url: =Irwin, David M. (20)\nZhang, Ya-Ping (12)\nMao, Yiqing (7)\nShen, Yong-Yi (6)\nWang, Xi (6)\nGuo, Tingting (5)\nIrwin, David M (5)\nJin, Ling (5)\nLi, Zhixin (4)\nSong, Rongjing (4)\nWu, Dong-Dong (4)\nHu, Ruobi (2)\nLiu, He-Qun (2)\nXie, Hai-Bing (2)\nZhang, Yizhuang (2)\nZhao, Shuyong (2)\nZhou, Tai-Cheng (2)\nZhou, Wei-Ping (2)\nAdeola, Adeniyi C. (1)\nBaker, Michelle L. (1)\nBao, Haihua (1)\nBegun, David J. (1)\nBiegel, Jason M (1)\nCheng, Lu-guang (1)\nChiang, Yu-Ting (1)\nColumbus, Joshua (1)\nFan, Ruo-xi (1)\nGe, Ri-Li (1)\nGeng, Chunyu (1)\n1. Genome-Wide Identification of Long Intergenic Noncoding RNA Genes and Their Potential Association with Domestication in Pigs Zhou, Zhong-Yin | Li, Ai-Min | Adeola, Adeniyi C. | Liu, Yan-Hu | Irwin, David M. | Xie, Hai-Bing | Zhang, Ya-Ping\nGenome Biology and Evolution 2014;6(6):1387-1392.\npig; lincRNA; domestication\n2. Relaxed Evolution in the Tyrosine Aminotransferase Gene Tat in Old World Fruit Bats (Chiroptera: Pteropodidae) Shen, Bin | Fang, Tao | Yang, Tianxiao | Jones, Gareth | Irwin, David M. | Zhang, Shuyi | Rokas, Antonis\n3. Differential expressed genes of change in glucose metabolism in the liver of GCK knockout mice Wang, Rong | Gao, Hui | Xu, Wei | Li, Hui | Mao, Yiqing | Wang, Yi | Wang, Xi | Irwin, David M. | Niu, Gang | Tan, Huanran\n4. The Wnt Signaling Pathway Effector TCF7L2 Controls Gut and Brain Proglucagon Gene Expression and Glucose Homeostasis Shao, Weijuan | Wang, Dingyan | Chiang, Yu-Ting | Ip, Wilfred | Zhu, Lingyun | Xu, Fenghao | Columbus, Joshua | Belsham, Denise D. | Irwin, David M. | Zhang, Haibo | Wen, Xiaoyan | Wang, Qinghua | Jin, Tianru\n5. Characterization of the gene expression profile of heterozygous liver-specific glucokinase knockout mice at a young age Guo, Tingting | Mao, Yiqing | Li, Hui | Wang, Xi | Xu, Wei | Song, Rongjing | Jia, Jianwei | Lei, Zhen | Irwin, David M. | Niu, Gang | Tan, Huanran\nBiomedicine & pharmacotherapy = Biomedecine & pharmacotherapie 2012;66(8):587-596.\nIn the liver, glucokinase (GCK) facilitates hepatic glucose uptake during hyperglycemia and is essential for the regulation of a network of glucose-responsive genes involved in glycolysis, glycogen synthesis, and lipogenesis. To better understand the consequences of changes in response to a liver-specific deficiency of GCK function we examined the expression profiles of genes involved in glucose metabolism in the liver, pancreas, muscle and adipose tissue in heterozygous liver-specific Gck knockout (Gckw/−) mice. Our results showed that with the development of a liver GCK deficiency, significant decreases in the mRNA levels for insulin receptor and Glut2 were observed in the liver, and HkII in muscle, while glucagon mRNA increased markedly in the pancreas. The levels of circulating glucagon hormone levels increased with increased mRNA levels. Depite a decrease in muscle HkII levels, the hexokinase activity level did not change. Our findings suggest that in liver-specific Gckw/− mice, peripheral tissues use different strategies to tackle with hyperglycemia even at a young age. By identifying the specific changes that occur in different tissues at an early stage of glucokinase deficiency, potentially we can develop interventions to prevent further progression to diabetes.\nPMID: 23085254 CAMSID: cams2717\nliver glucokinase; gene expression; diabetes\n6. Adaptive Evolution of the Hox Gene Family for Development in Bats and Dolphins Liang, Lu | Shen, Yong-Yi | Pan, Xiao-Wei | Zhou, Tai-Cheng | Yang, Chao | Irwin, David M. | Zhang, Ya-Ping | Hejnol, Andreas\nPLoS ONE 2013;8(6):e65944.