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Behavioural Brain Research|August 15, 2000
Expression of nicotinic acetylcholine receptors in Alzheimer's disease: postmortem investigations and experimental approachesA Wevers, L Burghaus, N Moser, et al.American Journal of Human Genetics|April 8, 2014
De novo mutations in the beta-tubulin gene TUBB2A cause simplified gyral patterning and infantile-onset epilepsyThomas D Cushion, Alex R Paciorkowski, Daniela T Pilz, et al.Open Forum Infectious Diseases|October 7, 2024
Effectiveness of the First and Second Severe Acute Respiratory Syndrome Coronavirus 2 Vaccine Dose: A Nationwide Cohort Study From Austria on Hybrid Versus Natural ImmunityAlena Chalupka, Uwe Riedmann, Lukas Richter, et al.Circulation. Cardiovascular Quality and Outcomes|November 15, 2012
Circulating 25-hydroxy-vitamin D and risk of cardiovascular disease: a meta-analysis of prospective studiesLu Wang, Yiqing Song, Joann E Manson, et al.Journal of Immunology (Baltimore, Md. : 1950)|September 6, 2007
Differential effects of CpG DNA on IFN-beta induction and STAT1 activation in murine macrophages versus dendritic cells: alternatively activated STAT1 negatively regulates TLR signaling in macrophagesKate Schroder, Martina Spille, Andreas Pilz, et al.Nutrients|June 21, 2017
Effects of Vitamin D Supplementation on IGF-1 and Calcitriol: A Randomized-Controlled TrialChristian Trummer, Verena Schwetz, Marlene Pandis, et al.The International Journal of Eating Disorders|October 23, 2023
Impaired implicit learning in adults with anorexia nervosaMarkus Wiener, Susanne A Bengesser, Jolana Wagner-Skacel, et al.Nutrition, Metabolism, and Cardiovascular Diseases : NMCD|October 11, 2021
Randomized trial of vitamin D versus placebo supplementation on markers of systemic inflammation in hypertensive patientsMartin R Grübler, Armin Zittermann, Nicolas D Verheyen, et al.Blood|January 28, 2006
Acute myeloid leukemia is associated with retroviral gene transfer to hematopoietic progenitor cells in a rhesus macaqueRuth Seggewiss, Stefania Pittaluga, Rima L Adler, et al.American Journal of Human Genetics|January 22, 2019
De Novo SOX4 Variants Cause a Neurodevelopmental Disease Associated with Mild DysmorphismAsh Zawerton, Baojin Yao, J Paige Yeager, et al.Pageof 177