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Artificial Organs|October 1, 1987
Albumin adsorption and retention on C18-alkyl-derivatized polyurethane vascular graftsR C Eberhart, M S Munro, G B Williams, et al.The Biochemical Journal|December 1, 1984
Calmodulin activation of adenylate cyclase in the mouse B16 melanomaS Mac Neil, S W Walker, H J Senior, et al.Journal of Fish Diseases|March 26, 2014
A mortality event in wrasse species (Labridae) associated with the presence of viral haemorrhagic septicaemia virusE S Munro, R E McIntosh, S J Weir, et al.The Journal of Investigative Dermatology|October 27, 1997
Loricrin mutation in Vohwinkel's keratoderma is unique to the variant with ichthyosisB P Korge, A Ishida-Yamamoto, C Pünter, et al.Scientific Reports|May 23, 2020
Characterisation of mexiletine's translational therapeutic index for suppression of ischaemia-induced ventricular fibrillation in the rat isolated heartLouise M Hesketh, Catherine D E Wilder, Niraja N Ranadive, et al.The Journal of Investigative Dermatology|December 18, 1998
Mutations in keratin K9 in kindreds with epidermolytic palmoplantar keratoderma and epidemiology in Northern IrelandS P Covello, A D Irvine, K E McKenna, et al.Jac-Antimicrobial Resistance|July 5, 2021
Improving paediatric antimicrobial stewardship in hospital-based settings: why, where and how?E Tanner, A P S Munro, J Gray, et al.Human Molecular Genetics|June 17, 1999
A missense mutation in connexin26, D66H, causes mutilating keratoderma with sensorineural deafness (Vohwinkel's syndrome) in three unrelated familiesE Maestrini, B P Korge, J Ocaña-Sierra, et al.The Journal of Investigative Dermatology|December 20, 2000
Mutant loricrin is not crosslinked into the cornified cell envelope but is translocated into the nucleus in loricrin keratodermaA Ishida-Yamamoto, H Kato, H Kiyama, et al.Nature Genetics|December 1, 1995
A mutation in the mucosal keratin K4 is associated with oral white sponge nevusE L Rugg, W H McLean, W E Allison, et al.Pageof 24