Targeting materials and strategies for RNA delivery
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[1] Yang Liu,et al. Development of delivery strategies for CRISPR‐Cas9 genome editing , 2023, BMEMat.
[2] Guoyong Liu,et al. Tuning the Organ Tropism of Polymersome for Spleen-Selective Nanovaccine Delivery to Boost Cancer Immunotherapy. , 2023, Advanced materials.
[3] P. Timashev,et al. Ferritin‐based drug delivery system for tumor therapy , 2023, BMEMat.
[4] D. McComb,et al. STING Agonist-Derived LNP-mRNA Vaccine Enhances Protective Immunity Against SARS-CoV-2 , 2023, Nano letters.
[5] Guangjun Nie,et al. Current advances in non‐viral gene delivery systems: Liposomes versus extracellular vesicles , 2023, BMEMat.
[6] Margaret M. Billingsley,et al. Ionizable Lipid Nanoparticles for In Vivo mRNA Delivery to the Placenta during Pregnancy. , 2023, Journal of the American Chemical Society.
[7] H. Cabral,et al. Polymer‐Based mRNA Delivery Strategies for Advanced Therapies , 2023, Advanced Healthcare Materials.
[8] Sean A. Dilliard,et al. Passive, active and endogenous organ-targeted lipid and polymer nanoparticles for delivery of genetic drugs , 2023, Nature Reviews Materials.
[9] Betty Y. S. Kim,et al. Intradermally delivered mRNA-encapsulating extracellular vesicles for collagen-replacement therapy , 2023, Nature Biomedical Engineering.
[10] Conroy Sun,et al. Peptide-guided lipid nanoparticles deliver mRNA to the neural retina of rodents and nonhuman primates , 2023, Science advances.
[11] D. Weissman,et al. Ionizable lipid nanoparticles deliver mRNA to pancreatic β cells via macrophage-mediated gene transfer , 2023, Science advances.
[12] Hiroki Tanaka,et al. Delivering mRNA to Secondary Lymphoid Tissues by Phosphatidylserine‐Loaded Lipid Nanoparticles , 2022, Advanced healthcare materials.
[13] L. Ferreira,et al. A Polymeric Nanoparticle Formulation for Targeted mRNA Delivery to Fibroblasts , 2022, Advanced science.
[14] H. Harashima,et al. Self-homing nanocarriers for mRNA delivery to the activated hepatic stellate cells in liver fibrosis. , 2022, Journal of controlled release : official journal of the Controlled Release Society.
[15] Z. Li,et al. Intracellular delivery of messenger RNA to macrophages with surfactant-derived lipid nanoparticles , 2022, Materials Today Advances.
[16] Jong Oh Kim,et al. Nano drug delivery systems for antisense oligonucleotides (ASO) therapeutics. , 2022, Journal of controlled release : official journal of the Controlled Release Society.
[17] Pratima Basak,et al. Preparation of selective organ-targeting (SORT) lipid nanoparticles (LNPs) using multiple technical methods for tissue-specific mRNA delivery , 2022, Nature Protocols.
[18] Shaoyi Jiang,et al. Zwitterionic Biomaterials. , 2022, Chemical reviews.
[19] Shaoyi Jiang,et al. Phosphatidylserine Lipid Nanoparticles Promote Systemic RNA Delivery to Secondary Lymphoid Organs. , 2022, Nano letters.
[20] S. Chatterjee,et al. Lipid Nanoparticle (LNP) Chemistry Can Endow Unique In Vivo RNA Delivery Fates within the Liver That Alter Therapeutic Outcomes in a Cancer Model. , 2022, Molecular pharmaceutics.
[21] Jeonghwan Kim,et al. Engineering Lipid Nanoparticles for Enhanced Intracellular Delivery of mRNA through Inhalation. , 2022, ACS nano.
[22] A. Aigner,et al. Therapeutic siRNA: State-of-the-Art and Future Perspectives , 2022, BioDrugs.
[23] James E. Dahlman,et al. Piperazine-derived lipid nanoparticles deliver mRNA to immune cells in vivo , 2022, Nature Communications.
[24] Xingxu Huang,et al. Helper-Polymer Based Five-Element Nanoparticles (FNPs) for Lung-Specific mRNA Delivery with Long-Term Stability after Lyophilization. , 2022, Nano letters.
