Works by Ellerby, Lisa M.
Results: 31
Coupling endoplasmic reticulum stress to the cell death program: role of the ER chaperone GRP78
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- FEBS Letters, 2002, v. 514, n. 2/3, p. 122, doi. 10.1016/S0014-5793(02)02289-5
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- Article
Caspase-mediated proteolysis of the polyglutamine disease protein ataxin-3.
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- Journal of Neurochemistry, 2004, v. 89, n. 4, p. 908, doi. 10.1111/j.1471-4159.2004.02369.x
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- Article
Kennedy's Disease: Caspase Cleavage of the Androgen Receptor Is aCrucial Event in Cytotoxicity.
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- Journal of Neurochemistry, 1999, v. 72, n. 1, p. 185, doi. 10.1046/j.1471-4159.1999.0720185.x
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- Article
Shift of the Cellular Oxidation-Reduction Potential in Neural Cells Expressing Bcl-2.
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- Journal of Neurochemistry, 1996, v. 67, n. 3, p. 1259, doi. 10.1046/j.1471-4159.1996.67031259.x
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- Article
Neurodegenerative disease: Cut to the chase.
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- Nature, 2006, v. 442, n. 7103, p. 641, doi. 10.1038/442641a
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- Article
Postnatal Conditional Deletion of Bcl11b in Striatal Projection Neurons Mimics the Transcriptional Signature of Huntington's Disease.
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- Biomedicines, 2022, v. 10, n. 10, p. N.PAG, doi. 10.3390/biomedicines10102377
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- Article
Novel probes for label-free detection of neurodegenerative GGGGCC repeats associated with amyotrophic lateral sclerosis.
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- Analytical & Bioanalytical Chemistry, 2019, v. 411, n. 26, p. 6995, doi. 10.1007/s00216-019-02075-8
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- Article
Histone deacetylase-3 interacts with ataxin-7 and is altered in a spinocerebellar ataxia type 7 mouse model.
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- Molecular Neurodegeneration, 2013, v. 8, n. 1, p. 1, doi. 10.1186/1750-1326-8-42
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- Article
Mitochondrial dysfunction in Huntington’s disease: the bioenergetics of isolated and in situ mitochondria from transgenic mice.
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- Journal of Neurochemistry, 2007, v. 101, n. 1, p. 241, doi. 10.1111/j.1471-4159.2006.04361.x
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- Article
A second cytotoxic proteolytic peptide derived from amyloid β-protein precursor.
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- Nature Medicine, 2000, v. 6, n. 4, p. 397, doi. 10.1038/74656
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- Article
Anti-cancer activity of targeted pro-apoptotic peptides.
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- Nature Medicine, 1999, v. 5, n. 9, p. 1032, doi. 10.1038/12469
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- Article
Structural Evaluation of a Novel Pro-apoptotic Peptide Coupled to CNGRC Tumor Homing Sequence by NMR.
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- Chemical Biology & Drug Design, 2006, v. 67, n. 6, p. 417, doi. 10.1111/j.1747-0285.2006.00394.x
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- Article
Do posttranslational modifications of CuZnSOD lead to sporadic amyotrophic lateral sclerosis?
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- Annals of Neurology, 1997, v. 42, n. 2, p. 135, doi. 10.1002/ana.410420202
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- Article
TYROBP/DAP12 knockout in Huntington's disease Q175 mice cell-autonomously decreases microglial expression of disease-associated genes and non-cell-autonomously mitigates astrogliosis and motor deterioration.
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- Journal of Neuroinflammation, 2024, v. 21, n. 1, p. 1, doi. 10.1186/s12974-024-03052-4
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- Article
A Genome-Scale RNA--Interference Screen Identifies RRAS Signaling as a Pathologic Feature of Huntington's Disease.
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- PLoS Genetics, 2012, v. 8, n. 11, p. 1, doi. 10.1371/journal.pgen.1003042
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- Article
Huntingtin Interacting Proteins Are Genetic Modifiers of Neurodegeneration.
