Genetically engineered microvesicles carrying suicide mRNA/protein inhibit schwannoma tumor growth. - Wikidata - wikimedia - TriplyDB

Genetically engineered microvesicles carrying suicide mRNA/protein inhibit schwannoma tumor growth.

Genetically engineered microvesicles carrying suicide mRNA/protein inhibit schwannoma tumor growth.

http://www.wikidata.org/entity/Q39293667

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Epigenetic Regulation of Oxidative Stress in Ischemic Stroke Extracellular Vesicles in Physiology, Pathology, and Therapy of the Immune and Central Nervous System, with Focus on Extracellular Vesicles Derived from Mesenchymal Stem Cells as Therapeutic Tools Texosome-based drug delivery system for cancer therapy: from past to present Tumor-derived exosomes in cancer progression and treatment failure From pathogenesis to clinical application: insights into exosomes as transfer vectors in cancer Extracellular vesicle-mediated delivery of molecular compounds into gametes and embryos: learning from nature Presence of Cx43 in extracellular vesicles reduces the cardiotoxicity of the anti-tumour therapeutic approach with doxorubicin Cell-derived vesicles for drug therapy and diagnostics: opportunities and challenges.Engineering Exosomes for Cancer Therapy.The role of extracellular vesicles in the progression of neurodegenerative disease and cancer FedExosomes: Engineering Therapeutic Biological Nanoparticles that Truly Deliver.Differential fates of biomolecules delivered to target cells via extracellular vesicles.Extracellular vesicles as shuttles of tumor biomarkers and anti-tumor drugs Stabilization of exosome-targeting peptides via engineered glycosylation.Gene therapy for the nervous system: challenges and new strategies.Therapeutic applications of extracellular vesicles: clinical promise and open questions.L Particles Transmit Viral Proteins from Herpes Simplex Virus 1-Infected Mature Dendritic Cells to Uninfected Bystander Cells, Inducing CD83 Downmodulation Delivery of Therapeutic Proteins via Extracellular Vesicles: Review and Potential Treatments for Parkinson's Disease, Glioma, and Schwannoma.A platform for actively loading cargo RNA to elucidate limiting steps in EV-mediated delivery.Synergy of homocysteine, microRNA, and epigenetics: a novel therapeutic approach for stroke.Dynamic biodistribution of extracellular vesicles in vivo using a multimodal imaging reporter.Current Perspectives on In Vivo Noninvasive Tracking of Extracellular Vesicles with Molecular Imaging.Small Luggage for a Long Journey: Transfer of Vesicle-Enclosed Small RNA in Interspecies Communication.Synthetic nucleic acids delivered by exosomes: a potential therapeutic for generelated metabolic brain diseases.MicroRNAs delivered by extracellular vesicles: an emerging resistance mechanism for breast cancer.Use of genetically modified mesenchymal stem cells to treat neurodegenerative diseases.Extracellular RNA mediates and marks cancer progression.Achieving the Promise of Therapeutic Extracellular Vesicles: The Devil is in Details of Therapeutic Loading.Extracellular vesicles derived from human vestibular schwannomas associated with poor hearing damage cochlear cells.Extracellular Vesicles in Brain Tumor Progression.Extracellular vesicles and intercellular communication within the nervous system.Biology and biogenesis of shed microvesicles.The Exosome - A Naturally Secreted Nanoparticle and its Application to Wound Healing.Re-Engineering Extracellular Vesicles as Smart Nanoscale Therapeutics.Advances in Anticancer Protein Delivery Using Micro-/ Nanoparticles.Extracellular vesicle-mediated suicide mRNA/protein delivery inhibits glioblastoma tumor growth in vivo.Extracellular vesicles for nucleic acid delivery: progress and prospects for safe RNA-based gene therapy.Exosomes in cancer theranostic: Diamonds in the rough.Exosomes and their Application in Biomedical Field: Difficulties and Advantages.Low active loading of cargo into engineered extracellular vesicles results in inefficient miRNA mimic delivery.

P2860

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P2860

Genetically engineered microvesicles carrying suicide mRNA/protein inhibit schwannoma tumor growth.

http://www.wikidata.org/entity/Q39293667

description

2012 nî lūn-bûn

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2012年の論文

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2012年論文

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2012年論文

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2012年論文

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2012年論文

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2012年論文

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2012年论文

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2012年论文

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2012年论文

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name

Genetically engineered microve ...... hibit schwannoma tumor growth.

@en

Genetically engineered microve ...... hibit schwannoma tumor growth.

@nl

type

label

Genetically engineered microve ...... hibit schwannoma tumor growth.

@en

Genetically engineered microve ...... hibit schwannoma tumor growth.

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prefLabel

Genetically engineered microve ...... hibit schwannoma tumor growth.

@en

Genetically engineered microve ...... hibit schwannoma tumor growth.

@nl

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Molecular Therapy

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Genetically engineered microve ...... hibit schwannoma tumor growth.

@en

P2093

Arda Mizrak

http://www.w3.org/2001/XMLSchema#string

Erdogan Pekcan Erkan

http://www.w3.org/2001/XMLSchema#string

Gary J Brenner

http://www.w3.org/2001/XMLSchema#string

Gokhan Baris Ozdener

http://www.w3.org/2001/XMLSchema#string

Mehmet Fatih Bolukbasi

http://www.w3.org/2001/XMLSchema#string

Okay Saydam

http://www.w3.org/2001/XMLSchema#string

Sibylle Madlener

http://www.w3.org/2001/XMLSchema#string

Thomas Ströbel

http://www.w3.org/2001/XMLSchema#string

Xandra O Breakefield

http://www.w3.org/2001/XMLSchema#string

P2860

Transfer of microRNAs by embryonic stem cell microvesicles

Embryonic stem cell-derived microvesicles reprogram hematopoietic progenitors: evidence for horizontal transfer of mRNA and protein delivery

Tumour microvesicles contain retrotransposon elements and amplified oncogene sequences

Unidirectional transfer of microRNA-loaded exosomes from T cells to antigen-presenting cells

Exosomal-like vesicles are present in human blood plasma

Glioblastoma microvesicles transport RNA and proteins that promote tumour growth and provide diagnostic biomarkers

Silica crystals and aluminum salts activate the NALP3 inflammasome through phagosomal destabilization

B lymphocytes secrete antigen-presenting vesicles

Exosome-mediated transfer of mRNAs and microRNAs is a novel mechanism of genetic exchange between cells

Early shutoff of host protein synthesis in cells infected with herpes simplex viruses

P304

101-108

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scholarly article

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10.1038/MT.2012.161

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P433

1

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21

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230713802

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22910294

http://www.w3.org/2001/XMLSchema#string

P921

genetic engineering

veteran suicide

P932

3538300

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