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13篇 您的检索式:作者名="Tairo"
    题名 作者 年代 出处 被引量
1Isolation of phospholipase D producing microorganisms with high transphosphatidylation activity显示文摘Tairo H Masanobu N Tadashi H 2000Biotechnology Letters2000,22,6:1
2Potyvirus complexes in sweetpotato:occurrence in Australia,serological and molecular resolution,and analysis of the sweet potato virus 2 (SPV2) component显示文摘Tairo F Jones RAC Valkonen JPT 0,,09:1
3Sweetpotato viruses: 15 years of progress on understanding and managing complex diseases显示文摘Clark C A Davis J A Abad J A Cuellar W J Fuentes S Kreuze J F Gibson R W Mukasa S Tugume A K Tairo F Valkonen J P T 2012Plant Disease2012,96,2:1
4Coat protein sequence analysis reveals occurrence of new strains of Sweet potato feathery mottle virus in Uganda and Tanzania显示文摘Mukasa SB Tairo F Kreuze JF 0,,01:1
5Unravelling the genetic diversity of the three main viruses involved in sweet potato virus disease(SPVD)and its practical implications显示文摘Tairo F Mukasa SB Jones RAC 0,,02:1
6Multiplex polymerase chain reaction for detection of herpes simplex vires type 1, and 2, cytomegalovirus,and varicella-zoste virus in ocular viral infections显示文摘Yan Zhang Tairo Kimura Keiko Fujiki 2003Jpn J Ophthalmol2003,47,:1
7Coat protein sequence analysis reveals occurrence of new strains of sweet potato feathery mottle virus in ugander and Tanzania显示文摘Mukasa S B Tairo F Kreuze J F 2003Virus Genes2003,27,:1
8Highly efficient production of enzymes of an extreme thermophile, Thermus thermophilus: A practical method to overexpress GC-rich genes in Escherichia coli显示文摘Masami Ishida Masasuke Yoshida Tairo Oshima 1997Extremophiles1997,,3:1
9Incidence of viruses infecting sweet potato in Tanzania 显示文摘Tairo F Kullaya A 2004Plant Disease2004,88,:1
10Reduction of NOx from combustion flue gases by superimposed barrier discharge plasma reactors 显示文摘URASHIMA Kuniko CHANG Jen-Shih ITO Tairo 1997IEEE Transactions on Industry Applications1997,33,3:1
11Impact of Frequency-Domain Optical Coherence Tomography Guidance for Optimal Coronary Stent Implantation in Comparison With Intravascular Ultrasound Guidance显示文摘Maoto Habara Kenya Nasu Mitsuyasu Terashima Hideaki Kaneda Daisuke Yokota Euihong Ko Tsuyoshi Ito Tairo Kurita Nobuyoshi Tanaka Masashi Kimura Tatsuya Ito Yoshihisa Kinoshita Etsuo Tsuchikane Keiko Asakura Yasushi Asakura Osamu Katoh Takahiko Suzuki 2012Circulation: Cardiovascular Interventions2012,,2:1
12Improvement of NOx Removal Rate Using Discharge Photocatalyst and UV Rays显示文摘 Yoshimoto Murata Daisuke Ito Yoshiyasu Ehara Haruo Kishida Tairo Ito 2004IEEJ Transactions on Fundamentals and Materials2004,124,10:1
13Dose escalation of external beam radiotherapy for high-risk prostate cancerdImpact of multiple high-risk factor显示文摘Objective:To retrospectively investigate the treatment outcomes of external beam radiotherapy with androgen deprivation therapy(ADT)in high-risk prostate cancer in three radiotherapy dose groups.Methods:Between 1998 and 2013,patients with high-risk prostate cancer underwent threedimensional conformal radiotherapy or intensity-modulated radiotherapy of 66 Gy,72 Gy,or 78 Gy with ADT.Prostate-specific antigen(PSA)relapse was defined using the Phoenix definition.PSA relapse-free survival(PRFS)was evaluated in each radiotherapy dose group.Moreover,high-risk patients were divided into H-1(patients with multiple high-risk factors)and H-2(patients with a single high-risk factor)as risk subgroups.Results:Two hundred and eighty-nine patients with a median follow-up period of 77.3 months were analyzed in this study.The median duration of ADT was 10.1 months.Age,Gleason score,T stage,and radiotherapy dose influenced PRFS with statistical significance both in univariate and multivariate analyses.The 4-year PRFS rates in Group-66 Gy,Group-72 Gy and Group-78 Gy were 72.7%,81.6%and 90.3%,respectively.PRFS rates in the H-1 subgroup differed with statistical significance with an increasing radiotherapy dose having a more favorable PRFS,while PRFS rates in H-2 subgroup did not differ with increase in radiotherapy dose.Conclusion:Dose escalation for high-risk prostate cancer in combination with ADT improved PRFS.PRFS for patients in the H-1 subgroup was poor,but dose escalation in those patients was beneficial,while dose escalation in the H-2 subgroup was not proven to be effective for improving PRFS.Rei Umezawa Koji Inaba Satoshi Nakamura Akihisa Wakita Hiroyuki Okamoto Keisuke Tsuchida Tairo Kashihara Kazuma Kobayashi Ken Harada Kana Takahashi Naoya Murakami Yoshinori Ito Hiroshi Igaki Keiichi Jingu Jun Itami 2019Asian Journal of Urology2019,6,2:0
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