维普中文期刊产品整合服务
25篇 您的检索式:作者名="Andrew Duncan"
    题名 作者 年代 出处 被引量
1Theileria annulata sporozoite surface antigen expressed in Escherichia coli elicits neutralizing antibody显示文摘Susanna W Andrew T Duncan B 1989PNAS1989,86,:1
2Microbes Central to Human Reproduction显示文摘Gregor Reid Patrizia Brigidi Jeremy P. Burton Nikhat Contractor Sylvia Duncan Emilie Fargier Colin Hill Sarah Lebeer Rocio Martín Andrew J. McBain Gil Mor Catherine O’Neill Juan Miguel Rodríguez Jonathan Swann Saskia Hemert Juliett Ansell 2015Am J Reprod Immunol2015,,1:1
3A PROSPECTIVE STUDY OF THE NATURAL HISTORY OF HEMATURIA ASSOCIATED WITH BENIGN PROSTATIC HYPERPLASIA AND THE EFFECT OF FINASTERIDE显示文摘STEPHEN J. FOLEY LEMKIE Z. SOLOMAN ANDREW W. WEDDERBURN KASHIF M. KASHIF DUNCAN SUMMERTON VANESSA BASKETTER SIMON A.V. HOLMES 2000The Journal of Urology2000,,2:1
4The effect of attitude on the development of adolescent cigarette use显示文摘Andrews JA Duncan SC 1998J Subst Abuse1998,10,:1
5Evaluation of oxi- dation and hydrogen permeation in Al-containing stainless steel al- loys 显示文摘Thad M Adams Paul Korinko Andrew Duncan 2006Materials Science and Engineering A2006,,424:1
6The long-term outcome of adult epilepsy surgery, patterns of seizure remission, and relapse: a cohort study显示文摘Jane de Tisi Gail S Bell Janet L Peacock Andrew W McEvoy William FJ Harkness Josemir W Sander John S Duncan 2011The Lancet2011,,9800:1
7Assessment of Dietary Intake and Trace Element Status in Patients with Ileal Pouch-Anal Anastomosis显示文摘Mohammad Sami H. Muhtaseb M.Sc. Andrew Duncan Ph.D. Dinesh K. Talwar Ph.D. Denis St. J. O’Reilly M.D. Ruth F. McKee M.D. John H. Anderson M.D. Ian G. Finlay M.D 2007Diseases of the Colon & Rectum2007,,10:1
8Recent sea-level contributions of the Antarctic and Greenland Ice sheets显示文摘Andrew Shepherd Duncan Wingham 2007Science2007,315,5818:1
9Genetic evidence for functional redundancy of Platelet/Endothelial cell adhesion molecule-1 (PECAM-1) : CD31-deficient mice reveal PECAM-l-dependent and PECAM-l-independent functions 显示文摘Duncan GS Andrew DP Takimoto H 1999J Immunol1999,162,5:1
10Structural Snapshots of Human HDAC8 ProvideInsights into the Class I His- tone Deacetylases显示文摘John RS Robert JS Bradley AK Clifford M Joseph DH Andy JJ Christine L Andrew A Joseph JB Ellen C Jie T Bi CS Erik V Robert W Ellen ML Douglas RD Gyorgy S Marc N Mark WK Ronald VS Duncan EM and Leslie WT 2004Structure2004,12,:1
11Generation of a monoclonal human single chain antibody fragment to hepatic stellate cells – a potential mechanism for targeting liver anti-fibrotic therapeutics显示文摘Lucy J. Elrick Val Leel Morgan G. Blaylock Linda Duncan Matthew R. Drever Gillian Strachan Keith A. Charlton Matthew Koruth Andrew J. Porter Matthew C. Wright 2005Journal of Hepatology2005,,6:1
12A Novel Method for Implementation of Frameless StereoEEG in Epilepsy Surgery显示文摘Mark Nowell Roman Rodionov Beate Diehl Tim Wehner Gergely Zombori Jane Kinghorn Sebastien Ourselin John Duncan Anna Miserocchi Andrew McEvoy 2014Neurosurgery2014,,:1
13Open repair of juxtarenal aortic aneurysms (JAA) remains a safe option in the era of fenestrated endografts显示文摘Andrew W. Knott Manju Kalra Audra A. Duncan Nanette R. Reed Thomas C. Bower Tanya L. Hoskin Gustavo S. Oderich Peter Gloviczki 2008Journal of Vascular Surgery2008,,:1
14A comparison of bispectral index and entropy monitoring,in patients undergoing embolization of cerebral artery aneurysms after subarachnoid haemorrhage显示文摘Duncan D Kelly KP Andrews PJD 2006Br J Anaesth2006,96,:1
15Impact of exclusive enteral nutrition on body composition and circulating micronutrients in plasma and erythrocytes of children with active Crohn’s disease显示文摘Konstantinos Gerasimidis Dinesh Talwar Andrew Duncan Pamela Moyes Elaine Buchanan Kamal Hassan Denis O’Reilly Paraic McGrogan Christine Ann Edwards 2011Inflamm Bowel Dis2011,,9:1
16The role of bulky substituents in the polymerization of ethylene using late transition metal catalysts: a comparative study of nickel and iron catalyst systems显示文摘George J.P Britovsek Simon P.D Baugh Olivier Hoarau Vernon C Gibson Duncan F Wass Andrew J.P White David J Williams 2002Inorganica Chimica Acta2002,,:1
17The order Herpesvirales显示文摘Andrew J. Davison Richard Eberle Bernhard Ehlers Gary S. Hayward Duncan J. McGeoch Anthony C. Minson Philip E. Pellett Bernard Roizman Michael J. Studdert Etienne Thiry 2009Archives of Virology2009,,1:1
