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1、英文投稿信模板投稿信模版一dear xx (editor):here is our paper submitted to (xx journal).the title: xxxxthe authors: xxxxxxandxxxin this paper, we .the authors claim that none of the material in the paper has been published or is under consideration for publication elsewhere.the corresponding author is dr. xxx and

2、 his address and other information is as following:address: department of xxx, xx university, ., p.r.chinae-mail: xxxxxtel: +86-xxx-xxxxxxxxfax: +86-xxx-xxxxxxxxthank you very much for consideration!sincerely yours,dr. xxx投稿信模版二dear prof. xxxxx,here within enclosed is our paper for conside

3、ration to be published on (journal name). the further information about the paper is in the following:the title: xxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxthe authors: xxxxx xxxxx and xxxxxthe authors claim that none of the material in the paper has been published or is under consideration for publication else

4、where.i am the corresponding author and my address and other information is as follows,address: department of xxxxxxxxx, tsinghua university,beijing, 10084,p.r.chinae-mail: xxxxxtel: 86-10-62785001fax: 86-10-62785001thank you very much for consideration!sincerely yours,dr. xxxxxx

5、xxxxx投稿信模版三(1)dear mr. *1. the work described has not been submitted elsewhere for publication, in whole or in part, and all the authors listed have approved the manuscript that is enclosed.2. i have read and have abided by the statement of ethical standards for manuscripts submitted to neuroscience

6、.kind regards.your sincerely,通讯作者(2)dear dr. 主编name:we submit our manuscript entitled 文章title to 杂志名for publication.接着简单介绍你文章的主要创新点和意义,不易过多,但要突出新意和关键点。all authors have seen the manuscript and approved to submit to your journal. thank you very much for your attention and consideration. sincerely your

7、s, 通讯作者(3)dear dr. 主编name:we submit our manuscript entitled文章title to 杂志名for publication.接着简单介绍你文章的主要创新点和意义,不易过多,但要突出新意和关键点。all authors have seen the manuscript and approved to submit to your journal. thank you very much for your attention and consideration. sincerely yours, 通讯作者(4)dr. *editor-in-ch

8、ief, *(add address) january 22, 2003 dear dr. *,enclosed herewith please find 3 copies of a ms by: *. * and * entitled: “*”, which we would like to submit for publication in the *.looking forward to your decision,with kind personal regards,sincerely yours,(5)dear prof. gil:this is a manuscript by *

9、and * entitled “.”. it is submitted to be considered for publication as a “.” in your journal. this paper is new. neither the entire paper nor any part of its content has been published or has been accepted elsewhere. it is not being submitted to any other journal.we believe the paper may be of part

10、icular interest to the readers of your journal as it .correspondence should be addressed to * at the following address, phone and fax number, and email address:.thanks very much for your attention to our paper. sincerely yours,*投稿信模版四(case)case 1dear editor,we would like to submit the enclosed manus

11、cript entitled gdnf acutely modulates neuronal excitability and a-type potassium channels in midbrain dopaminergic neurons, which we wish to be considered for publication in nature neuroscience.gdnf has long been thought to be a potent neurotrophic factor for the survival of midbrain dopaminergic ne

12、urons, which are degenerated in parkinsons disease. in this paper, we report an unexpected, acute effect of gdnf on a-type potassium channels, leading to a potentiation of neuronal excitability, in the dopaminergic neurons in culture as well as in adult brain slices. further, we show that gdnf regul

13、ates the k+ channels through a mechanism that involves activation of map kinase. thus, this study has revealed, for the first time, an acute modulation of ion channels by gdnf. our findings challenge the classic view of gdnf as a long-term survival factor for midbrain dopaminergic neurons, and sugge

14、st that the normal function of gdnf is to regulate neuronal excitability, and consequently dopamine release. these results may also have implications in the treatment of parkinsons disease. due to a direct competition and conflict of interest, we request that drs. xxx of harvard univ., and yy of yal

15、e univ. not be considered as reviewers. with thanks for your consideration, i am sincerely yours,case2dear editor,we would like to submit the enclosed manuscript entitled ca2+-binding protein frequenin mediates gdnf-induced potentiation of ca2+ channels and transmitter release, which we wish to be c

16、onsidered for publication in neuron. we believe that two aspects of this manuscript will make it interesting to general readers of neuron. first, we report that gdnf has a long-term regulatory effect on neurotransmitter release at the neuromuscular synapses. this provides the first physiological evi

17、dence for a role of this new family of neurotrophic factors in functional synaptic transmission. second, we show that the gdnf effect is mediated by enhancing the expression of the ca2+-binding protein frequenin. further, gdnf and frequenin facilitate synaptic transmission by enhancing ca2+ channel

18、activity, leading to an enhancement of ca2+ influx. thus, this study has identified, for the first time, a molecular target that mediates the long-term, synaptic action of a neurotrophic factor. our findings may also have general implications in the cell biology of neurotransmitter release.sincerely

19、 yours,case 3sample cover letterthe example used is the ijeb dear editor of the please type in journal title or acronym: enclosed is a paper, entitled mobile agents for network management. please accept it as a candidate for publication in the journal title. below are our responses to your submissio

