Engineering living therapeutics with synthetic biology
The steadfast advance of the synthetic biology field has enabled scientists to use genetically
engineered cells, instead of small molecules or biologics, as the basis for the development …
engineered cells, instead of small molecules or biologics, as the basis for the development …
The uptake of metal–organic frameworks: a journey into the cell
The application of metal–organic frameworks (MOFs) in drug delivery has advanced rapidly
over the past decade, showing huge progress in the development of novel systems …
over the past decade, showing huge progress in the development of novel systems …
FGF/FGFR signaling in health and disease
Y **e, N Su, J Yang, Q Tan, S Huang, M **… - Signal transduction and …, 2020 - nature.com
Growing evidences suggest that the fibroblast growth factor/FGF receptor (FGF/FGFR)
signaling has crucial roles in a multitude of processes during embryonic development and …
signaling has crucial roles in a multitude of processes during embryonic development and …
Longitudinal intravital imaging of mouse placenta
Studying placental functions is crucial for understanding pregnancy complications. However,
imaging placenta is challenging due to its depth, volume, and motion distortions. In this …
imaging placenta is challenging due to its depth, volume, and motion distortions. In this …
Nucleic acid delivery for therapeutic applications
Recent medical advances have exploited the ability to address a given disease at the
underlying level of transcription and translation. These treatment paradigms utilize nucleic …
underlying level of transcription and translation. These treatment paradigms utilize nucleic …
Engineering adeno-associated virus vectors for gene therapy
C Li, RJ Samulski - Nature Reviews Genetics, 2020 - nature.com
Adeno-associated virus (AAV) vector-mediated gene delivery was recently approved for the
treatment of inherited blindness and spinal muscular atrophy, and long-term therapeutic …
treatment of inherited blindness and spinal muscular atrophy, and long-term therapeutic …
Applications of genome editing technology in the targeted therapy of human diseases: mechanisms, advances and prospects
H Li, Y Yang, W Hong, M Huang, M Wu… - Signal transduction and …, 2020 - nature.com
Based on engineered or bacterial nucleases, the development of genome editing
technologies has opened up the possibility of directly targeting and modifying genomic …
technologies has opened up the possibility of directly targeting and modifying genomic …
Viral vector‐based gene therapies in the clinic
Gene therapies are currently one of the most investigated therapeutic modalities in both the
preclinical and clinical settings and have shown promise in treating a diverse spectrum of …
preclinical and clinical settings and have shown promise in treating a diverse spectrum of …
[HTML][HTML] Appraisal for the potential of viral and nonviral vectors in gene therapy: A review
Over the past few decades, gene therapy has gained immense importance in medical
research as a promising treatment strategy for diseases such as cancer, AIDS, Alzheimer's …
research as a promising treatment strategy for diseases such as cancer, AIDS, Alzheimer's …
Targeted nonviral delivery of genome editors in vivo
Cell-type-specific in vivo delivery of genome editing molecules is the next breakthrough that
will drive biological discovery and transform the field of cell and gene therapy. Here, we …
will drive biological discovery and transform the field of cell and gene therapy. Here, we …