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Postdoctoral Scholar in Structural Biology & Translational Medicine Are you a structural biologist looking to bridge the gap between fundamental discovery and real-world therapeutic applications
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Postdoctoral Positions for Computational Genomics, Cancer Genetics, and Translational Cancer Biology
mechanism-driven AI and agentic AI frameworks (iGenSig-AI, G2K) that integrate biological knowledge with cutting-edge machine learning to transform omics data into actionable therapeutic insights
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Postdoctoral position to study Polo kinase and centrosome abnormalities in cancer and other diseases
or HIV accessory proteins, is tightly linked to the development of aneuploidy and cancer. During the past several years, we have been taking cell biological, biochemical, biophysical, and structural
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-resolution imaging and spectroscopy of nanoparticles using advanced broad- and focused-beam transmission electron microscopy (TEM) techniques. 2. Structure–Catalysis Relationships at the Atomic Scale You will
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mechanisms in LC-MS/MS. The project addresses fundamental limitations in current proteomics workflows, which rely almost exclusively on positive ion mode and therefore systematically underrepresent acidic
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-resolved fluorescence methods for studying protein-protein interactions and protein structure-function relationships in live cells. This project will focus on elucidating the structure-function mechanisms
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as possible. Job description The project aims at determining in situ structures of axo-axonic synapses at the axon initial segment (AIS) of neurons through cryo-electron tomography (cryo-ET), and
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the mechanism of co-transcriptional splicing. The project aims to understand the mechanism of crosstalk between the transcription and splicing machineries using a combined biochemical and structural approach with
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knowledge of the mechanical behavior and microstructure of metals and their deformation mechanisms at high temperature Comprehensive knowledge and practical experience in mechanical testing
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Crosstalk: Which molecular mediators or physiological cues from the lymphatic microvasculature influence immune and structural cell behavior? (focus on epithelial, myeloid and stromal interactions) Immune and