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Peter Bross

Showing results (71-80 of 94) with videos related to

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Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|July 23, 2025
FDA approval summary: Lifileucel for unresectable or metastatic melanoma previously treated with an anti-PD-1 based immunotherapyLianne Hu, Chaohong Fan, Peter Bross, et al.
American Journal of Human Genetics|June 24, 2008
Mitochondrial hsp60 chaperonopathy causes an autosomal-recessive neurodegenerative disorder linked to brain hypomyelination and leukodystrophyDaniella Magen, Costa Georgopoulos, Peter Bross, et al.
Molecular Metabolism|August 15, 2024
HSP60 chaperone deficiency disrupts the mitochondrial matrix proteome and dysregulates cholesterol synthesisCagla Cömert, Kasper Kjær-Sørensen, Jakob Hansen, et al.
European Journal of Biochemistry|October 14, 2004
The Y42H mutation in medium-chain acyl-CoA dehydrogenase, which is prevalent in babies identified by MS/MS-based newborn screening, is temperature sensitiveLinda O'Reilly, Peter Bross, Thomas J Corydon, et al.
Stem Cells and Development|October 28, 2016
Mitochondrial Spare Respiratory Capacity Is Negatively Correlated with Nuclear Reprogramming EfficiencyYan Zhou, Rasha Abdelkadhem Al-Saaidi, Paula Fernandez-Guerra, et al.
Translational Psychiatry|August 8, 2022
The psychiatric risk gene BRD1 modulates mitochondrial bioenergetics by transcriptional regulationVeerle Paternoster, Cagla Cömert, Louise Sand Kirk, et al.
Circulation. Cardiovascular Genetics|April 8, 2014
Truncating plakophilin-2 mutations in arrhythmogenic cardiomyopathy are associated with protein haploinsufficiency in both myocardium and epidermisTorsten B Rasmussen, Peter H Nissen, Johan Palmfeldt, et al.
Human Mutation|February 6, 2013
Mutated desmoglein-2 proteins are incorporated into desmosomes and exhibit dominant-negative effects in arrhythmogenic right ventricular cardiomyopathyTorsten B Rasmussen, Johan Palmfeldt, Peter H Nissen, et al.
European Journal of Heart Failure|June 27, 2018
The clinical outcome of LMNA missense mutations can be associated with the amount of mutated protein in the nuclear envelopeRasha A Al-Saaidi, Torsten B Rasmussen, Rune I D Birkler, et al.
Molecular Genetics and Metabolism|May 1, 2012
MCAD deficiency in DenmarkBrage Storstein Andresen, Allan Meldgaard Lund, David Michael Hougaard, et al.
Pageof 10

Showing results (71-80 of 94) with videos related to

Sort By:
Pageof 10
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|July 23, 2025
FDA approval summary: Lifileucel for unresectable or metastatic melanoma previously treated with an anti-PD-1 based immunotherapyLianne Hu, Chaohong Fan, Peter Bross, et al.
American Journal of Human Genetics|June 24, 2008
Mitochondrial hsp60 chaperonopathy causes an autosomal-recessive neurodegenerative disorder linked to brain hypomyelination and leukodystrophyDaniella Magen, Costa Georgopoulos, Peter Bross, et al.
Molecular Metabolism|August 15, 2024
HSP60 chaperone deficiency disrupts the mitochondrial matrix proteome and dysregulates cholesterol synthesisCagla Cömert, Kasper Kjær-Sørensen, Jakob Hansen, et al.
European Journal of Biochemistry|October 14, 2004
The Y42H mutation in medium-chain acyl-CoA dehydrogenase, which is prevalent in babies identified by MS/MS-based newborn screening, is temperature sensitiveLinda O'Reilly, Peter Bross, Thomas J Corydon, et al.
Stem Cells and Development|October 28, 2016
Mitochondrial Spare Respiratory Capacity Is Negatively Correlated with Nuclear Reprogramming EfficiencyYan Zhou, Rasha Abdelkadhem Al-Saaidi, Paula Fernandez-Guerra, et al.
Translational Psychiatry|August 8, 2022
The psychiatric risk gene BRD1 modulates mitochondrial bioenergetics by transcriptional regulationVeerle Paternoster, Cagla Cömert, Louise Sand Kirk, et al.
Circulation. Cardiovascular Genetics|April 8, 2014
Truncating plakophilin-2 mutations in arrhythmogenic cardiomyopathy are associated with protein haploinsufficiency in both myocardium and epidermisTorsten B Rasmussen, Peter H Nissen, Johan Palmfeldt, et al.
Human Mutation|February 6, 2013
Mutated desmoglein-2 proteins are incorporated into desmosomes and exhibit dominant-negative effects in arrhythmogenic right ventricular cardiomyopathyTorsten B Rasmussen, Johan Palmfeldt, Peter H Nissen, et al.
European Journal of Heart Failure|June 27, 2018
The clinical outcome of LMNA missense mutations can be associated with the amount of mutated protein in the nuclear envelopeRasha A Al-Saaidi, Torsten B Rasmussen, Rune I D Birkler, et al.
Molecular Genetics and Metabolism|May 1, 2012
MCAD deficiency in DenmarkBrage Storstein Andresen, Allan Meldgaard Lund, David Michael Hougaard, et al.
Pageof 10