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7篇 您的检索式:作者名="Photini"
    题名 作者 年代 出处 被引量
1The new global map of human brucellosis显示文摘Georgios Pappas Photini Papadimitriou Nikolaos Akritidis Leonidas Christou Epameinondas V Tsianos 2006The Lancet Infectious Diseases2006,,2:3
2The new global map of human brucellosis显示文摘Georgios Pappas Photini Papadimitriou Nikolaos Akritidis Leonidas Christou Epameinondas V Tsianos 2006The Lancet Infectious Diseases2006,,2:1
3Malaria in India: The Center for the Study of Complex Malaria in India显示文摘Aparup Das Anupkumar R. Anvikar Lauren J. Cator Ramesh C. Dhiman Alex Eapen Neelima Mishra Bhupinder N. Nagpal Nutan Nanda Kamaraju Raghavendra Andrew F. Read Surya K. Sharma Om P. Singh Vineeta Singh Photini Sinnis Harish C. Srivastava Steven A. Sullivan 2011Acta Tropica2011,,3:1
4The regional production of cytokines and lactao in sepsis-related multiple organ failure显示文摘Douzinas EE Photini D Tsideniadou Pitariais MT 1997Am J Resp Crit Med1997,155,:1
5The regional production of cytokines and lactao in sepsis-related multiple organ failure显示文摘Douzinas EE Photini D Tsideniadou Pitariais MT 1997Am J Resp Crit Med1997,155,:1
6In vivo molecular mapping of the tumor microenvironment in an azoxymethane‐treated mouse model of colon carcinogenesis显示文摘Sarah J. Leung Photini S. Rice Jennifer K. Barton 2015Lasers Surg. Med2015,,:1
7Grapevine Phenological Quantitative Trait SSR Genotyping Using High-Throughput HRM-PCR Analysis显示文摘Discrimination among grapevine varieties based on quantitative traits,such as flowering,veraison and ripening dates is crucial for variety selection in the context of climate change and in breeding programs.These traits are under complex genetic control for which 6 linked SSR loci(VVS2,VVIn16,VMC7G3,VrZAG29,VMC5G7,and VVIB23)have been identified.Using these markers in HRM-PCR analysis,we assessed genetic diversity among a large collection of 192 grapevine varieties.The grapevine germplasm used encompasses the majority of Greek vineyard with 181 varieties,3 prominent foreign varieties and 11 varieties of Palestinian origin.The SSR markers used were highly polymorphic,displaying unique melting curves for unusually higher number of samples than generally observed in SSR analysis.This prompted us to examine sequence composition for selected samples and found that variation present as SNPs in the flanking sequences of SSR motifs was responsible for the observed polymorphism.Hence,HRM-PCR proved to be a tool of higher analytical power to distinguish genotypes surpassing the discrimination power of conventional gel-based SSR analysis.The study provides a better understanding of genetic variation of SSR marker loci associated to phenological traits in grapevine varieties,signifying an analytical methodology that may be of higher discrimination power in detection of polymorphism for utilization in breeding programs.Murad Awad Photini V.Mylona Alexios N.Polidoros 2020Phyton-International Journal of Experimental Botany2020,89,4:0
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