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Author Details

Cathleen Lutz
JAX Center for Precision Genetics
1990
81
35
PMIDPaper TitleJournal TitlePublished Year
36527789Efficient in vivo neuronal genome editing in the mouse brain using nanocapsules containing CRISPR-Cas9 ribonucleoproteins.Biomaterials2023
37579143Focused ultrasound-mediated brain genome editing.Proc Natl Acad Sci U S A2023
37398081Expression of ALS-PFN1 impairs vesicular degradation in iPSC-derived microglia.bioRxiv2023
36927019Mechanism of <i>STMN2</i> cryptic splice-polyadenylation and its correction for TDP-43 proteinopathies.Science2023
36712096Focused ultrasound-mediated brain genome editing.Res Sq2023
36689813MATR3 P154S knock-in mice do not exhibit motor, muscle or neuropathologic features of ALS.Biochem Biophys Res Commun2023
36638893Neurobehavioral deficits of mice expressing a low level of G127V mutant frataxin.Neurobiol Dis2023
36527789Efficient in vivo neuronal genome editing in the mouse brain using nanocapsules containing CRISPR-Cas9 ribonucleoproteins.Biomaterials2023
36433920New mouse models with hypomorphic SUMF1 variants mimic attenuated forms of multiple sulfatase deficiency.J Inherit Metab Dis2023
37579143Focused ultrasound-mediated brain genome editing.Proc Natl Acad Sci U S A2023
37398081Expression of ALS-PFN1 impairs vesicular degradation in iPSC-derived microglia.bioRxiv2023
36927019Mechanism of <i>STMN2</i> cryptic splice-polyadenylation and its correction for TDP-43 proteinopathies.Science2023
36689813MATR3 P154S knock-in mice do not exhibit motor, muscle or neuropathologic features of ALS.Biochem Biophys Res Commun2023
36712096Focused ultrasound-mediated brain genome editing.Res Sq2023
36433920New mouse models with hypomorphic SUMF1 variants mimic attenuated forms of multiple sulfatase deficiency.J Inherit Metab Dis2023
36638893Neurobehavioral deficits of mice expressing a low level of G127V mutant frataxin.Neurobiol Dis2023
34313795The Mutant Mouse Resource and Research Center (MMRRC): the NIH-supported National Public Repository and Distribution Archive of Mutant Mouse Models in the USA.Mamm Genome2022
36125045Promoting validation and cross-phylogenetic integration in model organism research.Dis Model Mech2022
35021077Stride-level analysis of mouse open field behavior using deep-learning-based pose estimation.Cell Rep2022
36552747Loss of Pex1 in Inner Ear Hair Cells Contributes to Cochlear Synaptopathy and Hearing Loss.Cells2022
34313795The Mutant Mouse Resource and Research Center (MMRRC): the NIH-supported National Public Repository and Distribution Archive of Mutant Mouse Models in the USA.Mamm Genome2022
36552747Loss of Pex1 in Inner Ear Hair Cells Contributes to Cochlear Synaptopathy and Hearing Loss.Cells2022
36125045Promoting validation and cross-phylogenetic integration in model organism research.Dis Model Mech2022
35021077Stride-level analysis of mouse open field behavior using deep-learning-based pose estimation.Cell Rep2022
32856432Regen med therapeutic opportunities for fighting COVID-19.Stem Cells Transl Med2021
33504650Impaired prenatal motor axon development necessitates early therapeutic intervention in severe SMA.Sci Transl Med2021
33472028A platform for experimental precision medicine: The extended BXD mouse family.Cell Syst2021
33463548Restoring mitofusin balance prevents axonal degeneration in a Charcot-Marie-Tooth type 2A model.J Clin Invest2021
32856432Regen med therapeutic opportunities for fighting COVID-19.Stem Cells Transl Med2021
33878035AAV9-mediated FIG4 delivery prolongs life span in Charcot-Marie-Tooth disease type 4J mouse model.J Clin Invest2021
33828315The NIH Somatic Cell Genome Editing program.Nature2021
33828315The NIH Somatic Cell Genome Editing program.Nature2021
33878035AAV9-mediated FIG4 delivery prolongs life span in Charcot-Marie-Tooth disease type 4J mouse model.J Clin Invest2021
33504650Impaired prenatal motor axon development necessitates early therapeutic intervention in severe SMA.Sci Transl Med2021