[25] X. Xiang,et al. Cancer-associated fibroblasts: Vital suppressors of the immune response in the tumor microenvironment. , 2022, Cytokine & growth factor reviews.
[26] B. Hoppe,et al. Improving Treatment Options for Primary Hyperoxaluria , 2022, Drugs.
[27] S. Mitragotri,et al. RNA therapeutics in the clinic , 2022, Bioengineering & translational medicine.
[28] Santosh K Bashyal,et al. Recent progresses in exosome-based systems for targeted drug delivery to the brain. , 2022, Journal of controlled release : official journal of the Controlled Release Society.
[29] J. Bacchetta,et al. Genetic assessment in primary hyperoxaluria: why it matters , 2022, Pediatric Nephrology.
[30] Timothy A. Miller,et al. Antisense Oligonucleotides for the Study and Treatment of ALS , 2022, Neurotherapeutics.
[31] D. Weissman,et al. Rational Design of Bisphosphonate Lipid-like Materials for mRNA Delivery to the Bone Microenvironment. , 2022, Journal of the American Chemical Society.
[32] Yi Hong,et al. Enhancing CRISPR/Cas gene editing through modulating cellular mechanical properties for cancer therapy , 2022, Nature Nanotechnology.
[33] Chunying Chen,et al. Chemical and Biophysical Signatures of the Protein Corona in Nanomedicine. , 2022, Journal of the American Chemical Society.
[34] M. Emdin,et al. RNA-targeting and gene editing therapies for transthyretin amyloidosis , 2022, Nature Reviews Cardiology.
[35] T. Sharp,et al. Anionic Lipid Nanoparticles Preferentially Deliver mRNA to the Hepatic Reticuloendothelial System , 2022, Advanced materials.
[36] Qiaobing Xu,et al. Lung-selective mRNA delivery of synthetic lipid nanoparticles for the treatment of pulmonary lymphangioleiomyomatosis , 2022, Proceedings of the National Academy of Sciences.
[37] M. Coelho,et al. Transferrin Receptor-Targeted Nanocarriers: Overcoming Barriers to Treat Glioblastoma , 2022, Pharmaceutics.
[38] Margaret A. Liu,et al. WHO informal consultation on regulatory considerations for evaluation of the quality, safety and efficacy of RNA-based prophylactic vaccines for infectious diseases, 20–22 April 2021 , 2022, Emerging microbes & infections.
[39] Jiancheng Wang,et al. Non-viral vectors for RNA delivery , 2022, Journal of Controlled Release.
[40] D. Weissman,et al. CAR T cells produced in vivo to treat cardiac injury , 2022, Science.
[41] D. Zack,et al. High-throughput and high-content bioassay enables tuning of polyester nanoparticles for cellular uptake, endosomal escape, and systemic in vivo delivery of mRNA , 2022, Science advances.
[42] Qiang Cheng,et al. On the mechanism of tissue-specific mRNA delivery by selective organ targeting nanoparticles , 2021, Proceedings of the National Academy of Sciences.
[43] James E. Dahlman,et al. Non-liver mRNA Delivery. , 2021, Accounts of chemical research.
[44] Jeonghwan Kim,et al. Chemistry of Lipid Nanoparticles for RNA Delivery. , 2021, Accounts of chemical research.
[45] W. Tarn,et al. Antisense Oligonucleotide-Based Therapy of Viral Infections , 2021, Pharmaceutics.
[46] M. Martínez-García,et al. Polymer-dendrimer hybrids as carriers of anticancer agents. , 2021, Current drug targets.
[47] R. Langer,et al. Nucleic Acid Delivery for Therapeutic Applications. , 2021, Advanced drug delivery reviews.
[48] B. Hoppe,et al. Safety, pharmacodynamics, and exposure-response modeling results from a first in human phase 1 study of nedosiran in primary hyperoxaluria. , 2021, Kidney international.
[49] James E. Dahlman,et al. Optimization of lipid nanoparticles for the delivery of nebulized therapeutic mRNA to the lungs , 2021, Nature Biomedical Engineering.
[50] P. Giangrande,et al. Advances in mRNA non-viral delivery approaches. , 2021, Advanced drug delivery reviews.
[51] K. Ganbarov,et al. SARS-CoV-2 (Covid-19) vaccines structure, mechanisms and effectiveness: A review , 2021, International Journal of Biological Macromolecules.
