Laustsen, M. M., Nørgaard, M., Lam, M. Q., Koefoed-Nielsen, P. & Staunstrup, N. H. (2022). The novel HLA class I allele, HLA-B*14:110, identified by next-generation sequencing. HLA, 100(5), 520-522. https://doi.org/10.1111/tan.14721

Le, L. T. M., Drakulic, S., Nyengaard, J. R., Golas, M. M. & Sander, B. (2022). Structural Organization of Human Full-Length PAR3 and the aPKC–PAR6 Complex. Molecular Biotechnology, 64(12), 1319-1327. https://doi.org/10.1007/s12033-022-00504-1

Leegaard, A., Gregersen, P. A., Nielsen, T., Bjerre, J. V. & Handrup, M. M. (2022). Succesful MEK-inhibition of severe hypertrophic cardiomyopathy in RIT1-related Noonan Syndrome. European Journal of Medical Genetics, 65(11), Article 104630. https://doi.org/10.1016/j.ejmg.2022.104630

DBDS Genomic Consortium (2022). Established risk loci for systemic lupus erythematosus at NCF2, STAT4, TNPO3, IRF5 and ITGAM associate with distinct clinical manifestations: A Danish genome-wide association study. Joint Bone Spine, 89(4), Article 105357. https://doi.org/10.1016/j.jbspin.2022.105357

Leth Bergholt, N., Demirel, A., Pedersen, M., Ding, M., Kragstrup, T. W., Andersen, T., Deleuran, B. W. & Foldager, C. B. (2022). Intermittent hypoxic therapy inhibits allogenic bone-graft resorption by inhibition of osteoclastogenesis in a mouse model. International Journal of Molecular Sciences , 23(1), Article 323. https://doi.org/10.3390/ijms23010323

Li, Z., Sun, C., Wang, F., Wang, X., Zhu, J., Luo, L., Ding, X., Zhang, Y., Ding, P., Wang, H., Pu, M., Li, Y., Wang, S., Qin, Q., Wei, Y., Sun, J., Wang, X., Luo, Y., Chen, D. & Qiu, W. (2022). Molecular mechanisms governing circulating immune cell heterogeneity across different species revealed by single-cell sequencing. Clinical and Translational Medicine, 12(1), Article e689. https://doi.org/10.1002/ctm2.689

Li, C., Zhang, Y., Leng, L., Pan, X., Zhao, D., Li, X., Huang, J., Bolund, L., Lin, G., Luo, Y. & Xu, F. (2022). The single-cell expression profile of transposable elements and transcription factors in human early biparental and uniparental embryonic development. Frontiers in Cell and Developmental Biology, 10, Article 1020490. https://doi.org/10.3389/fcell.2022.1020490

Lima, C. N., Oliveira, W. F., Silva, P. M. M., Filho, P. E. C., Juul-Madsen, K., Moura, P., Vorup-Jensen, T. & Fontes, A. (2022). Mannose-binding lectin conjugated to quantum dots as fluorescent nanotools for carbohydrate tracing. Methods and Applications in Fluorescence, 10(2), Article 025002. https://doi.org/10.1088/2050-6120/ac4e72

Lindahl, L. M., Iversen, L., Ødum, N. & Kilian, M. (2022). Staphylococcus aureus and Antibiotics in Cutaneous T-Cell Lymphoma. Dermatology, 238(3), 551-553. https://doi.org/10.1159/000517829

Lissel Isaksson, G., Bodilsen Nielsen, M., Hinrichs, G. R., Krogstrup, N. V., Zachar, R., Stubmark, H., Svenningsen, P., Madsen, K., Bistrup, C., Jespersen, B., Birn, H., Palarasah, Y. & Jensen, B. L. (2022). Proteinuria is accompanied by intratubular complement activation and apical membrane deposition of C3dg and C5b-9 in kidney transplant recipients. American Journal of Physiology: Renal Physiology, 322(2), F150-F163. https://doi.org/10.1152/ajprenal.00300.2021

Liu, C. C., Kim, Y. J., Teh, R., Garcia, A., Hamilton, E. J., Cornelius, F., Baxter, R. C. & Rasmussen, H. H. (2022). Displacement of Native FXYD Protein From Na⁺/K⁺-ATPase With Novel FXYD Peptide Derivatives: Effects on Doxorubicin Cytotoxicity. Frontiers in Oncology, 12, Article 859216. https://doi.org/10.3389/fonc.2022.859216

Lomholt, S. & Kragstrup, T. W. (2022). POS0420 A 10-COLOR FLOW CYTOMETRIC PANEL FOR IDENTIFYING SYNOVIAL FIBROBLAST SUBSETS IN RHEUMATOID ARTHRITIS. Annals of the Rheumatic Diseases, 81(Suppl 1), 465-465. https://doi.org/10.1136/annrheumdis-2022-eular.2119

