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In this subsection, we present an algorithm for integrating the above described scheduling disciplines for GBR and non-GBR bearers.
With this new precoding codebook design, the earlier described scheduling strategy remains same, i.e., for a UE to be scheduled in the multi-user MIMO mode, the eNodeB selects the second UE to be served on the same time-frequency resources (co-scheduled UE) such that the desired signal strength is maximized while interference strength is minimized for both the UEs.
Another described scheduling as "easy…because of low cost [and] evening [appointments]," explaining that these factors allow for frequent treatments.
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The majority of member sites of the INDEPTH‡ network, for example, describe scheduled random re-visits of primary sampling units as a method of data quality control, with the percentage of households re-visited ranging from 2% (Agincourt HDSS, South Africa) to between 5 and 10% (Nouna HDSS, Burkina Faso) (14, 33).
Of the 37 member sites of the Indepth network (International Network of field sites with continuous Demographic Evaluation of Populations and Their Health), 19 describe scheduled random re-visits of primary sampling units as a method of data quality control, with the percentage of households re-visited ranging from 2% (Agincourt DSS, South Africa) to between 5 and 10% (Nouna DSS, Burkina Faso).
The cohort was expanded according to the previously described schedule.
For each patient, all tumor and urine samples were collected by the same collector according to the above described schedule.
Twenty one experimental animals received 0.5 mg/kg Rapatar and 17 animals received PBS according to the above described schedule.
Mice with established tumors were treated with FV-162 at 30 and 100 mg/kg daily or with ONX-0912 at 30 mg/kg administered twice weekly by oral gavage similar to a previously described schedule for this drug.
In the combination arm B, according to the described schedule-dependent synergy (Aschele et al, 1998), the thymidilate synthase inhibitor was given on day 2, 24 h after irinotecan.
When our original pilot study of cisplatin and gemcitabine was initiated in 1995, this 28 day cycle with cisplatin given day 1 was the most well described schedule of delivery of this drug combination.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com