Bergmann, T., Liu, Y., Skov, J., Mogus, L., Lee, J., Pfisterer, U., Handfield, L. F., Asenjo-Martinez, A., Lisa-Vargas, I., Seemann, S. E., Lee, J. T. H., Patikas, N., Kornum, B. R.
, Denham, M., Hyttel, P., Witter, M. P., Gorodkin, J., Pers, T. H., Hemberg, M. ... Hall, V. J. (2022).
Production of human entorhinal stellate cell-like cells by forward programming shows an important role of Foxp1 in reprogramming.
Frontiers in Cell and Developmental Biology,
10, Article 976549.
https://doi.org/10.3389/fcell.2022.976549
Reimer, L., Gram, H., Jensen, N. M., Betzer, C., Yang, L., Jin, L., Shi, M., Boudeffa, D., Fusco, G., De Simone, A., Kirik, D., Lashuel, H. A., Zhang, J.
& Jensen, P. H. (2022).
Protein kinase R dependent phosphorylation of α-synuclein regulates its membrane binding and aggregation.
PNAS Nexus,
1(5), Article pgac259.
https://doi.org/10.1093/pnasnexus/pgac259
Singh, T., Poterba, T., Curtis, D., Akil, H., Al Eissa, M., Barchas, J. D., Bass, N., Bigdeli, T. B., Breen, G., Bromet, E. J., Buckley, P. F., Bunney, W. E., Bybjerg-Grauholm, J., Byerley, W. F., Chapman, S. B., Chen, W. J., Churchhouse, C., Craddock, N., Cusick, C. M. ... Daly, M. J. (2022).
Rare coding variants in ten genes confer substantial risk for schizophrenia.
Nature,
604(7906), 509-516.
https://doi.org/10.1038/s41586-022-04556-w
Ardalan, M., Chumak, T., Quist, A., Hermans, E.
, H.Rafati, A., Gravina, G., Marziyeh Jabbari Shiadeh, S., Svedin, P., Alabaf, S.
, Hansen, B., Wegener, G., Westberg, L. & Mallard, C. (2022).
Reelin cells and sex-dependent synaptopathology in autism following postnatal immune activation.
British Journal of Pharmacology,
179(17), 4400-4422.
https://doi.org/10.1111/bph.15859