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We performed genetic interaction analysis in these Aβ-expressing flies by analyzing the modification of Aβ-induced phenotypes in the presence of FKBP52 mutations.
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This study analyzes the modification of an existing process configuration train for Bio-SNG production using an indirectly-heated circulating fluidized bed gasifier.
To understand these modifications, we first analyze the modification of spontaneous dynamics by the learning process and then study the modification upon the injection of an input.
Finally, we analyzed the modification of Tlg1 mutants in which the cysteines have been moved away from the cytosolic border of the TMD.
To understand molecular mechanisms underlying cyclin D1 down-regulation by vorinostat in A549 cells, we analyzed the modification of H3K9 in response to vorinostat using chromatin immunoprecipitation.
Studies which analyzed the modification of the ifosfamide metabolism or the usage of novel substances such as the liposomal form of cisplatin or cilastatin are in their early stages [ 11, 28, 29].
To understand the mechanism underlying the cyclin D1 down-regulation in response to vorinostat, we analyzed the modification of H3K9 histone tail at the promoter of cyclin D1 using chromatin immune-precipitation (ChIP) in A549 cells.
The monofrequent oscillations of the system are studied in order to analyze the modifications of frequency and motion amplitude of the modal oscillations due to geometric non-linearities in the absence of internal resonance.
We are applying a combination of confocal imaging including photobleaching microscopy and computational methods to analyze the modifications of nuclear architecture and dynamics in parvovirus infected cells.
Furthermore, we analyzed the modifications of the protein moiety of NdCld incubated with chlorite in the presence and absence of methionine by mass spectrometry.
In this work, we analyzed the modifications of the photosynthetic apparatus in the Arabidopsis mutant chy1chy2lut2lut5, that accumulates β-xanthophylls despite disruption of the three chy1, chy2 and lut5 genes encoding carotene hydroxylases.
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