scispace - formally typeset
Y

Young Jik Kwon

Researcher at University of California, Irvine

Publications -  94
Citations -  5668

Young Jik Kwon is an academic researcher from University of California, Irvine. The author has contributed to research in topics: Transfection & Transduction (genetics). The author has an hindex of 29, co-authored 89 publications receiving 4643 citations. Previous affiliations of Young Jik Kwon include Stanford University & Case Western Reserve University.

Papers
More filters
Journal ArticleDOI

"Nanoantibiotics": a new paradigm for treating infectious diseases using nanomaterials in the antibiotics resistant era.

TL;DR: This review summarizes emerging efforts in combating against infectious diseases, particularly using antimicrobial NPs and antibiotics delivery systems as new tools to tackle the current challenges in treating infectious diseases.
Journal ArticleDOI

"Combo" nanomedicine: Co-delivery of multi-modal therapeutics for efficient, targeted, and safe cancer therapy

TL;DR: This review aims to provide an overview of developing multi-modal therapies using nanomaterials ("combo" nanomedicine) along with the rationale, up-to-date progress, further considerations, and the crucial roles of interdisciplinary approaches.
Journal ArticleDOI

Stimuli-responsive polymers and nanomaterials for gene delivery and imaging applications ☆

TL;DR: It is clear that developing novel multifunctional nonviral vectors, which transform their physico-chemical properties in response to various stimuli in a timely and spatially controlled manner, is highly desired to translate the promise of gene therapy for the clinical success.
Journal ArticleDOI

Efficient and targeted delivery of siRNA in vivo.

TL;DR: Major challenges in achieving efficient siRNA delivery in vivo are introduced and recent advances in overcoming them are discussed using chemically modified siRNA, viral siRNA vectors and nonviral siRNA carriers.
Journal ArticleDOI

Molecular genetics and emerging therapies for retinitis pigmentosa: Basic research and clinical perspectives

TL;DR: Development in gene editing technology and novel gene delivery carriers make gene therapy a promising therapeutic modality for RP and other hereditary retinal dystrophies in the future.