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Their blood MRSA isolates were submitted for determination of MICs to various antibiotics and multi-locus sequence types.
Blood was placed into EDTA and lithium heparin tubes immediately following collection, and heparinized blood was immediately submitted for determination of venous blood lactate using an automated blood gas analyzer (RapidLab 1265, Siemens Healthcare Diagnostics, Tarry Town, NY) for determination of venous blood lactate.
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Over each of the last five winters approximately 1,000 samples have been submitted for virological determination.
The annual number of rabid dogs correlated only weakly with total number of dogs submitted for testing; coefficient of determination (R) was 0.56.
Samples were submitted for laboratory investigation and serotype determination by using virus isolation, antigen ELISA, and reverse transcription PCR (RT-PCR).
Medicare claims are submitted for billing not research purposes, and the determination of interval to radiotherapy might not be precise.
An aliquot of the CSF was submitted for routine analysis: total and differential cells count (>5 cells/mm3); determination of protein, lactate and glucose, and microbiological tests for bacteria and fungi.
When phenotypic species determination was not possible, DNA specimens were submitted for identification to the University of Guelph (Ontario, Canada), where partial sequences of the cytochrome oxidase gene were generated and compared with those available from the Barcode of Life Data Systems (www.boldsystems.org).org
Specimens from nine patients were resected intraoperatively for ropivacaine determination and were rinsed to remove any residual blood before being submitted for analysis.
The stool specimens of 643 of these patients had been submitted for the identification of enteric pathogens; the remaining 57 stool specimens had been submitted for the determination of Staphylococcus aureus and Salmonella spp. intestinal carriage in healthy adults without diarrhea and no history of enteric disease in the past six months.
The U.S. Food & Drug Administration FDAA) has issued a final guidance document on the preclinical determination of abuse potential that must be conducted in animals for all new molecular entities (NMEs) submitted for a new drug application (NDA).
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