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Cell Stress & Chaperones|January 5, 2023
Second Virtual International Symposium on Cellular and Organismal Stress Responses, September 8-9, 2022Patricija van Oosten-Hawle, Sarah J Backe, Anat Ben-Zvi, et al.Diabetes|January 11, 2019
ADAMTS9 Regulates Skeletal Muscle Insulin Sensitivity Through Extracellular Matrix AlterationsAnne-Sofie Graae, Niels Grarup, Rasmus Ribel-Madsen, et al.Brain : a Journal of Neurology|February 2, 2023
BCKDK deficiency: a treatable neurodevelopmental disease amenable to newborn screeningTrine Tangeraas, Juliana R Constante, Paul Hoff Backe, et al.European Journal of Human Genetics : EJHG|January 19, 2018
Biallelic variants in KIF14 cause intellectual disability with microcephalyPeriklis Makrythanasis, Reza Maroofian, Asbjørg Stray-Pedersen, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 17, 2026
Biallelic SUPT4H1 Variants Cause a Multisystem Neurodevelopmental Disorder Associated with Disrupted TranscriptionChristina Canavati, Mari Oppebøen, Radha Verma, et al.Physical Review Letters|June 23, 2018
Probing Sizes and Shapes of Nobelium Isotopes by Laser SpectroscopyS Raeder, D Ackermann, H Backe, et al.American Journal of Human Genetics|June 17, 2014
PGM3 mutations cause a congenital disorder of glycosylation with severe immunodeficiency and skeletal dysplasiaAsbjørg Stray-Pedersen, Paul H Backe, Hanne S Sorte, et al.Pageof 24