Non-viral vectors for gene-based therapy
Gene-based therapy is the intentional modulation of gene expression in specific cells to
treat pathological conditions. This modulation is accomplished by introducing exogenous …
treat pathological conditions. This modulation is accomplished by introducing exogenous …
Enabling collaborative edge computing for software defined vehicular networks
Edge computing has great potential to address the challenges in mobile vehicular networks
by transferring partial storage and computing functions to network edges. However, it is still …
by transferring partial storage and computing functions to network edges. However, it is still …
Structure-guided chemical modification of guide RNA enables potent non-viral in vivo genome editing
Efficient genome editing with Cas9–sgRNA in vivo has required the use of viral delivery
systems, which have limitations for clinical applications. Translational efforts to develop other …
systems, which have limitations for clinical applications. Translational efforts to develop other …
Improving cloud gaming experience through mobile edge computing
With the development of 4G/5G technology and smart devices, more and more users begin
to play games via their mobile devices. As a promising way to enable users to play any …
to play games via their mobile devices. As a promising way to enable users to play any …
Joint optimization on trajectory, altitude, velocity, and link scheduling for minimum mission time in UAV-aided data collection
…, H Zhao, H Wang, F Gu, J Wei, H Yin… - IEEE Internet of Things …, 2019 - ieeexplore.ieee.org
Due to the flexibility in 3-D space and high probability of line-of-sight (LoS) in air-to-ground
communications, unmanned aerial vehicles (UAVs) have been considered as means to …
communications, unmanned aerial vehicles (UAVs) have been considered as means to …
The genome of the pear (Pyrus bretschneideri Rehd.)
The draft genome of the pear (Pyrus bretschneideri) using a combination of BAC-by-BAC and
next-generation sequencing is reported. A 512.0-Mb sequence corresponding to 97.1% of …
next-generation sequencing is reported. A 512.0-Mb sequence corresponding to 97.1% of …
Genome editing with Cas9 in adult mice corrects a disease mutation and phenotype
We demonstrate CRISPR-Cas9–mediated correction of a Fah mutation in hepatocytes in a
mouse model of the human disease hereditary tyrosinemia. Delivery of components of the …
mouse model of the human disease hereditary tyrosinemia. Delivery of components of the …
FDC: A secure federated deep learning mechanism for data collaborations in the Internet of Things
B Yin, H Yin, Y Wu, Z Jiang - IEEE Internet of Things Journal, 2020 - ieeexplore.ieee.org
With the explosive network data due to the advanced development of the Internet of Things (IoT),
the demand for multiparty computation is increasing. In addition, with the advent of …
the demand for multiparty computation is increasing. In addition, with the advent of …
Therapeutic genome editing by combined viral and non-viral delivery of CRISPR system components in vivo
The combination of Cas9, guide RNA and repair template DNA can induce precise gene
editing and the correction of genetic diseases in adult mammals. However, clinical …
editing and the correction of genetic diseases in adult mammals. However, clinical …
CRISPR-mediated direct mutation of cancer genes in the mouse liver
The study of cancer genes in mouse models has traditionally relied on genetically-engineered
strains made via transgenesis or gene targeting in embryonic stem cells 1 . Here we …
strains made via transgenesis or gene targeting in embryonic stem cells 1 . Here we …