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The lives of cells, recorded
A paradigm for biology is emerging in which cells can be genetically programmed to write
their histories into their own genomes. These records can subsequently be read, and the …
their histories into their own genomes. These records can subsequently be read, and the …
[HTML][HTML] Improving recombinant protein production in CHO cells using the CRISPR-Cas system
AK Kalkan, F Palaz, S Sofija, N Elmousa… - Biotechnology …, 2023 - Elsevier
Chinese hamster ovary (CHO) cells are among the most widely used mammalian cell lines
in the biopharmaceutical industry. Therefore, it is not surprising that significant efforts have …
in the biopharmaceutical industry. Therefore, it is not surprising that significant efforts have …
CRISPR detection of cardiac tumor-associated microRNAs
Y Fu, P Zhang, F Chen, Z **e, S **ao, Z Huang… - Molecular Biology …, 2025 - Springer
As multiple imaging modalities cannot reliably diagnose cardiac tumors, the molecular
approach offers alternative ways to detect rare ones. One such molecular approach is …
approach offers alternative ways to detect rare ones. One such molecular approach is …
Correction of F8 intron 1 inversion in hemophilia A patient-specific iPSCs by CRISPR/Cas9 mediated gene editing
Z Hu, Y Wu, R **ao, J Zhao, Y Chen, L Wu… - Frontiers in …, 2023 - frontiersin.org
Introduction: Hemophilia A (HA) is the most common genetic bleeding disorder caused by
mutations in the F8 gene encoding coagulation factor VIII (FVIII). As the second predominant …
mutations in the F8 gene encoding coagulation factor VIII (FVIII). As the second predominant …
A structural peculiarity of Antarctic fish IgM drives the generation of an engineered mAb by CRISPR/Cas9
IgM is the major circulating Ig isotype in teleost fish, showing in Antarctic fish unique features
such as an extraordinary long hinge region, which plays a crucial role in antibody structure …
such as an extraordinary long hinge region, which plays a crucial role in antibody structure …
Targeted integration in CHO cells using CRIS-PITCh/Bxb1 recombinase–mediated cassette exchange hybrid system
S Ghanbari, E Bayat, M Azizi, P Fard-Esfahani… - Applied Microbiology …, 2023 - Springer
Recombinant Chinese hamster ovary (CHO) cell line development for complex
biotherapeutic production is conventionally based on the random integration (RI) approach …
biotherapeutic production is conventionally based on the random integration (RI) approach …
Efficient DNA knock-in using AAV-mediated delivery with 2-cell embryo CRISPR-Cas9 electroporation
DJ Davis, JF McNew, H Maresca-Fichter… - Frontiers in Genome …, 2023 - frontiersin.org
Recent advances in CRISPR-Cas genome editing technology have been instrumental in
improving the efficiency to produce genetically modified animal models. In this study we …
improving the efficiency to produce genetically modified animal models. In this study we …
MAGIK: A rapid and efficient method to create lineage-specific reporters in human pluripotent stem cells
Precise insertion of fluorescent proteins into lineage-specific genes in human pluripotent
stem cells (hPSCs) presents challenges due to low knockin efficiency and difficulties in …
stem cells (hPSCs) presents challenges due to low knockin efficiency and difficulties in …
CRISPR-Cas9 genome editing of rat embryos using Adeno-Associated Virus (AAV) and 2-Cell embryo Electroporation
DJ Davis, JF McNew, JN Walls, CE Bethune… - Journal of Visualized …, 2024 - app.jove.com
Genome editing technology is widely used to produce genetically modified animals,
including rats. Cytoplasmic or pronuclear injection of DNA repair templates and CRISPR …
including rats. Cytoplasmic or pronuclear injection of DNA repair templates and CRISPR …
UV radiation enhanced encapsulation of superparamagnetic iron oxide nanoparticles (MNPs) in microparticles derived from tumor repopulating cells
QL Liang, H Liu, T Wang, CH Lau, J Wang… - Biochemical and …, 2024 - Elsevier
Extracellular vesicles (EVs) such as microparticles secreted by the cells can be manipulated
and used for delivering therapeutic drugs to target and eradicate cancer cells. However …
and used for delivering therapeutic drugs to target and eradicate cancer cells. However …