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Determination of the number of J/ψ events with J/ψ → inclusive decays

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Chinese Physics C 2012年第10期36卷 915-925页

作者：麦迪娜 M. N. Achasov D. J. Ambrose 安芬芬安琪安正华白景芝班勇 J. Becker N. Berger M. Bertani 边渐鸣 E. Boger o. Bondarenko I. Boyko R. A. Briere V. Bytev 蔡啸 A. Calcaterra 曹国富常劲帆 G. Chelkov 陈刚陈和生陈江川陈玛丽陈申见陈晔陈元柏程和平初元萍 D. Cronin-hennessy 代洪亮代建平 D. Dedovich 邓子艳 A. Denig I. Denysenko M. Destefanis 丁伟民丁勇董燎原董明义杜书先方建房双世 L. Fava F. Feldbauer 封常青 R. B. Ferroli 傅成栋傅金林高原宁耿聪 K. Goetzen 龚文煊 W. Gradl M. Greco 顾旻皓顾运厅管颖慧郭爱强郭立波郭玉萍韩艳良郝喜庆 F. A. harris 何康林何苗何振亚 T. held 衡月昆侯治龙胡海明胡继峰胡涛黄彬黄光明黄金书黄性涛黄燕萍 T. hussain 姬长胜纪全季晓斌季筱璐贾卢魁姜丽丽江晓山焦健斌焦铮金大鹏金山景繁凡 N. Kalantar-Nayestanaki M. Kavatsyuk W. Kuehn 赖蔚 J. S. Lange 潘振声李春花李澄李翠李德民李飞李刚李海波李家才李康李蕾李宁博李秋菊李绍莉李卫东李卫国李晓玲李小男李学潜李秀荣李志兵梁昊梁勇飞梁羽铁廖广瑞廖小涛刘北江 C. L. Liu 刘春秀刘春燕刘福虎刘芳刘峰刘虎刘宏邦刘汇慧刘怀民刘红薇刘觉平刘魁勇刘凯刘坤刘佩莲刘树彬刘翔刘晓海刘勇刘豫斌刘振安刘志强刘智青 h. Loehner 鲁公儒吕海江吕军光吕绮雯吕晓睿卢云鹏罗成林罗民兴罗涛罗小兰吕蒙马长利马凤才马海龙马秋梅马斯马天马晓妍 Y. Ma F. E. Maas M. Maggiora q. A. Malik 毛虎冒亚军毛泽普 J. G. Messchendorp 闵建闵天觉 R. E. Mitchell 莫晓虎 C. Morales Morales C. Motzko N. Yu. Muchnoi Y. Nefedov 宁洁 I. B. Nikolaev 宁哲马鹏欧阳群 S. Pacetti 卞正烷 M. Pelizaeus 彭海平 K. Peters 平加伦平荣刚 R. Poling E. Prencipe C. S. J. Pun 祁鸣钱森乔从丰秦小帅秦瑶秦中华邱进发 K. h. Rashid 荣刚阮向东 A. Sarantsev B. D. Schaefer J. Schulze 邵明沈成平沈肖雁盛华义 M. R. Shepherd 宋新颖 S. Spataro B. Spruck 孙德辉孙功星孙俊峰孙胜森孙晓东孙勇杰孙永昭孙志嘉孙振田唐昌建唐晓 E. h. Thorndike 田浩来 D. Toth M. Ullrich G. S. Varner 王斌王博群王科王亮亮王灵淑王萌王平王佩良王强王庆娟王思广王雄飞汪晓莲王雅迪王贻芳王亚乾王铮王志刚王至勇魏代会 P. Weidenkaff 文群刚文硕频 M. Werner U. Wiedner 伍灵慧吴宁吴硕星吴蔚吴智夏力钢肖振军谢宇广修青磊许国发徐光明徐昊徐庆君徐新平徐晔许志蕊薛飞薛镇严亮鄢文标颜永红杨洪勋杨涛杨迎杨永栩叶桦叶梅叶铭汉俞伯祥喻纯旭俞洁晟于帅鹏苑长征袁文龙袁野 A. A. Zafar A. Zallo 曾云张丙新张炳云张长春张达华张宏浩章红宇张杰张金国张敬庆张家文张建勇张景芝张雷张书华张太锐张晓杰张学尧张瑶张银鸿张艳硕张子平张振宇赵光赵海升赵京伟赵凯旋赵雷赵玲赵明刚赵强赵书俊赵天池赵祥虎赵豫斌赵政国 A. Zhemchugov 郑建平郑阳恒郑志鹏钟彬 J. Zhong 周莉周晓康周小蓉朱程朱凯朱科军朱世海朱相雷朱兴旺朱亚敏朱永生朱自安庄建邹冰松邹佳恒左嘉旭 Institute of high Energy Physics G.I. Budker Institute of Nuclear Physics SB RAS (BINP) Novosibirsk 630090 Russia University of Rochester Rochester New York 14627 USA University of Science and Technology of China Peking University Bochum Ruhr-University INFN Laboratori Nazionali di Frascati University of Minnesota Minneapolis Joint Institute for Nuclear Research also at the Moscow Institute of Physics and Technology Moscow Russia KVI/University of Groningen 9747 AA Groningen The Netherlands Carnegie Mellon University Nanjing University huangshan College University of Minnesota Minneapolis MN 55455 USA Johannes Gutenberg University of Mainz Johann-Joachim-Becher-Weg 45 55099 Mainz Germany on leave from the Bogolyubov Institute for Theoretical Physics Kiev Ukraine University of Turin and INFN Turin Italy Shandong University Liaoning University Zhengzhou University University of Piemonte orientale and INFN (Turin) Bochum Ruhr-University 44780 Bochum Germany Tsinghua University GSI helmholtzcentre for heavy Ion Research Gmbh D-64291 Darmstadt Germany Guangxi University Graduate University of Chinese Academy of Sciences Nankai University Nanjing Normal University University of hawaii Honolulu Hawaii 96822 USA huazhong Normal University henan Normal University University of the Punjab Universitaet Giessen 35392 Giessen Germany The University of hong Kong Pokfulam Hong Kong China hangzhou Normal University Seoul National University Sun Yat-Sen University Sichuan University The Chinese University of hong Kong Shatin N.T. Hong Kong China Carnegie Mellon University Pittsburgh PA 15213 USA Shanxi University henan University of Science and Technology Luoyang 471003 China Wuhan University Lanzhou University Zhejiang University helmholtz Institute Mainz J.J. Becherweg 45D 55099 Mainz Germany Indiana University Bloomington Indiana 47405 USA University of Perugia and INFN I-06100 Perugia Italy also at the PNPI Gatchina Russia now at Nagoya University Nagoya Japan China Center o