\n7. Long-term renal changes in the liver-specific glucokinase knockout mouse: implications for renal disease in MODY2 Gu, Yi | Mao, Yiqing | Li, Hui | Zhao, Shuyong | Yang, Yang | Gao, Hui | Yu, Jianqiang | Zhang, Xuemei | Irwin, David M. | Tan, Huanran\nTranslational research : the journal of laboratory and clinical medicine 2010;157(3):111-116.\nTo investigate the functional and structural renal changes in a long-term liver-specific glucokinase knockout mouse, model of MODY2. Hemizygous glucokinase knockout mice, gckw/− groups, were compared at 6-, 10- and 14-months to their age-matched normal littermates, gckw/w groups. To examine changes we compared body weight, fasting blood glucose, serum insulin and creatinine levels, as well as 24 h urine samples that were collected for urine volume and protein analysis between the two groups. Renal tissues were collected and stained with hemotoxylin-eosin and periodic-acid Schiff, for light microscopic observation. Expression of renal Transforming Growth Factor β1 (TGF-β1) was determined by Western blot. Our results show that fasting blood glucose levels were significantly higher in gckw/− mice compared to gckw/w mice (P<0.01) for all age groups. Compared to age-matched gckw/w mice, 10-month old gckw/− mice have significantly elevated body weights (P<0.01), and urine volume (P<0.05) and protein concentrations (P<0.01). Renal tubular casts were observed in 10- and 14-month gckw/− mice. Significant increase in mesangial matrix and thickening of the glomerular basement membrane was observed in gckw/− compared to age-matched gckw/w mice at 10 and 14 months. As mice age increases, the levels of renal TGF-β1 are observed in both gckw/− and gckw/w mice. Our results indicate that renal changes occur in the liver-specific glucokinase knockout mouse model of MODY2, and suggest that TGF-β1 may play a key role in pathogenesis of these renal changes.\nPMID: 21316027 CAMSID: cams2938\nMODY; Diabetic nephropathy; Animal models\n8. Differential Expression of Genes Associated with the Progression of Renal Disease in the Kidneys of Liver-Specific Glucokinase Gene Knockout Mice Xu, Wei | Li, Hui | Wang, Rong | Lei, Zhen | Mao, Yiqing | Wang, Xi | Zhang, Yizhuang | Guo, Tingting | Song, Rongjing | Zhang, Xiaojing | Jin, Ling | Li, Zhixin | Irwin, David M. | Niu, Gang | Tan, Huanran\nInternational Journal of Molecular Sciences 2013;14(3):6467-6486.\nLiver glucokinase (GCK) deficient mice possess mild renal complications associated with diabetes. To investigate the progression of kidney disease and identify candidate genes involved in the pathogenesis of renal damage, we examined changes in tissue structure and gene expression in the kidneys of liver-specific GCK knockout (gckw/−) mice and age-matched normal wild-type control (gckw/w) mice as they aged. Suppression subtractive hybridization (SSH) was used to identify candidate genes that showed a pattern of differential expression between kidneys of gckw/− and gckw/w mice at 60 weeks of age. Differential expression of the candidate genes was examined by real-time qPCR in liver-specific gckw/− and gckw/w mice at 16, 26, 40, 60, and 85 weeks of age. Among the candidate genes, only glutathione peroxidase-3 (GPX3) was confirmed to show differential expression by qPCR in the 60-week old mice, however two others genes, MALAT1 and KEG, showed significant changes at other ages. This study shows that liver-specific glucokinase deficient mice display changes in kidney morphology by 40 weeks of age, and that renal complication may be correlated with a reduction in GPX3 levels. Since decreased GPX3 mRNA expression was observed at 26 weeks, which is younger than the age when pathological changes can be seen in kidney biopsies, GPX3 may serve as an early marker for kidney damage.