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Niels Gregersen

Showing results (121-130 of 161) with videos related to

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ACS Photonics|July 26, 2022
Bright Quantum Dot Single-Photon Emitters at Telecom Bands Heterogeneously Integrated on SiPaweł Holewa, Aurimas Sakanas, Ugur M Gür, et al.
ACS Photonics|November 24, 2025
Toward Single-Photon Detection with Superconducting Niobium Diselenide NanowiresPietro Metuh, Athanasios Paralikis, Paweł Wyborski, et al.
International Journal of Neonatal Screening|August 27, 2021
Use of Molecular Genetic Analyses in Danish Routine Newborn ScreeningAllan Meldgaard Lund, Flemming Wibrand, Kristin Skogstrand, et al.
JIMD Reports|February 23, 2013
Normal Levels of Plasma Free Carnitine and Acylcarnitines in Follow-Up Samples from a Presymptomatic Case of Carnitine Palmitoyl Transferase 1 (CPT1) Deficiency Detected Through Newborn Screening in DenmarkLuise Borch, Allan Meldgaard Lund, Flemming Wibrand, et al.
Journal of Inherited Metabolic Disease|December 21, 2010
Toxic response caused by a misfolding variant of the mitochondrial protein short-chain acyl-CoA dehydrogenaseStinne P Schmidt, Thomas J Corydon, Christina B Pedersen, et al.
Prenatal Diagnosis|January 22, 2005
DNA-based prenatal diagnosis for severe and variant forms of multiple acyl-CoA dehydrogenation deficiencyRikke K J Olsen, Brage S Andresen, Ernst Christensen, et al.
Biomolecules|July 2, 2021
Bioenergetic and Proteomic Profiling of Immune Cells in Myalgic Encephalomyelitis/Chronic Fatigue Syndrome Patients: An Exploratory StudyPaula Fernandez-Guerra, Ana C Gonzalez-Ebsen, Susanne E Boonen, et al.
Molecular Genetics and Metabolism|November 11, 2017
An intronic variation in SLC52A1 causes exon skipping and transient riboflavin-responsive multiple acyl-CoA dehydrogenation deficiencySigne Mosegaard, Gitte Hoffmann Bruun, Karen Freund Flyvbjerg, et al.
American Journal of Human Genetics|March 19, 2002
Hereditary spastic paraplegia SPG13 is associated with a mutation in the gene encoding the mitochondrial chaperonin Hsp60Jens Jacob Hansen, Alexandra Dürr, Isabelle Cournu-Rebeix, et al.
The Journal of Biological Chemistry|April 11, 2008
The Hsp60-(p.V98I) mutation associated with hereditary spastic paraplegia SPG13 compromises chaperonin function both in vitro and in vivoPeter Bross, Søren Naundrup, Jakob Hansen, et al.
Pageof 17

Showing results (121-130 of 161) with videos related to

Sort By:
Pageof 17
ACS Photonics|July 26, 2022
Bright Quantum Dot Single-Photon Emitters at Telecom Bands Heterogeneously Integrated on SiPaweł Holewa, Aurimas Sakanas, Ugur M Gür, et al.
ACS Photonics|November 24, 2025
Toward Single-Photon Detection with Superconducting Niobium Diselenide NanowiresPietro Metuh, Athanasios Paralikis, Paweł Wyborski, et al.
International Journal of Neonatal Screening|August 27, 2021
Use of Molecular Genetic Analyses in Danish Routine Newborn ScreeningAllan Meldgaard Lund, Flemming Wibrand, Kristin Skogstrand, et al.
JIMD Reports|February 23, 2013
Normal Levels of Plasma Free Carnitine and Acylcarnitines in Follow-Up Samples from a Presymptomatic Case of Carnitine Palmitoyl Transferase 1 (CPT1) Deficiency Detected Through Newborn Screening in DenmarkLuise Borch, Allan Meldgaard Lund, Flemming Wibrand, et al.
Journal of Inherited Metabolic Disease|December 21, 2010
Toxic response caused by a misfolding variant of the mitochondrial protein short-chain acyl-CoA dehydrogenaseStinne P Schmidt, Thomas J Corydon, Christina B Pedersen, et al.
Prenatal Diagnosis|January 22, 2005
DNA-based prenatal diagnosis for severe and variant forms of multiple acyl-CoA dehydrogenation deficiencyRikke K J Olsen, Brage S Andresen, Ernst Christensen, et al.
Biomolecules|July 2, 2021
Bioenergetic and Proteomic Profiling of Immune Cells in Myalgic Encephalomyelitis/Chronic Fatigue Syndrome Patients: An Exploratory StudyPaula Fernandez-Guerra, Ana C Gonzalez-Ebsen, Susanne E Boonen, et al.
Molecular Genetics and Metabolism|November 11, 2017
An intronic variation in SLC52A1 causes exon skipping and transient riboflavin-responsive multiple acyl-CoA dehydrogenation deficiencySigne Mosegaard, Gitte Hoffmann Bruun, Karen Freund Flyvbjerg, et al.
American Journal of Human Genetics|March 19, 2002
Hereditary spastic paraplegia SPG13 is associated with a mutation in the gene encoding the mitochondrial chaperonin Hsp60Jens Jacob Hansen, Alexandra Dürr, Isabelle Cournu-Rebeix, et al.
The Journal of Biological Chemistry|April 11, 2008
The Hsp60-(p.V98I) mutation associated with hereditary spastic paraplegia SPG13 compromises chaperonin function both in vitro and in vivoPeter Bross, Søren Naundrup, Jakob Hansen, et al.
Pageof 17