The number of J/ψ events collected with the BES detector at the BEPC from June 12 to July 28, 2009 is determined to be （225.3 ± 2.8） × 10^ 6 using J/ψ→inclusive events, where the uncertainty is the systematic e... 详细信息

关键词： number of J/ψ events BES detector J/ψ →inclusive events

Dupilumab治疗常年性变应性鼻炎并发哮喘患者的疗效和安全性

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中华临床免疫和变态反应杂志 2018年第5期12卷 597-606页

作者： Steven F.Weinstein Rohit Katial Shyamalie Jayawardena Gianluca Pirozzi heribert Staudinger Laurent Eckert Vijay N.Joish Nikhil Amin Jaman Maroni Paul Rowe Neil M.h.Graham Ariel Teper 黄庭萱(翻译) 刘春涛(审校) 不详四川大学华西医院呼吸内科

背景Dupilumab是一种抗IL-4受体α亚基的抗体,可以阻断IL-4/IL-13的信号转导。IL-4/IL-13是2型/Th2型免疫疾病(如特应性/过敏性疾病)的关键驱动因子。一项重要的2b期临床研究(NCT01854047)显示,在使用了中高剂量吸入激素联合长效β2受... 详细信息

背景Dupilumab是一种抗IL-4受体α亚基的抗体,可以阻断IL-4/IL-13的信号转导。IL-4/IL-13是2型/Th2型免疫疾病(如特应性/过敏性疾病)的关键驱动因子。一项重要的2b期临床研究(NCT01854047)显示,在使用了中高剂量吸入激素联合长效β2受体激动剂(ICS/LABA)后仍控制不佳的持续性哮喘患者中,dupilumab可减少哮喘重度急性发作,改善患者的肺功能和生活质量,且耐受性良好。目的探讨在哮喘并发常年性变应性鼻炎(PAR)患者中,dupilumab对SNoT-22的总分及其中变应性鼻炎(AR)相关症状评分的影响。方法对2b临床研究中每2周(q2w) 200 mg和300 mg dupilumab治疗后的数据进行析因分析。这两种剂量的dupilumab目前正在3期临床研究(NCT02414854)中进行验证。PAR定义为:在研究开始时,患者出现对典型的常年性抗原产生特异性应答(Ig E≥0. 35 Ku/L)。结果总共241例(61%)患者患有PAR。与安慰剂相比,每两周300 mg dupilumab显著改善了在哮喘并发PAR的患者中SNoT-22的总分(最小二乘平均差,-5. 98; 95%CI,-10. 45～-1. 5; P=0. 009)和4项AR相关症状的评分(鼻塞,-0. 60; 95%CI,-0. 96～-0. 25;流鼻涕,-0. 67; 95%CI,-1. 04～-0. 31;打喷嚏,-0. 55; 95%CI,-0. 89～-0. 21;鼻后分泌物,-0. 49;95%CI,-0. 83～-0. 16; 4项评分都P oT-22总分(-1. 82; 95%CI,-6. 46～2. 83; P=0. 443)和AR相关的症状评分,但与安慰剂相比无统计学差异。在无PAR的哮喘患者中,dupilumab与安慰剂治疗这些评分无差异。结论每两周300 mg dupilumab治疗显著改善了在控制不佳的持续性哮喘并发PAR患者中的AR相关的鼻部症状。

关键词：哮喘变应性鼻炎常年性变应性鼻炎并发症 dupilumab 鼻部症状

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17q21遗传变异与哮喘相关

中国处方药 2008年第11期7卷 9-9页

作者： John W.holloway Gerard h.Koppelman Creaty

SNPs与哮喘的相关性仅存在于年龄为4岁或以下的儿童中,这一发现进一步证明,哮喘不是单一的一个疾病,而是几种不同疾病共同的临床表现。

关键词：哮喘遗传变异单核苷酸多态性 7号染色体长臂相互作用转录水平邻近基因跨膜蛋白

Refined families of Dothideomycetes:orders and families incertae sedis in Dothideomycetes

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Fungal Diversity 2020年第6期105卷 17-318页

作者： Sinang hongsanan Kevin D.hyde Rungtiwa Phookamsak Dhanushka N.Wanasinghe Eric h.C.McKenzie V.Venkateswara Sarma Robert Lücking Saranyaphat Boonmee Jayarama D.Bhat Ning-Guo Liu Danushka S.Tennakoon Dhandevi Pem Anuruddha Karunarathna Shu-hua Jiang Gareth E.B.Jones Alan J.L.Phillips Ishara S.Manawasinghe Saowaluck Tibpromma Subashini C.Jayasiri Diana Sandamali Ruvishika S.Jayawardena Nalin N.Wijayawardene Anusha h.Ekanayaka Rajesh Jeewon Yong-Zhong Lu Chayanard Phukhamsakda Asha J.Dissanayake xiang-Yu Zeng Zong-Long Luo qing Tian Kasun M.Thambugala Dongqin Dai Milan C.Samarakoon K.W.Thilini Chethana Damien