Publications

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Malik, A. R., Szydlowska, K., Nizinska, K., Asaro, A., van Vliet, E. A., Popp, O., Dittmar, G., Fritsche-Guenther, R., Kirwan, J. A., Nykjaer, A., Lukasiuk, K., Aronica, E. & Willnow, T. E. (2019). SorCS2 Controls Functional Expression of Amino Acid Transporter EAAT3 and Protects Neurons from Oxidative Stress and Epilepsy-Induced Pathology. Cell Reports, 26(10), 2792-2804.e6. https://doi.org/10.1016/j.celrep.2019.02.027
Mann, V., Grimm, D., Corydon, T. J., Krüger, M., Wehland, M., Riwaldt, S., Sahana, J., Kopp, S., Bauer, J., Reseland, J. E., Infanger, M., Mari Lian, A., Okoro, E. & Sundaresan, A. (2019). Changes in Human Foetal Osteoblasts Exposed to the Random Positioning Machine and Bone Construct Tissue Engineering. International Journal of Molecular Sciences , 20(6), Article 1357. https://doi.org/10.3390/ijms20061357
Martin, R. M., Ikeda, K., Cromer, M. K., Uchida, N., Nishimura, T., Romano, R., Tong, A. J., Lemgart, V. T., Camarena, J., Pavel-Dinu, M., Sindhu, C., Wiebking, V., Vaidyanathan, S., Dever, D. P., Bak, R. O., Laustsen, A., Lesch, B. J., Jakobsen, M. R., Sebastiano, V. ... Porteus, M. H. (2019). Highly Efficient and Marker-free Genome Editing of Human Pluripotent Stem Cells by CRISPR-Cas9 RNP and AAV6 Donor-Mediated Homologous Recombination. Cell Stem Cell, 24(5), 821-828.e5. https://doi.org/10.1016/j.stem.2019.04.001
Matchkov, V. V., Duy, N. T., Rajanathan, R., Jeppesen, P. B., Bouzinova, E. & Staehr, C. (2019). An abundance of the Na,K-ATPase modulates homeostasis of blood glucose.. 134-134. Abstract from The Annual Meeting of The Scandinavian Physiological Society 2019, Reykjavik, Iceland.
Mavroeidi, P., Arvanitaki, F., Karakitsou, A.-K., Vetsi, M., Kloukina, I., Zweckstetter, M., Giller, K., Becker, S., Sorrentino, Z. A., Giasson, B. I., Jensen, P. H., Stefanis, L. & Xilouri, M. (2019). Endogenous oligodendroglial alpha-synuclein and TPPP/p25α orchestrate alpha-synuclein pathology in experimental multiple system atrophy models. Acta Neuropathologica, 138(3), 415-441. https://doi.org/10.1007/s00401-019-02014-y
Meier, S. M., Trontti, K., Purves, K. L., Als, T. D., Grove, J., Laine, M., Pedersen, M. G., Bybjerg-Grauholm, J., Bækved-Hansen, M., Sokolowska, E., Mortensen, P. B., Hougaard, D. M., Werge, T., Nordentoft, M., Breen, G., Børglum, A. D., Eley, T. C., Hovatta, I., Mattheisen, M. & Mors, O. (2019). Genetic Variants Associated With Anxiety and Stress-Related Disorders: A Genome-Wide Association Study and Mouse-Model Study. Archives of General Psychiatry, 76(9), 924-932. https://doi.org/10.1001/jamapsychiatry.2019.1119
Meier, M., Knudsen, A. R., Andersen, K. J., Ludvigsen, M., Eriksen, P. L., Honoré, B. & Mortensen, F. V. (2019). Upregulation of ureagenesis may be pivotal for survival of post-hepatectomy liver failure in rats. Poster session presented at 13th Congress of the European – African Hepato-Pancreato-Biliary Association, Amsterdam, Netherlands.
Migliorini, L. B., Brüggemann, H., de Sales, R. O., Koga, P. C. M., de Souza, A. V., Martino, M. D. V., Galhardo, R. S. & Severino, P. (2019). Mutagenesis Induced by Sub-Lethal Doses of Ciprofloxacin: Genotypic and Phenotypic Differences Between the Pseudomonas aeruginosa Strain PA14 and Clinical Isolates. Frontiers in Microbiology, 10, Article 1553. https://doi.org/10.3389/fmicb.2019.01553
Minchiotti, L., Caridi, G., Campagnoli, M., Lugani, F., Galliano, M. & Kragh-Hansen, U. (2019). Diagnosis, Phenotype, and Molecular Genetics of Congenital Analbuminemia. Frontiers in Genetics, 10(MAR), Article 336. https://doi.org/10.3389/fgene.2019.00336