[52] R. Langer,et al. Lipid nanoparticles for mRNA delivery , 2021, Nature Reviews Materials.
[53] G. Song,et al. Therapeutic HNF4A mRNA attenuates liver fibrosis in a preclinical model. , 2021, Journal of hepatology.
[54] B. Cowling,et al. Comparative immunogenicity of mRNA and inactivated vaccines against COVID-19 , 2021, The Lancet Microbe.
[55] D. Matei,et al. The Ratio of Toxic-to-Nontoxic miRNAs Predicts Platinum Sensitivity in Ovarian Cancer , 2021, Cancer Research.
[56] Daniel G. Anderson,et al. Systemic delivery of mRNA and DNA to the lung using polymer-lipid nanoparticles. , 2021, Biomaterials.
[57] D. Weissman,et al. Highly efficient CD4+ T cell targeting and genetic recombination using engineered CD4+ cell-homing mRNA-LNPs , 2021, Molecular therapy : the journal of the American Society of Gene Therapy.
[58] A. Aljabali,et al. siRNA: Mechanism of action, challenges, and therapeutic approaches. , 2021, European journal of pharmacology.
[59] M. Imperiale,et al. Biology of Polyomavirus miRNA , 2021, Frontiers in Microbiology.
[60] S. Crooke,et al. Antisense technology: an overview and prospectus , 2021, Nature Reviews Drug Discovery.
[61] Mary E. Haas,et al. Lipid nanoparticle-mediated codelivery of Cas9 mRNA and single-guide RNA achieves liver-specific in vivo genome editing of Angptl3 , 2021, Proceedings of the National Academy of Sciences.
[62] Lukas Farbiak,et al. Membrane destabilizing ionizable phospholipids for organ selective mRNA delivery and CRISPR/Cas gene editing , 2021, Nature Materials.
[63] Q. Qian,et al. Therapeutic Mechanism of Nucleic Acid Drugs , 2021 .
[64] G. Ariceta,et al. Hepatic Lactate Dehydrogenase A: An RNA Interference Target for the Treatment of All Known Types of Primary Hyperoxaluria , 2021, Kidney international reports.
[65] K. Nam,et al. Engineered ionizable lipid nanoparticles for targeted delivery of RNA therapeutics into different types of cells in the liver , 2021, Science Advances.
[66] Zhujun Cheng,et al. The Risks of miRNA Therapeutics: In a Drug Target Perspective , 2021, Drug design, development and therapy.
[67] A. Waisman,et al. A noninflammatory mRNA vaccine for treatment of experimental autoimmune encephalomyelitis , 2021, Science.
[68] Jeonghwan Kim,et al. Self-assembled mRNA vaccines , 2021, Advanced Drug Delivery Reviews.
[69] Turkan Kopac,et al. Protein corona, understanding the nanoparticle-protein interactions and future perspectives: A critical review. , 2020, International journal of biological macromolecules.
[70] Qiang Cheng,et al. A Systematic Study of Unsaturation in Lipid Nanoparticles Leads to Improved mRNA Transfection In Vivo. , 2020, Angewandte Chemie.
[71] Nicholas A. Peppas,et al. Engineering precision nanoparticles for drug delivery , 2020, Nature reviews. Drug discovery.
[72] S. Solomon,et al. Novel antisense therapy targeting microRNA-132 in patients with heart failure: results of a first-in-human Phase 1b randomized, double-blind, placebo-controlled study , 2020, European heart journal.
[73] Siddharth Patel,et al. The effects of PEGylation on LNP based mRNA delivery to the eye , 2020, PloS one.
[74] M. Gyöngyösi,et al. CDR132L improves systolic and diastolic function in a large animal model of chronic heart failure , 2020, European heart journal.
[75] M. Wood,et al. Application of CRISPR-Cas9-Mediated Genome Editing for the Treatment of Myotonic Dystrophy Type 1. , 2020, Molecular therapy : the journal of the American Society of Gene Therapy.
[76] Michael Y. T. Chow,et al. Inhaled RNA Therapy: From Promise to Reality , 2020, Trends in Pharmacological Sciences.
[77] R. Langer,et al. Advances in oligonucleotide drug delivery , 2020, Nature Reviews Drug Discovery.
[78] Luis A. Barrera,et al. Functionalized lipid-like nanoparticles for in vivo mRNA delivery and base editing , 2020, Science Advances.
