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European Journal of Human Genetics : EJHG|March 27, 1999
Spectrum of mutations in fucosidosisP J Willems, H C Seo, P Coucke, et al.Nature Genetics|July 1, 1993
Identification of a common mutation in the carnitine palmitoyltransferase II gene in familial recurrent myoglobinuria patientsF Taroni, E Verderio, F Dworzak, et al.Genome Biology and Evolution|July 25, 2013
Recent recombination events in the core genome are associated with adaptive evolution in Enterococcus faeciumMark de Been, Willem van Schaik, Lu Cheng, et al.The Journal of Biological Chemistry|January 15, 2001
Novel frameshift mutations near short simple repeatsW H van Den Hurk, H J Willems, M Bloemen, et al.The European Journal of Surgery = Acta Chirurgica|April 1, 1992
Hyperparathyroidism associated with treatment of manic-depressive disorders by lithiumJ Nordenström, K Strigård, L Perbeck, et al.Pediatric Nephrology (Berlin, Germany)|July 1, 1987
The syndrome of hypertension and hyperkalaemia with normal glomerular function (Gordon's syndrome). A pathophysiological studyB Semmekrot, L Monnens, B G Theelen, et al.Human Molecular Genetics|May 1, 1996
X-linked liver glycogenosis type II (XLG II) is caused by mutations in PHKA2, the gene encoding the liver alpha subunit of phosphorylase kinaseJ Hendrickx, E Dams, P Coucke, et al.American Journal of Medical Genetics|August 1, 1988
Activation of fatty acid oxidation in the Silver-Russell syndrome and the Brachmann-de Lange syndromeP J Willems, I Dijkstra, H H Schierbeek, et al.Journal of Biomechanics|August 5, 1999
Skeletal muscle transverse strain during isometric contraction at different lengthsC C van Donkelaar, P J Willems, A M Muijtjens, et al.American Journal of Physiology. Endocrinology and Metabolism|September 12, 2001
Electrostimulation enhances FAT/CD36-mediated long-chain fatty acid uptake by isolated rat cardiac myocytesJ J Luiken, J Willems, G J van der Vusse, et al.Pageof 50