Loucif, H., Dagenais-Lussier, X., Avizonis, D., Choinière, L., Beji, C., Cassin, L., Routy, J.-P., Fritz, J. H., Olagnier, D. & van Grevenynghe, J. (2022). Autophagy-dependent glutaminolysis drives superior IL21 production in HIV-1-specific CD4 T cells. Autophagy, 18(6), 1256-1273. https://doi.org/10.1080/15548627.2021.1972403

Louise M Binderup, M., Smerdel, M., Borgwadt, L., Beck Nielsen, S. S., Madsen, M. G., Møller, H. U., Kiilgaard, J. F., Friis-Hansen, L., Harbud, V., Cortnum, S., Owen, H., Gimsing, S., Friis Juhl, H. A., Munthe, S., Geilswijk, M., Rasmussen, Å. K., Møldrup, U., Graumann, O., Donskov, F. ... Sunde, L. (2022). von Hippel-Lindau disease: Updated guideline for diagnosis and surveillance. European Journal of Medical Genetics, 65(8), Article 104538. https://doi.org/10.1016/j.ejmg.2022.104538

Łuczkowska, K., Taryma-Leśniak, O., Bińkowski, J., Sokołowska, K. E., Strapagiel, D., Jarczak, J., Paczkowska, E., Machaliński, B. & Wojdacz, T. K. (2022). Long-Term Treatment with Bortezomib Induces Specific Methylation Changes in Differentiated Neuronal Cells. Cancers, 14(14), Article 3402. https://doi.org/10.3390/cancers14143402

Lv, W., Pan, X., Han, P., Wang, Z., Feng, W., Xing, X., Wang, Q., Qu, K., Zeng, Y., Zhang, C., Xu, Z., Li, Y., Zheng, T., Lin, L., Liu, C., Liu, X., Li, H., Henriksen, R. A., Bolund, L. ... Luo, Y. (2022). Circle-Seq reveals genomic and disease-specific hallmarks in urinary cell-free extrachromosomal circular DNAs. Clinical and Translational Medicine, 12(4), Article e817. https://doi.org/10.1002/ctm2.817

Maccio, U., Mihic, A., Lenggenhager, D., Kolm, I., Mittmann, C., Heikenwälder, M., Lorentzen, A. & Mihic-Probst, D. (2022). Hypoxia and Ezrin Expression in Primary Melanoma Have High Prognostic Relevance. International Journal of Molecular Sciences , 23(18), Article 10745. https://doi.org/10.3390/ijms231810745

Magalhaes-Novais, S., Blecha, J., Naraine, R., Mikesova, J., Abaffy, P., Pecinova, A., Milosevic, M., Bohuslavova, R., Prochazka, J., Khan, S., Novotna, E., Sindelka, R., Machan, R., Dewerchin, M., Vlcak, E., Kalucka, J., Stemberkova Hubackova, S., Benda, A., Goveia, J. ... Rohlena, J. (2022). Mitochondrial respiration supports autophagy to provide stress resistance during quiescence. Autophagy, 18(10), 2409-2426. https://doi.org/10.1080/15548627.2022.2038898

Mahjani, B., Klei, L., Mattheisen, M., Halvorsen, M. W., Reichenberg, A., Roeder, K., Pedersen, N. L., Boberg, J., de Schipper, E., Bulik, C. M., Landén, M., Fundín, B., Mataix-Cols, D., Sandin, S., Hultman, C. M., Crowley, J. J., Buxbaum, J. D., Rück, C., Devlin, B. & Grice, D. E. (2022). The Genetic Architecture of Obsessive-Compulsive Disorder: Contribution of Liability to OCD From Alleles Across the Frequency Spectrum. American Journal of Psychiatry, 179(3), 216-225. https://doi.org/10.1176/appi.ajp.2021.21010101

Maihofer, A. X., Choi, K. W., Coleman, J. R. I., Daskalakis, N. P., Denckla, C. A., Ketema, E., Morey, R. A., Polimanti, R., Ratanatharathorn, A., Torres, K., Wingo, A. P., Zai, C. C., Aiello, A. E., Almli, L. M., Amstadter, A. B., Andersen, S. B., Andreassen, O. A., Arbisi, P. A., Ashley-Koch, A. E. ... Nievergelt, C. M. (2022). Enhancing Discovery of Genetic Variants for Posttraumatic Stress Disorder Through Integration of Quantitative Phenotypes and Trauma Exposure Information. Biological Psychiatry, 91(7), 626-636. https://doi.org/10.1016/j.biopsych.2021.09.020