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Application Deadline: Applications accepted all year round Details The deregulation of cell cycle progression is a common feature of cancer formation and progression. Cell/extracellular matrix (ECM) interaction
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methods for single-cell data analysis (tools developed by the team : https://github.com/cantinilab ). Single-cell high-throughput sequencing, extracting huge amounts molecular data from a cell, is creating
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relevant subject. To formally apply for a PhD, you must complete the University's application form using the following link: https://www.sheffield.ac.uk/postgraduate/phd/apply/applying All applicants should
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Investigating the role of Ect2 in pancreatic cancer cell proliferation and motility School of Biosciences PhD Research Project Self Funded Dr Helen Matthews Application Deadline: Applications
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French National Research Institute for Agriculture, Food, and the Environment (INRAE) | Nantes, Pays de la Loire | France | 3 days ago
Europe). You will then develop your own network of collaborations and apply for support within the institute, as well as from national and international sources. Where to apply Website https
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visit: https://recruit.apo.ucla.edu/JPF10738 The University of California is an Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration for employment without
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biophysical phenotypic analysis with fitness analysis and will therefore provide an in-depth characterization of the evolution of cell polarity. This will pave the way towards understanding how the vast
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Advanced Grant (2025 – 2030). We have developed in vivo single-cell CRISPR technologies to screen for dozens of molecular factors in liver macrophages in vivo. We will apply these technologies to unravel
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permanent cell-cycle arrest and release a secretome (https://doi.org/10.1016/j.celrep.2023.113181), which causes paracrine senescence and attracts immune cells to eliminate senescent cells. Despite
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-cell transcriptomics and modern statistical/AI methodology to address this gap using in-house developed cell atlases. We will develop and benchmark approaches that infer copy-number changes and CIN