33463548Restoring mitofusin balance prevents axonal degeneration in a Charcot-Marie-Tooth type 2A model.J Clin Invest2021
33472028A platform for experimental precision medicine: The extended BXD mouse family.Cell Syst2021
32220666The Loss of TBK1 Kinase Activity in Motor Neurons or in All Cell Types Differentially Impacts ALS Disease Progression in SOD1 Mice.Neuron2020
33315011A <i>Drosophila</i> screen identifies NKCC1 as a modifier of NGLY1 deficiency.Elife2020
33152279ACTIVating Resources for the COVID-19 Pandemic: In Vivo Models for Vaccines and Therapeutics.Cell Host Microbe2020
33113364Reduced GABAergic Neuron Excitability, Altered Synaptic Connectivity, and Seizures in a KCNT1 Gain-of-Function Mouse Model of Childhood Epilepsy.Cell Rep2020
32761777Loss of Tmem106b exacerbates FTLD pathologies and causes motor deficits in progranulin-deficient mice.EMBO Rep2020
32720893Regulation of BMP4/Dpp retrotranslocation and signaling by deglycosylation.Elife2020
32586831Mitochondrial damage and senescence phenotype of cells derived from a novel frataxin G127V point mutation mouse model of Friedreich's ataxia.Dis Model Mech2020
32577763Modelling and treating GRIN2A developmental and epileptic encephalopathy in mice.Brain2020
32504082Loss of TMEM106B leads to myelination deficits: implications for frontotemporal dementia treatment strategies.Brain2020
32498696COVID-19 preclinical models: human angiotensin-converting enzyme 2 transgenic mice.Hum Genomics2020
32418267TRPV4 Antagonism Prevents Mechanically Induced Myotonia.Ann Neurol2020
32313266Realizing the gains and losses in C9ORF72 ALS/FTD.Nat Neurosci2020
32240725Implications of increased S100β and Tau5 proteins in dystrophic nerves of two mdx mouse models for Duchenne muscular dystrophy.Mol Cell Neurosci2020
32220666The Loss of TBK1 Kinase Activity in Motor Neurons or in All Cell Types Differentially Impacts ALS Disease Progression in SOD1 Mice.Neuron2020
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Collaborators

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Columbia University.
Co-authored papers 6
Ritchie Ho
Co-authored papers 4
Kent C Lloyd
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Co-authored papers 3
Vivek M Philip
Center for Computational Sciences
Co-authored papers 3
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Co-authored papers 3
Laura G Reinholdt
Co-authored papers 3
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Co-authored papers 3
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Co-authored papers 3
Colin F Fletcher
Co-authored papers 2
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Center for Systems Neurogenetics of Addiction at The Jackson Laboratory
Co-authored papers 2
Robert E Braun
University of Maine
Co-authored papers 2
Stephen C Ekker
Co-authored papers 2
Calum A MacRae
Harvard Medical School and Cardiovascular Division, Brigham and Women's Hospital
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University of Tennessee Health Science Center
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Targacept Inc.
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Rosa Rademakers
University of Antwerp
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Anne M Dickinson
Translational and Clinical Research Institute, Newcastle University
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Carol J Bult
The Jackson Laboratory Cancer Center
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Gerald W Dorn
Co-authored papers 2
David B Goldstein
Institute for Genomic Medicine, Columbia University Irving Medical Center
Co-authored papers 2
Heather Gordish-Dressman
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Jacqueline K White
Wellcome Trust Sanger Institute
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Marla Weetall
Co-authored papers 1
John H Morrison
Co-authored papers 1
Chao-Ling Yang
Oregon Health & Science University
Co-authored papers 1
William C Skarnes
Wellcome Trust Sanger Institute
Co-authored papers 1
Gaelle Mercenne
University of Utah
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Release 1.2