Sentence examples for diverse dosages from inspiring English sources

and p.o. (3 mg/kg b.w).. (DOCX 15 kb) Additional file 4: Concentrations of DFC in feces after application of diverse dosages of ceftiofur i.m. (3 mg/kg b.w.; 1 mg/kg b.w. and 0.3 mg/kg b.w).

and p.o. (3 mg/kg b.w).. (DOCX 15 kb) Additional file 3: Concentrations of DFC in urine after application of diverse dosages of ceftiofur i.m. (3 mg/kg b.w.; 1 mg/kg b.w. and 0.3 mg/kg b.w).

(PPTX 108 kb) Additional file 2: Concentrations of DFC in plasma after application of diverse dosages of ceftiofur i.m. (3 mg/kg b.w.; 1 mg/kg b.w. and 0.3 mg/kg b.w).

and p.o. (3 mg/kg b.w).. (DOCX 17 kb) Additional file 6: Concentrations of DFC in the aerosol (sampled by air pumps) after application of diverse dosages of ceftiofur i.m. (3 mg/kg b.w.; 1 mg/kg b.w. and 0.3 mg/kg b.w).

and p.o. (3 mg/kg b.w).. (DOCX 14 kb) Additional file 5: Concentrations of DFC in the dust of the stable after application of diverse dosages of ceftiofur i.m. (3 mg/kg b.w.; 1 mg/kg b.w. and 0.3 mg/kg b.w).

Although the mechanism of male killing has been studied in detail only in a few bacterium host systems [ 7– 9], these studies suggested that mechanisms of male killing might be diverse: dosage compensation is suggested to be involved in Spiroplasma-induced male killing in Drosophila [ 7], whereas Arsenophonus is reported to target maternally inherited centrosomes to kill males in Nasonia [ 9].

Thus, it seems unlikely that exposure time directly contributes to triggering apoptosis since embryos that were irradiated with different energies for a given time period and, therefore, diverse total dosages, exhibited variable biological responses.

It thus did not come as a surprise that diverse epigenetic dosage compensation mechanisms have been discovered in several XX/XY systems as dissimilar as Drosophila, Mus and Caenorhabditis and much progress has been made to understand their evolutionary basis [ 7].

There is ample evidence for the preservation of multiple gene copies due to selection for increased gene dosage in diverse organisms [ 20].

The preferential retention of duplicate genes with these characteristics - stronger dosage constraints and more diverse interactions - supports the idea that expression dosage balance is important after WGD, and is consistent with other recent findings [ 13, 24- 27, 45, 50].

Transcriptome studies have revealed a plethora of non-coding RNAs, some of which have been implicated in diverse regulatory processes such as dosage compensation, genomic imprinting and RNAi.