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That halts passenger train service and forces Mr. Pratt and his fellow passengers to transfer to express buses, to once again endure (and mostly shrug off) a topographical drama less spectacular but far more common than the potentially deadly earthquakes, avalanches and tsunamis that loom in anxious minds across the Pacific Northwest: mudslides.
Blocking VEGF, by means of lentiviral gene transfer to express an anti-VEGF antibody in RPE cells, inhibits outer BRB breakdown and retinal degeneration, as illustrated by functional, behavioral and morphometric analysis.
The present study sought to dissect the molecular basis of the impressive therapeutic effects of IL-17 sequestration reported in Nguyen et al. [ 7], who showed that sequestration of IL-17 by using Adenoviral gene transfer to express a fusion protein called IL-17R Fc IL-17R Fcfunctimproveshistological metrics in the Aec1/Aec2 model ofunction].
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A detailed 3D model of the MOCVD reactor is developed, which includes a reaction kinetic mechanism to describe the gas-phase and surface reactions occurring in the reactor, and a comprehensive heat transfer scheme to express the heat transfer between the inner reactor wall and the outer tube cooling gas.
A construct containing a bovine lactoferrin cDNA was used to transform wheat using an Agrobacterium-mediated DNA transfer system to express this antimicrobial protein in transgenic wheat.
The hMSC lines were generated from the human telomerase reverse transcriptase-immortalized single-cell derived hMSC line SCP-1 and genetically modified using lentiviral gene transfer to stably express the bsAb CD33 CD3.
One goal of gene transfer may be to express a functional gene when the endogenous gene is inactive.
The reconstructed embryos, which were obtained by somatic cell nuclear transfer and confirmed to express the four fluorescent proteins evenly, were transplanted into seven recipient gilts.
A baculovirus transfer vector designed to express EGFP (enhanced green fluorescent protein) in mammalian cells was created by cloning EGFP under control of the CAG promoter in the vector pTriEx™-1.1 between the Ncol and Bsu36I sites.
Genetic engineering in adoptively transferred T cells to express antigen-specific chimeric antigen receptors (CARs) has proved highly powerful and efficacious in inducing sustained responses in patients with refractory malignancies, as exemplified by the success of CD19-targeting CAR-T treatment in patients with relapsed acute lymphoblastic leukemia.
Sequence confirmed constructs were transferred into BL21 to express the recombinant peptides.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com