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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.
Current Medicinal Chemistry|September 23, 2010
Emerging roles for riboflavin in functional rescue of mitochondrial β-oxidation flavoenzymesBárbara J Henriques, Rikke K Olsen, Peter Bross, et al.
FEBS Letters|January 12, 2011
A polymorphic position in electron transfer flavoprotein modulates kinetic stability as evidenced by thermal stressBárbara J Henriques, Mark T Fisher, Peter Bross, 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.
Neonatology|July 20, 2018
Biomarker Discovery by Mass Spectrometry in Cerebrospinal Fluid and Plasma after Global Hypoxia-Ischemia in Newborn PigletsKasper Jacobsen Kyng, Anders Valdemar Edhager, Tine Brink Henriksen, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease|February 7, 2021
Bezafibrate activation of PPAR drives disturbances in mitochondrial redox bioenergetics and decreases the viability of cells from patients with VLCAD deficiencyMartin Lund, Kathrine G Andersen, Robert Heaton, et al.
Optics Express|April 11, 2014
Bright single photon source based on self-aligned quantum dot-cavity systemsSebastian Maier, Peter Gold, Alfred Forchel, et al.
The Journal of Clinical Endocrinology and Metabolism|July 11, 2002
Autosomal dominant neurohypophyseal diabetes insipidus due to substitution of histidine for tyrosine(2) in the vasopressin moiety of the hormone precursorSøren Rittig, Charlotte Siggaard, Metin Ozata, et al.
Gene|January 15, 2021
Electron transfer flavoprotein and its role in mitochondrial energy metabolism in health and diseaseBárbara J Henriques, Rikke Katrine Jentoft Olsen, Cláudio M Gomes, et al.
Clinical Endocrinology|December 18, 2003
Impaired trafficking of mutated AVP prohormone in cells expressing rare disease genes causing autosomal dominant familial neurohypophyseal diabetes insipidusJane H Christensen, Charlotte Siggaard, Thomas J Corydon, et al.
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