BioInfoBank Library


 
author name recommending commenting favorite    papers recom. cited
0 0 0 131 0 527 [Update]
0 0 0 2 0 0 [Update]
0 0 0 11 0 62 [Update]
0 0 0 2 0 0 [Update]
0 0 0 2 0 0 [Update]
0 0 0 1 0 0 [Update]
0 0 0 1 0 1 [Update]
0 0 0 6 0 52 [Update]
0 0 0 1 0 12 [Update]
0 0 0 7 0 7 [Update]
0 0 0 1 0 0 [Update]
0 0 0 14 0 31 [Update]
0 0 0 6 0 17 [Update]
0 0 0 1 0 1 [Update]
0 0 0 9 0 2 [Update]
0 0 0 2 0 0 [Update]
0 0 0 56 0 80 [Update]
0 0 0 1 0 2 [Update]
1 0 0 62 1 295 [Update]
0 0 0 5 0 28 [Update]
0 0 0 1 0 0 [Update]

Latest Paper:

go to Pubmedgo to Scholargo to Googleshow EndNote Citationshow BibTex Citation
Department of Respiratory & Critical Care Medicine, Peking University People's Hospital, Beijing 100044, China.
BACKGROUND The extended spectrum β-lactamase (ESBL)-producing Escherichia coli (E. coli) and Klebsiella pneumoniae (K. pneumoniae) are the major pathogens causing pneumonia and have a significant impact on the clinical course. Limited data exist on molecular characterization of ESBL-producing E. coli and K. pneumoniae that cause pneumonia. The aim of this study was to investigate the comprehensive multilevel characteristics of E. coli and K. pneumoniae causing pneumonia in China for the first time. METHODS E. coli (17) and K. pneumoniae (21) isolates responsible for pneumonia were isolated from 1270 specimens collected in a prospective multi-center study in eight teaching hospitals in China from June to December in 2007. The susceptibilities, ESBL confirmation, sequence typing, bla(CTX-M) and bla(SHV) genes, their genetic environment and plasmid Inc/rep types were determined. RESULTS Sixteen E. coli (94.1%) and eleven K. pneumoniae (52.4%) isolates were ESBL producers. About 77.8% and 66.7% of them were resistance to ciprofloxacin and levofloxacin, and 100% were susceptible to imipenem. The most prevalent ESBL gene was CTX-M-14, followed by SHV-2, CTX-M-15, CTX-M-3, CTX-M-65, SHV-12, SHV-26 and SHV-28. SHV-1 and SHV-11 were also detected and coexisted with bla(CTX-Ms) in five strains, and three strains contained only SHV-1. All CTX-M-14 were detected ISEcp1 upstream and nine were found IS903 downstream and the majority of them (64.3%) were carried by IncF plasmids. All bla(SHV) were flanked by recF and deoR, located on IncF, IncN, IncX and IncH plasmids. Two SHV-2, one SHV-1 and the only SHV-28 were further preceded by IS26. Genes lacY and lacZ were detected at further upstream of two bla(SHV-1). The K. pneumoniae carrying SHV-28 was susceptible to β-lactams, and no mutations or deletions in gene or promoter sequences were identified to account for susceptibility. Multilocus sequence typing experiments showed the ESBL-producing strains were genetically diverse. CONCLUSIONS The rate of occurrence of bla(ESBL) in E. coli and K. pneumoniae causing pneumonia was high, and bla(CTX-M-14) was dominant and probably mobilized by ISEcp1 mainly on IncF plasmids. Importantly, unexpressed bla(ESBL) genes may occur in susceptible isolates and hence may have clinical implications.
go to Publishergo to Pubmedgo to Scholargo to Googleshow EndNote Citationshow BibTex Citation
School of Life Science, Huainan Normal University, Huainan, P.R. China. chengrunw66@yahoo.com.cn.
