Showing 8,781 - 8,800 results of 44,926 for search '(( significant ((amount decrease) OR (point decrease)) ) OR ( significant changes decrease ))', query time: 0.80s Refine Results
  1. 8781

    DataSheet7_Novel Starting Points for Human Glycolate Oxidase Inhibitors, Revealed by Crystallography-Based Fragment Screening.ZIP by Sabrina R. Mackinnon (12496324)

    Published 2022
    “…<p>Primary hyperoxaluria type I (PH1) is caused by AGXT gene mutations that decrease the functional activity of alanine:glyoxylate aminotransferase. …”
  2. 8782

    DataSheet6_Novel Starting Points for Human Glycolate Oxidase Inhibitors, Revealed by Crystallography-Based Fragment Screening.ZIP by Sabrina R. Mackinnon (12496324)

    Published 2022
    “…<p>Primary hyperoxaluria type I (PH1) is caused by AGXT gene mutations that decrease the functional activity of alanine:glyoxylate aminotransferase. …”
  3. 8783

    DataSheet4_Novel Starting Points for Human Glycolate Oxidase Inhibitors, Revealed by Crystallography-Based Fragment Screening.ZIP by Sabrina R. Mackinnon (12496324)

    Published 2022
    “…<p>Primary hyperoxaluria type I (PH1) is caused by AGXT gene mutations that decrease the functional activity of alanine:glyoxylate aminotransferase. …”
  4. 8784

    DataSheet5_Novel Starting Points for Human Glycolate Oxidase Inhibitors, Revealed by Crystallography-Based Fragment Screening.ZIP by Sabrina R. Mackinnon (12496324)

    Published 2022
    “…<p>Primary hyperoxaluria type I (PH1) is caused by AGXT gene mutations that decrease the functional activity of alanine:glyoxylate aminotransferase. …”
  5. 8785

    DataSheet1_Novel Starting Points for Human Glycolate Oxidase Inhibitors, Revealed by Crystallography-Based Fragment Screening.PDF by Sabrina R. Mackinnon (12496324)

    Published 2022
    “…<p>Primary hyperoxaluria type I (PH1) is caused by AGXT gene mutations that decrease the functional activity of alanine:glyoxylate aminotransferase. …”
  6. 8786

    DataSheet3_Novel Starting Points for Human Glycolate Oxidase Inhibitors, Revealed by Crystallography-Based Fragment Screening.ZIP by Sabrina R. Mackinnon (12496324)

    Published 2022
    “…<p>Primary hyperoxaluria type I (PH1) is caused by AGXT gene mutations that decrease the functional activity of alanine:glyoxylate aminotransferase. …”
  7. 8787

    DataSheet2_Novel Starting Points for Human Glycolate Oxidase Inhibitors, Revealed by Crystallography-Based Fragment Screening.ZIP by Sabrina R. Mackinnon (12496324)

    Published 2022
    “…<p>Primary hyperoxaluria type I (PH1) is caused by AGXT gene mutations that decrease the functional activity of alanine:glyoxylate aminotransferase. …”
  8. 8788

    Tendency chart of monthly FVC mean. by Yichuan Zhang (2888345)

    Published 2024
    “…The degradation and improvement are primarily slight. The most significant improvement in monthly FVC occurs in March-April, with a predominant type of significant improvement in FVC changes. …”
  9. 8789
  10. 8790

    Temperature-Responsive Peptide–Nucleotide Coacervates by Tiemei Lu (4244926)

    Published 2021
    “…We derive a simple relation between the temperature and salt concentration at the critical point based on a mean-field model of phase separation. …”
  11. 8791

    Temperature-Responsive Peptide–Nucleotide Coacervates by Tiemei Lu (4244926)

    Published 2021
    “…We derive a simple relation between the temperature and salt concentration at the critical point based on a mean-field model of phase separation. …”
  12. 8792
  13. 8793
  14. 8794
  15. 8795
  16. 8796
  17. 8797
  18. 8798
  19. 8799
  20. 8800

    Organometallic Synthesis of 2,3,6,7-Tetrasubstituted 1,8-Bis(dimethylamino)naphthalenes for Investigation of the Double Buttressing Effect in Proton Sponges by Andrey V. Marchenko (14193336)

    Published 2022
    “…Using X-ray diffraction and basicity measurements, we showed that due to the high conformational mobility of the methoxy groups, the most striking manifestations of double BE are the strong planarization of <i>peri</i>-NMe<sub>2</sub> groups and a significant decrease in basicity, while the length and the other properties of the intramolecular NHN hydrogen bond in the corresponding protonated species undergo minor changes.…”