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15篇 您的检索式:作者名="Pooja D"
    题名 作者 年代 出处 被引量
1Emodin suppresses Wnt signaling in hu- man colorectal cancer cells SW480 and SW620显示文摘Pooja T Karunagaran D 2014Eur J Pharmacol2014,14,2:1
2Emodin suppresses Wnt signaling in human eoloreetal cancer cells SW480 and SW6201显示文摘Pooja T Karunagaran D 2014Eur J Pharmaeol2014,742,:1
3Emodin suppresses Wnt signaling in human colorectal cancer cells SW480 and SW620 显示文摘Pooja T Karunagaran D 2014Eur J Pharmacol2014,742,11:1
4Enhanced luminescence of Y3Al5O12:Ce^3+ nanophosphor for white light-emitting diodes显示文摘Haranath D Harish Chander Pooja Sharma Singh S 2006Applied Physics Letters2006,89,17:1
5Phenolic compounds, antioxidant activity and insulinotropic effect of extracts prepared from grape (Vitis vinifera E) byproducts 显示文摘Pooja D Pandurang A Kaushik B 2015Journal of Food Science and Technology2015,52,1:1
6Functionalized goldnanoparticles and their biomedical applications显示文摘Pooja M T Komal V Vida A D 2011Nanomaterials2011,1,:1
7Emodin suppresses Wnt signaling in humancolorectal cancer cells SW480 and SW620显示文摘POOJA T KARUNAGARAN D 2014Eur J Pharmacol2014,742,:1
8Trastuzumab-grafted PAMAM dendrimers for the selective delivery of anti-cancer drugs to HER2-positive breast cancer 显示文摘Kulhari H Pooja D Shrivastava S 2016Sci Rep2016,6,23:1
9Fluid flow and heat transfer in curved tubes with temperature-dependent properties 显示文摘Vimal Kumar Pooja Gupta Nigam K D P 2007Industrial and Engineering Chemistry Re- search2007,46,10:1
10Fluid flow andheat transfer in curved tubes with temperature-dependentproperties显示文摘Kumar Vimal Gupta Pooja Nigam K D P 2007Industrial and Engineering Chemistry Research2007,46,10:1
11Management of chemotherapy-induced nausea and vomiting显示文摘Pooja D Swati S Deepika H 2010Indian Pediatrics2010,47,2:1
12Xanthan Gum Stabilized Gold Nanopartieles: Characterization, Bioeompatibility, Stability and Cytotoxicity 显示文摘Pooja D Panyaram S Kulhari H 2014Carbohydr Polym2014,110,:1
13Emodin suppresses Wnt signaling in human colorectal cancer cells SW480 and SW620显示文摘Pooja T Karunagaran D 2014Eur J Pharmacol2014,742,:1
14An international survey of classification and treatment choices for group D retinoblastoma显示文摘AIM: To determine which IIRC scheme was used by retinoblastoma centers worldwide and the percentage of D eyes treated primarily with enucleation versus globe salvaging therapies as well as to correlate trends in treatment choice to IIRC version used and geographic region.METHODS: An anonymized electronic survey was offered to 115 physicians at 39 retinoblastoma centers worldwide asking about IIRC classification schemes and treatment patterns used between 2008 and 2012. Participants were asked to record which version of the IIRC was used for classification, how many group D eyes were diagnosed, and how many eyes were treated with enucleation versus globe salvaging therapies. Averages of eyes per treatment modality were calculated and stratified by both IIRC version and geographic region. Statistical significance was determined by Chi-square, ANOVA and Kruskal-Wallis tests using Prism.RESULTS: The survey was completed by 29% of physicians invited to participate. Totally 1807 D eyes were diagnosed. Regarding IIRC system, 27% of centers used the Children's Hospital of Los Angeles(CHLA) version, 33% used the Children's Oncology Group(COG) version, 23% used the Philadelphia version, and 17% were unsure. The rate for primary enucleation varied between 0 and 100% and the mean was 29%. By IIRC version, primary enucleation rates were: Philadelphia, 8%; COG, 34%; and CHLA, 37%. By geographic region, primary enucleation rates were: Latin America, 57%; Asia, 40%; Europe, 36%; Africa, 10%, US, 8%; and Middle East, 8%. However, systemic chemoreduction was used more often than enucleation in all regions except Latin America with a mean of 57% per center(P<0.0001). CONCLUSION: Worldwide there is no consensus on which IIRC version is used, systemic chemoreduction was the most frequently used initial treatment during the study period followed by enucleation and primary treatment modality, especially enucleation, varied greatly with regards to IIRC version used and geographic region.Christina Scelfo Jasmine H Francis Vikas Khetan Thomas Jenkins Brian Marr David H Abramson Carol L Shields Jacob Pe’er Francis Munier Jesse Berry J.William Harbour Andrey Yarovoy Evandro Lucena Timothy G Murray Pooja Bhagia Evelyn Paysse Samuray Tuncer Guillermo L Chantada Annette C Moll Tatiana Ushakova David A Plager Islamov Ziyovuddin Carlos A Leal Miguel A Materin Xun-Da Ji Jose W Cursino Rodrigo Polania Hayyam Kiratli Charlotta All-Ericsson Rejin Kebudi Santosh G Honavar Vicktoria Vishnevskia-Dai Sidnel Epelman Anthony B Daniels Jeanie D Ling Fousseyni Traore Marco A Ramirez-Ortiz 2017International Journal of Ophthalmology(English edition)2017,10,6:0
15Sequence analysis of VP4 genes of wild type and culture adapted human rotavirus G1P[8]strains显示文摘Objective:To conduct a comparative analysis of the VP4 gene sequences of Indian wild type (06361,0613158,061060 and 0715880) and cell culture adapted(06361-CA,0613158-CA.061060- CA and 0715880-CA) G1P[8]rotavirus strains.Methods:Full-length VP4 genes of each of the four wild type G1P[8]rotavirus strains and their cell culture adapted counterparts displaying consistent cytopathic effect were subjected to RT-PCR amplification and nucleotide sequencing. Results:All four cell culture adapted G1P[8]rotavirus strains showed nucleotide and amino acid substitutions in the VP4 gene as compared to their wild type strains.The number of substitutions however,varied from 1-64 and 1-13 respectively.The substitutions were distributed in both VP5* and VP8* subunits of VP4 gene respectively of permeabilizalion and hemagglutinaling activity. The presence of unique amino acid substitutions was identified in two of the four wild type(V377G. S387N in 061060 and 1644L in 0715880) and all four cell culture adapted(A46V in 0613158-CA. T60R in 06361-CA,L237V.G389V and Q480H in 061060-CA and S615G and T625P in 0715880-CA) strains for the first time in the VP4 gene of P[8]specificity.Amino acid substitutions generated increase in the hydrophilicity in the cell culture adapted rotavirus strains as compared to their corresponding wild type strains.Conclusions:Amino acid substitutions detected in the VP4 genes of G1P[8]rotavirus strains from this study together with those from other studies highlight occurrence of only strain and/or host specific substitutions during cell culture adaptation. Further evaluation of such substitutions for their role in attenuation,immunogenicity and conformation is needed for the development of newer rolavirus vaccines.Ritu Arora Ganesh S Dhale Pooja R Patil Shobha D Chitambar 2011Asian Pacific Journal of Tropical Medicine2011,4,7:0
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