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Peter Bross

Showing results (81-90 of 94) with videos related to

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Journal of Human Genetics|October 31, 2006
Single-nucleotide variations in the genes encoding the mitochondrial Hsp60/Hsp10 chaperone system and their disease-causing potentialPeter Bross, Zhijie Li, Jakob Hansen, et al.
Frontiers in Molecular Biosciences|October 25, 2016
Effects of a Mutation in the <i>HSPE1</i> Gene Encoding the Mitochondrial Co-chaperonin HSP10 and Its Potential Association with a Neurological and Developmental DisorderAnne S Bie, Paula Fernandez-Guerra, Rune I D Birkler, et al.
Nature Metabolism|October 16, 2025
Interaction of sortilin with apolipoprotein E3 enables neurons to use long-chain fatty acids as alternative metabolic fuelAnna K Greda, Jemila P Gomes, Vanessa Schmidt-Krueger, et al.
Diabetes, Obesity & Metabolism|May 13, 2018
Metformin targets brown adipose tissue in vivo and reduces oxygen consumption in vitroPeter Breining, Jonas B Jensen, Elias I Sundelin, et al.
Nature Communications|July 30, 2025
De novo pyrimidine biosynthesis inhibition synergizes with BCL-X<sub>L</sub> targeting in pancreatic cancerHuan Zhang, Naiara Santana-Codina, Qijia Yu, et al.
Oncogene|August 6, 2022
A genome-wide CRISPR-Cas9 knockout screen identifies novel PARP inhibitor resistance genes in prostate cancerMalene Blond Ipsen, Ea Marie Givskov Sørensen, Emil Aagaard Thomsen, et al.
Cellular and Molecular Life Sciences : CMLS|January 13, 2016
Enhanced genome editing in mammalian cells with a modified dual-fluorescent surrogate systemYan Zhou, Yong Liu, Dianna Hussmann, et al.
Human Genetics|June 5, 2008
The ACADS gene variation spectrum in 114 patients with short-chain acyl-CoA dehydrogenase (SCAD) deficiency is dominated by missense variations leading to protein misfolding at the cellular levelChristina B Pedersen, Steen Kølvraa, Agnete Kølvraa, et al.
Journal of Medical Genetics|November 5, 2024
Heterozygous de novo variants in <i>HSPD1</i> cause hypomyelinating leukodystrophy through impaired HSP60 oligomerisationMarina Eskin-Schwartz, Shaikah Seraidy, Eyal Paz, et al.
Cell Chemical Biology|August 21, 2018
APD-Containing Cyclolipodepsipeptides Target Mitochondrial Function in Hypoxic Cancer CellsKristian Mark Jacobsen, Nikolaj Lilholm Villadsen, Thomas Tørring, et al.
Pageof 10

Showing results (81-90 of 94) with videos related to

Sort By:
Pageof 10
Journal of Human Genetics|October 31, 2006
Single-nucleotide variations in the genes encoding the mitochondrial Hsp60/Hsp10 chaperone system and their disease-causing potentialPeter Bross, Zhijie Li, Jakob Hansen, et al.
Frontiers in Molecular Biosciences|October 25, 2016
Effects of a Mutation in the <i>HSPE1</i> Gene Encoding the Mitochondrial Co-chaperonin HSP10 and Its Potential Association with a Neurological and Developmental DisorderAnne S Bie, Paula Fernandez-Guerra, Rune I D Birkler, et al.
Nature Metabolism|October 16, 2025
Interaction of sortilin with apolipoprotein E3 enables neurons to use long-chain fatty acids as alternative metabolic fuelAnna K Greda, Jemila P Gomes, Vanessa Schmidt-Krueger, et al.
Diabetes, Obesity & Metabolism|May 13, 2018
Metformin targets brown adipose tissue in vivo and reduces oxygen consumption in vitroPeter Breining, Jonas B Jensen, Elias I Sundelin, et al.
Nature Communications|July 30, 2025
De novo pyrimidine biosynthesis inhibition synergizes with BCL-X<sub>L</sub> targeting in pancreatic cancerHuan Zhang, Naiara Santana-Codina, Qijia Yu, et al.
Oncogene|August 6, 2022
A genome-wide CRISPR-Cas9 knockout screen identifies novel PARP inhibitor resistance genes in prostate cancerMalene Blond Ipsen, Ea Marie Givskov Sørensen, Emil Aagaard Thomsen, et al.
Cellular and Molecular Life Sciences : CMLS|January 13, 2016
Enhanced genome editing in mammalian cells with a modified dual-fluorescent surrogate systemYan Zhou, Yong Liu, Dianna Hussmann, et al.
Human Genetics|June 5, 2008
The ACADS gene variation spectrum in 114 patients with short-chain acyl-CoA dehydrogenase (SCAD) deficiency is dominated by missense variations leading to protein misfolding at the cellular levelChristina B Pedersen, Steen Kølvraa, Agnete Kølvraa, et al.
Journal of Medical Genetics|November 5, 2024
Heterozygous de novo variants in <i>HSPD1</i> cause hypomyelinating leukodystrophy through impaired HSP60 oligomerisationMarina Eskin-Schwartz, Shaikah Seraidy, Eyal Paz, et al.
Cell Chemical Biology|August 21, 2018
APD-Containing Cyclolipodepsipeptides Target Mitochondrial Function in Hypoxic Cancer CellsKristian Mark Jacobsen, Nikolaj Lilholm Villadsen, Thomas Tørring, et al.
Pageof 10