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Author Details
Full Name
Lisa M Ellerby
Affiliation
Buck Institute for Research on Aging
ORCID
Career Start Year
1990
Papers
100
H Index
53
Expertise
CM4AI Collaborator
Nevan J Krogan (CM4AI)
PMID
Paper Title
Journal Title
Published Year
37586438
Therapeutic targeting of HYPDH/PRODH2 with N-propargylglycine offers a Hyperoxaluria treatment opportunity.
Biochim Biophys Acta Mol Basis Dis
2024
36950837
Molecular and Cellular Crosstalk between Bone and Brain: Accessing Bidirectional Neural and Musculoskeletal Signaling during Aging and Disease.
J Bone Metab
2023
36289639
Postnatal Conditional Deletion of <i>Bcl11b</i> in Striatal Projection Neurons Mimics the Transcriptional Signature of Huntington's Disease.
Biomedicines
2022
35424746
PNA microprobe for label-free detection of expanded trinucleotide repeats.
RSC Adv
2022
34024231
Modulating FKBP5/FKBP51 and autophagy lowers HTT (huntingtin) levels.
Autophagy
2021
33663567
Pluripotent stem cell-derived models of neurological diseases reveal early transcriptional heterogeneity.
Genome Biol
2021
34609283
Unbiased identification of novel transcription factors in striatal compartmentation and striosome maturation.
Elife
2021
34403156
Striatal Cholinergic Dysregulation after Neonatal Decrease in X-Linked Dystonia Parkinsonism-Related TAF1 Isoforms.
Mov Disord
2021
34089390
N-Propargylglycine: a unique suicide inhibitor of proline dehydrogenase with anticancer activity and brain-enhancing mitohormesis properties.
Amino Acids
2021
34286353
Correction to: N-Propargylglycine: a unique suicide inhibitor of proline dehydrogenase with anticancer activity and brain-enhancing mitohormesis properties.
Amino Acids
2021
34081916
Neuronal intranuclear inclusion disease: Polyglycine protein is the culprit.
Neuron
2021
33156570
FOXO3 targets are reprogrammed as Huntington's disease neural cells and striatal neurons face senescence with p16<sup>INK4a</sup> increase.
Aging Cell
2020
31894829
Characterization and application of fluidic properties of trinucleotide repeat sequences by wax-on-plastic microfluidics.
J Mater Chem B
2020
30594931
Rac1 Activity Is Modulated by Huntingtin and Dysregulated in Models of Huntington's Disease.
J Huntingtons Dis
2019
31907874
Repeat Expansion Disorders: Mechanisms and Therapeutics.
Neurotherapeutics
2019
31792895
Modeling Polyglutamine Expansion Diseases with Induced Pluripotent Stem Cells.
Neurotherapeutics
2019
31435686
Novel probes for label-free detection of neurodegenerative GGGGCC repeats associated with amyotrophic lateral sclerosis.
Anal Bioanal Chem
2019
31541002
Nuclear Receptor Nr4a1 Regulates Striatal Striosome Development and Dopamine D<sub>1</sub> Receptor Signaling.
eNeuro
2019
30994454
Mutant huntingtin impairs PNKP and ATXN3, disrupting DNA repair and transcription.
Elife
2019
29459817
Altered Expression of Matrix Metalloproteinases and Their Endogenous Inhibitors in a Human Isogenic Stem Cell Model of Huntington's Disease.
Front Neurosci
2018
28533375
KEAP1-modifying small molecule reveals muted NRF2 signaling responses in neural stem cells from Huntington's disease patients.
Proc Natl Acad Sci U S A
2017
27041503
Acetylated Tau Obstructs KIBRA-Mediated Signaling in Synaptic Plasticity and Promotes Tauopathy-Related Memory Loss.
Neuron
2016
26428226
iPSC-based drug screening for Huntington's disease.
Brain Res
2016
26025364
Integration-independent Transgenic Huntington Disease Fragment Mouse Models Reveal Distinct Phenotypes and Life Span in Vivo.