The present study combined chemical analyses and biological measurements to investigate biphasic effects of La on Cd stress in leaves of Vicia faba seedlings, which were hydroponically cultivated for 15 d in the combination of 6 µM CdCl(2) and 2 to 480 µM La(NO(3))(3), respectively. The results showed that contents of Cd first elevated above and then declined below the 6 µM single Cd treatment when 2 to 30 µM extraneous La were combined. Contents of mineral nutrients altered differentially and became imbalanced. No distinct band was observed in catalase (CAT), guaiacol peroxidase (GPX), or ascorbate peroxidase (APX) patterns, but in superoxide dismutase (SOD) isozymes by the supplementation with 8 to 480 µM of extraneous La. Superoxide dismutase and APX activities changed as a U-shaped curve, however, CAT and GPX changed as an inverted U-shaped curve along with increasing La. Moreover, heat shock protein 70 (HSP 70) production was reduced below the single treatment of Cd at 2 to 8 µM of extraneous La and enhanced thereafter. Thus, La at lower concentrations promote antioxidation against Cd stress; La at higher concentrations turned to prooxidant effects, implicating potential ecological risk. Heat shock protein 70, combined with the antioxidant enzymes, constitutes an integrative defense system, which can be used to estimate the degree of antioxidation or prooxidation of extraneous La- to Cd-induced oxidative stress in the seedlings. Environ. Toxicol. Chem. © 2012 SETAC.
go to Publishergo to Pubmedgo to Scholargo to Googleshow EndNote Citationshow BibTex Citation
Department of Otorhinolaryngology, The First Affiliated Hospital, Sun Yat-sen University, 58 Zhongshan Road, Guangzhou 510080, PR China; Institute of Otorhinolaryngology, Sun Yat-sen University, Guangzhou 510080, PR China.
BACKGROUND: Recently, in vitro and in vivo models have identified that microRNAs (miRNAs), which are extensively expressed in the inner ear, play important roles in inner ear development and function. However, the function of miRNA in vertebrate tissue is not well understood. RESULTS: The current study used an in vitro model of embryonic mouse inner ear in a stem/progenitor cell culture to demonstrate that: 1) miR-182 is expressed during differentiation of inner ear stem/progenitor cell into a hair cell-like fate, 2) ectopic miR-182 promotes inner ear stem/progenitor cell differentiation into a hair cell-like fate, and 3) the function of miR-182 may be associated with its putative target Tbx1, a transcription factors that have been implicated in inner ear development and hair cell fate. CONCLUSIONS: Our findings suggest that miR-182 could regulate inner ear progenitor cell differentiation and that miRNAs are important regulators of hair cell differentiation, providing new targets for hair cell repair.
go to Pubmedgo to Scholargo to Googleshow EndNote Citationshow BibTex Citation
[My paper] A Adare, S Afanasiev, C Aidala, N N Ajitanand, Y Akiba, H Al-Bataineh, J Alexander, K Aoki, Y Aramaki, E T Atomssa, R Averbeck, T C Awes, B Azmoun, V Babintsev, M Bai, G Baksay, L Baksay, K N Barish, B Bassalleck, A T Basye, S Bathe, V Baublis, C Baumann, A Bazilevsky, S Belikov, R Belmont, R Bennett, A Berdnikov, Y Berdnikov, A A Bickley, J S Bok, K Boyle, M L Brooks, H Buesching, V Bumazhnov, G Bunce, S Butsyk, C M Camacho, S Campbell, C-H Chen, C Y Chi, M Chiu, I J Choi, R K Choudhury, P Christiansen, T Chujo, P Chung, O Chvala, V Cianciolo, Z Citron, B A Cole, M Connors, P Constantin, M Csanád, T Csörgő, T Dahms, S Dairaku, I Danchev, K Das, A Datta, G David, A