20、n requirements. 1. title and the central theme of the article. paper title: mobile agents for network management. this study reviews the concepts of mobile agents and distributed network management system. it proposes a mobile agent-based implementation framework and creates a prototype system to de

21、monstrate the superior performance of a mobile agent-based network over the conventional client-server architecture in a large network environment.2. which subject/theme of the journal the material fits new enabling technologies (if no matching subject/theme, enter subject highly related to subject

22、of journal but not listed by please type in journal title or acronym) 3. why the material is important in its field and why the material should be published in please type in journal title or acronym? the necessity of having an effective computer network is rapidly growing alongside the implementati

23、on of information technology. finding an appropriate network management system has become increasingly important todays distributed environment. however, the conventional centralized architecture, which routinely requests the status information of local units by the central server, is not sufficient

24、 to manage the growing requests. recently, a new framework that uses mobile agent technology to assist the distributed management has emerged. the mobile agent reduces network traffic, distributes management tasks, and improves operational performance. given todays bandwidth demand over the internet

25、, it is important for the journal title/acronym readers to understand this technology and its benefits. this study gives a real-life example of how to use mobile agents for distributed network management. it is the first in the literature that reports the analysis of network performance based on an

26、operational prototype of mobile agent-based distributed network. we strongly believe the contribution of this study warrants its publication in the journal title/acronym.4. names, addresses, and email addresses of four expert referees. prof. dr. william gates chair professor of information technolog

27、y 321 johnson hall premier university lancaster, ny 00012-6666, usaphone: +1-888-888-8888 - fax: +1-888-888-8886 e-mail: expertise: published a related paper (tcp/ip and osi: four strategies for interconnection) in cacm, 38(3), pp. 188-198.relationship: i met dr. gate only once at

28、 a conference in 1999. i didnt know him personally.assoc prof. dr. john adams director of network research center college of business australian university 123, harbor drive sydney, australia 56789 phone: +61-8-8888-8888 - fax: +61-8-8888-8886 e-mail: .auexpertise: published a related pa

29、per (creating mobile agents) in ieee tose, 18(8), pp. 88-98. relationship: none. i have never met dr. adams.assoc prof. dr. chia-ho chen chair of mis department college of management open university888, putong road keelung, taiwan100 phone: +886-2-8888-8888 - fax: +886-2-8888-8886 e-mail: chchenou.e

30、du.twexpertise: published a related paper (network management for e-commerce) in ij electronic business, 1(4), pp. 18-28.relationship: former professor, dissertation chairman.mr. frank young partner, abc consulting 888, seashore highway won kok, kowloon hong kong phone: +852-8888-8888 - fax: +852-88

31、88-8886 e-mail: expertise: mr. young provides consulting services extensively to his clients regarding network management practices. relationship: i have worked with mr. young in several consulting projects in the past three years. finally, this paper is our original unpublished work a

32、nd it has not been submitted to any other journal for reviews. sincerely, johnny smith投稿信模版五dear editor,herewith we are very pleased to submit a manuscript entitled above to you for your kind considereation for publication in xxx(杂志名). we ensure you that this ms has not been submitted elsewhere for

33、consideration of publication.thank you.sincerely yoursxxx投稿信模版六dear dr:enclosed are three copies of a manuscript by rose n dipaola,donna agallo,and tom nroberts titled“hepatitis c virus infection in long-term transfusion patients”it is submitted to be considered for publication as a“original article

34、 in your journalthis paper is?neither the entire paper nor any part of its content has been published or has been accepted elsewhereit is not being submitted to any other journalwe believe the paper may be of particular interest to the readers of your journal because the study it reports stated the

35、hcv infection rate among long-term transfusion patients is higher than that of the general population and of short-term transfusion patients correspondence and phone calls about the paper should be directed to rose ndipaola at the following address,phone and fax number,and e-mail address:rose n dipa

36、ola,md institute of internal medicine cleveland clinic foundation 9500 euclid avecleveland,oh44195,usa tel:1-216-444-5360 fax:1-216-444-9580 e-mail:dipaocesmtp ccf. org thanks very much for your attention to our papersincerely yours,rose ndipaola投稿信模版七(一个老外写的)plos genetics(plos遗传学期刊)i submit the acc

37、ompanying manuscript entitled “gain and loss of multiple genes during the evolution of helicobacter pylori” by h. gressmann et al. for publication in plos genetics.this manuscript presents the global variability within h. pylori in terms of presence or absence of almost all the genes within the two

38、currently available genome sequences. the strains tested are representative of the global genetic diversity within h. pylori and also represent the diverse populations that exist in that organism. global analyses of genomic content are very rare indeed for bacterial species and are new for h. pylori

39、. by including isolates from the most closely related species, h. acinonychis, as an outgroup, it was possible to deduce that most variable genes were probably present in the last common ancestor of h. pylori and have subsequently been lost in individual isolates. in some cases, the same genes were

40、lost in phylogenetically distinct groupings, reflecting convergent evolution. however, the cag pai was acquired later, after subpopulations had formed. these conclusions are important for concepts about changes in gene content within species and for the acquisition of pathogenicity islands.we also perform a head-to-head comparison of population structure indicated by whole genome microarrays versus that indicated by sequences of 7 housekeeping gene fragments. the comparison indicates that microarrays yield distorted population structures and are less s

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