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Experimental Cell Research|September 5, 2013
The LMNA mutation p.Arg321Ter associated with dilated cardiomyopathy leads to reduced expression and a skewed ratio of lamin A and lamin C proteinsRasha Al-Saaidi, Torsten B Rasmussen, Johan Palmfeldt, et al.Methods in Molecular Biology (Clifton, N.J.)|August 12, 2010
Protein misfolding and cellular stress: an overviewNiels Gregersen, Peter BrossMethods in Molecular Biology (Clifton, N.J.)|August 12, 2010
A cellular viability assay to monitor drug toxicityJakob Hansen, Peter BrossFrontiers in Molecular Biosciences|September 16, 2016
Disease-Associated Mutations in the HSPD1 Gene Encoding the Large Subunit of the Mitochondrial HSP60/HSP10 Chaperonin ComplexPeter Bross, Paula Fernandez-GuerraBiochemical and Biophysical Research Communications|June 28, 2005
Differential degradation of variant medium-chain acyl-CoA dehydrogenase by the protein quality control proteases Lon and ClpXPJakob Hansen, Niels Gregersen, Peter BrossMolecular Biotechnology|September 20, 2005
Protein misfolding, aggregation, and degradation in diseaseNiels Gregersen, Lars Bolund, Peter BrossAPMIS. Supplementum|July 24, 2003
Protein quality control in the endoplasmic reticulumMalene Munk Jørgensen, Peter Bross, Niels GregersenCurrent Topics in Medicinal Chemistry|January 24, 2013
Molecular chaperone disorders: defective Hsp60 in neurodegenerationPeter Bross, Raffaella Magnoni, Anne Sigaard BiePageof 9