Altered ryanodine receptor expression in mild cognitive impairment and Alzheimer's disease AM Bruno, JY Huang, DA Bennett, RA Marr, ML Hastings, GE Stutzmann Neurobiology of aging 33 (5), 1001. e1-1001. e6, 2012 | 151 | 2012 |
Hepatitis C virus inhibits DNA damage repair through reactive oxygen and nitrogen species and by interfering with the ATM-NBS1/Mre11/Rad50 DNA repair pathway in monocytes and … K Machida, G McNamara, KTH Cheng, J Huang, CH Wang, L Comai, ... The Journal of Immunology 185 (11), 6985-6998, 2010 | 124 | 2010 |
Neprilysin-2 is an important β-amyloid degrading enzyme D Hafez, JY Huang, AM Huynh, S Valtierra, E Rockenstein, AM Bruno, ... The American journal of pathology 178 (1), 306-312, 2011 | 85 | 2011 |
Hepatitis C virus (HCV)-induced immunoglobulin hypermutation reduces the affinity and neutralizing activities of antibodies against HCV envelope protein K Machida, Y Kondo, JY Huang, YC Chen, KTH Cheng, Z Keck, S Foung, ... Journal of virology 82 (13), 6711-6720, 2008 | 62 | 2008 |
Hepatitis C virus has a genetically determined lymphotropism through co-receptor B7. 2 CL Chen, JY Huang, CH Wang, SM Tahara, L Zhou, Y Kondo, ... Nature communications 8 (1), 13882, 2017 | 46 | 2017 |
Altered NEP2 expression and activity in mild cognitive impairment and Alzheimer's disease JY Huang, DM Hafez, BD James, DA Bennett, RA Marr Journal of Alzheimer's Disease 28 (2), 433-441, 2012 | 38 | 2012 |
F-spondin gene transfer improves memory performance and reduces amyloid-β levels in mice DM Hafez, JY Huang, JC Richardson, E Masliah, DA Peterson, RA Marr Neuroscience 223, 465-472, 2012 | 36 | 2012 |
Human membrane metallo-endopeptidase-like protein degrades both beta-amyloid 42 and beta-amyloid 40 JY Huang, AM Bruno, CA Patel, AM Huynh, KD Philibert, MJ Glucksman, ... Neuroscience 155 (1), 258-262, 2008 | 32 | 2008 |
PARP6 is a regulator of hippocampal dendritic morphogenesis JY Huang, K Wang, A Vermehren-Schmaedick, JP Adelman, MS Cohen Scientific reports 6 (1), 18512, 2016 | 27 | 2016 |
CRISPR-Cas9 generated Pompe knock-in murine model exhibits early-onset hypertrophic cardiomyopathy and skeletal muscle weakness JY Huang, SH Kan, EK Sandfeld, ND Dalton, AD Rangel, Y Chan, ... Scientific reports 10 (1), 10321, 2020 | 14 | 2020 |
Characterization of PARP6 function in knockout mice and patients with developmental delay A Vermehren-Schmaedick, JY Huang, M Levinson, MB Pomaville, S Reed, ... Cells 10 (6), 1289, 2021 | 9 | 2021 |
Base editing corrects the common Salla disease SLC17A5 c. 115C> T variant JF Harb, CL Christensen, SH Kan, AK Rha, P Andrade-Heckman, ... Molecular Therapy-Nucleic Acids 34, 2023 | 4 | 2023 |
CRISPR-mediated generation and characterization of a Gaa homozygous c.1935C>A (p.D645E) Pompe disease knock-in mouse model recapitulating human … S Kan, JY Huang, J Harb, A Rha, ND Dalton, C Christensen, Y Chan, ... Scientific Reports 12 (1), 21576, 2022 | 4 | 2022 |
Improvement of Hypertrophic Cardiomyopathy in Two Different Pompe Knock-In Murine Models with Weekly Enzyme Replace Therapy S Kan, J Harb, ND Dalton, E Torres, Y Chan, JW Huang, RY Wang MOLECULAR THERAPY 30 (4), 469-469, 2022 | | 2022 |
Prime Editing Corrects the Gaa c. 1826dupA Mutation in a C2C12 Mouse Myoblast Line of Infantile Onset Pompe Disease A Rha, J Huang, S Kan, J Harb, C Christensen, R Wang MOLECULAR THERAPY 30 (4), 123-124, 2022 | | 2022 |
CRISPR-mediated generation and characterization of the GAA homozygous c. 1935c> a (p. d645e) Pompe disease knock-in mouse model JF Harb, S Kan, JY Huang, AK Rha, ND Dalton, CL Christensen, Y Chan, ... Molecular Genetics and Metabolism 135 (2), S54, 2022 | | 2022 |
Prime editing corrects the c. 1826dupA mutation in infantile-onset Pompe disease AK Rha, JY Huang, SH Kan, J Harb, C Christensen, RY Wang Molecular Genetics and Metabolism 135 (2), S104-S105, 2022 | | 2022 |
Longitudinal assessment and immune response to recombinant GAA in CRISPR-Cas9 generated Pompe disease knock-in mice JY Huang, SH Kan, EK Sandfeld, Y Chan, AD Rangel, E Torres, ... Molecular Genetics and Metabolism 129 (2), S75-S76, 2020 | | 2020 |
Genomic correction of Pompe disease knock-in mouse myoblasts via CRISPR-Cas9 homology-directed repair EK Sandfeld, JY Huang, SH Kan, RY Wang Molecular Genetics and Metabolism 129 (2), S143, 2020 | | 2020 |
CRISPR-Cas9 generated Pompe knock-in murine model exhibits early-onset cardiomyopathy and impaired skeletal muscle function JY Huang, SH Kan, AD Rangel, Y Chan, J Davis-Turak, ND Dalton, ... bioRxiv, 780320, 2019 | | 2019 |