Adeno-associated virus as a delivery vector for gene therapy of human diseases
JH Wang, DJ Gessler, W Zhan, TL Gallagher… - Signal Transduction and …, 2024 - nature.com
Adeno-associated virus (AAV) has emerged as a pivotal delivery tool in clinical gene
therapy owing to its minimal pathogenicity and ability to establish long-term gene expression …
therapy owing to its minimal pathogenicity and ability to establish long-term gene expression …
Thirty years of baculovirus–insect cell protein expression: from dark horse to mainstream technology
MM Van Oers, GP Pijlman… - Journal of General …, 2015 - microbiologyresearch.org
In December 1983, a seminal paper appeared on the overexpression of human IFN-β in
insect cells with a genetically engineered baculovirus. The finding that baculoviruses …
insect cells with a genetically engineered baculovirus. The finding that baculoviruses …
[HTML][HTML] MSC based gene delivery methods and strategies improve the therapeutic efficacy of neurological diseases
H Zhou, Y He, W Xiong, S Jing, X Duan, Z Huang… - Bioactive materials, 2023 - Elsevier
Mesenchymal stem cells (MSCs) are promising seed cells for neural regeneration therapy
owing to their plasticity and accessibility. They possess several inherent characteristics …
owing to their plasticity and accessibility. They possess several inherent characteristics …
Scientific Opinion on the update of the list of QPS‐recommended biological agents intentionally added to food or feed as notified to EFSA
EFSA Panel on Biological Hazards (BIOHAZ)… - EFSA …, 2017 - Wiley Online Library
EFSA is requested to assess the safety of a broad range of biological agents in the context of
notification for market authorisation as sources of food and feed additives, food enzymes …
notification for market authorisation as sources of food and feed additives, food enzymes …
Engineering mesenchymal stem cells for regenerative medicine and drug delivery
Researchers have applied mesenchymal stem cells (MSC) to a variety of therapeutic
scenarios by harnessing their multipotent, regenerative, and immunosuppressive properties …
scenarios by harnessing their multipotent, regenerative, and immunosuppressive properties …
[HTML][HTML] In vivo genome editing in animals using AAV-CRISPR system: applications to translational research of human disease
Adeno-associated virus (AAV) has shown promising therapeutic efficacy with a good safety
profile in a wide range of animal models and human clinical trials. With the advent of …
profile in a wide range of animal models and human clinical trials. With the advent of …
Spatial control of in vivo CRISPR–Cas9 genome editing via nanomagnets
The potential of clustered regularly interspaced short palindromic repeats (CRISPR)–
CRISPR associated protein 9 (Cas9)-based therapeutic genome editing is hampered by …
CRISPR associated protein 9 (Cas9)-based therapeutic genome editing is hampered by …
Protein production using the baculovirus‐insect cell expression system
A Contreras‐Gómez, A Sánchez‐Mirón… - Biotechnology …, 2014 - Wiley Online Library
The baculovirus‐insect cell expression system is widely used in producing recombinant
proteins. This review is focused on the use of this expression system in developing …
proteins. This review is focused on the use of this expression system in developing …
Research progress of engineered mesenchymal stem cells and their derived exosomes and their application in autoimmune/inflammatory diseases
X Zhu, D Ma, B Yang, Q An, J Zhao, X Gao… - Stem cell research & …, 2023 - Springer
Autoimmune/inflammatory diseases affect many people and are an important cause of
global incidence and mortality. Mesenchymal stem cells (MSCs) have low immunogenicity …
global incidence and mortality. Mesenchymal stem cells (MSCs) have low immunogenicity …
CRISPR technologies for stem cell engineering and regenerative medicine
CRISPR/Cas9 system exploits the concerted action of Cas9 nuclease and programmable
single guide RNA (sgRNA), and has been widely used for genome editing. The Cas9 …
single guide RNA (sgRNA), and has been widely used for genome editing. The Cas9 …