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Postdoctoral Researcher RNA Biology and Therapeutics in Kidney Disease
Job Description & How to Apply Below
Location:
Stony Brook, New York, United States Institution:
Department of Medicine, Stony Brook University.
The Aboudehen Laboratory at Stony Brook University (SBU) is seeking a highly motivated Postdoctoral Research Fellow to investigate RNA regulatory mechanisms and develop RNA-based therapeutic strategies for autosomal dominant polycystic kidney disease (ADPKD). ADPKD is dosage-sensitive disease and is caused primarily by mutations in PKD1, in which reductions in functional PKD1 below a critical threshold causes renal cysts. Our research program has two complementary themes:
- Long noncoding RNA (lncRNA) in ADPKD: determining how disease-associated lncRNAs regulate cystogenesis and identifying the pathways through which they modify disease.
- PKD1 mRNA biology: defining how RNA-binding proteins, RNA-RNA interactions, and other post-transcriptional mechanisms regulate PKD1 mRNA and protein expression.
- Investigate lncRNAs using mouse genetics, cell models, and RNA interaction assays.
- Studying RNA-binding proteins and regulatory RNAs that control PKD1 expression, including mapping interactions and binding sites using eCLIP/CLIP-based approaches.
- Validation of therapeutic targets in genetically engineered mouse models of PKD and primary ADPKD cells.
- Development of RNA-targeted therapeutic approaches, including antisense oligonucleotide.
- Applicants should have a PhD or equivalent degree in RNA biology, molecular biology, cell biology, genetics, biochemistry, biomedical sciences, or a related discipline.
- Candidates should have strong molecular and cellular biology skills, a demonstrated ability to conduct independent research, and a strong interest in RNA regulation and disease mechanisms.
Preference will be given to candidates with strong hands-on experience in RNA biology and RNA-based assays, particularly:
- eCLIP, iCLIP, CLIP-seq, or related RNA-protein interaction and binding-site mapping approaches.
- RNA-targeting technologies, including siRNA, antisense oligonucleotides.
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