Ertz Mingkwan Doilom Jian-Kui(Jack)Liu Sergio Pérez-ortega Ave Suija Chanokned Senwanna Subodini N.Wijesinghe Mekala Niranjan Sheng-Nan Zhang hiran A.Ariyawansa hong-Bo Jiang Jin-Feng Zhang Chada Norphanphoun Nimali Ide Silva Vinodhini Thiyagaraja huang Zhang Jadson D.P.Bezerra Ricardo Miranda-González AndréAptroot hiroyuki Kashiwadani Dulanjalee harishchandra Emmanuël Sérusiaux Pranami DAbeywickrama Dan-Feng Bao Bandarupalli Devadatha hai-xia Wu Kwang hee Moon Cecile Gueidan Felix Schumm Digvijayini Bundhun Ausana Mapook Jutamart Monkai Chitrabhanu S.Bhunjun Putarak Chomnunti Satinee Suetrong Napalai Chaiwan Monika C.Dayarathne Jing Yang Achala R.Rathnayaka Jian-Chu xu Jiesheng Zheng Gang Liu Yao Feng Ning xie Guangdong Provincial Key Laboratory for Plant Epigenetics Shenzhen Key Laboratory of Microbial Genetic EngineeringCollege of Life Science and OceanographyShenzhen UniversityShenzhen 518060People’s Republic of China Center of Excellence in Fungal Research Mae Fah Luang UniversityChiang Rai 57100Thailand CAS Key Laboratory for Plant Diversity and Biogeography of East Asia(KLPB) Kunming Institute of BotanyChinese Academy of ScienceKunming 650201YunnanPeople’s Republic of China East and Central Asia Regional office World Agroforestry Centre(ICRAF)Kunming 650201YunnanPeople’s Republic of China Centre for Mountain Futures(CMF) Kunming Institute of BotanyKunming 650201YunnanPeople’s Republic of China Department of Entomology and Plant Pathology Faculty of AgricultureChiang Mai UniversityChiang Mai 50002Thailand Institute of Plant health Zhongkai University of Agriculture and EngineeringHaizhu DistrictGuangzhou 510225People’s Republic of China World Agroforestry Centre East and Central Asia132 Lanhei RoadKunming 650201YunnanPeople’s Republic of China Manaaki Whenua-Landcare Research Private Mail Bag 92170AucklandNew Zealand Fungal Biotechnology Lab Department of BiotechnologySchool of Life SciencesPondicherry UniversityKalapetPondicherry 605014India School of Science Mae Fah Luang UniversityChiang Rai 57100Thailand Botanischer Garten und Botanisches Museum Freie Universität BerlinKönigin-Luise-Straße 6-814195 BerlinGermany 13128/1-J Azad Co-Op Housing SocietyCurcaP.O.Goa Velha 403108India Faculty of Agriculture Natural Resources and EnvironmentNaresuan UniversityPhitsanulok 65000Thailand Guizhou Key Laboratory of Agricultural Biotechnology Guizhou Academy of Agricultural SciencesGuiyang 550006People’s Republic of China School of Life Science and Technology University of Electronic Science and Technology of ChinaChengdu 611731People’s Republic of China State Key Laboratory of Mycology Institute of MicrobiologyChinese Academy of SciencesBeijing 100101People’s Republic of C