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- PLoS Genetics, 2007, v. 3, n. 5, p. e82, doi. 10.1371/journal.pgen.0030082
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- Article
FOXO3 targets are reprogrammed as Huntington's disease neural cells and striatal neurons face senescence with p16<sup>INK4a</sup> increase.
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- Aging Cell, 2020, v. 19, n. 11, p. 1, doi. 10.1111/acel.13226
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- Article
Polyglutamine Disease Modeling: Epitope Based Screen for Homologous Recombination using CRISPR/Cas9 System.
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- PLoS Currents, 2014, p. 369, doi. 10.1371/currents.hd.0242d2e7ad72225efa72f6964589369a
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- Article
Pluripotent stem cell-derived models of neurological diseases reveal early transcriptional heterogeneity.
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- Genome Biology, 2021, v. 22, n. 1, p. 1, doi. 10.1186/s13059-021-02301-6
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- Article
Altered Expression of Matrix Metalloproteinases and Their Endogenous Inhibitors in a Human Isogenic Stem Cell Model of Huntington's Disease.
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- Frontiers in Neuroscience, 2018, p. 1, doi. 10.3389/fnins.2017.00736
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- Article
Unbiased identification of novel transcription factors in striatal compartmentation and striosome maturation.
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- eLife, 2021, p. 1, doi. 10.7554/eLife.65979
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- Article
Proteolytic cleavage of ataxin-7 promotes SCA7 retinal degeneration and neurological dysfunction.
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- Human Molecular Genetics, 2015, v. 24, n. 14, p. 3908, doi. 10.1093/hmg/ddv121
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- Article
Correction to: N-Propargylglycine: a unique suicide inhibitor of proline dehydrogenase with anticancer activity and brain-enhancing mitohormesis properties.
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- 2021
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- Correction Notice
N-Propargylglycine: a unique suicide inhibitor of proline dehydrogenase with anticancer activity and brain-enhancing mitohormesis properties.
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- Amino Acids, 2021, v. 53, n. 12, p. 1927, doi. 10.1007/s00726-021-03012-9
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- Article
Caspase-6 Activity in a BACHD Mouse Modulates Steady-State Levels of Mutant Huntingtin Protein But Is Not Necessary for Production of a 586 Amino Acid Proteolytic Fragment.
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- Journal of Neuroscience, 2012, v. 32, n. 22, p. 7454, doi. 10.1523/JNEUROSCI.6379-11.2012
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- Article
Posttranslational Modification of Ataxin-7 at Lysine 257 Prevents Autophagy-Mediated Turnover of an N-Terminal Caspase-7 Cleavage Fragment.
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- Journal of Neuroscience, 2009, v. 29, n. 48, p. 15134, doi. 10.1523/JNEUROSCI.4720-09.2009
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- Article
Polyglutamine-Expanded Androgen Receptor Truncation Fragments Activate a Bax-Dependent Apoptotic Cascade Mediated by DP5/Hrk.
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- Journal of Neuroscience, 2009, v. 29, n. 7, p. 1987, doi. 10.1523/JNEUROSCI.4072-08.2009
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- Article
Mitochondrial-Dependent Ca<sup>2+</sup> Handling in Huntington's Disease Striatal Cells: Effect of Histone Deacetylase Inhibitors.
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- Journal of Neuroscience, 2006, v. 26, n. 43, p. 11174, doi. 10.1523/JNEUROSCI.3004-06.2006
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- Article
Striatal Cholinergic Dysregulation after Neonatal Decrease in X‐Linked Dystonia Parkinsonism‐Related TAF1 Isoforms.
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- Movement Disorders, 2021, v. 36, n. 12, p. 2780, doi. 10.1002/mds.28750
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- Article
Modulating FKBP5/FKBP51 and autophagy lowers HTT (huntingtin) levels.
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- Autophagy, 2021, v. 17, n. 12, p. 4119, doi. 10.1080/15548627.2021.1904489
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- Article
Autophagy.
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- Autophagy, 2010, v. 6, n. 2, p. 312, doi. 10.4161/auto.6.2.11139
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- Article