Publications by authors named "Jia-Jun Mei"
Purpose: The causes of anemia and the common side effects of cancer are multifactorial. Malnutrition is one of the alleged components of the aforementioned complications. This study planned to investigate the relationship among biochemical markers, Patient-Generated Subjective Global Assessment (PG-SGA), and anemia in cancer patients.
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- * Using whole-genome sequencing data from 31 ESCCs, researchers discovered deletions and translocations as the main types of SVs, with significant disruption of cancer-related genes like CDKN2A and NOTCH1.
- * The analysis highlighted genomic phenomena such as chromothripsis and breakage-fusion-bridge events, which contribute to cancer progression in ESCCs, and suggested that these findings could aid in prevention, diagnosis, and treatment strategies.
Aim: To observe different histomorphologic changes of ulcerative colitis (UC) rats that were treated with four regulating-intestine prescriptions (FRIP), to investigate the curative effects of FRIP and to analyze their treatment mechanism.
Methods: The UC rat model was made by the method of 2,4-dinitro chloro benzene (DNCB) immunity and acetic acid local enema. Ninety-eight SD rats were randomly divided into seven groups, namely, the normal control group, model group, salicylazosulfapyridine (SASP) group, Wumeiwan (WMW) group, Baitouwengtang (BTWT) group, Senglingbaishusan (SLBSS) group, and Tongxieyaofang (TXYF) group.
[The role of enterogenous endotoxemia in the pathogenesis of non-alcoholic steatohepatitis].
Zhonghua Gan Zang Bing Za Zhi
October 2004
Aim: To inquire into the effects and mechanism of Zuogui Wan (Pills for Kidney Yin) on neurocyte apoptosis in nuclei of arcuate hypothalamus (ARN) of monosodium glutamate (MSG)-liver regeneration rats, and the mechanism of liver regeneration by using optic microscope, electron microscope and in situ end labeling technology to adjust nerve-endocrine-immunity network.
Methods: Neurocyte apoptosis in ARN of the experiment rats was observed by using optic microscope, electron microscope and in situ end labeling technology. Expression of TGF-beta1 in ARN was observed by using immunohistochemistry method.