\nglucokinase (GCK); MODY2; differentially expressed genes; kidney; Gpx3\n9. Signature of Balancing Selection at the MC1R Gene in Kunming Dog Populations Wang, Guo-dong | Cheng, Lu-guang | Fan, Ruo-xi | Irwin, David M. | Tang, Shu-sheng | Peng, Jian-guo | Zhang, Ya-ping | Yao, Yong-Gang\n10. Genome-Wide Scans for Candidate Genes Involved in the Aquatic Adaptation of Dolphins Sun, Yan-Bo | Zhou, Wei-Ping | Liu, He-Qun | Irwin, David M. | Shen, Yong-Yi | Zhang, Ya-Ping\nGenome Biology and Evolution 2012;5(1):130-139.\nSince their divergence from the terrestrial artiodactyls, cetaceans have fully adapted to an aquatic lifestyle, which represents one of the most dramatic transformations in mammalian evolutionary history. Numerous morphological and physiological characters of cetaceans have been acquired in response to this drastic habitat transition, such as thickened blubber, echolocation, and ability to hold their breath for a long period of time. However, knowledge about the molecular basis underlying these adaptations is still limited. The sequence of the genome of Tursiops truncates provides an opportunity for a comparative genomic analyses to examine the molecular adaptation of this species. Here, we constructed 11,838 high-quality orthologous gene alignments culled from the dolphin and four other terrestrial mammalian genomes and screened for positive selection occurring in the dolphin lineage. In total, 368 (3.1%) of the genes were identified as having undergone positive selection by the branch-site model. Functional characterization of these genes showed that they are significantly enriched in the categories of lipid transport and localization, ATPase activity, sense perception of sound, and muscle contraction, areas that are potentially related to cetacean adaptations. In contrast, we did not find a similar pattern in the cow, a closely related species. We resequenced some of the positively selected sites (PSSs), within the positively selected genes, and showed that most of our identified PSSs (50/52) could be replicated. The results from this study should have important implications for our understanding of cetacean evolution and their adaptations to the aquatic environment.\nTursiops truncates; aquatic adaptation; positive selection; branch-site model\n11. Multiple Episodes of Convergence in Genes of the Dim Light Vision Pathway in Bats Shen, Yong-Yi | Lim, Burton K. | Liu, He-Qun | Liu, Jie | Irwin, David M. | Zhang, Ya-Ping | Warrant, Eric James\n12. Long term liver specific glucokinase gene defect induced diabetic cardiomyopathy by up regulating NADPH oxidase and down regulating insulin receptor and p-AMPK Li, Hui | Wang, Xi | Mao, Yiqing | Hu, Ruobi | Xu, Wei | Lei, Zhen | Zhou, Na | Jin, Ling | Guo, Tingting | Li, Zhixin | Irwin, David M | Niu, Gang | Tan, Huanran\nCardiovascular Diabetology 2014;13:24.\nThe liver-specific glucokinase knockout (gckw/–) mouse experiences long-term hyperglycemia and insulin resistance. This study was designed to evaluate the functional and structural changes in the myocardium of 60 week-old gckw/– mice, and to investigate the effect of rosiglitazone on the myocardium in this model.