Denisov, A Deshpande, E J Desmond, O Dietzsch, A Dion, M Donadelli, O Drapier, A Drees, K A Drees, J M Durham, A Durum, D Dutta, S Edwards, Y V Efremenko, F Ellinghaus, T Engelmore, A Enokizono, H En'yo, S Esumi, B Fadem, D E Fields, M Finger, M Finger Jr, F Fleuret, S L Fokin, Z Fraenkel, J E Frantz, A Franz, A D Frawley, K Fujiwara, Y Fukao, T Fusayasu, I Garishvili, A Glenn, H Gong, M Gonin, Y Goto, R Granier de Cassagnac, N Grau, S V Greene, M Grosse Perdekamp, T Gunji, H-Å Gustafsson, J S Haggerty, K I Hahn, H Hamagaki, J Hamblen, R Han, J Hanks, E P Hartouni, E Haslum, R Hayano, X He, M Heffner, T K Hemmick, T Hester, J C Hill, M Hohlmann, W Holzmann, K Homma, B Hong, T Horaguchi, D Hornback, S Huang, T Ichihara, R Ichimiya, J Ide, Y Ikeda, K Imai, M Inaba, D Isenhower, M Ishihara, T Isobe, M Issah, A Isupov, D Ivanischev, B V Jacak, J Jia, J Jin, B M Johnson, K S Joo, D Jouan, D S Jumper, F Kajihara, S Kametani, N Kamihara, J Kamin, J H Kang, J Kapustinsky, K Karatsu, D Kawall, M Kawashima, A V Kazantsev, T Kempel, A Khanzadeev, K M Kijima, B I Kim, D H Kim, D J Kim, E Kim, E J Kim, S H Kim, Y J Kim, E Kinney, K Kiriluk, A Kiss, E Kistenev, L Kochenda, B Komkov, M Konno, J Koster, D Kotchetkov, A Kozlov, A Král, A Kravitz, G J Kunde, K Kurita, M Kurosawa, Y Kwon, G S Kyle, R Lacey, Y S Lai, J G Lajoie, A Lebedev, D M Lee, J Lee, K Lee, K B Lee, K S Lee, M J Leitch, M A L Leite, E Leitner, B Lenzi, X Li, P Liebing, L A Linden Levy, T Liška, A Litvinenko, H Liu, M X Liu, B Love, R Luechtenborg, D Lynch, C F Maguire, Y I Makdisi, A Malakhov, M D Malik, V I Manko, E Mannel, Y Mao, H Masui, F Matathias, M McCumber, P L McGaughey, N Means, B Meredith, Y Miake, A C Mignerey, P Mikeš, K Miki, A Milov, M Mishra, J T Mitchell, A K Mohanty, Y Morino, A Morreale, D P Morrison, T V Moukhanova, J Murata, S Nagamiya, J L Nagle, M Naglis, M I Nagy, I Nakagawa, Y Nakamiya, T Nakamura, K Nakano, J Newby, M Nguyen, R Nouicer, A S Nyanin, E O'Brien, S X Oda, C A Ogilvie, M Oka, K Okada, Y Onuki, A Oskarsson, M Ouchida, K Ozawa, R Pak, V Pantuev, V Papavassiliou, I H Park, J Park, S K Park, W J Park, S F Pate, H Pei, J-C Peng, H Pereira, V Peresedov, D Yu Peressounko, C Pinkenburg, R P Pisani, M Proissl, M L Purschke, A K Purwar, H Qu, J Rak, A Rakotozafindrabe, I Ravinovich, K F Read, K Reygers, V Riabov, Y Riabov, E Richardson, D Roach, G Roche, S D Rolnick, M Rosati, C A Rosen, S S E Rosendahl, P Rosnet, P Rukoyatkin, P Ružička, B Sahlmueller, N Saito, T Sakaguchi, K Sakashita, V Samsonov, S Sano, T Sato, S Sawada, K Sedgwick, J Seele, R Seidl, A Yu Semenov, R Seto, D Sharma, I Shein, T-A Shibata, K Shigaki, M Shimomura, K Shoji, P Shukla, A Sickles, C L Silva, D Silvermyr, C Silvestre, K S Sim, B K Singh, C P Singh, V Singh, M Slunečka, R A Soltz, W E Sondheim, S P Sorensen, I V Sourikova, N A Sparks, P W Stankus, E Stenlund, S P Stoll, T Sugitate, A Sukhanov, J Sziklai, E M Takagui, A Taketani, R Tanabe, Y Tanaka, K Tanida, M J Tannenbaum, S Tarafdar, A Taranenko, P Tarján, H Themann, T L Thomas, M Togawa, A Toia, L Tomášek, H Torii, R S Towell, I Tserruya, Y Tsuchimoto, C Vale, H Valle, H W van Hecke, E Vazquez-Zambrano, A Veicht, J Velkovska, R Vértesi, A A Vinogradov, M Virius, V Vrba, E Vznuzdaev, X R Wang, D Watanabe, K Watanabe, Y Watanabe, F Wei, R Wei, J Wessels, S N White, D Winter, J P Wood, C L Woody, R M Wright, M Wysocki, W Xie, Y L Yamaguchi, K Yamaura, R Yang, A Yanovich, J Ying, S Yokkaichi, Z You, G R Young, I Younus, I E Yushmanov, W A Zajc, C Zhang, S Zhou, L Zolin
University of Colorado, Boulder, Colorado 80309, USA.