Numerous new taxa and classifications of Dothideomycetes have been published following the last monograph of families of Dothideomycetes in 2013.A recent publication by honsanan et *** 2020 expanded information of families in Dothideo-mycetidae and Pleosporomycetidae with modern *** this paper,we provide a refined updated document on orders and families incertae sedis of *** family is provided with an updated description,notes,including figures to represent the morphology,a list of accepted genera,and economic and ecological *** also provide phylogenetic trees for each *** this study,31 orders which consist 50 families are assigned as orders incertae sedis in Dothideomycetes,and 41 families are treated as families incertae sedis due to lack of molecular or morphological *** new order,Catinellales,and four new families,Catinellaceae,Morenoinaceae Neobuelliellaceae and Thyrinulaceae are *** genera(Neobuelliella,Pseudomicrothyrium,Flagellostrigula,Swinscowia,Macroconstrictolumina,Pseudobogoriella,and Schummia)are *** new species(Acrospermum urticae,Bogoriella complexoluminata,Dothiorella ostryae,Dyfrolomyces distoseptatus,Macroconstrictolumina megalateralis,Patellaria microspora,and Pseu-domicrothyrium thailandicum)are introduced base on morphology and phylogeny,together with two new records/reports and five new collections from different *** new combinations are also provided in this paper.

关键词： Abrothallales Ascrospermales Asterinales Botryosphaeriales Catinellales Cladoriellales Collemopsidiales Dyfrolomycetales Eremithallales Eremomycetales Jahnulales Kirschsteiniotheliales Lembosinales Lichenotheliales Microthyriales Minutisphaerales Monoblastiales Murramarangomycetales new family new genera new order new species Parmulariales Patellariales Phaeotrichales Phylogeny Stigmatodiscales Strigulales Superstratomycetales Taxonomy Trypetheliales Tubeufiales Valsariales Venturiales Zeloasperisporiales

Prognostic impact of molecular markers in a series of 220 primary glioblastomas

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中国神经肿瘤杂志 2006年第1期4卷 7-7页

作者： houillier C Lejeune J Benouaic h-Amiel A Laigle-Donadey F Criniere E Mokhtari K Thillet J Delattre JY hoang-xuan K Sanson M Mazarin Neurology Service and INSERM U711 Biology of Neuronal and GlialInteractions Paris France.

BACKGRoUND: In contrast to ofigodendrogliomas, molecular predictors of prognosis have not been consistently found in glioblastomas. however, genetic studies show that glioblastomas consist of several genetic subtypes and raise the possibility that molecular alterations could be predictive of survival. METhoDS: A search for loss of heterozygosity (Loh) on chromosome 1p, 9p, 10q, 19q, EGFR (epidermal growth factor receptor), CDK4, and MDM2 (mouse double minute) amplifications, CDKN2A (INK4A/ARF) homozygous deletions, p53 expression, was performed in a series of 220 primary glioblastomas.