[79] Daniel G. Anderson,et al. Delivery of Tissue-Targeted Scalpels: Opportunities and Challenges for In Vivo CRISPR/Cas-Based Genome Editing. , 2020, ACS nano.
[80] Qiaobing Xu,et al. Imidazole-based Synthetic Lipidoids for In Vivo mRNA Delivery into Primary T Lymphocytes. , 2020, Angewandte Chemie.
[81] Qiang Cheng,et al. Theranostic dendrimer-based lipid nanoparticles containing PEGylated BODIPY dyes for tumor imaging and systemic mRNA delivery in vivo. , 2020, Journal of controlled release : official journal of the Controlled Release Society.
[82] Qiaobing Xu,et al. Neurotransmitter-derived lipidoids (NT-lipidoids) for enhanced brain delivery through intravenous injection , 2020, Science Advances.
[83] J. Karp,et al. BBB pathophysiology independent delivery of siRNA in traumatic brain injury , 2020, bioRxiv.
[84] E. Olson,et al. Systemic nanoparticle delivery of CRISPR-Cas9 ribonucleoproteins for effective tissue specific genome editing , 2020, Nature Communications.
[85] W. Saltzman,et al. Polymeric vehicles for nucleic acid delivery. , 2020, Advanced drug delivery reviews.
[86] J. Heyes,et al. Lipid nanoparticles for nucleic acid delivery: Current perspectives. , 2020, Advanced drug delivery reviews.
[87] Khalid A. Hajj,et al. A potent branched-tail lipid nanoparticle enables multiplexed mRNA delivery and gene editing in vivo. , 2020, Nano letters.
[88] R. Bahal,et al. Role of Lipid-Based and Polymer-Based Non-Viral Vectors in Nucleic Acid Delivery for Next-Generation Gene Therapy , 2020, Molecules.
[89] J. Knuuti,et al. Synthetic mRNA Encoding VEGF-A in Patients Undergoing Coronary Artery Bypass Grafting: Design of a Phase 2a Clinical Trial , 2020, Molecular therapy. Methods & clinical development.
[90] Bruna dos Santos Rodrigues,et al. In Vitro and In Vivo characterization of CPP and transferrin modified liposomes encapsulating pDNA. , 2020, Nanomedicine : nanotechnology, biology, and medicine.
[91] J. Yewdell,et al. Decoding mRNA translatability and stability from the 5′ UTR , 2020, Nature Structural & Molecular Biology.
[92] Qiang Cheng,et al. Selective ORgan Targeting (SORT) nanoparticles for tissue specific mRNA delivery and CRISPR/Cas gene editing , 2020, Nature Nanotechnology.
[93] Qiang Cheng,et al. Lipid‐Modified Aminoglycosides for mRNA Delivery to the Liver , 2020, Advanced healthcare materials.
[94] James E. Dahlman,et al. Nanoparticles containing constrained phospholipids deliver mRNA to liver immune cells in vivo without targeting ligands , 2020, Bioengineering & translational medicine.
[95] Siddharth Patel,et al. Naturally-occurring cholesterol analogues in lipid nanoparticles induce polymorphic shape and enhance intracellular delivery of mRNA , 2020, Nature Communications.
[96] A. Ortiz,et al. Pelacarsen for lowering lipoprotein(a): implications for patients with chronic kidney disease , 2020, Clinical kidney journal.
[97] L. Scott. Givosiran: First Approval , 2020, Drugs.
[98] R. Gemeinhart,et al. Toward understanding polymer micelle stability: Density ultracentrifugation offers insight into polymer micelle stability in human fluids. , 2019, Journal of controlled release : official journal of the Controlled Release Society.
[99] Do Won Hwang,et al. Systemic delivery of microRNA-21 antisense oligonucleotides to the brain using T7-peptide decorated exosomes. , 2019, Journal of controlled release : official journal of the Controlled Release Society.
[100] C. Vanhove,et al. Non-viral delivery of chemically modified mRNA to the retina: Subretinal versus intravitreal administration. , 2019, Journal of controlled release : official journal of the Controlled Release Society.
[101] T. Andresen,et al. Targeting the transferrin receptor for brain drug delivery , 2019, Progress in Neurobiology.
[102] B. Newland,et al. Highly branched poly(β-amino ester) delivery of minicircle DNA for transfection of neurodegenerative disease related cells , 2019, Nature Communications.
