Objective Two single nucleotide polymorphisms(SNPs)in TBX1 gene,G2857C(rs737868)and G2963A(rs28649236),were chosen to investigate their distribution in contruncal defects(CTD)patients and normal controls in order to determine the relationship between TBX1 gene and CTD.
All patients were mobilized by chemotherapy plus recombination human granulocyte colony-stimulating factor (rhG-CSF), and then PBSCs were collected by a separator CS-3000 plus or COBE spectra-4. The grafts were cryopreserved in 10% dimethyl sulfoxide(DMSD) and stored in liquid nitrogen.
Methods To observe the alternation of 260 children patients with bronchopneumonia (severe pneumonia 110, mild pneumonia 150) platelet count (PLT), platelet hema-tocrit (PCT) , mean platelet volume (MPV) , platelet distribution width (PDW) , and compared it with 100 normal control-groups.
Genomic DNA was extracted from blood samples of healthy controls and from patients with HBV infection.
The immunoassay was used to check the BALP of the blood serum that was from 42 primary osteosarcoma patients.
The patients were followed up from five months to 49 months with an average of 24.3 months.
Detection of abnormal myocardial perfusion is crucial to the prognosis of patients with coronary artery disease (CAD) after they have undergone percutaneous coronary intervention (PCI).
For those patients with acute or total occlusion, the levels of myocardial perfusion before and after PCI were similar, as determined by IC-MCE and visually analyzed from 61 segments (P >amp;lt; 0.05).