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關於Ph.D.直招:
這種博士招生信息一般是由導師自己或者秘書刊登,會具體說明獎學金金額及合同年限,會給出具體研究方向、目的及方法,有的甚至直接給出研究計劃。這類博士職位的研究方向比較確定,獎學金金額也比較高,導師對於申請者科研能力及專業匹配性要求很高。
【瑞士】蘇黎世聯邦理工學院(QS排名6)
PhD Position: Lasers and the proton’s magnetic structure
相關專業:物理
項目簡介:
The department of Physics at ETH Zurich offers a 4-year PhD position in the group of Prof. K. Kirch, 「Precision Physics at Low Energy「.Highly accurate measurements of atomic transitions can be used as precise probes of low-energy properties of the nuclei. As the Bohr radius of hydrogen-like atoms decreases with increasing orbiting particle mass, the muonic atoms (hydrogen-like atoms formed by a negative muon and a nucleus) have enhanced sensitivity to nuclear structure effects. The goal of this project is to measure the hyperfine splitting in muonic hydrogen by means of laser spectroscopy to deduce information concerning the proton’s magnetic structure. This experiment at the intersection of particle, atomic and nuclear physics requires developing cutting-edge laser technologies, especially in the thin-disk laser and the mid- infrared laser domains. The thin-disk laser is a workhorse in the high-power industrial laser sector, and mid-infrared laser sources have many applications, including spectroscopy, remote sensing, surgery and numerous other bio-medical applications. In this project, we focus on energy-scaling of these lasers while constraining operation to single-frequency mode, with the potential of transferring this technology to industry.In this project you will participate within a group of about 5 members to the development of a complex laser system, including high-power thin-disk lasers and lasers based on nonlinear optical procesess (optical parameteric oscillators and amplifiers). Using the developed laser system you will measure the hyperfine splitting in muonic hydrogen together within the international CREMA collaboration. Data analysis and extraction of the nuclear information will conclude your PhD.Other important aspects will be the dissemination of the results in peer reviewed articles and at conferences, the co-supervision of undergraduate students and participation in teaching activities at ETH.This project offers a multidisciplinary environment spanning from fundamental research in particle and atomic physics to applied cutting-edge laser technologies. The project will allow development of technical, organisational and educational skills as well as problem solving and data analysis capabilities. The experience gained will be optimal for careers both in academia and in industry.ETH Zurich is one of the world’s leading universities specialising in science and technology. We are renowned for our excellent education, cutting-edge fundamental research and direct transfer of new knowledge into society. Over 30,000 people from more than 120 countries find our university to be a place that promotes independent thinking and an environment that inspires excellence. Located in the heart of Europe, yet forging connections all over the world, we work together to develop solutions for the global challenges of today and tomorrow.Further information about the project can be found on our websites: ( http://edm.ethz.ch/research/laser-spectroscopy-of-muonic-atoms.html ) & ( http://www.psi.ch/en/ltp/hypermu ).
申請截止時間:招滿即止
PhD opening in microfluidics and ex vivo tissue culture
相關專業:生物工程、計算機科學、電子信息工程
項目簡介:
The Bio Engineering Laboratory at the Department Biosystems Science and Engineering is seeking a highly motivated and enthusiastic PhD student with expertise in microtechnological fabrication (cleanroom) and microfluidics, who will want to work in a highly interdisciplinary and international environment in Basel, Switzerland.In the framework of an Innosuisse project, involving academic and industrial research partners, the student will develop a microfluidic platform for the ex-vivo culturing of organotypic tissue slices and for monitoring, in real-time, the effects of anti-cancer drug compounds on the tissue model.Standard analysis methods (fluorescence microscopy, immunofluorescence staining, supernatant sampling and analysis) will be used to analyze and continuously monitor tissue status and viability. The microfluidic devices will be developed and tested in a collaborative effort with an industrial and an academic partner. The work will be performed in close collaboration with engineers and biologists. A state-of-the art microtechnological cleanroom, a broad spectrum of engineering and testing equipment, as well as cell-culture and biological facilities are available in the group and Department.ETH Zurich is one of the world’s leading universities specialising in science and technology. We are renowned for our excellent education, cutting-edge fundamental research and direct transfer of new knowledge into society. Over 30,000 people from more than 120 countries find our university to be a place that promotes independent thinking and an environment that inspires excellence. Located in the heart of Europe, yet forging connections all over the world, we work together to develop solutions for the global challenges of today and tomorrow.The position is planned for 3 - 4 years (PhD).
