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Lipids and lipid derivatives for RNA delivery
RNA-based therapeutics have shown great promise in treating a broad spectrum of
diseases through various mechanisms including knockdown of pathological genes …
diseases through various mechanisms including knockdown of pathological genes …
Strategies in the delivery of Cas9 ribonucleoprotein for CRISPR/Cas9 genome editing
S Zhang, J Shen, D Li, Y Cheng - Theranostics, 2021 - pmc.ncbi.nlm.nih.gov
CRISPR/Cas9 genome editing has gained rapidly increasing attentions in recent years,
however, the translation of this biotechnology into therapy has been hindered by efficient …
however, the translation of this biotechnology into therapy has been hindered by efficient …
The mRNA vaccine revolution: COVID-19 has launched the future of vaccinology
During the COVID-19 pandemic, mRNA (mRNA) vaccines emerged as leading vaccine
candidates in a record time. Nonreplicating mRNA (NRM) and self-amplifying mRNA (SAM) …
candidates in a record time. Nonreplicating mRNA (NRM) and self-amplifying mRNA (SAM) …
Polymers for cytosolic protein delivery
J Lv, Q Fan, H Wang, Y Cheng - Biomaterials, 2019 - Elsevier
Cytosolic protein delivery offers opportunities to develop protein-based therapeutics
specifically modulate intracellular processes, especially those linked to 'undruggable'targets …
specifically modulate intracellular processes, especially those linked to 'undruggable'targets …
Develo** biodegradable lipid nanoparticles for intracellular mRNA delivery and genome editing
Conspectus Since the US Food and Drug Administration (FDA) granted emergency use
authorization for two mRNA vaccines against SARS-CoV-2, mRNA-based technology has …
authorization for two mRNA vaccines against SARS-CoV-2, mRNA-based technology has …
Imidazole‐based synthetic lipidoids for in vivo mRNA delivery into primary T lymphocytes
Engineering T lymphocytes is an emerging approach in a variety of biomedical applications.
However, delivering large biologics to primary T lymphocytes directly in vivo is technically …
However, delivering large biologics to primary T lymphocytes directly in vivo is technically …
Carrier strategies boost the application of CRISPR/Cas system in gene therapy
Z Xu, Q Wang, H Zhong, Y Jiang, X Shi, B Yuan… - …, 2022 - Wiley Online Library
Emerging clustered regularly interspaced short palindromic repeat/associated protein
(CRISPR/Cas) genome editing technology shows great potential in gene therapy. However …
(CRISPR/Cas) genome editing technology shows great potential in gene therapy. However …
Nanocarrier‐mediated cytosolic delivery of biopharmaceuticals
Biopharmaceuticals have emerged to play a vital role in disease treatment and have shown
promise in the rapidly expanding pharmaceutical market due to their high specificity and …
promise in the rapidly expanding pharmaceutical market due to their high specificity and …
[HTML][HTML] Tailoring combinatorial lipid nanoparticles for intracellular delivery of nucleic acids, proteins, and drugs
Lipid nanoparticle (LNP)-based drug delivery systems have become the most clinically
advanced non-viral delivery technology. LNPs can encapsulate and deliver a wide variety of …
advanced non-viral delivery technology. LNPs can encapsulate and deliver a wide variety of …
In situ cancer vaccination using lipidoid nanoparticles
In situ vaccination is a promising strategy for cancer immunotherapy owing to its
convenience and the ability to induce numerous tumor antigens. However, the advancement …
convenience and the ability to induce numerous tumor antigens. However, the advancement …