1
Multivariable logistic regression was used to identify factors independently associated with willingness to use rt-PA in the ideal setting.
2
This might complement future efforts to standardize MDR1 detection methods using RT-PCR.
3
Gene and protein expression levels were analyzed using RT-qPCR and western blot.
4
Successful transfection was confirmed by using RT-PCR and western blot analysis.
5
We validated the expression of several of the miRs using RT-PCR.
6
TGF-beta1expression was studied using RT-PCR and secretion was quantified using ELISA.
7
The detection of minor archaeal populations was greater using RT-T-RFLP instead of T-RFLP.
8
The labor-specific expression of 4 genes was confirmed using RT-PCR and Northern blot analysis.
9
The validity of results obtained using RT qPCR is reliant on accurate data normalization.
10
The results were analyzed using RT-qPCR and western blot analysis.
11
The expression of ECR and let-7 was measured using RT-qPCR.
12
We therefore used RT-PCR to detect this molecular event in a prospective study including 890 children.
13
Using RT, we observe enhanced antioxidant capability of activated neurons and dynamic glutathione changes during ferroptosis.
14
Key genes implicated in the starch, pectin, and cellulose degradation were further investigated using RT-qPCR analysis.
15
The expression of mRNAs or proteins associated with adipogenesis was measured using RT-PCR and Western blotting analysis.
16
Methods: By using RT-PCR, the seven fragments contained about 1000 nucleotides in the complete genome were sequenced.