\n60 week-old gckw/– mice were randomly divided into 3 groups: gckw/–, gckw/– mice treated with insulin (1 U/kg) and gckw/– mice treated with rosiglitazone (18 mg/kg). Insulin or rosiglitazone treatment was for 4 weeks. Gckw/w litermates were used as controls. Echocardiography, electrocardiogram, biochemical, histopathological, ultrastructural, real time PCR and Western blot studies were performed to examine for structural and functional changes.\nLong-term liver-specific gck knockout in mice elicits hyperglycaemia and insulin resistance. Compared to age matched gckw/w mice, 60 week-old gckw/– mice showed decreased LV internal dimension, increased posterior wall thickness, lengthened PR and QRS intervals, up-regulated MLC2 protein expression, decreased SOD activity, increased MDA levels and up-regulated Cyba mRNA. Morphological studies revealed that there was an increase in the amount of PAS and Masson positively stained material, as did the number and proportion of the cell occupied by mitochondria in the gckw/– mice. Western blot analysis revealed that the levels of the insulin receptor, Akt, phosphorylated AMPK beta and phosphorylated ACC were reduced in gckw/– mice. These effects were partly attenuated or ablated by treatment with rosiglitazone.\nOur results indicate that changes in the myocardium occur in the liver-specific glucokinase knockout mouse and suggest that reduced glucokinase expression in the liver may induce diabetic cardiomyopathy by up regulating NADPH oxidase and down regulating insulin receptor and p-AMPK protein levels. Rosiglitazone treatment may protect against diabetic cardiomyopathy by altering the levels of a set of proteins involved in cardiac damage.\nLiver-specific glucokinase knockout; Diabetic cardiomyopathy; Rosiglitazone; Insulin receptor; AMPK\n13. De Novo Origin of Human Protein-Coding Genes Wu, Dong-Dong | Irwin, David M. | Zhang, Ya-Ping | Begun, David J.\n14. Evolution of the mammalian lysozyme gene family Irwin, David M | Biegel, Jason M | Stewart, Caro-Beth\nBMC Evolutionary Biology 2011;11:166.\n15. Correlated Evolution among Six Gene Families in Drosophila Revealed by Parallel Change of Gene Numbers Wu, Dong-Dong | Irwin, David M. | Zhang, Ya-Ping\nGenome Biology and Evolution 2011;3:396-400.\nProteins involved in a pathway are likely to evolve in a correlated fashion, and coevolving gene families tend to undergo complementary gains and losses. Accordingly, gene copy numbers (i.e., repertoire size) tend to show parallel changes during the evolution of coevolving gene families. To test and verify this hypothesis, here we describe positive correlations among the repertoire sizes of six gene families, that is, trypsin-like serine protease, odorant-binding protein, odorant receptor, gustatory receptor, cytochrome P450, and glutathione S-transferase after excluding the possibility of phylogenetic constraint and random drift. The observed correlations are indicative of parallel changes in the repertoire sizes of the six gene families that are due to similar demands for the quantity of these different genes in different lineages of Drosophila. In conclusion, we propose that the correlated evolution among these six gene families in Drosophila is a signature of a parallel response to ecological adaptation.\ncorrelated evolution; Drosophila; gene family\n16. An Over Expression APP Model for Anti-Alzheimer Disease Drug Screening Created by Zinc Finger Nuclease Technology Zhang, Xiaojing | Li, Hui | Mao, Yiqing | Li, Zhixin | Wang, Rong | Guo, Tingting | Jin, Ling | Song, Rongjing | Xu, Wei | Zhou, Na | Zhang, Yizhuang | Hu, Ruobi | Wang, Xi | Huang, Huakang | Lei, Zhen | Niu, Gang | Irwin, David M. | Tan, Huanran | Holscher, Christian\n17. Parallel and Convergent Evolution of the Dim-Light Vision Gene RH1 in Bats (Order: Chiroptera) Shen, Yong-Yi | Liu, Jie | Irwin, David M. | Zhang, Ya-Ping | Scheffler, Konrad\nPLoS ONE 2010;5(1):e8838.