J Biol Chem
2015
26651603
Genomic Analysis Reveals Disruption of Striatal Neuronal Development and Therapeutic Targets in Human Huntington's Disease Neural Stem Cells.
Stem Cell Reports
2015
26390242
Critical role of acetylation in tau-mediated neurodegeneration and cognitive deficits.
Nat Med
2015
25859008
Proteolytic cleavage of ataxin-7 promotes SCA7 retinal degeneration and neurological dysfunction.
Hum Mol Genet
2015
24761311
Polyglutamine Disease Modeling: Epitope Based Screen for Homologous Recombination using CRISPR/Cas9 System.
PLoS Curr
2014
24160175
Histone deacetylase-3 interacts with ataxin-7 and is altered in a spinocerebellar ataxia type 7 mouse model.
Mol Neurodegener
2013
22649225
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.
J Neurosci
2012
23393546
Pizotifen Activates ERK and Provides Neuroprotection in vitro and in vivo in Models of Huntington's Disease.
J Huntingtons Dis
2012
23209424
A genome-scale RNA-interference screen identifies RRAS signaling as a pathologic feature of Huntington's disease.
PLoS Genet
2012
22966490
Guidelines for the use and interpretation of assays for monitoring autophagy.
Autophagy
2012
22748967
Genetic correction of Huntington's disease phenotypes in induced pluripotent stem cells.
Cell Stem Cell
2012
22917535
Responses of human embryonic stem cells and their differentiated progeny to ionizing radiation.
Biochem Biophys Res Commun
2012
22511757
Inhibition of lipid signaling enzyme diacylglycerol kinase epsilon attenuates mutant huntingtin toxicity.
J Biol Chem
2012
21685499
Mass spectrometric identification of novel lysine acetylation sites in huntingtin.
Mol Cell Proteomics
2011
20104018
Autophagy: polyQ toxic fragment turnover.
Autophagy
2010
21037797
Characterization of Human Huntington's Disease Cell Model from Induced Pluripotent Stem Cells.
PLoS Curr
2010
21095569
Identification and evaluation of small molecule pan-caspase inhibitors in Huntington's disease models.
Chem Biol
2010
20670829
Matrix metalloproteinases are modifiers of huntingtin proteolysis and toxicity in Huntington's disease.
Neuron
2010
20086007
Proteolysis of mutant huntingtin produces an exon 1 fragment that accumulates as an aggregated protein in neuronal nuclei in Huntington disease.
J Biol Chem
2010
19228953
Polyglutamine-expanded androgen receptor truncation fragments activate a Bax-dependent apoptotic cascade mediated by DP5/Hrk.
J Neurosci
2009
19955365
Posttranslational modification of ataxin-7 at lysine 257 prevents autophagy-mediated turnover of an N-terminal caspase-7 cleavage fragment.
J Neurosci
2009
19617626
Calpain-1 cleaves and activates caspase-7.
J Biol Chem
2009
19679066
IGF-1: elixir for motor neuron diseases.
Neuron
2009
17394466
Mitochondrial dysfunction in Huntington's disease: the bioenergetics of isolated and in situ mitochondria from transgenic mice.
J Neurochem
2007
17537594
A neuroglobin-overexpressing transgenic mouse.
Gene
2007
17646170
Proteolytic cleavage of ataxin-7 by caspase-7 modulates cellular toxicity and transcriptional dysregulation.
J Biol Chem
2007
17500595
Huntingtin interacting proteins are genetic modifiers of neurodegeneration.
PLoS Genet
2007
1 - 50 of 100
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Co-authored papers
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Cellstan-Immunoquant Inc.
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Christopher C Benz
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Co-authored papers
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David A Greenberg
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Co-authored papers
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Wadih Arap
Rutgers Cancer Institute of New Jersey
Co-authored papers
2
Tara E Tracy
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Co-authored papers
2
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Gladstone Institutes
Co-authored papers
2
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2
Renata Pasqualini
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Sakura Minami
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