Materias dentro de su búsqueda.
Mostrando 1,301 - 1,320 Resultados de 205,982 Para Buscar 'Will*', tiempo de consulta: 0.98s Limitar resultados
  1. 1301
    Enlace del recurso
    Enlace del recurso
    Enlace del recurso
    Online Artículo Texto
    Breakeven, Cost Benefit, Cost Effectiveness, and Willingness to Pay for Web-Based Versus Face-to-Face Education Delivery for Health Professionals
  2. 1302
    “…The neurodevelopmental disorder Williams–Beuren syndrome is caused by spontaneous ∼1.5 Mb deletions comprising 25 genes on human chromosome 7q11.23. …”
    Enlace del recurso
    Enlace del recurso
    Enlace del recurso
    Online Artículo Texto
    Induced chromosome deletions cause hypersociability and other features of Williams–Beuren syndrome in mice
  3. 1303
    por Meyer-Lindenberg, Andreas
    Publicado 2009
    Enlace del recurso
    Enlace del recurso
    Enlace del recurso
    Online Artículo Texto
    More than the sum of its parts: new mouse models for dissecting the genetic complexities of Williams–Beuren syndrome
  4. 1304
    Enlace del recurso
    Enlace del recurso
    Enlace del recurso
    Online Artículo Texto
    Look Who’s (Not) Talking: Diabetic patients’ willingness to discuss self-care with physicians
  5. 1305
    “…We demonstrate that beliefs about willpower–whether willpower is viewed as a limited or non-limited resource–impact sustained learning on a strenuous mental task. …”
    Enlace del recurso
    Enlace del recurso
    Enlace del recurso
    Online Artículo Texto
    Theories of Willpower Affect Sustained Learning
  6. 1306
    “…Williams syndrome (WS) is a developmental disorder of genetic origin, with characteristic cognitive and personality profiles. …”
    Enlace del recurso
    Enlace del recurso
    Enlace del recurso
    Online Artículo Texto
    Social Cognition in Williams Syndrome: Relations between Performance on the Social Attribution Task and Cognitive and Behavioral Characteristics
  7. 1307
    “…Using a CRC mouse xenograft model, in the present study we evaluated the effect of the ethanol extract of Hedyotis diffusa Willd (EEHDW) on tumor growth in vivo and investigated the underlying molecular mechanisms. …”
    Enlace del recurso
    Enlace del recurso
    Enlace del recurso
    Online Artículo Texto
    Hedyotis diffusa Willd Inhibits Colorectal Cancer Growth in Vivo via Inhibition of STAT3 Signaling Pathway
  8. 1308
    “…The interaction of platelet glycoprotein (GP) Ib-IX with von Willebrand factor (VWF) exposed at the injured vessel wall or atherosclerotic plaque rupture initiates platelet transient adhesion to the injured vessel wall, which triggers intracellular signaling cascades leading to platelet activation and thrombus formation. 14-3-3ζ has been verified to regulate the VWF binding function of GPIb-IX by interacting with the cytoplasmic domains of GPIb-IX. …”
    Enlace del recurso
    Enlace del recurso
    Enlace del recurso
    Online Artículo Texto
    Role of 14-3-3ζ in Platelet Glycoprotein Ibα-von Willebrand Factor Interaction-Induced Signaling
  9. 1309
    “…The purpose of this study was to investigate the willingness to pay (WTP) for IV-PCA and the relationship between patients' characteristics and WTP in Korea. …”
    Enlace del recurso
    Enlace del recurso
    Enlace del recurso
    Online Artículo Texto
    The willingness of patients to pay for intravenous patient-controlled analgesia in Korea
  10. 1310
    “…Williams Syndrome is a genetically determined neurodevelopmental disorder characterized by an uneven cognitive profile and surprisingly large neurobehavioral differences among individuals. …”
    Enlace del recurso
    Enlace del recurso
    Enlace del recurso
    Online Artículo Texto
    Perceptual Learning in Williams Syndrome: Looking Beyond Averages
  11. 1311
    “…BACKGROUND: In type 1 von Willebrand Disease (VWD) patients, von Willebrand Factor (VWF) levels and bleeding symptoms are highly variable. …”
    Enlace del recurso
    Enlace del recurso
    Enlace del recurso
    Online Artículo Texto
    Effect of Genetic Variation in STXBP5 and STX2 on von Willebrand Factor and Bleeding Phenotype in Type 1 von Willebrand Disease Patients
  12. 1312
    por McDaid, Lisa M., Hart, Graham J.
