BackgroundCurrent antiretroviral therapy against human immunodeficiency virus (HIV-1) reduces viral load and thereby prevents viral spread, but it cannot eradicate proviral genomes from infected cells.
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Graphene-Based Nanosystem for Targeted Delivery of Anti-Sense miRNA-21 on Hepatocellular Carcinoma Cells. [PDF]
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Cell-penetrating antibody enhances nuclear delivery of triplex-forming oligonucleotides targeting HER2-positive cancers. [PDF]
Minnah A +5 more
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Decoding the genetic blueprints of neurological disorders: disease mechanisms and breakthrough gene therapies. [PDF]
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The role of exosomes as oligonucleotide delivery system for managing α-synuclein in Parkinson's disease: A systematic review of <i>in vivo</i> studies. [PDF]
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Advances in gene therapy for mitochondrial genetic disorders: current status and clinical implementation challenges. [PDF]
Lyu L, Qie B, He Y, Chen F, Liu B.
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Can Gene Therapy Transform the Treatment Landscape of Posterior Segment Eye Diseases? A Comprehensive Review of Recent Advancements. [PDF]
Chen KY, Chan HC, Chan CM.
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Tau-Targeted Therapeutic Strategies: Mechanistic Targets, Clinical Pipelines, and Analysis of Failures. [PDF]
Shen X, Li H, Zhang B, Li Y, Zhu Z.
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Human-Induced Pluripotent Stem Cell Models for Amyloid Cardiomyopathy: From Mechanistic Insights to Therapeutic Discovery. [PDF]
Liu Y, Riaz M.
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