J Agric Food Chem
February 2024
Biochem Biophys Res Commun
June 2014
A number of JmjC domain-containing histone demethylases have been identified and biochemically characterized in mammalian. JMJD2A is a transcriptional cofactor and enzyme that catalyzes demethylation of histone H3 lysines 9 and 36. Here in this study, we aim to explore the role of JMJD2A in human gastric cancer.
View Article and Find Full Text PDFBiochem Biophys Res Commun
June 2014
Objective: To evaluate the therapeutic effect and security of CT guided unilateral percutaneous vertebroplasty (PVP) for the treatment of osteoporotic vertebral compression fracture (OVCF) in senile patients.
Methods: From April 2009 to June 2010, 26 patients undergoing CT guided unilateral percutaneous vertebroplasty were analyzed retrospectively. There were 9 males and 17 females,ranging in age from 60 to 85 years with an average of (67.
The olfactory sense plays a key role in animals'life time. The main gene related with olfaction was olfactory receptor (OR) gene. This review introduced the structure, expression regulation, distribution, molecular evolution and polymorphism of OR gene.
View Article and Find Full Text PDFA total of 1139 trees from 8 clear-cut stands dominated by fir, spruce, and pine in the Changbai Mountains were selected to study the relationships between the coefficient of variation of diameter and height and the competition index of the three main coniferous tree species in the Mountains. For the test tree species, the variation of height vs. diameter class was relatively small, while the variations of diameter and height vs.
View Article and Find Full Text PDFObjective: To study the function of Loa22 gene from virulent serovar Lai. L. interrogans by expressing its protein.
View Article and Find Full Text PDFSichuan Da Xue Xue Bao Yi Xue Ban
May 2008
Xi Bao Yu Fen Zi Mian Yi Xue Za Zhi
February 2008
Aim: To compare the immunogenicity of vaccine strategies about combined DNA prime-BCG boost and DNA or BCG vaccination only.
Methods: BALB/c mice were divided into four groups each containing 6 mice, and all mice received three immunizations at 2 weeks interval. One group of mice was vaccinated with PBS (PBS group); one group was vaccinated twice at 0 week and 2 weeks with combined DNA expressing two mycobacterial antigens, ESAT-6 and antigen 85A respectively; and then boosted with BCG at 4 weeks (DNA/BCG group); another group was vaccinated twice with combined DNA at 0 week, 2 weeks and 4 weeks(DNA/DNA group); and the final group received PBS twice at 0 week and 2 weeks and then vaccinated with BCG at 4 weeks(BCG group).
Xi Bao Yu Fen Zi Mian Yi Xue Za Zhi
February 2008
Aim: To construct the eukaryotic experssion vector of LipL32 gene from Leptospira serovar Lai and express the recombinant plasmid in COS-7 cell.
Methods: The LipL32 gene was amplified from Leptospira strain 017 genomic DNA by PCR and cloned into pcDNA3.1, through restriction nuclease enzyme digestion.
Sichuan Da Xue Xue Bao Yi Xue Ban
March 2007
Sichuan Da Xue Xue Bao Yi Xue Ban
March 2007
Objective: To screen and construct the recombinant Bacillus Calmette-Guerin (rBCG) strain expressing and secreting the human interleukin 12 (rBCG-12).
Methods: IL-12 complete gene including p40 and p35 subunits was amplified by PCR from a plasmid pORF-h IL-12 and cloned into E. coli-Mycobacteria shuttle vector pMV361.
Sichuan Da Xue Xue Bao Yi Xue Ban
January 2007
Nan Fang Yi Ke Da Xue Xue Bao
January 2007
Objective: The mechanism by which M.tuberculosis persists and survives in host macrophage is not fully understood, however, the M. tuberculosis chromosome-encoded TA loci perform functions possibly of signaling to these processes.
View Article and Find Full Text PDFXi Bao Yu Fen Zi Mian Yi Xue Za Zhi
November 2006
Aim: To clone and construct the eukaryotic expression plasmids containing different subunits of human IL-12 and to investigate its expression following transient transfection into COS-7 cells.
Methods: Human leukaemia cells (HL-60 and THP-1) were stimulated by DMSO, IFN-gamma and LPS, and the target genes including IL-12 p40 and p35 subunits were amplified by RT-PCR. P40 and p35 fragments were then connected and the recombinant plasmids pcDNA-p40, pcDNA-p35 and pcDNA-p40-p35 were constructed by double restriction enzymes digestion and connection.