Flow coefficients v_{n} for n=2, 3, 4, characterizing the anisotropic collective flow in Au+Au collisions at sqrt[s_{NN}]=200  GeV, are measured relative to event planes Ψ_{n}, determined at large rapidity. We report v_{n} as a function of transverse momentum and collision centrality, and study the correlations among the event planes of different order n. The v_{n} are well described by hydrodynamic models which employ a Glauber Monte Carlo initial state geometry with fluctuations, providing additional constraining power on the interplay between initial conditions and the effects of viscosity as the system evolves. This new constraint can serve to improve the precision of the extracted shear viscosity to entropy density ratio η/s.
Allergy. 2012 Jan 9;:   22229716 
go to Publishergo to Pubmedgo to Scholargo to Googleshow EndNote Citationshow BibTex Citation
Otorhinolaryngology Hospital, the First Affiliated Hospital of Sun Yat-sen University, Otorhinolaryngology Institute of Sun Yat-sen University, Guangzhou, China.
BACKGROUND: MicroRNAs (miRNAs) are known to regulate the inflammatory response in various cell types. However, the ability of miRNAs to modulate dendritic cells (DCs) function for allergen immunotherapy is unclear. OBJECTIVE: To assess the role of miR-23b in the regulation of ovalbumin (OVA)-induced DC differentiation and function and to investigate the related molecular mechanisms. METHODS: Bone marrow-derived dendritic cells (BMDCs) were generated from murine bone marrow progenitor cells and subsequently stimulated with OVA to examine the profile of miRNA expression. After transfection with miR-23b reagents, DCs were evaluated for endocytic ability, surface marker expression, cytokine secretion and CD4+ T-cell differentiation. The possible roles of the Notch and NF-κB signalling pathways were also evaluated. Human monocyte-derived dendritic cells (MDDCs) were similarly evaluated as well. RESULTS: Significant upregulation of miR-23b was observed in BMDCs pulsed with OVA. Following miR-23b transfection, BMDCs showed decreased OVA uptake, increased IL-10 production, decreased IL-12 production and an enhanced capacity to promote FoxP3+ CD4+ T regulatory cells (Tregs) differentiation. In addition, inactivation of the Notch1 and NF-κB signalling pathways were observed. Conversely, inhibition of miR-23b in BMDCs resulted in the opposite effects. In human MDDCs, miRNA23b transfection similarly increased IL-10 and decreased IL-12 production, and that treated human MDDCs induced increased FoxP3+ CD4+ T cells. CONCLUSION: Our findings provide evidence that miR-23b is capable of inducing tolerogenic DC activity and Treg responses in vitro through the inhibition of the Notch1 and NF-κB signalling pathways; thus, miR-23b might represent a therapeutic target for the management of allergic diseases.
go to Publishergo to Pubmedgo to Scholargo to Googleshow EndNote Citationshow BibTex Citation
*Attending Physician, §§Professor, Department of Anesthesiology, Renji Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai, China. †Associate Professor,#Research Assistant, State Key Laboratory of Oncogenes and Related Genes, Shanghai Cancer Institute, Shanghai Jiao Tong University, Shanghai, China. ‡Associate Professor, ‖Resident, Eastern Hepatobiliary Surgery Hospital, the Second Military Medical University, Shanghai, China, ‡‡Professor, State Key Laboratory of Oncogenes and Related Genes, Shanghai Cancer Institute, Shanghai Jiao Tong University, and Eastern Hepatobiliary Surgery Hospital, the Second Military Medical University. §Attending Physician, Department of Anesthesiology, Shanghai Pneumology Hospital, Tongji University, Shanghai, China.**Associate Professor, Putuo Hospital, Shanghai University of Traditional Chinese Medicine. ††Attending Physician, Department of Nuclear Medicine, Renji Hospital, School of Medicine, Shanghai Jiao Tong University.