[103] A. Jimeno,et al. Abstract CT210: A Phase I, open-label, multicenter, dose escalation study of mRNA-2752, a lipid nanoparticle encapsulating mRNAs encoding human OX40L, IL-23, and IL-36γ, for intratumoral injection alone and in combination with immune checkpoint blockade , 2019, Clinical Trials.
[104] Jordan J. Green,et al. Cancer‐Targeting Nanoparticles for Combinatorial Nucleic Acid Delivery , 2019, Advanced materials.
[105] Gaurav Sahay,et al. Lipid nanoparticles for delivery of messenger RNA to the back of the eye. , 2019, Journal of controlled release : official journal of the Controlled Release Society.
[106] Ryan L Setten,et al. The current state and future directions of RNAi-based therapeutics , 2019, Nature Reviews Drug Discovery.
[107] Manish R. Patel,et al. A phase I multicenter study to assess the safety, tolerability, and immunogenicity of mRNA-4157 alone in patients with resected solid tumors and in combination with pembrolizumab in patients with unresectable solid tumors. , 2019, Journal of Clinical Oncology.
[108] B. Rothen‐Rutishauser,et al. Polymer-Coated Gold Nanospheres Do Not Impair the Innate Immune Function of Human B Lymphocytes in Vitro. , 2019, ACS Nano.
[109] Jingwen Sun,et al. Copper Sulfide Facilitates Hepatobiliary Clearance of Gold Nanoparticles through the Copper-Transporting ATPase ATP7B. , 2019, ACS nano.
[110] Hao Yin,et al. Genome Editing with mRNA Encoding ZFN, TALEN, and Cas9. , 2019, Molecular therapy : the journal of the American Society of Gene Therapy.
[111] I. Sahu,et al. Recent Developments in mRNA-Based Protein Supplementation Therapy to Target Lung Diseases. , 2019, Molecular therapy : the journal of the American Society of Gene Therapy.
[112] Daniel G Anderson,et al. Delivering the Messenger: Advances in Technologies for Therapeutic mRNA Delivery. , 2019, Molecular therapy : the journal of the American Society of Gene Therapy.
[113] D. Offen,et al. Golden Exosomes Selectively Target Brain Pathologies in Neurodegenerative and Neurodevelopmental Disorders. , 2019, Nano letters.
[114] Khalid A. Hajj,et al. Branched-Tail Lipid Nanoparticles Potently Deliver mRNA In Vivo due to Enhanced Ionization at Endosomal pH. , 2019, Small.
[115] C. Bennett. Therapeutic Antisense Oligonucleotides Are Coming of Age. , 2019, Annual review of medicine.
[116] Robert Langer,et al. Inhaled Nanoformulated mRNA Polyplexes for Protein Production in Lung Epithelium , 2019, Advanced materials.
[117] I. Papangeli,et al. CRISPR/Cas9 gene-editing: Research technologies, clinical applications and ethical considerations. , 2018, Seminars in perinatology.
[118] N. Pedemonte,et al. Chemically modified hCFTR mRNAs recuperate lung function in a mouse model of cystic fibrosis , 2018, Scientific Reports.
[119] Dan Peer,et al. Cell specific delivery of modified mRNA expressing therapeutic proteins to leukocytes , 2018, Nature Communications.
[120] Philip J. Santangelo,et al. High-throughput in vivo screen of functional mRNA delivery identifies nanoparticles for endothelial cell gene editing , 2018, Proceedings of the National Academy of Sciences.
[121] Hao Zhou,et al. Zinc Coordinated Cationic Polymers Break Up the Paradox between Low Molecular Weight and High Transfection Efficacy. , 2018, Biomacromolecules.
[122] Kaitlyn Sadtler,et al. Optimization of a Degradable Polymer-Lipid Nanoparticle for Potent Systemic Delivery of mRNA to the Lung Endothelium and Immune Cells. , 2018, Nano letters.
[123] Daniel G. Anderson,et al. Customizable Lipid Nanoparticle Materials for the Delivery of siRNAs and mRNAs. , 2018, Angewandte Chemie.
[124] K. Garber. Alnylam launches era of RNAi drugs , 2018, Nature Biotechnology.
[125] C. Mayr. What Are 3' UTRs Doing? , 2018, Cold Spring Harbor perspectives in biology.
