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Plos One|November 8, 2019
Protein synthesis rates of muscle, tendon, ligament, cartilage, and bone tissue in vivo in humansJoey S J Smeets, Astrid M H Horstman, Georges F Vles, et al.
Journal of the American Society of Nephrology : JASN|July 1, 1997
Mutation in mitochondrial tRNA(Leu(UUR)) gene associated with progressive kidney diseaseJ J Jansen, J A Maassen, F J van der Woude, et al.
The American Journal of Clinical Nutrition|September 12, 2021
Amino acid removal during hemodialysis can be compensated for by protein ingestion and is not compromised by intradialytic exercise: a randomized controlled crossover trialFloris K Hendriks, Joey S J Smeets, Janneau M X van Kranenburg, et al.
Biochemical and Biophysical Research Communications|August 17, 2000
Combined enzymatic complex I and III deficiency associated with mutations in the nuclear encoded NDUFS4 geneS M Budde, L P van den Heuvel, A J Janssen, et al.
Journal of Medical Genetics|December 1, 1992
Linkage analysis with chromosome 15q11-13 markers shows genomic imprinting in familial Angelman syndromeE J Meijers-Heijboer, L A Sandkuijl, H G Brunner, et al.
American Journal of Physiology. Endocrinology and Metabolism|January 16, 2019
Dietary feeding pattern does not modulate the loss of muscle mass or the decline in metabolic health during short-term bed restMarlou L Dirks, Joey S J Smeets, Andrew M Holwerda, et al.
Physics in Medicine and Biology|October 27, 2016
Towards clinical application: prompt gamma imaging of passively scattered proton fields with a knife-edge slit cameraM Priegnitz, S Barczyk, L Nenoff, et al.
International Journal of Obesity (2005)|May 21, 2008
Common SNPs in LEP and LEPR associated with birth weight and type 2 diabetes-related metabolic risk factors in twinsN Y Souren, A D Paulussen, A Steyls, et al.
Human Mutation|April 29, 1999
Novel KCNQ1 and HERG missense mutations in Dutch long-QT familiesR J Jongbloed, A A Wilde, J L Geelen, et al.
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