A novel heterozygous variant in ERLIN2 causes autosomal dominant pure hereditary spastic paraplegia von Rydning, S. L., Dudesek, A., Rimmele, F., Funke, C., Krüger, S., Biskup, S., Vigeland, M. D., Hjorthaug, H. S., Sejersted, Y., Tallaksen, C., Selmer, K. K., Kamm, C.

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Genetic and clinical variations in a Norwegian sample diagnosed with Rett syndrome von Henriksen, Mari Wold, Breck, Hilde, Sejersted, Yngve, Diseth, Trond, von Tetzchner, Stephen, Paus, Benedicte, Skjeldal, Ola H.

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Whole Genome Expression in Newborn Mouse Brain Tissue after Hypoxia and Reoxygenation von Wollen, E J, Wright, M S, Gunther, C -C, Bik-Multanowski, M, Madetko-Talowska, A, Sejersted, Y, Kwinta, P, Pietrzyk, J J, Saugstad, O D

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349 Hypoxia and Reoxygenation Induce Alterations in Whole Genome Expression in Lung Tissue of the Newborn Mouse von Wollen, E J, Sejersted, Y, Wright, M S, Gunther, C C, Pietrzyk, J J, Bik-Multanowski, M, Madetko-Talowska, A, Kwinta, P, Saugstad, O D

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Stretch Harmonizes Sarcomere Strain Across the Cardiomyocyte von Li, Jia, Sundnes, Joakim, Hou, Yufeng, Laasmaa, Martin, Ruud, Marianne, Unger, Andreas, Kolstad, Terje R., Frisk, Michael, Norseng, Per Andreas, Yang, Limin, Setterberg, Ingunn E., Alves, Estela S., Kalakoutis, Michaeljohn, Sejersted, Ole M., Lanner, Johanna T., Linke, Wolfgang A., Lunde, Ida G., de Tombe, Pieter P., Louch, William E.

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Silicon Nanoparticle Ensembles for Lithium-Ion Batteries Elucidated by Small-Angle Neutron Scattering von Lai, Samson Y, Knudsen, Kenneth D, Sejersted, Benjamin T, Ulvestad, Asbjørn, Mæhlen, Jan Petter, Koposov, Alexey Y

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Mice carrying a conditional Serca2 super(f) super(l) super(o) super(x) allele for the generation of Ca super(2) super(+) handling-deficient mouse models von Andersson, K B, Finsen, A V, Sjaland, C, Winer, L H, Sjaastad, I, Odegaard, A, Louch, W E, Wang, Y, Chen, J, Chien, K R, Sejersted, OM, Christensen, G

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