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Peter Bross

Showing results (41-50 of 94) with videos related to

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The FEBS Journal|April 12, 2005
Actin mutations in hypertrophic and dilated cardiomyopathy cause inefficient protein folding and perturbed filament formationSøren Vang, Thomas J Corydon, Anders D Børglum, et al.
The Journal of Biological Chemistry|September 25, 2003
Misfolding, degradation, and aggregation of variant proteins. The molecular pathogenesis of short chain acyl-CoA dehydrogenase (SCAD) deficiencyChristina Bak Pedersen, Peter Bross, Vibeke Stenbroen Winter, et al.
Cell Stress & Chaperones|October 3, 2006
Reduced heat shock response in human mononuclear cells during aging and its association with polymorphisms in HSP70 genesRipudaman Singh, Steen Kølvraa, Peter Bross, et al.
Biogerontology|June 11, 2004
Association between low self-rated health and heterozygosity for -110A > C polymorphism in the promoter region of HSP70-1 in aged Danish twinsRipudaman Singh, Steen Kølvraa, Peter Bross, et al.
Cell Stress & Chaperones|February 16, 2020
An inventory of interactors of the human HSP60/HSP10 chaperonin in the mitochondrial matrix spaceAnne Sigaard Bie, Cagla Cömert, Roman Körner, et al.
Neurobiology of Disease|March 8, 2013
Late onset motoneuron disorder caused by mitochondrial Hsp60 chaperone deficiency in miceRaffaella Magnoni, Johan Palmfeldt, Jane H Christensen, et al.
The Journal of Clinical Investigation|October 3, 2013
Leptin regulation of Hsp60 impacts hypothalamic insulin signalingAndré Kleinridders, Hans P M M Lauritzen, Siegfried Ussar, et al.
Molecular Genetics & Genomic Medicine|October 22, 2014
Selected reaction monitoring as an effective method for reliable quantification of disease-associated proteins in maple syrup urine diseasePaula Fernández-Guerra, Rune I D Birkler, Begoña Merinero, et al.
Cold Spring Harbor Molecular Case Studies|June 14, 2020
A recurrent de novo <i>HSPD1</i> variant is associated with hypomyelinating leukodystrophyCagla Cömert, Lauren Brick, Debbie Ang, et al.
Journal of Neurology|April 11, 2007
A novel mutation in the HSPD1 gene in a patient with hereditary spastic paraplegiaJakob Hansen, Kirsten Svenstrup, Debbie Ang, et al.
Pageof 10

Showing results (41-50 of 94) with videos related to

Sort By:
Pageof 10
The FEBS Journal|April 12, 2005
Actin mutations in hypertrophic and dilated cardiomyopathy cause inefficient protein folding and perturbed filament formationSøren Vang, Thomas J Corydon, Anders D Børglum, et al.
The Journal of Biological Chemistry|September 25, 2003
Misfolding, degradation, and aggregation of variant proteins. The molecular pathogenesis of short chain acyl-CoA dehydrogenase (SCAD) deficiencyChristina Bak Pedersen, Peter Bross, Vibeke Stenbroen Winter, et al.
Cell Stress & Chaperones|October 3, 2006
Reduced heat shock response in human mononuclear cells during aging and its association with polymorphisms in HSP70 genesRipudaman Singh, Steen Kølvraa, Peter Bross, et al.
Biogerontology|June 11, 2004
Association between low self-rated health and heterozygosity for -110A > C polymorphism in the promoter region of HSP70-1 in aged Danish twinsRipudaman Singh, Steen Kølvraa, Peter Bross, et al.
Cell Stress & Chaperones|February 16, 2020
An inventory of interactors of the human HSP60/HSP10 chaperonin in the mitochondrial matrix spaceAnne Sigaard Bie, Cagla Cömert, Roman Körner, et al.
Neurobiology of Disease|March 8, 2013
Late onset motoneuron disorder caused by mitochondrial Hsp60 chaperone deficiency in miceRaffaella Magnoni, Johan Palmfeldt, Jane H Christensen, et al.
The Journal of Clinical Investigation|October 3, 2013
Leptin regulation of Hsp60 impacts hypothalamic insulin signalingAndré Kleinridders, Hans P M M Lauritzen, Siegfried Ussar, et al.
Molecular Genetics & Genomic Medicine|October 22, 2014
Selected reaction monitoring as an effective method for reliable quantification of disease-associated proteins in maple syrup urine diseasePaula Fernández-Guerra, Rune I D Birkler, Begoña Merinero, et al.
Cold Spring Harbor Molecular Case Studies|June 14, 2020
A recurrent de novo <i>HSPD1</i> variant is associated with hypomyelinating leukodystrophyCagla Cömert, Lauren Brick, Debbie Ang, et al.
Journal of Neurology|April 11, 2007
A novel mutation in the HSPD1 gene in a patient with hereditary spastic paraplegiaJakob Hansen, Kirsten Svenstrup, Debbie Ang, et al.
Pageof 10