Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Niels Gregersen

Showing results (51-60 of 161) with videos related to

Pageof 17
Sort By:
Biochimica Et Biophysica Acta. Molecular and Cell Biology of Lipids|November 10, 2022
Odd- and even-numbered medium-chained fatty acids protect against glutathione depletion in very long-chain acyl-CoA dehydrogenase deficiencyMartin Lund, Robert Heaton, Iain P Hargreaves, et al.
Nanoscale|February 22, 2023
Performance of the nanopost single-photon source: beyond the single-mode modelMartin Arentoft Jacobsen, Yujing Wang, Luca Vannucci, et al.
International Journal of Molecular Sciences|June 3, 2020
Riboflavin Deficiency-Implications for General Human Health and Inborn Errors of MetabolismSigne Mosegaard, Graziana Dipace, Peter Bross, et al.
Molecular Genetics and Metabolism|June 3, 2004
Homozygosity for a severe novel medium-chain acyl-CoA dehydrogenase (MCAD) mutation IVS3-1G > C that leads to introduction of a premature termination codon by complete missplicing of the MCAD mRNA and is associated with phenotypic diversity ranging from sudden neonatal death to asymptomatic statusStanley H Korman, Alisa Gutman, Rivka Brooks, et al.
Optics Express|March 27, 2021
Time-bin entangled photon pairs from quantum dots embedded in a self-aligned cavityLaia Ginés, Carlo Pepe, Junior Gonzales, et al.
Journal of Child Neurology|July 19, 2012
An infant with ethylmalonic encephalopathy masquerading as a hematologic disorderEvangelos Pavlou, Persephone Augoustides-Savvopoulou, Niels Gregersen, et al.
Human Mutation|June 20, 2003
Clear relationship between ETF/ETFDH genotype and phenotype in patients with multiple acyl-CoA dehydrogenation deficiencyRikke K J Olsen, Brage S Andresen, Ernst Christensen, et al.
Pituitary|June 15, 2012
A novel variation in the AVP gene resulting in familial neurohypophyseal diabetes insipidus in a large Italian kindredCamilla Birkegaard, Jane H Christensen, Alberto Falorni, et al.
NPJ 2D Materials and Applications|September 13, 2024
Tailoring polarization in WSe<sub>2</sub> quantum emitters through deterministic strain engineeringAthanasios Paralikis, Claudia Piccinini, Abdulmalik A Madigawa, et al.
Optics Letters|April 30, 2016
Spectral symmetry of Fano resonances in a waveguide coupled to a microcavityAndreas Dyhl Osterkryger, Jakob Rosenkrantz de Lasson, Mikkel Heuck, et al.
Pageof 17

Showing results (51-60 of 161) with videos related to

Sort By:
Pageof 17
Biochimica Et Biophysica Acta. Molecular and Cell Biology of Lipids|November 10, 2022
Odd- and even-numbered medium-chained fatty acids protect against glutathione depletion in very long-chain acyl-CoA dehydrogenase deficiencyMartin Lund, Robert Heaton, Iain P Hargreaves, et al.
Nanoscale|February 22, 2023
Performance of the nanopost single-photon source: beyond the single-mode modelMartin Arentoft Jacobsen, Yujing Wang, Luca Vannucci, et al.
International Journal of Molecular Sciences|June 3, 2020
Riboflavin Deficiency-Implications for General Human Health and Inborn Errors of MetabolismSigne Mosegaard, Graziana Dipace, Peter Bross, et al.
Molecular Genetics and Metabolism|June 3, 2004
Homozygosity for a severe novel medium-chain acyl-CoA dehydrogenase (MCAD) mutation IVS3-1G > C that leads to introduction of a premature termination codon by complete missplicing of the MCAD mRNA and is associated with phenotypic diversity ranging from sudden neonatal death to asymptomatic statusStanley H Korman, Alisa Gutman, Rivka Brooks, et al.
Optics Express|March 27, 2021
Time-bin entangled photon pairs from quantum dots embedded in a self-aligned cavityLaia Ginés, Carlo Pepe, Junior Gonzales, et al.
Journal of Child Neurology|July 19, 2012
An infant with ethylmalonic encephalopathy masquerading as a hematologic disorderEvangelos Pavlou, Persephone Augoustides-Savvopoulou, Niels Gregersen, et al.
Human Mutation|June 20, 2003
Clear relationship between ETF/ETFDH genotype and phenotype in patients with multiple acyl-CoA dehydrogenation deficiencyRikke K J Olsen, Brage S Andresen, Ernst Christensen, et al.
Pituitary|June 15, 2012
A novel variation in the AVP gene resulting in familial neurohypophyseal diabetes insipidus in a large Italian kindredCamilla Birkegaard, Jane H Christensen, Alberto Falorni, et al.
NPJ 2D Materials and Applications|September 13, 2024
Tailoring polarization in WSe<sub>2</sub> quantum emitters through deterministic strain engineeringAthanasios Paralikis, Claudia Piccinini, Abdulmalik A Madigawa, et al.
Optics Letters|April 30, 2016
Spectral symmetry of Fano resonances in a waveguide coupled to a microcavityAndreas Dyhl Osterkryger, Jakob Rosenkrantz de Lasson, Mikkel Heuck, et al.
Pageof 17