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Mostrando 621 - 640 Resultados de 1,026 Para Buscar '"Saga"', tiempo de consulta: 0.21s Limitar resultados
  1. 621
    “…Tra1 is a component of the Saccharomyces cerevisiae SAGA and NuA4 complexes and a member of the PIKK family, which contain a C-terminal phosphatidylinositol 3-kinase-like (PI3K) domain followed by a 35-residue FATC domain. …”
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    Mutational analysis of the C-terminal FATC domain of Saccharomyces cerevisiae Tra1
  2. 622
    “…From this process, two highly specific IgG1(κ) MAbs were obtained, one against the polysaccharide (DHG.01) and one against the protein (SagA.01). Both MAbs exhibited good opsonic killing against the target bacterial strains: DHG.01 showed 90% killing against E. faecalis type 2, and SagA.01 showed 40% killing against E. faecium 11231/6. …”
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    Development of Opsonic Mouse Monoclonal Antibodies against Multidrug-Resistant Enterococci
  3. 623
    “…We find that the mutant’s phenotypes are due to disruption of a gene, which we call StArch Granules Abnormal 1 (SAGA1) because starch sheath granules, or plates, in mutants lacking SAGA1 are more elongated and thinner than those of wild type. …”
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    A Rubisco-binding protein is required for normal pyrenoid number and starch sheath morphology in Chlamydomonas reinhardtii
  4. 624
    “…Nonstop is a component of the Spt-Ada-Gcn5-acetyltransferase (SAGA) transcriptional coactivator complex, but SAGA’s histone acetyltransferase module, which does not bind to expanded or merlin, is dispensable for migration. …”
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    Drosophila USP22/nonstop polarizes the actin cytoskeleton during collective border cell migration
  5. 625
    “…Suppression of TBP dynamics via removal of the Mot1 ATPase partially restores normal transcriptional activity to Med16-depleted cells, suggesting that cMed/tail separation results in an imbalance in the levels of PIC formation at SAGA-requiring and TFIID-dependent genes. We propose that the preferential regulation of SAGA-requiring genes by tailed Mediator helps maintain a proper balance of transcription between these genes and those more dependent on TFIID.…”
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    Connection of core and tail Mediator modules restrains transcription from TFIID-dependent promoters
  6. 626
    “…Fifteen years of undergraduate medical education curriculum reform at Saga Medical School was evaluated by measuring medical students’ communication and interpersonal skills with a patient satisfaction questionnaire developed by the American Board of Internal Medicine. …”
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    Improvement in medical students’ communication and interpersonal skills as evaluated by patient satisfaction questionnaire after curriculum reform
  7. 627
    “…The transcriptional coactivators Mediator and two histone acetyltransferase (HAT) complexes, NuA4 and SAGA, play global roles in transcriptional activation. …”
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    Distinct patterns of histone acetyltransferase and Mediator deployment at yeast protein-coding genes
  8. 628
    “…The epigenetic modulatory SAGA complex is involved in various developmental and stress responsive pathways in plants. …”
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    Diversification of the Histone Acetyltransferase GCN5 through Alternative Splicing in Brachypodium distachyon
  9. 629
    “…METHODS: We evaluated the feasibility and effectiveness of SAGA in a hybrid phase 1/2, randomized controlled trial. …”
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    Improving sensitivity to eye gaze cues in adolescents on the autism spectrum using serious game technology: A randomized controlled trial
  10. 630
    por Romero Curtis, Maribel
    Publicado 2004
    Libro
    Los niños índigo /
  11. 631
    por Frey, Avery G, Eide, David J
    Publicado 2012
    “…Coactivator recruitment was highly interdependent such that mutations disrupting SAGA impaired recruitment of SWI/SNF and vice versa. …”
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    Zinc-responsive coactivator recruitment by the yeast Zap1 transcription factor
  12. 632
    “…Here, we show that Gad8 physically interacts with proteins that regulate transcription, including subunits of the Spt-Ada-Gcn5-acetyltransferase (SAGA) complex and the BET bromodomain protein Bdf2. …”
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    TOR complex 2 contributes to regulation of gene expression via inhibiting Gcn5 recruitment to subtelomeric and DNA replication stress genes
  13. 633
    “…Here, we report that the SAGA DUB module and TREX-2 distinctly regulate yeast replicative lifespan in a Sir2-dependent and -independent manner, respectively. …”
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    Sus1 maintains a normal lifespan through regulation of TREX-2 complex-mediated mRNA export
  14. 634
    “…In addition, the presented results underline that open-source software, such as SAGA GIS and SNAP can provide satisfactory results for vegetation coverage dynamics.…”
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    The normalized difference vegetation index (NDVI) of the Zat valley, Marrakech: comparison and dynamics
  15. 635
    “…Statistically significant difference was detected between SAGA and FAGA values of operated knees in both groups (p<0.05). …”
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    Comparison of MRI Results of Grafts Obtained by Unilateral Anterior Cruciate Ligament Reconstruction Either Using Anteromedial Portal Only or Transtibial Method with Contralateral Healthy Knee: Tibial Tunnel or Graft Insertion?
  16. 636
    “…We previously developed the In Vitro Immortalization Assay (IVIM) and Surrogate Assay for Genotoxicity Assessment (SAGA) for pre-clinical genotoxicity prediction of integrating vectors. …”
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    Development of an in vitro genotoxicity assay to detect retroviral vector-induced lymphoid insertional mutants
  17. 637
    “…Sus1 is a transcription export factor and part of both the SAGA and the TREX-2 complex. The competitive exchange of Sus1 molecule between SAGA and TREX-2 complex modulates their function which is credited to structural plasticity of Sus1. …”
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    An insight into structural plasticity and conformational transitions of transcriptional co-activator Sus1
  18. 638
    por Kumano, S
    Publicado 1994
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    $\phi$ radiative decays and scalar meson structure
  19. 639
    por Saitô, S, Uehara, M
    Publicado 1993
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    Nonstatic effect on the intersoliton potential and the 1/N expansion
  20. 640
    por Saitô, S, Uehara, M
    Publicado 1993
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    Recalculation of electromagnetic polarizabilities of the nucleon in the Skyrme model
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