Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Lukas Farbiak"'
Autor:
Xueliang Yu, Shuai Liu, Qiang Cheng, Sang M. Lee, Tuo Wei, Di Zhang, Lukas Farbiak, Lindsay T. Johnson, Xu Wang, Daniel John Siegwart
Publikováno v:
Pharmaceutics, Vol 13, Iss 11, p 1914 (2021)
Messenger RNA (mRNA) has generated great attention due to its broad potential therapeutic applications, including vaccines, protein replacement therapy, and immunotherapy. Compared to other nucleic acids (e.g., siRNA and pDNA), there are more opportu
Externí odkaz:
https://doaj.org/article/d4c84e7de6404a5fad7c36abe82adb46
Autor:
Di Zhang, Guoxun Wang, Xueliang Yu, Tuo Wei, Lukas Farbiak, Lindsay T. Johnson, Alan Mark Taylor, Jiazhu Xu, Yi Hong, Hao Zhu, Daniel J. Siegwart
Publikováno v:
Nature Nanotechnology. 17:777-787
Genome editing holds great potential for cancer treatment due to the ability to precisely inactivate or repair cancer-related genes. However, delivery of CRISPR/Cas to solid tumours for efficient cancer therapy remains challenging. Here we targeted t
Autor:
Norbert Pardi, Daria Strelkova, Jason B. Miller, Mariah L. Arral, Khalid A. Hajj, Kathryn A. Whitehead, Namit Chaudhary, Daniel J. Siegwart, Drew Weissman, Mohamad-Gabriel Alameh, Jilian R. Melamed, Lukas Farbiak
Publikováno v:
J Control Release
Therapeutic mRNA has the potential to revolutionize the treatment of myriad diseases and, in 2020, facilitated the most rapid vaccine development in history. Among the substantial advances in mRNA technology made in recent years, the incorporation of
Autor:
Osamah Mian, Lindsay T. Johnson, Erick D. Guerrero, Xu Wang, Martha Marquez Ramirez, Ester Alvarez Benedicto, Lukas Farbiak, Daniel J. Siegwart
Publikováno v:
Biomater Sci
Lipid nanoparticles (LNPs) have been established as an essential platform for nucleic acid delivery. Efforts have led to the development of vaccines that protect against SARS-CoV-2 infection using LNPs to deliver messenger RNA (mRNA) coding for the v
Autor:
Lindsay T, Johnson, Di, Zhang, Kejin, Zhou, Sang M, Lee, Shuai, Liu, Sean A, Dilliard, Lukas, Farbiak, Sumanta, Chatterjee, Yu-Hsuan, Lin, Daniel J, Siegwart
Publikováno v:
Molecular pharmaceutics. 19(11)
Within the field of lipid nanoparticles (LNPs) for RNA delivery, the focus has been mainly placed on organ level delivery, which can mask cellular level effects consequential to therapeutic applications. Here, we studied a pair of LNPs with similar p
Autor:
Shuai Liu, Lindsay T. Johnson, Xueliang Yu, Daniel J. Siegwart, Tuo Wei, Lukas Farbiak, Qiang Cheng
Publikováno v:
Nature materials
Endosomal escape remains a fundamental barrier hindering the advancement of nucleic acid therapeutics. Taking inspiration from natural phospholipids that comprise biological membranes, we report the combinatorial synthesis of multi-tailed ionizable p
Autor:
Lindsay T. Johnson, Qiang Cheng, Daniel J. Siegwart, Tuo Wei, Sean A. Dilliard, Lukas Farbiak
Publikováno v:
Nature nanotechnology
CRISPR/Cas gene editing and messenger RNA (mRNA)-based protein replacement therapy hold tremendous potential to effectively treat disease-causing mutations with diverse cellular origin. However, it is currently impossible to rationally design nanopar
Autor:
Qiang, Cheng, Tuo, Wei, Lukas, Farbiak, Lindsay T, Johnson, Sean A, Dilliard, Daniel J, Siegwart
Publikováno v:
Nature nanotechnology. 15(4)
CRISPR-Cas gene editing and messenger RNA-based protein replacement therapy hold tremendous potential to effectively treat disease-causing mutations with diverse cellular origin. However, it is currently impossible to rationally design nanoparticles
Autor:
Sang M. Lee, Lindsay T. Johnson, Daniel J. Siegwart, Tuo Wei, Lukas Farbiak, Ester Álvarez-Benedicto, Qiang Cheng
Publikováno v:
Adv Mater
Clustered regularly interspaced short palindromic repeat (CRISPR)/CRISPR-associated (Cas) protein gene editing is poised to transform the treatment of genetic diseases. However, limited progress has been made toward precise editing of DNA via homolog
Autor:
Shuyuan Zhang, Kejin Zhou, Daniel J. Siegwart, Yonglong Wei, Lukas Farbiak, Yuemeng Jia, Hao Zhu, Tuo Wei, Qiang Cheng
Publikováno v:
Advanced Materials. 30:1805308
mRNA-mediated protein replacement represents a promising concept for the treatment of liver disorders. Children born with fumarylacetoacetate hydrolase (FAH) mutations suffer from Hepatorenal Tyrosinemia Type 1 (HT-1) resulting in renal dysfunction,