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Rachael Miller
Rachael Miller
UMass Chan Medical School
Verifisert e-postadresse på umassmed.edu
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Exosomes produced from 3D cultures of MSCs by tangential flow filtration show higher yield and improved activity
RA Haraszti, R Miller, M Stoppato, YY Sere, A Coles, MC Didiot, ...
Molecular Therapy 26 (12), 2838-2847, 2018
3572018
A divalent siRNA chemical scaffold for potent and sustained modulation of gene expression throughout the central nervous system
JF Alterman, BMDC Godinho, MR Hassler, CM Ferguson, D Echeverria, ...
Nature biotechnology 37 (8), 884-894, 2019
1542019
Optimized cholesterol-siRNA chemistry improves productive loading onto extracellular vesicles
RA Haraszti, R Miller, MC Didiot, A Biscans, JF Alterman, MR Hassler, ...
Molecular Therapy 26 (8), 1973-1982, 2018
832018
Serum deprivation of mesenchymal stem cells improves exosome activity and alters lipid and protein composition
RA Haraszti, R Miller, ML Dubuke, HE Rockwell, AH Coles, E Sapp, ...
Iscience 16, 230-241, 2019
752019
Hydrophobicity of lipid-conjugated siRNAs predicts productive loading to small extracellular vesicles
A Biscans, RA Haraszti, D Echeverria, R Miller, MC Didiot, M Nikan, ...
Molecular Therapy 26 (6), 1520-1528, 2018
402018
Safe and efficient silencing with a Pol II, but not a Pol lII, promoter expressing an artificial miRNA targeting human huntingtin
EL Pfister, KO Chase, H Sun, LA Kennington, F Conroy, E Johnson, ...
Molecular Therapy-Nucleic Acids 7, 324-334, 2017
332017
Chemical engineering of therapeutic siRNAs for allele-specific gene silencing in Huntington’s disease models
F Conroy, R Miller, JF Alterman, MR Hassler, D Echeverria, ...
Nature communications 13 (1), 5802, 2022
132022
Mutant huntingtin messenger RNA forms neuronal nuclear clusters in rodent and human brains
S Ly, MC Didiot, CM Ferguson, AH Coles, R Miller, K Chase, D Echeverria, ...
Brain Communications 4 (6), fcac248, 2022
92022
Allele-specific knockdown of mutant huntingtin protein via editing at coding region single nucleotide polymorphism heterozygosities
SR Oikemus, EL Pfister, E Sapp, KO Chase, LA Kennington, E Hudgens, ...
Human Gene Therapy 33 (1-2), 25-36, 2022
72022
Structurally constrained phosphonate internucleotide linkage impacts oligonucleotide-enzyme interaction, and modulates siRNA activity and allele specificity
K Yamada, S Hildebrand, SM Davis, R Miller, F Conroy, E Sapp, J Caiazzi, ...
Nucleic Acids Research 49 (21), 12069-12088, 2021
72021
Extended Nucleic Acid (exNA): A Novel, Biologically Compatible Backbone that Significantly Enhances Oligonucleotide Efficacy in vivo.
K Yamada, VN Hariharan, J Caiazzi, R Miller, C Furguson, E Sapp, ...
bioRxiv, 2023
52023
Allele-specific knockdown of mutant HTT protein via editing at coding region SNP heterozygosities
S Oikemus, EL Pfister, E Sapp, KO Chase, LA Kennington, E Hudgens, ...
22021
Extended Nucleic Acid (exNA): A Novel, Biologically Compatible Backbone that Significantly Enhances Oligonucleotide Efficacy in vivo
VN Hariharan, J Caiazzi, R Miller, C Ferguson, E Sapp, H Fakih, Q Tang, ...
Research Square, 2023
12023
Nacc1 mutation in mice models rare neurodevelopmental disorder with underlying synaptic dysfunction
MA Deehan, JM Kothuis, E Sapp, K Chase, Y Ke, C Seeley, M Iuliano, ...
Journal of Neuroscience 44 (14), 2024
2024
mRNA nuclear clustering leads to a difference in mutant huntingtin mRNA and protein silencing by siRNAs in vivo
SJ Allen, D O'Reilly, R Miller, E Sapp, A Summers, J Paquette, DE Moreno, ...
bioRxiv, 2024.04. 24.590997, 2024
2024
Awake intracerebroventricular delivery and safety assessment of oligonucleotides in a large animal model
HR Benatti, RD Prestigiacomo, T Taghian, R Miller, R King, MJ Gounis, ...
Molecular Therapy-Methods & Clinical Development 31, 2023
2023
Rapalog-Mediated Regulation of an AAV miRNA Targeting Huntingtin in a HD Transgenic Mouse Model
R Miller, E Pfister, E Sapp, M DiFiglia, N Aronin, C Mueller
MOLECULAR THERAPY 28 (4), 70-71, 2020
2020
Engineered exosomes for non-viral delivery of RNA therapeutics to brain
RA Haraszti, MC Didiot, A Biscans, R Miller, M Dubuke, H Rockwell, ...
HUMAN GENE THERAPY 28 (12), A16-A16, 2017
2017
ARRDC1-and Histone-Enriched Exosomes Released from Starved Stem Cells Improve siRNA Transfer to Neurons
RA Haraszti, R Miller, MC Didiot, M Dubuke, J Leszyk, SA Shaffer, ...
MOLECULAR THERAPY 25 (5), 218-219, 2017
2017
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Artikler 1–19