申請截止時間:招滿即止
申請截止時間:2020-12-31
PhD Position in the field of Hosts, Pathogens and Global Health相關專業:生物工程、生命科學、生物醫學工程、公共衛生與預防醫學The School of Biological Sciences, in partnership with Edinburgh Infectious Diseases, is delighted to open applications to the sixth cohort of students on this Wellcome Trust funded four-year PhD programme.Students will be supported to combine research in a UK and developing country setting, or take interdisciplinary approaches that combine epidemiological, molecular and evolutionary mechanisms. Students will address global health challenges by understanding how infectious agents are spread, cause disease, interact with the immune and other body systems, or evolve to overcome our therapeutic interventions.Description of the programmeYear one: teaching and research rotation projectsIn the first year of the programme students will attend a series of taught sessions and carry out two 15-week research projects in the main themes of study:⒈Molecular biology and immunology⒉Epidemiology, evolutionary biology and ecologyAt the end of the first year, reports from these research projects, plus a mock grant proposal based on their chosen PhD project, will be assessed for the MSc by Research degree awarded by the University of Edinburgh.Years two to four: main research projectDuring the three main years of study, projects shared between Edinburgh-based supervisors and their international collaborators will provide the opportunity for some students to undertake research projects in a disease endemic setting. Projects that link disciplines (for example, evaluating molecular reagents in an epidemiological study), will also be strongly encouraged.倪冉教授課題組致力於通過數值方法(如Monte Carlo,分子動力學模擬)以及理論分析研究軟物質物理。目前的研究方向包括DNA修飾膠體粒子的組裝,活力物質的動態組裝,2D體系中的相變以及仿生體系的組裝,可能的新方向包括流體力學模擬、深度學習在軟物質以及統計物理中的應用,研究方向也可以雙方討論決定。更多信息歡迎訪問課題組網站:https://www.ntu.edu.sg/home/r.ni 。現課題組招一名2021年1月入學的博士生。
陳國樑副教授實驗室有多個研究方向,主要包括以下幾個方面:基於有機熱敏電阻和電晶體的高靈敏度生物傳感器的研究;有機器件的大規模製造技術;基於微電子機械技術(MEMS)的微電極製造;微尺度熱傳導有機傳感器;除上述研究之外,陳教授近年來逐步將研究領域擴展到傳感器及微電極的生物應用領域。目前,我們正在籌建一支神經生物學方向的研究團隊。該團隊主要負責新型微電極的研發及應用測試,神經電生理平臺的搭建。加入我們你能得到什麼:1) 充足的研究經費:陳教授帶領的研究團隊目前擁有RGC/GRF 及香港科創署的多項經費支持,加入我們的團隊完全不用擔心科研經費不足的情況出現;2) 可觀的薪資待遇:由於擁有充足的經費支持,我們可以為符合條件的申請者提供碩士21萬,博士25萬,博後38萬港幣的年薪。解除大家在香港高物價高消費生活的後顧之憂;3) 專業的團隊指導和自由的研究環境:目前我們神經生物方向的小團隊主要有三名成員,一名生物醫學工程方向的博後, 一名碩士研究生和一名本科在讀生。加入我們,在共同進行科學研究的同時,還可以帶你一起玩轉香港的風土人情。
招生類型:香港中文大學,化學系,全日制四年制博士研究生兩-三名課題組研究方向主要包括新型低維無機納米材料的溼化學法合成,以及新型納米材料在催化、新能源轉化等領域的應用。歡迎熱愛科學研究的同學們加入。香港中文大學(The Chinese University of Hong Kong)成立於1963年,是一所亞洲頂尖、享譽國際的公立研究型綜合大學,也是香港第一所研究型大學。在qs 2021年世界大學排名榜中,位居全球第43位,在路透社亞太區最具創新力大學排名中連續多年排在全港首位。中大校園俯瞰吐露港,是全港校園中佔地最大的,最綠意盎然的校園。相關專業:計算機工程、計算機科學、電子信息工程、地理科學學院介紹:https://www.polyu.edu.hk/aae/ 。申請要求:有大地測量、導航定位、電子信息或計算機相關背景,有工程開發和編程經驗,有論文發表經驗。雅思6.5,或者託福80。申請截止時間:招滿即止
PhD Position: Analysis of pathogen determinants recognized by the hypervariable immune receptor DscamBackground: To mount an immune response, host organisms must first recognize the pathogen with which they are infected. The first line of defense against pathogen infection in animals is provided through the innate immune response. Many aspects of this response are conserved in invertebrates making the fruitfly Drosophila with its sophisticated genetic tools a model of choice. The fundamental knowledge obtained about the innate immune response in fruitflies has even been recognized by a Nobel prize. Recently, the