Showing 1,321 - 1,340 results of 1,428 for search '(((((pina OR ping) OR pin) OR ssspingl) OR ((sminge OR spine) OR nine)) OR (mingna OR peng))', query time: 0.19s Refine Results
  1. 1321

    Building AC/DC microgrid design by Li, ChengJing

    Published 2017
    Get full text
    Final Year Project (FYP)
  2. 1322
  3. 1323
  4. 1324

    Flexible Composites with Rare-Earth Element Doped Polycrystalline Particles for Piezoelectric Nanogenerators by Fan, Yanzhe, Jia, Zihan, Zhang, Zhuo, Gu, Shengfei, Du, Wenya, Lin, Dabin

    Published 2024
    “…Herein, we successfully demonstrated a flexible piezoelectric nanogenerator (PENG) designed by the co-doped rare-earth element ceramics (RE-PMN-PT) embedded in PVDF and PDMS composite film and attained a significant output performance while avoiding electrical poling process. …”
    Get full text
    Article
  5. 1325
  6. 1326
  7. 1327
  8. 1328
  9. 1329
  10. 1330
  11. 1331
  12. 1332
  13. 1333

    The Cognitive Underpinnings of Legal Complexity by Martínez, Eric

    Published 2024
    “…Corpus analyses reveal that legal contracts are laden with psycholinguistically complex structures at a strikingly higher rate than nine baseline genres of English. Experimental evidence further reveals that some of these structures, such as center-embedded syntax, inhibit recall and comprehension of legal content more than others, suggesting that difficulties in understanding legal content result largely from working-memory limitations imposed by long-distance syntactic dependencies as opposed to a mere lack of specialized legal knowledge. …”
    Get full text
    Thesis
  14. 1334

    Novel mutation G324C in WNT1 mapped in a large Pakistani family with severe recessively inherited Osteogenesis Imperfecta by Kausar, Mehran, Saima Siddiqi, Muhammad Yaqoob, Sajid Mansoor, Makitie, Outi, Asif Mir, Khor, Chiea Chuen, Foo, Jia Nee, Anees, Mariam

    Published 2019
    “…In silico characterization of WNT1 mutation was performed using multiple platforms. Results:Nine affected family members exhibited severe bone deformities, recurrent fractures, short stature and low bone mineral density. …”
    Get full text
    Get full text
    Journal Article
  15. 1335

    Molecular characterisation of alpha-thalassaemia in patients investigated for hypochromic microcytic indices in Hospital Universiti Sains Malaysia by Vijian, Divashini

    Published 2023
    “…The prevalence of α-thalassaemia in this study was 47.1 %. Thirty-nine and 1.4 percent of patients were found to have heterozygous and homozygous α- thalassaemia mutations, respectively, with 6.6 percent being compound heterozygous. …”
    Get full text
    Thesis
  16. 1336
  17. 1337
  18. 1338
  19. 1339
  20. 1340