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Data from: Heme pathway evolution in kinetoplastid protists
负责人:
关键词:
heme;Prokinetoplastina;endosymbiosis;Kinetoplastea;Evolution;lateral gene transfer;Perkinsela;Paramoeba pemaquidensis
DOI:
doi:10.5061/dryad.664cp
摘要:
ng the evolutionary history of the group. Interestingly, in both parasitic and free-living kinetoplastids, the heme pathway—a core metabolic pathway in a wide range
Data from: Identification of glucose kinase dependent and independent pathways for carbon control of primary metabolism, development
负责人:
关键词:
secondary metabolites;Streptomyces coelicolor;carbon catabolite repression;quantitative proteomics;glucose kinase
DOI:
doi:10.5061/dryad.62j0q
摘要:
. Carbon catabolite repression (CCR), a main signaling pathway underlying this phenomenon, was so far considered fully dependent on the glycolytic enzyme glucose kinase (Glk). Her
Data from: High throughput functional genomics identifies modulators of TCE metabolite genotoxicity and candidate susceptibility genes
负责人:
关键词:
trichloroethylene;toxicogenomics;DNA damage and repair mechanisms;susceptibility genes;high-throughput testing;Saccharomyces cerevisiae
DOI:
doi:10.5061/dryad.p8k18
摘要:
by reactive metabolites in humans. Our approach illustrates the potential for high-throughput in vitro functional profiling in yeast to elucidate toxicity path
Data from: Deconstruction of archaeal genome depict strategic consensus in core pathways coding sequence assembly
负责人:
关键词:
metabolic pathway;codon context;Archaea;codon usage
DOI:
doi:10.5061/dryad.sv70f
摘要:
was performed. These organisms differed in their physiological attributes, particularly oxygen tolerance and energy metabolism. We explored the diversity
Data from: From the cover: three-dimensional (3d) heparg spheroid model with physiologically relevant xenobiotic metabolism competence and hepat
负责人:
关键词:
DOI:
doi:10.5061/dryad.s05v3
摘要:
ng differentiated HepaRG cells that achieve and maintain physiologically relevant levels of xenobiotic metabolism (CYP1A2, CYP2B6, and CYP3A4/5). This invitro model
Data from: Oncogene inference optimization using constraint-based modelling incorporated with protein expression in normal and tumour tissues
负责人:
关键词:
differential evolution;Flux balance analysis;multiple-level optimization;Cancer cell metabolism
DOI:
doi:10.5061/dryad.364vk23
摘要:
modi cations of cancer cells result in the abnormal regulation of cellular metabolic pathways that are different when compared to normal cells. Suc
Data from: The complete genome sequence of the thermophilic bacterium Laceyella sacchari FBKL4.010 reveals the basis for tetramet
负责人:
关键词:
Laceyella sacchari;antiSMASH analysis;Microbiology;Complete genome;Moutai-flavor Daqu;Tetramethylpyrazine;Liquor-making
DOI:
doi:10.5061/dryad.82gn3m6
摘要:
hylpyrazine metabolic pathway. Metabolic pathways relevant to tetramethylpyrazine synthesis were also reconstructed based on the Kyoto Encyclopedia of Genes and Genomes (KEGG
Data from: Developmental plasticity in metabolism but not in energy reserve accumulation in a seasonally polyphenic butterfly
负责人:
关键词:
Allometry;Pieris napi;direct development;diapause;Metabolic Rate;fat reserve;Holocene;polyphenism
DOI:
doi:10.5061/dryad.1f8m3q1
摘要:
use. The metabolic divergence appeared only in the final instar, that is, after the induction of developmental pathway that takes place in the penultimate insta
Data from: Rewiring of embryonic glucose metabolism via suppression of pfk-1/aldolase during mouse chorioallantoic branching
负责人:
关键词:
Lin28a;mouse;development;imaging mass spectrometry;chorioallantoic branching;energy metabolism
DOI:
doi:10.5061/dryad.fj0qj
摘要:
Adapting the energy metabolism state to changing bioenergetic demands is essential for mammalian development accompanying massive cell proli
Data from: Plastic transcriptomes stabilize immunity to pathogen diversity: the jasmonic acid and salicylic acid networks within the Arabidopsis
负责人:
关键词:
Plant-pathogen interaction;Arabidopsis thaliana;Botrytis cinerea;transcriptome;network;Innate immunity;Jasmonate signaling;Salicylic acid signaling
DOI:
doi:10.5061/dryad.7gd5q
摘要:
t plants utilize major defense hormone pathways to buffer disease resistance, but not the metabolic or transcriptional responses to genetic

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