Drosophila Down syndrome cell adhesion molecule (Dscam) gene has been shown to act as pattern recognition receptor in phagocytosis, in addition to its role in neuronal wiring [1, 2]. The Dscam gene generates through alternative splicing over 36』000 different isoforms by inclusion of a single exon in each of the variable regions (Fig 1). Intriguingly, the splicing pattern of Dscam changes upon infection to express isoforms with a higher affinity towards the pathogen in mosquitoes [3]. We anticipate that Dscam splicing is also altered in Drosophila upon pathogen exposure to dramatically increase inclusion of specific isoforms. We currently don’t know the identity of the pathogen molecules recognized by Dscam, or how pathogens impact on adapting Dscam alternative splicing for pathogen recognition and if the same mechanism is also used in the human innate immune response. Objectives: 1) Identify pathogens and conditions that induce preferential inclusion of single variable exons in Drosophila Dscam 2) Determine pathogen components that are recognized by Dscam and impact on its alternative splicing 3) Determine the mechanism(s) through which pathogens impact on alternative splicing regulation Project description: From a wide array of pathogens available from the Institute of Microbiology and Infection at the University of Birmingham we will first identify those that induce inclusion of a narrow range of exons in the three variable regions as they are indicative of high affinity interactions. For this analysis we developed highly efficient Molecular Biology tools, including high throughput sequencing for efficient analysis [4]. Once we have obtained a broader choice of pathogens we will identify the bacterial molecules impacting on Dscam alternative splicing and determine if they bind to Dscam using genetic, molecular and biochemical approaches. Alternative splicing is thought to provide a major mechanism for adaptation of cell function to changing environments, e.g. during infection. The Dscam splicing pattern is initially established in a predefined ratios, but probabilistically at a cellular level [4, 5]. We will establish a GFP-based Dscam alternative splicing reporter to identify the pathways, how pathogens lead to adaptive changes in alternative splicing during an innate immune response. For more information about research in our laboratory, please visit: http://www.biosciences-labs.bham.ac.uk/soller/ http://www.birmingham.ac.uk/staff/profiles/biosciences/soller-matthias.aspx【英國】利茲大學(QS排名91)
Cell polarity is a fundamental cellular property that determines the form and function of the organs and tissues in our bodies. While it is well-studied in single cells, a major frontier in cell and developmental biology is in understand how cell polarity can be established and coordinated between cells in a tissue. Planar polarity is an example of such coordination, whereby cells in a sheet all acquire the same orientation. The core and Fat-Dachsous pathways that control planar polarity have been studied extensively in the Strutt lab using the model organism Drosophila melanogaster. This work has given insights into the bulk protein behaviours, however single molecule dynamics have not been possible to measure due to technological limitations. In collaboration with the Cadby lab, this project will use quantitative approaches to fluorescence microscopy in vivo: fluorescence correlation spectroscopy (fcs) and single particle tracking (spt) to determine single protein dynamics using the Drosophila pupal wing model of planar polarity establishment. This project aligns with current super-resolution microscopy and molecular genetics projects within the lab. Key words: Cell biology, developmental biology, biophysics, Drosophila, super resolution microscopy, single particle tracking
