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analysis of multiple disease-specific datasets and contribute to the development of novel methodologies in this space. The ideal applicant will have a strong background in bioinformatics methods and a keen
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translate extracellular cues sensed by GPCRs into specific phenotypic outputs. Developing quantitative proteomics approaches to capture the spatiotemporal organization of signaling networks and combining
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features. Using our recently developed chromosome engineering approach, we have created isogenic stem cell lines that allow us to precisely isolate the effects of the chromosomal abnormality from other
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chromosome 8p that results in neurodevelopmental delays, epilepsy, and other clinical features. Using our recently developed chromosome engineering approach, we have created isogenic stem cell lines that allow
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resilience. Additionally, SURI has established a network of stakeholders, including private firms, city governments, and international development institutions. The Postdoctoral Scholar will help extend
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in human biology and evolution, our work seeks to uncover the molecular logic underlying human-specific neuronal differentiation and synaptic connectivity and to translate these insights
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using in vivo Perturb-seq. This project is related to a new NIH-funded Program Project Grant aimed at identifying differences and similarities in gene function across vascular cell types and diseases, as
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: Investigating the biological mechanisms governing urothelial exfoliation and regeneration. Optimizing stem cell engraftment after urothelial exfoliation Developing diagnostic and therapeutic tools to improve
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physiological roles do these channels play in the eye? 3) Do these ion channels mediate the development of glaucoma and other ocular diseases? The successful applicant will lead a project investigating the role
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state-of-the art micro-fluidic platforms developed at Stanford by the Fordyce lab. Individuals should have experience with molecular cloning, next generation sequencing, experience with enzyme kinetic