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共检索到113条 ,权限内显示50条;
Data from: Selective clearance of the inner nuclear membrane protein emerin by vesicular transport during ER stress
- 负责人：
- DOI：
- doi:10.5061/dryad.n0r525h
- 摘要：
- proteins of the INM and ER are degraded through shared or distinct pathways in mammalian cells. We applied dynamic proteomics to profile protein half-live
Data from: Protein degradation rate in Arabidopsis thaliana leaf growth and development
- 负责人：
- DOI：
- doi:10.5061/dryad.q3h85
- 摘要：
- . From this information, we have calculated the protein turnover energy costs in different leaves and their key determinants within the proteome.
Data from: Long-lived metabolic enzymes in the crystalline lens identified by pulse-labeling of mice and mass spectrometry
- 负责人：
- DOI：
- doi:10.5061/dryad.r6h8dr2
- 摘要：
- is unclear. We sought to measure the global protein turnover rates in the eye using dietary nitrogen-15 (15N)-labeling of mice between 3 and 15 weeks of age
Data from: Isotopic turnover rates and diet-tissue discrimination depend on feeding habits of freshwater snails
- 负责人：
- DOI：
- doi:10.5061/dryad.tt84b23
- 摘要：
- y be influenced by diet quality, growth, and other factors. We measured the effect of dietary protein content on diet-tissue discrimination and tissue turnover
Data from: A proteomic strategy for global analysis of plant protein complexes
- 负责人：
- DOI：
- doi:10.5061/dryad.3r8p4
- 摘要：
- Global analyses of protein complex assembly, composition, and location are needed to fully understand how cells coordinate diverse metabolic
Data from: Separating golgi proteins from cis to trans reveals underlying properties of cisternal localization
- 负责人：
- DOI：
- doi:10.5061/dryad.89s4n70
- 摘要：
- differences in surface charge of intact cisternae to perform separation of early to late Golgi sub-compartments. We determine protein and glycan abundance
Data from: Tracking transcription factor mobility and interaction in Arabidopsis roots with fluorescence correlation spectroscopy
- 负责人：
- DOI：
- doi:10.5061/dryad.50410
- 摘要：
- To understand complex regulatory processes in multicellular organisms, it is critical to be able to quantitatively analyze protein move
Data from: A proteomic method to extract, concentrate, digest, and enrich peptides from fossils with colored (humic) substances for mass spectro
- 负责人：
- DOI：
- doi:10.5061/dryad.3tv1523
- 摘要：
- to separate from proteins in solution, and interfere with analyses of fossil proteomes. We introduce a method combining multiple recent advances in extraction
Data from: Quantitative proteomic analysis reveals posttranslational responses to aneuploidy in yeast
- 负责人：
- DOI：
- doi:10.5061/dryad.65364
- 摘要：
- strains. We show that although protein levels largely scale with gene copy number, subunits of multi-protein complexes are notable exceptions. Posttranslational
Data from: Regulation of HBEGF by micro-RNA for survival of developing human trophoblast cells
- 负责人：
- DOI：
- doi:10.5061/dryad.gf1bq
- 摘要：
- by western blotting. Results: Protein turnover studies, using 10 ?g/ml cyclohexamide, 1 ?g/ml lactocystin, or 100 ?g/ml MG132, demonstrated faster HBEGF degradation