\nRhodopsin, encoded by the gene Rhodopsin (RH1), is extremely sensitive to light, and is responsible for dim-light vision. Bats are nocturnal mammals that inhabit poor light environments. Megabats (Old-World fruit bats) generally have well-developed eyes, while microbats (insectivorous bats) have developed echolocation and in general their eyes were degraded, however, dramatic differences in the eyes, and their reliance on vision, exist in this group. In this study, we examined the rod opsin gene (RH1), and compared its evolution to that of two cone opsin genes (SWS1 and M/LWS). While phylogenetic reconstruction with the cone opsin genes SWS1 and M/LWS generated a species tree in accord with expectations, the RH1 gene tree united Pteropodidae (Old-World fruit bats) and Yangochiroptera, with very high bootstrap values, suggesting the possibility of convergent evolution. The hypothesis of convergent evolution was further supported when nonsynonymous sites or amino acid sequences were used to construct phylogenies. Reconstructed RH1 sequences at internal nodes of the bat species phylogeny showed that: (1) Old-World fruit bats share an amino acid change (S270G) with the tomb bat; (2) Miniopterus share two amino acid changes (V104I, M183L) with Rhinolophoidea; (3) the amino acid replacement I123V occurred independently on four branches, and the replacements L99M, L266V and I286V occurred each on two branches. The multiple parallel amino acid replacements that occurred in the evolution of bat RH1 suggest the possibility of multiple convergences of their ecological specialization (i.e., various photic environments) during adaptation for the nocturnal lifestyle, and suggest that further attention is needed on the study of the ecology and behavior of bats.\n18. Correction: Molecular evolution of the keratin associated protein gene family in mammals, role in the evolution of mammalian hair Wu, Dong-Dong | Irwin, David M | Zhang, Ya-Ping\nBMC Evolutionary Biology 2009;9:213.\nCorrection to Wu DD, Irwin DM, Zhang YP: Molecular evolution of the keratin associated protein gene family in mammals, role in the evolution of mammalian hair. BMC Evol Biol 2008, 8:241.\n19. CHIP promotes Runx2 degradation and negatively regulates osteoblast differentiation Li, Xueni | Huang, Mei | Zheng, Huiling | Wang, Yinyin | Ren, Fangli | Shang, Yu | Zhai, Yonggong | Irwin, David M. | Shi, Yuguang | Chen, Di | Chang, Zhijie\nThe Journal of Cell Biology 2008;181(6):959-972.\n20. Evolution of conserved secondary structures and their function in transcriptional regulation networks Xie, Hai-Bing | Irwin, David M | Zhang, Ya-Ping\nBMC Genomics 2008;9:520.\n21. Molecular evolution of the keratin associated protein gene family in mammals, role in the evolution of mammalian hair Wu, Dong-Dong | Irwin, David M | Zhang, Ya-Ping\nBMC Evolutionary Biology 2008;8:241.\n22. Evolution of Hepatic Glucose Metabolism: Liver-Specific Glucokinase Deficiency Explained by Parallel Loss of the Gene for Glucokinase Regulatory Protein (GCKR) Wang, Zhao Yang | Jin, Ling | Tan, Huanran | Irwin, David M. | Brusgaard, Klaus\n23. Draft genome sequence of the Tibetan antelope Ge, Ri-Li | Cai, Qingle | Shen, Yong-Yi | San, A | Ma, Lan | Zhang, Yong | Yi, Xin | Chen, Yan | Yang, Lingfeng | Huang, Ying | He, Rongjun | Hui, Yuanyuan | Hao, Meirong | Li, Yue | Wang, Bo | Ou, Xiaohua | Xu, Jiaohui | Zhang, Yongfen | Wu, Kui | Geng, Chunyu | Zhou, Weiping | Zhou, Taicheng | Irwin, David M. | Yang, Yingzhong | Ying, Liu | Bao, Haihua | Kim, Jaebum | Larkin, Denis M. | Ma, Jian | Lewin, Harris A. | Xing, Jinchuan | Platt, Roy N. | Ray, David A. | Auvil, Loretta | Capitanu, Boris | Zhang, Xiufeng | Zhang, Guojie | Murphy, Robert W. | Wang, Jun | Zhang, Ya-Ping | Wang, Jian\nNature Communications 2013;4:1858-.