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Molecular & Cellular Proteomics : MCP|February 8, 2012
Candidate hippocampal biomarkers of susceptibility and resilience to stress in a rat model of depressionKim Henningsen, Johan Palmfeldt, Sofie Christiansen, et al.The Journal of Clinical Endocrinology and Metabolism|September 10, 2004
Differential cellular handling of defective arginine vasopressin (AVP) prohormones in cells expressing mutations of the AVP gene associated with autosomal dominant and recessive familial neurohypophyseal diabetes insipidusJane H Christensen, Charlotte Siggaard, Thomas J Corydon, et al.European Journal of Pediatrics|March 30, 2018
Novel and recurrent variants in AVPR2 in 19 families with X-linked congenital nephrogenic diabetes insipidusShivani Joshi, Helene Kvistgaard, Konstantinos Kamperis, et al.Biochimica Et Biophysica Acta. Molecular Basis of Disease|November 5, 2018
Deficiency of the mitochondrial sulfide regulator ETHE1 disturbs cell growth, glutathione level and causes proteome alterations outside mitochondriaNavid Sahebekhtiari, Paula Fernandez-Guerra, Zahra Nochi, et al.Molecular Genetics and Metabolism|April 23, 2003
Expression of short-chain acyl-CoA dehydrogenase (SCAD) proteins in the liver of SCAD deficient mice after hydrodynamic gene transferDavid A Holm, Frederik Dagnaes-Hansen, Henrik Simonsen, et al.Forensic Science International|September 24, 2013
Heat stress and sudden infant death syndrome--stress gene expression after exposure to moderate heat stressMarianne Cathrine Rohde, Thomas Juhl Corydon, Jakob Hansen, et al.Forensic Science International|January 1, 2014
Characteristics of human infant primary fibroblast cultures from Achilles tendons removed post-mortemMarianne Cathrine Rohde, Thomas Juhl Corydon, Jakob Hansen, et al.Proteomics|February 13, 2016
Quantitative proteomics suggests metabolic reprogramming during ETHE1 deficiencyNavid Sahebekhtiari, Michelle M Thomsen, Jens J Sloth, et al.Nano Letters|September 7, 2018
All-Optical Mapping of the Position of Quantum Dots Embedded in a Nanowire AntennaRomain Fons, Andreas D Osterkryger, Petr Stepanov, et al.Journal of Inherited Metabolic Disease|May 19, 2010
High-resolution melting analysis, a simple and effective method for reliable mutation scanning and frequency studies in the ACADVL geneRikke Katrine Jentoft Olsen, Steven F Dobrowolski, Margrethe Kjeldsen, et al.Pageof 21