6 results on '"Jin, W.-R."'
Search Results
2. Gene expression profiling in the human hypothalamus-pituitary-adrenal axis and full-length cDNA cloning
- Author
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Hu, R.-M., Han, Z.-G., Song, H.-D., Peng, Y.-D., Huang, Q.-H., Ren, S.-X., Gu, Y.-J., Huang, C.-H., Li, Y.-B., Jiang, C.-L., Fu, G., Zhang, Q.-H., Gu, B.-W., Dai, M., Mao, Y.-F., Gao, G.-F., Rong, R., Ye, M., Zhou, J., Xu, S.-H., Gu, J., Shi, J.-X., Jin, W.-R., Zhang, C.-K., Wu, T.-M., Huang, G.-Y., Chen, Z., Chen, M.-D., and Chen, J.-L.
- Subjects
Gene expression -- Research ,Hypothalamic-pituitary-adrenal axis -- Genetic aspects ,Science and technology - Abstract
The primary neuroendocrine interface, hypothalamus and pituitary, together with adrenals, constitute the major axis responsible for the maintenance of homeostasis and the response to the perturbations in the environment. The gene expression profiling in the human hypothalamus-pituitary-adrenal axis was catalogued by generating a large amount of expressed sequence tags (ESTs), followed by bioinformatics analysis (http://www.chgc.sh.cn/ database). Totally, 25,973 sequences of good quality were obtained from 31,130 clones (83.4%) from cDNA libraries of the, hypothalamus, pituitary, and adrenal glands. After eliminating 5,347 sequences corresponding to repetitive elements and mtDNA, 20,626 ESTs could be assembled into 9,175 clusters (3,979, 3,074, and 4,116 clusters in hypothalamus, pituitary, and adrenal glands, respectively) when overlapping ESTs were integrated. Of these clusters, 2,777 (30.3%) corresponded to known genes, 4,165 (44.8%) to dbESTs, and 2,233 (24.3%) to novel ESTs. The gene expression profiles reflected well the functional characteristics of the three levels in the hypothalamus-pituitary-adrenal axis, because most of the 20 genes with highest expression showed statistical difference in terms of tissue distribution, including a group of tissue-specific functional markers. Meanwhile, some findings were made with regard to the physiology of the axis, and 200 full-length cDNAs of novel genes were cloned and sequenced. All of these data may contribute to the understanding of the neuroendocrine regulation of human life.
- Published
- 2000
3. Langmuir-Blodgett films of three new biferrocene derivatives and their electrocatalysis
- Author
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Zhang, C.-R., Yang, K.-Z., and Jin, W.-R.
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- 1996
- Full Text
- View/download PDF
4. Preliminary results of tubal surgery with pregnancy outcome.
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Xiu JX, Bin LY, Jin WR, Min ZY, Jun L, and Hong XK
- Subjects
- Abortion, Spontaneous, Adult, China, Fallopian Tube Diseases pathology, Female, Humans, Laparoscopy methods, Pregnancy, Pregnancy Outcome, Pregnancy, Ectopic, Severity of Illness Index, Fallopian Tube Diseases surgery, Infertility, Female surgery
- Abstract
Purpose of Investigation: To assess the preliminary results of tubal surgery and its effect on pregnancy outcome., Materials and Methods: The study included 440 patients with unilateral or bilateral tubal disease as the only cause of the infertility. All patients undergoing a laparoscopy for infertility were studied in reproductive surgery centre. The fallopian tube was classified into class I-IV. The studied outcomes were live birth, ectopic pregnancy, and miscarriage. After 12 months, cumulative conception rate was calculated., Results: In the 440 patients, 172 patients with mild salpinx abnormality (class I) had a 34% cumulative pregnancy rate, 151 patients with moderate salpinx abnormality (class II) had a 16% cumulative pregnancy rate, and 77 patients with severe salpinx abnormality (class III) had a 10% cumulative pregnancy rate. No intrauterine pregnancies were observed in the severe group of 40 patients (class IV)., Conclusion: Surgical laparoscopy is helpful for class I and II tubal abnormality, while it is not for class III and IV abnormalities.