申請截止時間:2021/1/10
3 year PhD Studentship in Enabling Next Generation Additive ManufacturingTitle: Additive Manufacturing (3D Printing) of multi-functional scaffold and tissue models through multi-material projection micro stereolithography (pµSLA)Project description: The successful applicant will participate in a fully funded programme to look into the production of high accuracy multi-functionalized scaffold and tissue models mimicking actual body parts. The ability to fabricate and customise these models not only helps increasing the accuracy of in vitro assessment, reducing the need of in vivo test (i.e. organ on a chip, organoids), but also opens the vista of real organ printing.Projection Micro stereolithography (puSLA) is a high resolution (~2µm) Additive Manufacturing (AM) technique that has been commercialised in recent years. It enables the user to create centimeter-scale devices with extreme feature resolution approaching those of single mammalian cells. Although not currently commercialized, the puSLA process also has the capability to integrate multiple materials through a customised fluidic cell unit. The successful applicant will work on a project including the development and optimization of a highly efficient multi-material printing unit for puSLA. Based on the new unit, high accuracy mutli-material devices will be produced for in vitro assessment to investigate their unique mechanical performance and cell response brought by micron scale 3D printing.The person appointed will work as part of a dynamic interdisciplinary team focussed on developing cutting edge polymer technologies as part of the CfAM. The CfAM is a large interdisciplinary group active in the area of Additive Manufacturing and 3D Printing. Comprising of around 100 academics, post-doctoral researchers and PhD students, it is one of the largest research centres for additive manufacturing and 3D printing worldwide. The Centre engages with a broad range of academics from across the UK and a significant number of industrial partners to deliver on an industrially prioritised research agenda – this particular project is part of a large, collaborative EPSRC Programme Grant looking at Next Generation Additive Manufacturing (EP/P031684/1).申請截止時間:2021/1/31
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註:為了提供更加專業化和細分的留學信息,我們開通了歐洲各國家的留學公眾號,歡迎大家及時關注,我們將會在各國家留學公眾號上發布該國留學的具體信息。各國家留學公眾號如下:
歐洲留學公眾號:Study-in-EU
歐洲獎學金公眾號:EU-Grant
荷蘭留學公眾號:Study-in-Holland
比利時留學公眾號:Study-in-Belgium
德國留學公眾號:Edu-in-Germany
法國留學公眾號:Edu-in-France
瑞士留學公眾號:StudyInSwitzerland
北歐留學公眾號:Study-in-NorthEurope
義大利留學公眾號:Edu-in-Italy
西班牙留學公眾號:Study-in-Spain
英國留學公眾號:Edu-in-UK
捷克留學 波蘭留學與匈牙利留學:Study-in-MidEurope
香港與新加坡留學公眾號:Edu-in-HK
日本與韓國留學公眾號:Study-in-EastAsia
北美留學公眾號:NorthAmerica-Adviser
澳洲留學公眾號:Edu-in-Australia
我們的微博帳號:留歐之星 我們的抖音帳號:留歐之星我們的官網:www.study-in-europe.net我們的知乎帳號:留歐之星,留歐之星-荷蘭留學,留歐之星-瑞士留學,留歐之星-北歐留學,留歐之星-德國留學,留歐之星-比利時留學,留歐之星-法國留學,留歐之星-義大利留學,留歐之星-西班牙留學