1
The complete coding region of LOXL1 was sequenced using the PCR-based Sanger method.
2
Samples were cultivated and processed using the PCR technique.
3
Forty-one Brazilian women with stages II and III breast cancer using the PCR-RFLP analysis were evaluated.
4
Two hundred and ninety-nine base pair fragments from the second exon of HLA-DPB1 genes were selectively amplified using the PCR-primers.
5
Among 419 febrile episodes, 35 cases of malaria were detected using the PCR-based pooling strategy and 40 cases using microscopy.
6
Amplification of genomic DNA, using the PCR, demonstrated that the deletion included exons 22 and 23 of the C3 gene.