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- 2015
5. Genomic sequence and expression analyses of human chromatin assembly factor 1 p150 gene.
- Author
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Dong H, Lin W, Zhang CK, Xiong H, Fu G, Jin WR, Chen R, Chen Z, Qi ZT, and Huang GM
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- 3T3 Cells, Alternative Splicing, Amino Acid Sequence, Animals, Base Sequence, COS Cells, Chromatin Assembly Factor-1, Computational Biology, DNA chemistry, DNA genetics, DNA, Complementary genetics, Humans, Luciferases genetics, Luciferases metabolism, Mice, Molecular Sequence Data, Promoter Regions, Genetic genetics, Protein Subunits, Recombinant Fusion Proteins genetics, Recombinant Fusion Proteins metabolism, Sequence Alignment, Sequence Analysis, DNA, Sequence Homology, Amino Acid, Transcription Factors, Chromosomal Proteins, Non-Histone, DNA-Binding Proteins genetics, Genes genetics
- Abstract
Chromatin assembly factor-1 (CAF-1) plays essential roles in eukaryotic chromatin assembly during DNA replication (Smith and Stillman, 1989. Cell 58, 15-25), (Krude, 1999. Eur. J. Biochem. 263, 1-5). Its p150 subunit, involved in interaction with histone H3 and H4, is critical to the CAF-1 nucleosome assembly activity. In this study, we sequenced a 96-kb genomic DNA region that includes a 42.8-kb CAF-1 p150 subunit gene (CHAF1A), and a 41.1-kb EEN gene. A scripted bioinformatics analysis pipeline (research agent) has been set up to annotate the BAC sequence with a set of integrated algorithms. The CAF-1 p150 subunit gene contains 15 exons and 14 introns. The promoter region is characterized by deletional analyses, revealing a potential repressor. Tissue-correlated alternative splicing forms of the transcript was initially identified by EST clustering analysis, then confirmed by RT-PCR which resulted more splicing forms than computational prediction.
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- 2001
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6. Feasibility and clinical significance of real-time quantitative RT-PCR assay of PML-RARalpha fusion transcript in patients with acute promyelocytic leukemia.
- Author
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Gu BW, Hu J, Xu L, Yan H, Jin WR, Zhu YM, Zhao WL, Niu C, Cao Q, Su XY, Gu J, Ying HY, Chen Y, Xiong SM, Shen ZX, Chen Z, and Chen SJ
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- Adolescent, Adult, Aged, Antineoplastic Agents administration & dosage, Bone Marrow pathology, Child, Disease Progression, Disease-Free Survival, Feasibility Studies, Female, Humans, Leukemia, Promyelocytic, Acute drug therapy, Leukemia, Promyelocytic, Acute genetics, Male, Middle Aged, Neoplasm Proteins genetics, Neoplasm, Residual diagnosis, Neoplasm, Residual genetics, Oncogene Proteins, Fusion genetics, Prognosis, RNA, Messenger analysis, Reproducibility of Results, Sensitivity and Specificity, Leukemia, Promyelocytic, Acute diagnosis, Neoplasm Proteins analysis, Oncogene Proteins, Fusion analysis, Reverse Transcriptase Polymerase Chain Reaction standards
- Abstract
Introduction: To study the relationship between the expression level of the PML-RARalpha fusion transcripts and the clinical status and efficiency of the therapy in acute promyelocytic leukemia (APL) patients, we applied a very sensitive and specific real-time Reverse Transcription Polymerase Chain Reaction (RT-PCR) system to quantify the dose of PML-RARalpha fusion transcripts in a series of APL patients at distinct disease stages., Materials and Methods: A total of 31 APL patients (19 males and 12 females; aged from 8 to 74 years) from eight hospitals in Shanghai were analysed. Real-time Quantitative RT-PCR was used to measure the normalized dose (DoseN) of PML-RARalpha fusion transcripts., Results: A wide range of PML-RARalpha DoseN above 1 x 10(3) was noted in 25 newly diagnosed patients. PML-RARalpha DoseN was significantly decreased after remission induction with ATRA, ATRA/chemotherapy or As2O3 and further reduced after consolidation. The fact that all patients with long disease free survival had a constantly low PML-RARalpha DoseN below 2 x 10(2) and a higher level predicted impending relapse suggests that this value could serve as a 'threshold' for molecular remission. PML-RARalpha DoseN was also of prognostic value in a group of relapsed patients, since good response to As2O3 reinduction was accompanied by a remarkable reduction of fusion transcript level, whereas patients with high PML-RARalpha Dose(N) after the second CR tended to relapse again rapidly., Conclusion: These results confirm that real-time RT-PCR assay for PML-RARalpha transcripts in APL patients is useful in reflecting leukemic burden, assessing response to treatment and indicating the ultimate clinical outcome or curability of disease.
- Published
- 2001
- Full Text
- View/download PDF
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