\n24. Genome-Wide Scan for Bats and Dolphin to Detect Their Genetic Basis for New Locomotive Styles Shen, Yong-Yi | Zhou, Wei-Ping | Zhou, Tai-Cheng | Zeng, Yan-Ni | Li, Gui-Mei | Irwin, David M. | Zhang, Ya-Ping | Baker, Michelle L.\n25. Expression of the Human Glucokinase Gene: Important Roles of the 5′ Flanking and Intron 1 Sequences Wang, Yi | Guo, Tingting | Zhao, Shuyong | Li, Zhixin | Mao, Yiqing | Li, Hui | Wang, Xi | Wang, Rong | Xu, Wei | Song, Rongjing | Jin, Ling | Li, Xiuli | Irwin, David M. | Niu, Gang | Tan, Huanran | Mummidi, Srinivas\nTo better understand the liver-specific expression of the human glucokinase gene we compared the structures of this gene from diverse mammals. Much of the sequence located between the 5′ pancreatic beta-cell-specific and downstream liver-specific promoters of the glucokinase genes is composed of repetitive DNA elements that were inserted in parallel on different mammalian lineages. The transcriptional activity of the liver-specific promoter 5′ flanking sequences were tested with and without downstream intronic sequences in two human liver cells lines, HepG2 and L-02. While glucokinase liver-specific 5′ flanking sequences support expression in liver cell lines, a sequence located about 2000 bases 3′ to the liver-specific mRNA start site represses gene expression. Enhanced reporter gene expression was observed in both cell lines when cells were treated with fetal calf serum, but only in the L-02 cells was expression enhanced by insulin.


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url: =Experimental study on cross linkage damage of biological molecules in old rats--《CHINESE JOURNAL OF CERIATRICS》1996年06期\nExperimental study on cross linkage damage of biological molecules in old rats\nGuo Yubin;Xu Guixiang;Zhang Kechun,et al.(Department of Biochemistry, Hunan College of Traditional Chinese Medicine,Changsha 410007)\nObjective To explore the relation between aging and the cross linkage damage of biological molecules(DNA, protein).Metbod Old (18 months) and young(5 months) rats of Wistar strain were used and DNA was prepared from the liver of the tats. The melting temperature(Tm)and the hyperchromic effect of DNA were measured. In addition, the thermal contraction temperature, the collagen deposition capacity and the soluble collagen content in caudal tendon were assaied to explore the relation between aging and the cross linkage damage in collagen.Results The Tm(73.2 ±1.1℃)and the hyperchromic effect (1.42±0.08) of hepatic DNA in young rats were lower than those in old rats (74.3±1.0℃,1.45±0.03).the difference of Tm between old and young rats was significant(P0.05).The thermal contraction temperature(67.2±1.6℃) and the collagen deposition capacity(613.6±74.6μg/mg)in caudal tendon of old rats were higher than those of young rats (64.1± 2.3℃,529.7±46.3μg/mg) (P0.01). The soluble collagen content in caudal tendon of young rats (51.5±3.8μg/mg) was a little higher than that of old rats (50.5±3.3μg/mg) (P0.05).Conclusions These results suggest that the cross linkage damage of DNA and collagen increase in old rats.