer׳s disease. | Data Brief | 2016 |
| 26024860 | Modeling the complex pathology of Alzheimer's disease in Drosophila. | Exp Neurol | 2015 |
| 26253732 | Anti-Aβ single-chain variable fragment antibodies exert synergistic neuroprotective activities in Drosophila models of Alzheimer's disease. | Hum Mol Genet | 2015 |
| 24523910 | Combined pharmacological induction of Hsp70 suppresses prion protein neurotoxicity in Drosophila. | PLoS One | 2014 |
| 25152487 | KCNC3(R420H), a K(+) channel mutation causative in spinocerebellar ataxia 13 displays aberrant intracellular trafficking. | Neurobiol Dis | 2014 |
| 24810400 | Launching Hsp70 neuroprotection: two drugs better than one. | Cell Cycle | 2014 |
| 23524378 | Purification of transcripts and metabolites from Drosophila heads. | J Vis Exp | 2013 |
| 23681549 | pâ¿¿TubHA4C, a new versatile vector for constitutive expression in Drosophila. | Mol Biol Rep | 2013 |
| 23771030 | Polar substitutions in helix 3 of the prion protein produce transmembrane isoforms that disturb vesicle trafficking. | Hum Mol Genet | 2013 |
| 22288402 | Drosophila models of proteinopathies: the little fly that could. | Curr Pharm Des | 2012 |
| 22528838 | Differential activation of the ER stress factor XBP1 by oligomeric assemblies. | Neurochem Res | 2012 |
| 21393248 | Amyloid-beta42 interacts mainly with insoluble prion protein in the Alzheimer brain. | J Biol Chem | 2011 |
| 21980555 | Pulling rabbits to reveal the secrets of the prion protein. | Commun Integr Biol | 2011 |
| 21389082 | The ER stress factor XBP1s prevents amyloid-beta neurotoxicity. | Hum Mol Genet | 2011 |
| 20083902 | Exploring prion protein biology in flies: genetics and beyond. | Prion | 2010 |
| 20817727 | Sequence-dependent prion protein misfolding and neurotoxicity. | J Biol Chem | 2010 |
| 19503596 | In vivo generation of neurotoxic prion protein: role for hsp70 in accumulation of misfolded isoforms. | PLoS Genet | 2009 |
| 17984172 | Comparative analysis of genetic modifiers in Drosophila points to common and distinct mechanisms of pathogenesis among polyglutamine diseases. | Hum Mol Genet | 2008 |
| 12537575 | Assessing the impact of comparative genomic sequence data on the functional annotation of the Drosophila genome. | Genome Biol | 2002 |
| 11091089 | Conserved overlapping and reciprocal expression of msh/Msx1 and apterous/Lhx2 in Drosophila and mice. | Mech Dev | 2000 |
| 10835358 | The level of DLDB/CHIP controls the activity of the LIM homeodomain protein apterous: evidence for a functional tetramer complex in vivo. | EMBO J | 2000 |
| 10051612 | Conservation of the expression and function of apterous orthologs in Drosophila and mammals. | Proc Natl Acad Sci U S A | 1999 |
| 9735354 | Lhx2, a vertebrate homologue of apterous, regulates vertebrate limb outgrowth. | Development | 1998 |
| 9843490 | The relative expression amounts of apterous and its co-factor dLdb/Chip are critical for dorso-ventral compartmentalization in the Drosophila wing. | EMBO J | 1998 |
| 9697309 | Protein complex formation between Msx1 and Lhx2 homeoproteins is incompatible with DNA binding activity. | Differentiation | 1998 |
| 8524221 | Ubiquitous and neuronal DNA-binding proteins interact with a negative regulatory element of the human hypoxanthine phosphoribosyltransferase gene. | Mol Cell Biol | 1995 |
| 7523686 | 5'-flanking sequences of the human HPRT gene direct neuronal expression in the brain of transgenic mice. | J Neurosci Res | 1994 |
| 8094629 | Association between genetic variation at the porphobilinogen deaminase gene and schizophrenia. | Schizophr Res | 1993 |