MATERIALS AND METHODS: A total of thirty participants with LC of non-small cell and small
cell type were included along with twenty healthy controls. Ribonucleic acid (RNA) isolated …

The present study aimed to examine 10 housekeeping genes (HKGs), including 18s
ribosomal RNA (18S), glyceraldehyde‑3‑phosphate dehydrogenase (GAPDH), ribosomal …

The concentration of circulating DNA (cirDNA) in blood plasma and cell-surface-bound
fractions of lung cancer patients and healthy individuals was measured using real-time PCR …

Non-small cell lung carcinoma (NSCLC) is one of the leading causes of death from cancer in
both Eastern and Western countries. For patients with stage I NSCLC, full lobar or more …

Identification of molecular markers often leads to important clinical applications such as
early diagnosis, prognosis, and drug targeting. Lung cancer, the leading cause of cancer …

This study attempts to identify a suitable endogenous control gene for real-time RT-PCR in
nonsmall cell lung cancer (NSCLC) tissues. Expression of seven common endogenous …

To identify differentially expressed genes in lung squamous cell carcinomas (SCCs), the
suppression subtractive hybridization method (SSH) was performed comparing six lung …

Lung cancer is a common cancer, and expression profiling can provide an accurate
indication to advance the medical intervention. However, this requires the availability of …

Personalized medicine has become essential in the treatment of lung cancer. However, the
lung cancer-related gene expression profiles in non-small cell lung cancer (NSCLC) …

Background In real-time RT quantitative PCR (qPCR) the accuracy of normalized data is
highly dependent on the reliability of the reference genes (RGs). Failure to use an …