BACKGROUND:: Recent advances have indicated a complex interplay between the autonomic nervous system and the innate immune system. Targeting neural networks for the treatment of sepsis is being developed as a therapeutic strategy. Because electroacupuncture at select acupoints can modulate activities of the autonomic nervous system, we tested the hypothesis that electroacupuncture at specific acupoints could modulate systemic inflammatory responses and improve survival via its impact on the autonomic nervous system in a rat model of sepsis. METHODS:: Sprague-Dawley male rats received electroacupuncture for 45 min before and at 1, 2, or 4 h after a lethal dose of intraperitoneal lipopolysaccharide injection (6 mg/kg). Outcomes included survival and systemic cytokine responses. Also, the possible roles of neural circuitry, including the hypothalamic-pituitary-adrenal axis and the autonomic nervous system, were evaluated. RESULTS:: Electroacupuncture pretreatment at the Hegu acupoints significantly attenuate systemic inflammatory responses and improve survival rate from 20% to 80% in rats with lethal endotoxemia. Such a site-specific effect requires the activation of muscarinic receptors in the central nervous system, but not increasing central sympathetic tone. In the periphery synergistic, rather than independent, action of the sympathetic and parasympathetic systems is also necessary. CONCLUSIONS:: Electroacupuncture pretreatment has a dramatic survival-enhancing effect in rats with lethal endotoxemia, which involves the activation of efferent neural circuits of the autonomic nervous system (e.g., cholinergic antiinflammatory pathway). This approach could be developed as a prophylactic treatment for sepsis or perioperative conditions related to excessive inflammation.
go to Publishergo to Pubmedgo to Scholargo to Googleshow EndNote Citationshow BibTex Citation
Xin Lv, Jian-Gang Song, Xiang-Rui Wang, Department of Anesthesiology, Renji Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai 200127, China.
AIM To investigate the role of hepatic peroxisome proliferator-activated receptor-γ (PPAR-γ) in increased susceptibility to endotoxin-induced toxicity in rats with bile duct ligation during endotoxemia. METHODS Male Sprague-Dawley rats were subjected to bile duct ligation (BDL). Sham-operated animals served as controls. DNA binding were determined by polymerase chain reaction, Western blotting analysis, and electrophoretic mobility shift assay, respectively. BDL and sham-operated rats received a non-lethal dose of intraperitoneal lipopolysaccharide (LPS) injection (3 mg/kg, i.p.). Additionally, the potential beneficial effects of the PPAR-γ agonist rosiglitazone were determined in BDL and sham-operated rats treated with a non-lethal dose of LPS. Survival was assessed in BDL rats treated with a non-lethal dose of LPS and in sham-operated rats treated at a lethal dose of LPS (6 mg/kg, i.p.). RESULTS PPAR-γ activity in rats undergoing BDL was significantly lower than in the sham-controls. Hepatic PPAR-γ gene expression was downregulated at both the mRNA and protein levels. In a parallel group, serum levels of pro-inflammatory cytokines were nearly undetectable in the sham-operated rats. When challenged with a non-lethal dose of LPS (3 mg/kg), the BDL rats had approximately a 2.4-fold increase in serum IL-6, a 2.7 fold increase in serum TNF-α, 2.2-fold increase in serum IL-1 and 4.2-fold increase in serum ALT. The survival rate was significantly lower as compared with that in sham-operated group. Additionally, rosiglitazone significantly reduced the concentration of TNF-α, IL-1β, IL-6 and ALT in sham-operated rats, but not in BDL rats, in response to LPS (3 mg/kg). Also, the survival was improved by rosiglitazone in sham-operated rats challenged with a lethal dose of LPS, but not in BDL rats, even with a non-lethal dose of LPS (3 mg/kg). CONCLUSION Obstructive jaundice downregulates hepatic PPAR-γ expression, which in turn may contribute to hypersensitivity towards endotoxin.
go to Publishergo to Pubmedgo to Scholargo to Googleshow EndNote Citationshow BibTex Citation
Department of Neurosurgery, The First Affiliated Hospital of Nanjing Medical University, 300 Guangzhou Road, Nanjing, 210029, Jiangsu Province, People's Republic of China.
