Researcher Portfolio

Heninger, Anne-Kristin

Max Planck Institute of Molecular Cell Biology and Genetics, Max Planck Society

Researcher Profile

Position: Max Planck Institute of Molecular Cell Biology and Genetics, Max Planck Society

Researcher ID: https://pure.mpg.de/cone/persons/resource/persons219235

External references

WorldCat Search for Heninger, Anne-Kristin

Google Scholar Search for Heninger, Anne-Kristin

Publications

: Spiegel, A., Lauber, C., Bachmann, M., Heninger, A.-K., Klose, C., Simons, K., Sarov, M., & Gerl, M. J. (2022). A set of gene knockouts as a resource for global lipidomic changes. Scientific reports, 12(1): 10533. doi:10.1038/s41598-022-14690-0. [PubMan] : Schubert, T., Reisch, N., Naumann, R., Reichardt, I., Landgraf, D., Quitter, F., Thirumalasetty, S. R., Heninger, A.-K., Sarov, M., Peitzsch, M., Huebner, A., & Koehler, K. (2022). CYP21A2 Gene Expression in a Humanized 21-Hydroxylase Mouse Model Does Not Affect Adrenocortical Morphology and Function. Journal of the Endocrine Society, 6(6): bvac062. doi:10.1210/jendso/bvac062. [PubMan] : Vaid, S., Camp, J. G., Hersemann, L., Oegema, C. E., Heninger, A.-K., Winkler, S., Brandl, H., Sarov, M., Treutlein, B., Huttner, W., & Namba, T. (2018). A novel population of Hopx-dependent basal radial glial cells in the developing mouse neocortex. Development (Cambridge, England), 145(20): dev169276. doi:10.1242/dev.169276. [PubMan] : Eugster, A., Lindner, A., Catani, M., Heninger, A.-K., Dahl, A., Klemroth, S., Kühn, D., Dietz, S. M., Bickle, M., Ziegler, A.-G., & Bonifacio, E. (2015). High Diversity in the TCR Repertoire of GAD65 Autoantigen-Specific Human CD4+ T Cells. Journal of Immunology (Baltimore, Md.: 1950), 194(6), 2531-2538. [PubMan] : Slabicki, M., Theis, M., Krastev, D., Samsonov, S., Mundwiller, E., Junqueira, M., Paszkowski-Rogacz, M., Teyra, J., Heninger, A.-K., Poser, I., Prieur, F., Truchetto, J., Confavreux, C., Marelli, C., Durr, A., Camdessanche, J. P., Brice, A., Shevchenko, A., Pisabarro, M. T., Stevanin, G., & Buchholz, F. (2010). A genome-scale DNA repair RNAi screen identifies SPG48 as a novel gene associated with hereditary spastic paraplegia. PLoS Biology, 8(6): e1000408. [PubMan] : Ding, L., Paszkowski-Rogacz, M., Nitzsche, A., Slabicki, M. M., Heninger, A.-K., Vries, I. d., Kittler, R., Junqueira, M., Shevchenko, A., Schulz, H., Hubner, N., Doss, M. X., Sachinidis, A., Hescheler, J., Iacone, R., Anastassiadis, K., Stewart, A. F., Pisabarro, M. T., Caldarelli, A., Poser, I., Theis, M., & Buchholz, F. (2009). A genome-scale RNAi screen for Oct4 modulators defines a role of the Paf1 complex for embryonic stem cell identity. Cell Stem Cell, 4(5), 403-415. [PubMan] : Kittler, R., Surendranath, V., Heninger, A.-K., Slabicki, M., Theis, M., Putz, G., Franke, K., Caldarelli, A., Grabner, H., Kozak, K., Wagner, J., Rees, E., Korn, B., Frenzel, C., Sachse, C., Sönnichsen, B., Guo, J., Schelter, J., Burchard, J., Linsley, P. S., Jackson, A. L., Habermann, B., & Buchholz, F. (2007). Genome-wide resources of endoribonuclease-prepared short interfering RNAs for specific loss-of-function studies. Nature Methods, 4(4), 337-344. [PubMan] : Heninger, A.-K., Kozak, K., Kittler, R., Wagner, J., Lohmann, A., Poser, I., Grabner, H., Krausz, E., & Buchholz, F. (2006). RNAi Libraries for Functional Genomics. Genetic Engineering News, 26(19), 22-23. [PubMan] : Kittler, R., Putz, G., Pelletier, L., Poser, I., Heninger, A.-K., Drechsel, D., Fischer, S., Konstantinova, I., Habermann, B., Grabner, H., Yaspo, M.-L., Himmelbauer, H., Korn, B., Neugebauer, K., Pisabarro, M. T., & Buchholz, F. (2004). An endoribonuclease-prepared siRNA screen in human cells identifies genes essential for cell division. Nature, 432(7020), 1036-1040. [PubMan]