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A novel role for the 3\u2032-5\u2032 exoribonuclease Dis3L2 in controlling cell proliferation and tissue growth
负责人:
关键词:
Biochemistry Cell Biology Genetics Molecular Biology 69999 Biological Sciences not elsewhere classified Developmental Biology
DOI:
doi:10.6084/m9.figshare.3830103
摘要:
ssive cell proliferation can lead to diseases such as cancer. We have shown that the exoribonuclease Dis3L2 is required for the correct regulation of prolifer
Phylogenetic analysis and virulence determinant of the host-adapted Staphylococcus aureus<\/i> lineage ST188 in China
负责人:
关键词:
Ecology Microbiology 59999 Environmental Sciences not elsewhere classified 69999 Biological Sciences not elsewhere classified Cancer 110309 Infectious Diseases Plant Biology 60506 Virology
DOI:
doi:10.6084/m9.figshare.7937831
摘要:
demonstrated that ST188 might evolve from livestock, and there was no significant genomic or virulence difference between ST188 isolated from livestock
Data from: Fadraciclib (CYC065), a novel CDK inhibitor, targets key pro-survival and oncogenic pathways in cancer
负责人:
关键词:
DOI:
doi:10.5061/dryad.44j0zpc9v
摘要:
preclinical pharmacology data support its therapeutic potential in CDK9- or CDK2-dependent cancers and as a rational combination with BCL2 inhibi
Data from: Identification of biomarkers for Barcelona Clinic Liver Cancer staging and overall survival of patients with hepatocellular carcinoma
负责人:
关键词:
homo species;Hepatocellular carcinoma;Holocene
DOI:
doi:10.5061/dryad.10m4k6q
摘要:
. Significantly enriched gene ontology biological process terms included RNA processing, non-coding RNA processing and phosphodiester bond hydrolysis
Data from: Synthesis of gypsogenin derivatives with capabilities to arrest cell cycle and induce apoptosis in human cancer cells
负责人:
关键词:
Gypsogenin derivatives;Cell cycle arrest;Cytotoxic activity;apoptosis
DOI:
doi:10.5061/dryad.35j3j
摘要:
e found to be much lower than those of the other derivatives and parent compound. These compounds were submitted to an extensive biological testing and proved
Sparks Et Al, Heterogeneity In Tumor Chromatin-Doxorubicin Binding Revealed By In Vivo Fluorescence Lifetime Imaging Confocal Endomicroscopy: In Vivo
负责人:
关键词:
Sparks et al, Heterogeneity in tumor chromatin-doxorubicin binding revealed by in vivo fluorescence lifetime imaging confocal endomicroscopy
DOI:
doi:10.5281/zenodo.1249022
摘要:
then peritoneal tumors were exposed by minor surgery and inspected with the CEM.All animal model procedures were approved by The Francis Crick Institute Biological
Data from:A computational study of cancer hyperthermia based on vascular magnetic nanoconstructs
负责人:
关键词:
embedded multiscale method;cancer hyperthermia;nanotechnology;finite element simulations;heat and mass transfer
DOI:
doi:10.5061/dryad.20c5c
摘要:
and heat transport in biological tissues. The model is defined at the scale of the tumour microenvironment and an advanced computational scheme called the embedded
Data from: Aneuploidy causes non-genetic individuality
负责人:
关键词:
Down Syndrome;Mus musculus;aneuploidy;gene dosage effects;Cancer;cell-to-cell variability;biological noise;Saccharomyces cerevisiae;non-genetic heterogeneity
DOI:
doi:10.5061/dryad.30mv0
摘要:
gene copy number imbalances, suggesting that subtle changes in gene expression impact the robustness of biological networks and cause alternate behaviors
Additional file 1: Table S1. of Loss of maternal ANNEXIN A10 via a 34-kb deleted-type copy number variation is associated with embryonic mortality
负责人:
关键词:
Cancer Space Science Medicine Genetics Evolutionary Biology 69999 Biological Sciences not elsewhere classified 19999 Mathematical Sciences not elsewhere classified Plant Biology Computational Biology
DOI:
doi:10.6084/m9.figshare.c.3627914_d6.v1
摘要:
by cows that received a second round of AI at 18\u201329 days (D), 30\u201360 D, 61\u201390 D, 91\u2013140 D, and 141 D\u2013parturition after the 1st AI
Data from: Identifying metabolic subpopulations from population level mass spectrometry
负责人:
关键词:
DOI:
doi:10.5061/dryad.gf80t
摘要:
can lead to disease and aging. In addition, metabolic heterogeneity can have biological consequences, such as differences in outcomes and drug

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