PURPOSE: Recently, several microRNAs (miRNAs) were reported to be involved in the modulation of glioma development. The aim of our study was to determine the effect of miR-181d on the growth of glioma and to investigate whether this growth is modulated by targeting K-ras and Bcl-2. METHODS: Real-time PCR was used to analyze the expression of miR-181d in human glioma samples and glioma cell lines. Apoptosis, cell cycle, and proliferation (MTT) assays were performed to assess the phenotypic changes in glioma cells. Immunohistochemistry was used to determine the expression of K-ras and Bcl-2 in glioma tissues, and a luciferase reporter assay was carried out to confirm whether K-ras and Bcl-2 are direct targets of miR-181d. Western blotting was used to identify the potential signaling pathways affected glioma cell growth by miR-181d. In vivo, xenograft tumors were examined for an anti-glioma effect of miR-181d. RESULTS: MiR-181d was down-regulated in human glioma samples and up-regulated in transfected glioma cells. Ectopic expression of miR-181d suppressed proliferation and triggered cell cycle arrest and apoptosis in glioma cell lines. K-ras and Bcl-2 were identified as direct targets of miR-181d and were up-regulated in glioma samples. The results showed evidence linking the tumor suppressor activity of miR-181d in glioma cells with the K-ras-related PI3K/AKT and MAPK/ERK pathways. Furthermore, xenograft tumors from miR-181d-treated U251 cells were suppressed in vivo. CONCLUSION: MiR-181d may act as a glioma suppressor by targeting K-ras and Bcl-2.
go to Pubmedgo to Scholargo to Googleshow EndNote Citationshow BibTex Citation
CSIRO Information and Communications Technology Centre, P.O. Box 76, Epping, New South Wales 1710, Australia.
We study phase transitions and relevant order parameters via statistical estimation theory using the Fisher information matrix. The assumptions that we make limit our analysis to order parameters representable as a negative derivative of thermodynamic potential over some thermodynamic variable. Nevertheless, the resulting representation is sufficiently general and explicitly relates elements of the Fisher information matrix to the rate of change in the corresponding order parameters. The obtained relationships allow us to identify, in particular, second-order phase transitions via divergences of individual elements of the Fisher information matrix. A computational study of random Boolean networks supports the derived relationships, illustrating that Fisher information of the magnetization bias (that is, activity level) is peaked in finite-size networks at the critical points, and the maxima increase with the network size. The framework presented here reveals the basic thermodynamic reasons behind similar empirical observations reported previously. The study highlights the generality of Fisher information as a measure that can be applied to a broad range of systems, particularly those where the determination of order parameters is cumbersome.
go to Publishergo to Pubmedgo to Scholargo to Googleshow EndNote Citationshow BibTex Citation
1] School of Public Health and Primary Care, The Chinese University of Hong Kong, Hong Kong SAR, China [2] Fujian Center for Control and Prevention of Occupational diseases and Chemical Poisoning, Fuzhou, Fujian, China.
To investigate the association between lead powder use, as folk skin care, and blood lead level (BLL) in children, we studied 222 children up to 14-years old living in a Chinese rural area and administered a face to face interview with their parents to collect information on lead powder use and other potential exposure. We measured children's BLL at baseline and 2 years later after an intervention. The children were divided into three categories according to their use of lead powder: regular use, irregular use and never use. We applied multivariate linear regression to determine the association between lead powder use and elevated BLL. The average BLL of all children was 18 μg/dl; 56% of them had BLL of 10 μg/dl or higher. Lead powder use was significantly associated with elevated BLL. After adjusting for potential confounders the BLL of regular and irregular users was higher than non-users by 3.11 μg/dl and 1.47 μg/dl, respectively. Duration of lead powder use was positively associated with BLL, but the time since last use was inversely associated. A significant BLL reduction was observed 2 years later, and the greatest reduction (21 μg/dl) was seen in the youngest group of regular users. This study showed that traditional use of lead powder for a skin care purpose was a major contributor to elevated BLL in these children.Journal of Exposure Science and Environmental Epidemiology advance online publication, 14 December 2011; doi:10.1038/jes.2011.46.
Polish News
2012-05-23 20:11:33 © BioInfoBank Institute