Showing results (31-40 of 43) with videos related to
Sort By:
Pageof 5
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|June 20, 2018
Cilia protein IFT88 regulates extracellular protease activity by optimizing LRP-1-mediated endocytosisClarissa R Coveney, Isabella Collins, Megan Mc Fie, et al.Scientific Reports|December 19, 2013
Surface topography regulates wnt signaling through control of primary cilia structure in mesenchymal stem cellsR J McMurray, A K T Wann, C L Thompson, et al.Journal of Tissue Engineering|April 28, 2025
Engineering growth factor gradients to drive spatiotemporal tissue patterning in organ-on-a-chip systemsTimothy Hopkins, Swati Midha, Simon Grossemy, et al.The Journal of Physiology|July 23, 2009
Signal pathways regulating hyaluronan secretion into static and cycled synovial joints of rabbitsK R Ingram, A K T Wann, R M Wingate, et al.FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|January 7, 2012
Primary cilia mediate mechanotransduction through control of ATP-induced Ca2+ signaling in compressed chondrocytesAngus K T Wann, Ning Zuo, Courtney J Haycraft, et al.Undersea Biomedical Research|July 1, 1990
Exposure to high pressure may produce the 5-HT behavioral syndrome in ratsB Wardley-Smith, S Hudson, C J Doré, et al.Arthritis Research & Therapy|December 26, 2015
Hedgehog signalling does not stimulate cartilage catabolism and is inhibited by Interleukin-1βClare L Thompson, Riana Patel, Terri-Ann N Kelly, et al.Toxicology|September 21, 2010
Bacterial metabolic 'toxins': a new mechanism for lactose and food intolerance, and irritable bowel syndromeA K Campbell, S B Matthews, N Vassel, et al.Luminescence : the Journal of Biological and Chemical Luminescence|February 25, 2012
Enzymatic activity of albumin shown by coelenterazine chemiluminescenceN Vassel, C D Cox, R Naseem, et al.Journal of the American College of Cardiology|June 7, 2000
Homozygosity for a HERG potassium channel mutation causes a severe form of long QT syndrome: identification of an apparent founder mutation in the FinnsK Piippo, P Laitinen, H Swan, et al.Pageof 5