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The elucidation of these signal transduction systems and, more importantly, their interrelations in the early stages of the HPV-dependent transformation processes could provide indications for novel therapeutic strategies and/or a potential marker test for the clinical determination of pre-cancer, HPV-transformed cells in the cervix.
It was introduced as the first serum tumor marker test for ovarian cancer patients in 1983 [10], [11], [12], [13].
From September 2000 a marker test for the CVM-defect has been available and from February 2001 a direct gene test [ 2].
Blood tests are routinely used for biomarker determination and are widely accepted, and it is reasoned that the transition to an initial blood tumour marker test for CRC screening would improve uptake due its less invasive nature than either FOBT or flexible sigmoidoscopy.
Breed differences in both odds of infection and control of virus once infected have suggested a host genetic basis for susceptibility to OvLV (Herrmann-Hoesing et al. 2008; Blacklaws 2012), and recent work has identified the first genetic marker test for odds of OvLV infection based on the TMEM154 gene (Heaton et al. 2012, 2013).
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Thus, we are able to directly compare sensitivity and specificity of the proteomic expression profiles to currently available single marker tests for D-dimer.
The present study achieved the novel identification of two clinically useful marker tests for oncological colorectal surgery complications.
The purpose of this study was to conduct a structured review of the diagnostic performance of non-invasive marker tests for the detection of mesothelioma in patients with suspected mesothelioma.
A single-marker test for linkage between marker and QTL considers marker allele frequency differences between high and low groups.
This suggests that the use of tests such as maternal serum α-fetoprotein, alkaline phosphatase, and granulocyte colony-stimulating factor as a group or adding their results to fetal fibronectin test and cervical length test results may enhance our ability to predict spontaneous preterm birth and that the development of a multiple-marker test for spontaneous preterm birth is feasible.
Among the 6 markers tested for GS3, RGS1 was associated with GL, GW and LWR in all the six environments.
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Justyna Jupowicz-Kozak
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