[126] R. Tarran,et al. The epithelial sodium channel (ENaC) as a therapeutic target for cystic fibrosis lung disease , 2018, Expert opinion on therapeutic targets.
[127] Robert Langer,et al. Ionizable Amino‐Polyesters Synthesized via Ring Opening Polymerization of Tertiary Amino‐Alcohols for Tissue Selective mRNA Delivery , 2018, Advanced materials.
[128] S. Solomon,et al. Patisiran, an RNAi Therapeutic, for Hereditary Transthyretin Amyloidosis , 2018, The New England journal of medicine.
[129] E. Salido,et al. Specific Inhibition of Hepatic Lactate Dehydrogenase Reduces Oxalate Production in Mouse Models of Primary Hyperoxaluria , 2018, Molecular therapy : the journal of the American Society of Gene Therapy.
[130] R. Waymouth,et al. Enhanced mRNA delivery into lymphocytes enabled by lipid-varied libraries of charge-altering releasable transporters , 2018, Proceedings of the National Academy of Sciences.
[131] Yizhou Dong,et al. Co-delivery of mRNA and SPIONs through amino-ester nanomaterials , 2018, Nano Research.
[132] O. Farokhzad,et al. Nanotechnology-Based Strategies for siRNA Brain Delivery for Disease Therapy. , 2018, Trends in biotechnology.
[133] W. Harrington,et al. A Single Administration of CRISPR/Cas9 Lipid Nanoparticles Achieves Robust and Persistent In Vivo Genome Editing. , 2018, Cell reports.
[134] P. Trivedi,et al. Advances in siRNA delivery in cancer therapy , 2018, Artificial cells, nanomedicine, and biotechnology.
[135] J. Lieberman,et al. A modular platform for targeted RNAi therapeutics , 2018, Nature Nanotechnology.
[136] B. Kumar,et al. Promising Targets in Anti-cancer Drug Development: Recent Updates. , 2018, Current medicinal chemistry.
[137] Yoosoo Yang,et al. Cancer‐derived exosomes as a delivery platform of CRISPR/Cas9 confer cancer cell tropism‐dependent targeting , 2017, Journal of controlled release : official journal of the Controlled Release Society.
[138] Qiang Cheng,et al. Systemic mRNA Delivery to the Lungs by Functional Polyester-based Carriers. , 2017, Biomacromolecules.
[139] Daniel G. Anderson,et al. Structure-guided chemical modification of guide RNA enables potent non-viral in vivo genome editing , 2017, Nature Biotechnology.
[140] Khalid A. Hajj,et al. Tools for translation: non-viral materials for therapeutic mRNA delivery , 2017 .
[141] Jiayi Pan,et al. Dendrimers as Nanocarriers for Nucleic Acid and Drug Delivery in Cancer Therapy , 2017, Molecules.
[142] Kimberly J. Hassett,et al. Efficient Targeting and Activation of Antigen-Presenting Cells In Vivo after Modified mRNA Vaccine Administration in Rhesus Macaques , 2017, Molecular therapy : the journal of the American Society of Gene Therapy.
[143] J. Ulmer,et al. Mechanism of action of mRNA-based vaccines , 2017, Expert review of vaccines.
[144] S. Newman. Drug delivery to the lungs: challenges and opportunities. , 2017, Therapeutic delivery.
[145] Bin Li,et al. Biodegradable Amino-Ester Nanomaterials for Cas9 mRNA Delivery in Vitro and in Vivo. , 2017, ACS applied materials & interfaces.
[146] Shuai Liu,et al. Alkylated branched poly(β-amino esters) demonstrate strong DNA encapsulation, high nanoparticle stability and robust gene transfection efficacy. , 2017, Journal of materials chemistry. B.
[147] Wenxin Wang,et al. Biodegradable Highly Branched Poly(β-Amino Ester)s for Targeted Cancer Cell Gene Transfection. , 2017, ACS biomaterials science & engineering.
[148] Mark W. Tibbitt,et al. Synthesis and Biological Evaluation of Ionizable Lipid Materials for the In Vivo Delivery of Messenger RNA to B Lymphocytes , 2017, Advanced materials.
[149] P. Cullis,et al. Lipid Nanoparticle Systems for Enabling Gene Therapies. , 2017, Molecular therapy : the journal of the American Society of Gene Therapy.
