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Do you have a passion for genetics and a drive to uncover the genetic underpinnings of complex traits and diseases? We are seeking a curious and motivated postdoctoral researcher in statistical
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qualified applicant to receive consideration for employment without regard to race, color, religion, sex, gender identity or expression, national origin, sexual orientation, genetic information, disability
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of lncRNAs with various proteins, lipids and microRNAs etc. Research platforms in the laboratory include human embryonic stem (ES) cells, patient-derived induced pluripotent stem (iPS) cells, mouse genetic
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interested in the dynamics of beta-cell heterogeneity, islet organization and cell-cell interaction in fetal and neonatal development. The Dhawan lab utilizes genetic mouse models, molecular biology, imaging
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Borrelia burgdorferi using genetics, genomics, microbiology, and biochemistry. The successful candidate will join the Lemieux and Steere laboratories to explore novel aspects of Borrelia burgdorferi
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, religion, sex, gender identity or expression, national origin, sexual orientation, genetic information, disability, age, ancestry, military service, protected veteran status, or other characteristics
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genetic screen (e.g., metabolic pathway, mitochondria structure) 2) Understanding the role of innate immunity during leukemogenesis as well as disease relapse in order to design novel inhibitors
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interspecies chemical signalling bacteria/fungus-virus interactions in the soil soil microbiology microbial community modelling and plant genetics in the context of microbial interactions. This position will
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Nature Careers | Northern British Columbia Fort Nelson, British Columbia | Canada | about 2 months ago
Medical Genetics, Faculty of Medicine Faculty of Medicine University of British Columbia Successful candidates will join the laboratory of Dr. Bruce Carleton and the multi-centre research team
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research institute in the United States. The VBRI is a leader in the field of thrombosis, hemostasis, benign/malignant hematology and genetic disorders like Sickle Cell Disease, VWF disease and hemophilia