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Niels Gregersen

Showing results (131-140 of 161) with videos related to

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Physical Review Letters|January 30, 2016
On-Demand Single Photons with High Extraction Efficiency and Near-Unity Indistinguishability from a Resonantly Driven Quantum Dot in a MicropillarXing Ding, Yu He, Z-C Duan, et al.
Cell Chemical Biology|August 19, 2017
Ketone Body Acetoacetate Buffers Methylglyoxal via a Non-enzymatic Conversion during Diabetic and Dietary KetosisTrine Salomón, Christian Sibbersen, Jakob Hansen, et al.
Human Molecular Genetics|June 4, 2013
Secondary coenzyme Q10 deficiency and oxidative stress in cultured fibroblasts from patients with riboflavin responsive multiple Acyl-CoA dehydrogenation deficiencyNanna Cornelius, Colleen Byron, Iain Hargreaves, et al.
Ugeskrift for Laeger|July 4, 2019
[Myalgic encephalomyelitis or chronic fatigue syndrome]Louise Brinth, Henrik Nielsen, Kim Varming, et al.
Journal of Inherited Metabolic Disease|May 11, 2021
Variants in the ethylmalonyl-CoA decarboxylase (ECHDC1) gene: a novel player in ethylmalonic aciduria?Sarah Fogh, Graziana Dipace, Anne Bie, et al.
ACS Photonics|February 26, 2024
On-Demand Generation of Indistinguishable Photons in the Telecom C-Band Using Quantum Dot DevicesDaniel A Vajner, Paweł Holewa, Emilia Zięba-Ostój, et al.
Journal of Inherited Metabolic Disease|May 6, 2010
Antioxidant dysfunction: potential risk for neurotoxicity in ethylmalonic aciduriaChristina B Pedersen, Zarazuela Zolkipli, Søren Vang, 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.
The Journal of Biological Chemistry|June 26, 2019
Mitochondrial fatty acid oxidation and the electron transport chain comprise a multifunctional mitochondrial protein complexYudong Wang, Johan Palmfeldt, Niels Gregersen, et al.
American Journal of Human Genetics|February 3, 2007
Seemingly neutral polymorphic variants may confer immunity to splicing-inactivating mutations: a synonymous SNP in exon 5 of MCAD protects from deleterious mutations in a flanking exonic splicing enhancerKarsten Bork Nielsen, Suzette Sørensen, Luca Cartegni, et al.
Pageof 17

Showing results (131-140 of 161) with videos related to

Sort By:
Pageof 17
Physical Review Letters|January 30, 2016
On-Demand Single Photons with High Extraction Efficiency and Near-Unity Indistinguishability from a Resonantly Driven Quantum Dot in a MicropillarXing Ding, Yu He, Z-C Duan, et al.
Cell Chemical Biology|August 19, 2017
Ketone Body Acetoacetate Buffers Methylglyoxal via a Non-enzymatic Conversion during Diabetic and Dietary KetosisTrine Salomón, Christian Sibbersen, Jakob Hansen, et al.
Human Molecular Genetics|June 4, 2013
Secondary coenzyme Q10 deficiency and oxidative stress in cultured fibroblasts from patients with riboflavin responsive multiple Acyl-CoA dehydrogenation deficiencyNanna Cornelius, Colleen Byron, Iain Hargreaves, et al.
Ugeskrift for Laeger|July 4, 2019
[Myalgic encephalomyelitis or chronic fatigue syndrome]Louise Brinth, Henrik Nielsen, Kim Varming, et al.
Journal of Inherited Metabolic Disease|May 11, 2021
Variants in the ethylmalonyl-CoA decarboxylase (ECHDC1) gene: a novel player in ethylmalonic aciduria?Sarah Fogh, Graziana Dipace, Anne Bie, et al.
ACS Photonics|February 26, 2024
On-Demand Generation of Indistinguishable Photons in the Telecom C-Band Using Quantum Dot DevicesDaniel A Vajner, Paweł Holewa, Emilia Zięba-Ostój, et al.
Journal of Inherited Metabolic Disease|May 6, 2010
Antioxidant dysfunction: potential risk for neurotoxicity in ethylmalonic aciduriaChristina B Pedersen, Zarazuela Zolkipli, Søren Vang, 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.
The Journal of Biological Chemistry|June 26, 2019
Mitochondrial fatty acid oxidation and the electron transport chain comprise a multifunctional mitochondrial protein complexYudong Wang, Johan Palmfeldt, Niels Gregersen, et al.
American Journal of Human Genetics|February 3, 2007
Seemingly neutral polymorphic variants may confer immunity to splicing-inactivating mutations: a synonymous SNP in exon 5 of MCAD protects from deleterious mutations in a flanking exonic splicing enhancerKarsten Bork Nielsen, Suzette Sørensen, Luca Cartegni, et al.
Pageof 17