关键词：星形细胞瘤原发型分子标记预测

高阶成像参数可改善T2/FLAIR不匹配征预测弥漫性低级别胶质瘤亚型即IDh突变与无1p19q共缺失的价值

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国际医学放射学杂志 2020年第2期 249-249页

作者： M.K.Lee J.E.Park Y.Jo S.Y.Park S.J.Kim h.S.Kim 冀晓莉 Department of Radiology and Research Institute of Radiology Asan Medical Center University of Ulsan College of Medicine

目的 T2/FLAIR不匹配征与高阶影像学参数结合可提高对弥漫性低级别胶质瘤分子亚型的判断能力。本研究评价表观扩散系数(ADC)、脑血容量(CBV)对T2/FLAIR不匹

关键词： T2/FLAIR CBV ADC AUC 低级别胶质瘤成像参数弥漫性 IDh

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接受心脏移植者的LMNA突变

世界核心医学期刊文摘（心脏病学分册） 2005年第8期1卷 26-26页

作者： Pethig K. Genschel J. Peters T. et al. h. h.- J. Schmidt 王永兴 Med. Klin. m.S. Gastroenterol. H. Charité Campus Mitte DE- 10098Berlin Germany

Lamin A and C are components of the nuclear envelope, located at the nucleoplasmatic surface of the inner nuclear membrane within cells. Recently,mutations within LMNA encoding lamin A/C have been associated with various disease entities including cardiomyopathy. We screened heart transplant recipients suffering from dilated cardiomyopathy(DCM) with a positive family history of LMNA mutations. Four index patients and one relative belonging to four unrelated families carrying LMNA mutations were identified. The mutations p.q355x and p.S22L have not been reported before, whereas p.R190W has already been reported in other studied DCM cohorts. In the patients of the present study, the mean age at manifestation of heart disease was 37.6 years(range 30- 45 years), with progression to end- stage heart failure requiring transplantation at a mean age of 45.8 years(range 35- 54 years). Three patients presented initially with atrial fibrillation. These data confirm the involvement of LMNA mutations in patients with DCM and extend the mutational spectrum of LMNA. The p.R190W mutation has been reported in different populations and may therefore be useful for analyzing the impact of a specific LMNA mutation on the phenotype of muscle disease.

关键词：移植者 LMNA 心肌病内核膜阳性家族史心房纤颤研究人群突变谱内层核浆

常染色体隐性遗传脊髓小脑共济失调症和周围神经病变伴甲胎蛋白升高

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世界核心医学期刊文摘（神经病学分册） 2005年第1期1卷 8-8页

作者： Izatt L. Németh A.h. Meesaq A. 张勇 Department of Clinical Genetics Guy’ s St. Thomas’ Hosp. NHS Trust St Thomas Street London SE1 9RT United Kingdom

We describe three patients from two families with progressive spinocerebellar ataxia, peripheral neuropathy, raised α fetoprotein (AFP) and hypercholesterolaemia. Two siblings had identical clinical features, with late childhood onset of symptoms and slow progression, requiring crutches to walk at ages 37 and 38 years. Another patient developed ataxia aged 13 years and became wheel chair bound by 20 years of age. Although they all had raised serum AFP levels, their clinical, immunological, biochemical, cytogenetic and molecular genetic studies failed to support a diagnosis ofAtaxia Telangiectasia. Extensive investigation including imaging, biochemical and genetic studies excluded other known ataxias. Their clinical features most closely resemble the phenotype of a single consanguineous Japanese family with four individuals affected by spinocerebellar ataxia, peripheral neuropathy, raised AFP and hypercholesterolaemia. homozygosity mapping has identified a locus in this Japanese family at 9q34. haplotype analysis of our cases demonstrated possible linkage to 9q34, suggesting these may be the first Caucasian families described with this disorder.

关键词：共济失调症脊髓小脑甲胎蛋白高胆固醇血症分子遗传学同胞兄弟首例报道细胞遗传学影像学免疫学

Cav1.2,Cav1.3,and Cav2.1 in the mouse hippocampus during and after pilocarpine-induced status epilepticus

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Cav1.2,Cav1.3,and Cav2.1 in the mouse hippocampus during and...