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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.
Experimental Cell Research|September 5, 2013
The LMNA mutation p.Arg321Ter associated with dilated cardiomyopathy leads to reduced expression and a skewed ratio of lamin A and lamin C proteinsRasha Al-Saaidi, Torsten B Rasmussen, Johan Palmfeldt, 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.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|December 20, 2024
FDA Approval Summary: Nadofaragene Firadenovec-vncg for Bacillus Calmette-Guérin-Unresponsive Non-Muscle-Invasive Bladder CancerLaronna Colbert, Yuxia Jia, Anurag Sharma, 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.
Danish Medical Journal|January 8, 2020
Danish expanded newborn screening is a successful preventive public health programmeAllan Lund, Flemming Wibrand, Kristin Skogstrand, et al.
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