[150] Raghu Kalluri,et al. Exosomes Facilitate Therapeutic Targeting of Oncogenic Kras in Pancreatic Cancer , 2017, Nature.
[151] Shuai Liu,et al. Bioreducible Zinc(II)-Coordinative Polyethylenimine with Low Molecular Weight for Robust Gene Delivery of Primary and Stem Cells. , 2017, Journal of the American Chemical Society.
[152] W. Baumgartner,et al. Generation‐6 hydroxyl PAMAM dendrimers improve CNS penetration from intravenous administration in a large animal brain injury model , 2017, Journal of controlled release : official journal of the Controlled Release Society.
[153] Robert Langer,et al. Lipid Nanoparticle Assisted mRNA Delivery for Potent Cancer Immunotherapy. , 2017, Nano letters.
[154] S. Dowdy. Overcoming cellular barriers for RNA therapeutics , 2017, Nature Biotechnology.
[155] Hao Zhu,et al. Non-Viral CRISPR/Cas Gene Editing In Vitro and In Vivo Enabled by Synthetic Nanoparticle Co-Delivery of Cas9 mRNA and sgRNA. , 2017, Angewandte Chemie.
[156] Daniel G Anderson,et al. Polymer-Lipid Nanoparticles for Systemic Delivery of mRNA to the Lungs. , 2016, Angewandte Chemie.
[157] Y. Yeo,et al. Pharmacokinetics and biodistribution of recently-developed siRNA nanomedicines. , 2016, Advanced drug delivery reviews.
[158] Vladimir P Torchilin,et al. Mixed Nanosized Polymeric Micelles as Promoter of Doxorubicin and miRNA-34a Co-Delivery Triggered by Dual Stimuli in Tumor Tissue. , 2016, Small.
[159] C. Rudolph,et al. A Single Methylene Group in Oligoalkylamine-Based Cationic Polymers and Lipids Promotes Enhanced mRNA Delivery. , 2016, Angewandte Chemie.
[160] Özlem Türeci,et al. Systemic RNA delivery to dendritic cells exploits antiviral defence for cancer immunotherapy , 2016, Nature.
[161] K. Whitehead,et al. Lipidoid Tail Structure Strongly Influences siRNA Delivery Activity , 2016 .
[162] Thomas D. Schmittgen,et al. Effects of local structural transformation of lipid-like compounds on delivery of messenger RNA , 2016, Scientific Reports.
[163] Mark W. Tibbitt,et al. Bioinspired Alkenyl Amino Alcohol Ionizable Lipid Materials for Highly Potent In Vivo mRNA Delivery , 2016, Advanced materials.
[164] Jun Zhu,et al. Inferred miRNA activity identifies miRNA-mediated regulatory networks underlying multiple cancers , 2015, Bioinform..
[165] Mauro Ferrari,et al. Principles of nanoparticle design for overcoming biological barriers to drug delivery , 2015, Nature Biotechnology.
[166] G. Salzano,et al. Multifunctional Polymeric Micelles Co-loaded with Anti–Survivin siRNA and Paclitaxel Overcome Drug Resistance in an Animal Model of Ovarian Cancer , 2015, Molecular Cancer Therapeutics.
[167] G. Szabo,et al. Exosome-mediated delivery of functionally active miRNA-155 inhibitor to macrophages. , 2014, Nanomedicine : nanotechnology, biology, and medicine.
[168] Meg Duroux,et al. A comprehensive overview of exosomes as drug delivery vehicles - endogenous nanocarriers for targeted cancer therapy. , 2014, Biochimica et biophysica acta.
[169] V. Kim,et al. TAIL-seq: genome-wide determination of poly(A) tail length and 3' end modifications. , 2014, Molecular cell.
[170] Robert Langer,et al. Lipopeptide nanoparticles for potent and selective siRNA delivery in rodents and nonhuman primates , 2014, Proceedings of the National Academy of Sciences.
[171] Ronald A. Li,et al. Modified mRNA directs the fate of heart progenitor cells and induces vascular regeneration after myocardial infarction , 2013, Nature Biotechnology.
[172] Shigeo Matsuda,et al. Maximizing the Potency of siRNA Lipid Nanoparticles for Hepatic Gene Silencing In Vivo** , 2012, Angewandte Chemie.
