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Both studies that recently reported the role of SAMHD1 as an HIV-1 restriction factor in resting CD4+ T lymphocytes agree on the overall relevance of this cellular enzyme in limiting the efficiency of HIV-1 RT.
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The differential expression of cellular factors in resting and activated T cells has been proposed as an explanation for these observations (reviewed in [6], [7]), but conclusive evidence for their role has been lacking.
The parotid saliva variables except for the same factors in resting parotid saliva and derived secretion rates for some components in both salivas (see Methods).
With these limitations in mind, it is clear that further resting-state fMRI investigations, are needed to understand and partition the complex and interacting influences of these factors in resting functional connectivity, particularly in the setting of TLE.
Here, we systematically investigated the effects of >50 million variations from five strains of mice on mRNA, nascent transcription, transcription start sites, and transcription factor binding in resting and activated macrophages.
To further address the possible expansion of Treg cells upon exposure to TCDD as documented in mice [8], [9], we assessed the frequency of CD4+ T cells simultaneously expressing high levels of the IL-2 receptor subunit CD25 and the Treg-specific transcription factor FoxP3 in resting conditions [32].
For workaholics, nutrition and fitness are the last things in mind when you still have to factor in rest, family and leisure activities.
A substantial reduction in PA levels from early/mid adulthood to late adulthood is a critical factor that leads to a reduction in energy requirements for older adults; another critical factor is a decrease in resting metabolic rate (RMR) owing to aging-related loss of fat free mass.
The transcription factor GATA3 was expressed in resting cells while T-BET was upregulated on activation concurrent with the change in cytokine expression profile.
Recently, apolipoprotein B mRNA editing enzyme catalytic polypeptide 3G (APOBEC3G – A3G) has been put forth as the post-entry restriction factor responsible for HIV1 restriction in resting CD4+ T cells [8].
It is less clear whether the inhibition of nocturnal reflux events is also attributable to inhibition of TLOSRs, or whether other factors, such as an increase in resting LOS pressure which was apparent from animal studies using MTEP and MPEP, 12 may play an additional role.
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CEO of Professional Science Editing for Scientists @ prosciediting.com