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Stanford Cancer Center Pediatrics Postdoc Appointment Term: Two years Appointment Start Date: 1/1/2026 Group or Departmental Website: http://www.sheltzerlab.org (link is external) How to Submit Application
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disease. They are also conducting advanced CRISPR screens to interrogate the complex genetic basis of these disorders. The lab has been supported by the ERC for the past 15 years. Now we are seeking a
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Website: https://med.stanford.edu/stankovic-lab.html (link is external) https://hellerlab-stanford.net/ (link is external) How to Submit Application Materials: Please send the following materials in a
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, or Pharmacology; - Demonstrated record of scientific achievements (publications and patents). Desired Qualifications: - Experience with gene editing (CRISPR), cellular and biochemical assays, cloning, expression
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genetics, transgenics/CRISPR approaches, neurophysiology, comparative/evolutionary biology. About the School/Department/Institute/Project Queen Mary University of London is a research-intense university and
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genetics, transgenics/CRISPR approaches, neurophysiology, comparative/evolutionary biology. About the School/Department/Institute/Project Queen Mary University of London is a research-intense university and
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to conduct functional genomics analysis in insects. The successful candidate will conduct RNAi or CRISPR/Cas9 experiments in a lepidopteran species to investigate detoxification functions. The candidate may
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models. In addition, it will use Crispr-Cas9 approach to knockdown important transcription factors, such as Snail and Twist, in triple-negative breast cancer cell lines to examine the functional role and
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progression and therapy resistance. This position will leverage cutting-edge approaches including spatial transcriptomics, CRISPR-based functional genomic screening, and patient-derived xenograft (PDX) models
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funds. Continued employment is contingent on the renewal of funding. Essential Functions Assists in designing CRISPRs targeting genes associated with neurological disorders, generates CRISPR-Cas9 mutants