\n1 ;高龄肺癌病人术前心肺功能不全与术后并发症的护理[J];Journal of Nurses Training;2001-09\n2 CHEN Zhao-he, YANG De-zhong (The Institute of Drug of Guangzhou Military Logistics Department, Guangzhou 510500, China);Effect and Harm of Trace Elements on the Old People Health[J];Trace Elements Science;2002-08\n3 Li Linghui;The comprehensive nursing for elderly stroke patients with dysphagia[J];Journal of Nurses Training;2011-16\n4 Chen Yuanwu (Department of Physical Culture);HUMBLE OPINION ON THE HARMFUL EFFECTS OF STRENUOUS PHYSICAL EXERCISE ON HUMAN BODY'S HEALTH[J];Journal of Hubei University(Natural Science Edition);1993-02\n5 ZHANG Gui-min,TANG Wen-jie,BAN Jing,MA Li-xin (School of Life Science,Hubei University,Wuhan 430062,China);An efficient protocol for extraction of fungal chromosomal DNA[J];Journal of Hubei University(Natural Science);2006-01\n6 JIN Culling, YING Jie, LIUMin;Application of Breath Training Device in the Elderly During Perioperation[J];Journal of Nursing Science;2004-06\n7 Jiang Xiaun;Yao Kaitai Cancer Research Institute Hunan Medical University;A SIMPLIEIED TECHNIQUE OF DNA-DNA IN SITU HYBRIDIZATION ON PARAFFIN SECTIONS WITH A BIOTINYLATED PROBE[J];BULLETIN OF HUNAN MEDICAL UNIVERSITY;1994-02\n8 Zhang Ming1 Zhai Chaoyang2 Zhao Chengyu1 Wan Qian21Department of Medical Biology and Cell Biology,School of BasicMedical Sciences (Chengdu 610041);  2.Laboratory of Molecular Biology;Properties of Chromosomal DNA of Termitomyces albuminosus[J];JOURNAL OF WEST CHINA UNIVERSITY OF MEDICAL SCIENCES;1997-04\n9 Song Qilin et al (Department of Metabolic Disease);Biomarker Expressed in Three dimension Method of Aging[J];JOURNAL OF HARBIN MEDICAL UNIVERSITY;1997-01\n10 ZHONG Shi-jun, OU Gang-wei, GE Zheng-long (Department of Biochemistry, Zunyi Medical College, Zunyi 563003, China);Influence of high glucose concentration on the expression of TGF-β gene,excretion of LN and colage-IV in HUVEC[J];Basic Medical Sciences and Clinics;2004-04\n1 Han Mingxiang et al;Primary Research of Model "Dificiency-Blood Stasis-Senility[J];Journal of Anhui Traditional Chinese Medical College;1992-03\n4 Yao Xuedong, Lin Qiren, Shi Jinxing, et al (Department of Orthopaedics, The Affiliated 2nd Hospital, Fujian Medical University, Quanzhou, 362000);Experimental Study of Collagenase in the Prevention of Adhesion of Intrathecal Tendon[J];JOURNAL OF FUJIAN MEDICAL UNIVERSITY;1999-02\n5 DENG Yue e\_+1,JI Li jin\_+2\_;(1.Dept.of Modern Medicine,FCTCM,Fuzhou,Fujian 350003,China;\_;2.Dept.of Traditional Chinese Medicine,FCTCM,Fuzhou,Fujian 350003,China) \_;;Study Correlation Between Emotion and Spleen & Stomach[J];Journal of Fujian College of Traditional Chinese Medicine;2003-03\n7 SHI Yu, JIANG Xian, LI Li. Department of Dermatology, Huaxi Hospital of Sichuan University, Chengdu 610041, China;Wrinkles and Skin Photoaging[J];International Journal of Dermatology and Venereology;2006-03\n8 Du Qingyun;Ning Wangrong;Zhang Mingqiong;Lin Xiaofang (Department of Pharmacy,the 175th Hospital of PLA,);Study of Turmeric Volatile Oil Decreasing Human Face Skin Roughness[J];STRAIT PHARMACEUTICAL JOURNAL;1999-01\n9 LI Yi, WANG Canling Department of Physiology,Nanyang Medical College,Nanyan 473058;Effects of Liuwei Dihuang Tang on skin senility in mice[J];Journal of Zhengzhou University(Science Medical);2005-06\n10 ZHAO Lei,WEI Xiaodong,GE Tangdong,LIU Miao,ZHANG Pengxia(The College of Basic Medicine of Jiamusi University,Jiamusi 154007,China);Effects of Astragalus Root serum on senile cell antioxidation and p16 expression[J];Heilongjiang Medicine and Pharmacy;2006-05


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