    Publicado 2011
    “…Having an STI in the past 12 months remained significantly associated with being willing to participate in all three study types. There were no associations between sexual risk behaviour and willingness. …”
    Enlace del recurso
    Enlace del recurso
    Enlace del recurso
    Online Artículo Texto
    Willingness to Participate in Future HIV Prevention Studies Among Gay and Bisexual Men in Scotland, UK: A Challenge for Intervention Trials
  13. 1313
    por Yang, Zhenya, Li, Zhiyong
    Publicado 2012
    “…In this study, based on gene library and ∫-LIBSHUFF analysis, the spatial distribution of prokaryotic symbionts and nitrogen cycling genes in the cortex and endosome sections of sponge Astrosclera willeyana were investigated. A significance difference of bacterial phylotypes between the cortex and endosome was revealed. …”
    Enlace del recurso
    Enlace del recurso
    Enlace del recurso
    Online Artículo Texto
    Spatial distribution of prokaryotic symbionts and ammoxidation, denitrifier bacteria in marine sponge Astrosclera willeyana
  14. 1314
    “…Imaging of the brain revealed dolichoectasia of arteries of the circle of Willis coexisting with a fusiform aneurysm of the basilar artery. …”
    Enlace del recurso
    Enlace del recurso
    Online Artículo Texto
    Dolichoectasia of the circle of Willis arteries and fusiform aneurysm of basilar artery – case report and review of the literature
  15. 1315
    “…CONCLUSIONS: Pediatric patients and their families are often willing to share electronic health information to support health improvement, but remain cautious. …”
    Enlace del recurso
    Enlace del recurso
    Enlace del recurso
    Online Artículo Texto
    Willingness to share personal health record data for care improvement and public health: a survey of experienced personal health record users
  16. 1316
    por Jin, Dong-Kyu
    Publicado 2012
    “…Prader-Willi syndrome (PWS) is a complex multisystem genetic disorder characterized by hypothalamic-pituitary dysfunction. …”
    Enlace del recurso
    Enlace del recurso
    Enlace del recurso
    Online Artículo Texto
    Endocrine problems in children with Prader-Willi syndrome: special review on associated genetic aspects and early growth hormone treatment
  17. 1317
    “…Seventy-nine percent either strongly or somewhat agreed that they know what to do in the event of a disaster, and the majority was willing to report for duty in the event of a disaster. …”
    Enlace del recurso
    Enlace del recurso
    Enlace del recurso
    Online Artículo Texto
    Health care workers and disaster preparedness: barriers to and facilitators of willingness to respond
  18. 1318
    por Asada, Kosuke, Itakura, Shoji
    Publicado 2012
    “…Autism spectrum disorders (ASD) and Williams syndrome (WS) both are neurodevelopmental disorders, each with a unique social phenotypic pattern. …”
    Enlace del recurso
    Enlace del recurso
    Enlace del recurso
    Online Artículo Texto
    Social Phenotypes of Autism Spectrum Disorders and Williams Syndrome: Similarities and Differences
  19. 1319
    Enlace del recurso
    Enlace del recurso
    Enlace del recurso
    Online Artículo Texto
    General anesthetic management of Prader-Willi syndrome patient undergoing middle cerebral artery-superficial temporal artery anastomosis
  20. 1320
    “…The imprinted Snurf–Snrpn chromosomal domain contains two large arrays of tandemly repeated, paternally expressed box C/D small-nucleolar RNA (snoRNA) genes: the SNORD115 (H/MBII-52) and SNORD116 (H/MBII-85) gene clusters believed to play key roles in the fine-tuning of serotonin receptor (5-HT2C) pre-mRNA processing and in the etiology of the Prader–Willi Syndrome (PWS), respectively. SNORD115 and SNORD116 were recently proposed to undergo significant conversion into shorter RNA species, the so-called psnoRNAs. …”
    Enlace del recurso
    Enlace del recurso
    Enlace del recurso
    Online Artículo Texto
    The SNORD115 (H/MBII-52) and SNORD116 (H/MBII-85) gene clusters at the imprinted Prader–Willi locus generate canonical box C/D snoRNAs
Herramientas de búsqueda: RSS