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Data from: High-resolution chemical dissection of a model eukaryote reveals targets, pathways and gene functions
- 负责人:
- DOI:
- doi:10.5061/dryad.v5m8v
- 摘要:
- to small molecules. Using an optimized platform, we provide the relative sensitivities of the heterozygous and homozygous deletion collections for nearly 1800
Development of targeted therapies for peroxisome biogenesis disorders
- 负责人:
- 关键词:
- Molecular Biology peroxisome biogenesis disorders peroxins PEX1 high-content screening small molecules induced pluripotent stem cells HepG2 cells Pex1-p.G844D mouse
- DOI:
- doi:10.25549/usctheses-c40-298640
- 摘要:
- available. ? In this dissertation, I described the identification and characterization of small molecules that enhance peroxisome assembly and functi
Genetic and chemical characterization of two highly-reducing polyketide synthase clusters from Aspergillus species
- 负责人:
- 关键词:
- Pharmaceutical Sciences natural products biosynthesis Aspergillus citreoviridin aspernidgulenes
- DOI:
- doi:10.25549/usctheses-c40-499283
- 摘要:
- l secondary metabolites. The first goal is important because understanding the biosynthesis of complex organic molecules can inspire biomimetic synthesis strategies. Furt
Data from: Genome mining reveals the genus Xanthomonas to be a promising reservoir for new bioactive non-ribosomally synthesized peptides
- 负责人:
- 关键词:
- DOI:
- doi:10.5061/dryad.gh7h8
- 摘要:
- Background: Various bacteria can use non-ribosomal peptide synthesis (NRPS) to produce peptides or other small molecules. Conserved features
Data from: Random sequences are an abundant source of bioactive RNAs or peptides
- 负责人:
- DOI:
- doi:10.5061/dryad.6f356
- 摘要:
- t random sequences may become an effective new source of molecules for studying cellular functions, as well as for pharmacological activity screening.
Data from: Proteolytic processing of palmitoylated Hedgehog peptides specifies the 3-4 intervein region of the Drosophila wing
- 负责人:
- DOI:
- doi:10.5061/dryad.6b058n7
- 摘要:
- on. Hence, palmitoylated membrane anchors restrict morphogen spread until site-specific processing switches membrane-bound Hh into bioactive forms
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