18Multiple quantitative trait loci contribute to resistance to bacterial canker incited by Pseudomonas syringae pv.actinidiae in kiwifruit(Actinidia chinensis)显示文摘Pseudomonas syringae pv.actinidiae(Psa)biovar 3,a virulent,canker-inducing pathogen is an economic threat to the kiwifruit(Actinidia spp.)industry worldwide.The commercially grown diploid(2×)A.chinensis var.chinensis is more susceptible to Psa than tetraploid and hexaploid kiwifruit.However information on the genetic loci modulating Psa resistance in kiwifruit is not available.Here we report mapping of quantitative trait loci(QTLs)regulating resistance to Psa in a diploid kiwifruit population,derived from a cross between an elite Psa-susceptible‘Hort16A’and a resistant male breeding parent P1.Using high-density genetic maps and intensive phenotyping,we identified a single QTL for Psa resistance on Linkage Group(LG)27 of‘Hort16A’revealing 16–19%phenotypic variance and candidate alleles for susceptibility and resistance at this loci.In addition,six minor QTLs were identified in P1 on distinct LGs,exerting 4–9%variance.Resistance in the F1 population is improved by additive effects from‘Hort16A’and P1 QTLs providing evidence that divergent genetic pathways interact to combat the virulent Psa strain.Two different bioassays further identified new QTLs for tissue-specific responses to Psa.The genetic marker at LG27 QTL was further verified for association with Psa resistance in diploid Actinidia chinensis populations.Transcriptome analysis of Psa-resistant and susceptible genotypes in field revealed hallmarks of basal defense and provided candidate RNA-biomarkers for screening for Psa resistance in greenhouse conditions.Jibran Tahir Stephen Hoyte Heather Bassett Cyril Brendolise Abhishek Chatterjee Kerry Templeton Cecilia Deng Ross Crowhurst Mirco Montefiori Ed Morgan Andrew Wotton Keith Funnell Claudia Wiedow Mareike Knaebel Duncan Hedderley Joel Vanneste John McCallum Kirsten Hoeata Amardeep Nath David Chagné Luis Gea Susan E.Gardiner 2019Horticulture Research2019,6,1:0
19Aneuploidy in pluripotent stem cells and implications for cancerous transformation显示文摘Jie Na Duncan Baker Jing Zhang Peter W. Andrews Ivana Barbaric 2014Protein & Cell2014,5,8:0
20Rationally designed mariner vectors for functional genomic analysis of Actinobacillus pleuropneumoniae and other Pasteurellaceae species by transposon-directed insertion-site sequencing (TraDIS)显示文摘Comprehensive identification of conditionally essential genes requires efficient tools for generating high-density transposon libraries that, ideally, can be analysed using next-generation sequencing methods such as Transposon Directed Insertion-site Sequencing (TraDIS). The Himar1 (mariner) transposon is ideal for generating near-saturating mutant libraries, especially in AT-rich chromosomes, as the requirement for integration is a TA dinucleotide, and this transposon has been used for mutagenesis of a wide variety of bacteria. However, plasmids for mariner delivery do not necessarily work well in all bacteria. In particular, there are limited tools for functional genomic analysis of Pasteurellaceae species of major veterinary importance, such as swine and cattle pathogens, Actinobacillus pleuropneumoniae and Pasteurella multocida, respectively. Here, we developed plasmids, pTsodCPC9 and pTlacPC9 (differing only in the promoter driving expression of the transposase gene), that allow delivery of mariner into both these pathogens, but which should also be applicable to a wider range of bacteria. Using the pTlacPC9 vector, we have generated, for the first time, saturating mariner mutant libraries in both A. pleuropneumoniae and P. multocida that showed a near random distribution of insertions around the respective chromosomes as detected by TraDIS. A preliminary screen of 5000 mutants each identified 8 and 14 genes, respectively, that are required for growth under anaerobic conditions. Future high-throughput screening of the generated libraries will facilitate identification of mutants required for growth under different conditions, including in vivo, highlighting key virulence factors and pathways that can be exploited for development of novel therapeutics and vaccines.Janine T.Bossé Yanwen Li Leon G.Leanse Liqing Zhou Roy R.Chaudhuri Sarah E.Peters Jinhong Wang Gareth A.Maglennon Matthew T.G.Holden Duncan J.Maskell Alexander W.Tucker Brendan W.Wren Andrew N.Rycroft Paul R.Langford on behalf of the BRaDPT consortium 2021Animal Diseases2021,1,4:0
返回顶部 每页显示:
共2页 首页 上一页 第1页 下一页 末页 /2 跳转

网站首页 | 关于我们 | 联系我们 | 产品服务 | 客服中心 | 广告服务 | 版权声明 | 网站联盟 | 友情链接 | 售卡网点

版权所有© 渝B2-20050021-1 渝公网安备 50019002500403号 违法和不良信息举报中心

互联网出版许可证 新出网证(渝)字10号 全国400电话 - 免长途话费