[173] M. Wood,et al. Exosome nanotechnology: An emerging paradigm shift in drug delivery , 2011, BioEssays : news and reviews in molecular, cellular and developmental biology.
[174] Joseph M. DeSimone,et al. Using mechanobiological mimicry of red blood cells to extend circulation times of hydrogel microparticles , 2011, Proceedings of the National Academy of Sciences.
[175] B. Campbell,et al. RNA interference: a chemist's perspective. , 2010, Chemical Society reviews.
[176] Leaf Huang,et al. Stealth nanoparticles: high density but sheddable PEG is a key for tumor targeting. , 2010, Journal of controlled release : official journal of the Controlled Release Society.
[177] P. Devarajan,et al. Particle shape: a new design parameter for passive targeting in splenotropic drug delivery. , 2010, Journal of pharmaceutical sciences.
[178] F. Dammacco,et al. Targeted therapies in cancer , 2018, Surgery (Oxford).
[179] Sei-Young Lee,et al. Shaping nano-/micro-particles for enhanced vascular interaction in laminar flows , 2009, Nanotechnology.
[180] J. Cavaille,et al. C19MC microRNAs are processed from introns of large Pol-II, non-protein-coding transcripts , 2009, Nucleic acids research.
[181] J. Watts,et al. Chemically modified siRNA: tools and applications. , 2008, Drug discovery today.
[182] M Ferrari,et al. The effect of shape on the margination dynamics of non-neutrally buoyant particles in two-dimensional shear flows. , 2008, Journal of biomechanics.
[183] J. Steitz,et al. Switching from Repression to Activation: MicroRNAs Can Up-Regulate Translation , 2007, Science.
[184] M. Bawendi,et al. Renal clearance of quantum dots , 2007, Nature Biotechnology.
[185] V. Rotello,et al. Drug and gene delivery using gold nanoparticles , 2007 .
[186] U. Şahin,et al. Modification of antigen-encoding RNA increases stability, translational efficacy, and T-cell stimulatory capacity of dendritic cells. , 2006, Blood.
[187] Shubiao Zhang,et al. Toxicity of cationic lipids and cationic polymers in gene delivery. , 2006, Journal of controlled release : official journal of the Controlled Release Society.
[188] Fumiyoshi Yamashita,et al. The role of dioleoylphosphatidylethanolamine (DOPE) in targeted gene delivery with mannosylated cationic liposomes via intravenous route. , 2005, Journal of controlled release : official journal of the Controlled Release Society.
[189] C. Porter,et al. Subcutaneous drug delivery and the role of the lymphatics. , 2005, Drug discovery today. Technologies.
[190] D. Bartel. MicroRNAs Genomics, Biogenesis, Mechanism, and Function , 2004, Cell.
[191] Laurence Zitvogel,et al. Exosomes: composition, biogenesis and function , 2002, Nature Reviews Immunology.
[192] N. Sonenberg,et al. The major mRNA‐associated protein YB‐1 is a potent 5′ cap‐dependent mRNA stabilizer , 2001, The EMBO journal.
[193] A. Fire,et al. Potent and specific genetic interference by double-stranded RNA in Caenorhabditis elegans , 1998, Nature.
[194] N. Sonenberg,et al. eIF4G Dramatically Enhances the Binding of eIF4E to the mRNA 5′-Cap Structure* , 1997, The Journal of Biological Chemistry.
[195] H. J. Kim,et al. Engineered Lipid Nanoparticles for the Treatment of Pulmonary Fibrosis by Regulating Epithelial‐Mesenchymal Transition in the Lungs , 2023 .
[196] P. Dřevínek,et al. Antisense oligonucleotide eluforsen is safe and improves respiratory symptoms in F508DEL cystic fibrosis. , 2019, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.
[197] P. Cullis,et al. Liposomal drug delivery systems: from concept to clinical applications. , 2013, Advanced drug delivery reviews.
[198] Warren C W Chan,et al. Strategies for the intracellular delivery of nanoparticles. , 2011, Chemical Society reviews.
[199] M. Stephenson,et al. Inhibition of Rous sarcoma virus replication and cell transformation by a specific oligodeoxynucleotide. , 1978, Proceedings of the National Academy of Sciences of the United States of America.
[200] Zwitterionic Phospholipidation of Cationic Polymers Facilitates Systemic mRNA Delivery to Spleen and Lymph Nodes , 2022 .