Suchergebnisse

Gajos, M.; Jasnovidova, O.; van Bömmel, A.; Freier, S.; Vingron, M.; Mayer, A.: Conserved DNA sequence features underlie pervasive RNA polymerase pausing. Nucleic Acids Research (London) 49 (8), S. 4402 - 4420 (2021)

Voisin, N.; Schnur, R. E.; Douzgou , S.; Hiatt, S. M.; Rustad, C. F.; Brown, N. J.; Earl, D. L.; Keren, B.; Levchenko, O.; Geuer, S. et al.; Verheyen, S.; Johnson , D.; Zarate, Y. A.; Hančárová, M.; Amor, D. J.; Bebin, E. M.; Blatterer, J.; Brusco, A.; Cappuccio, G.; Charrow, J.; Chatron, N.; Cooper, G. M.; Courtin, T.; Dadali, E.; Delafontaine, J.; Del Giudice, E.; Doco, M.; Douglas, G.; Eisenkölbl, A.; Funari, T.; Giannuzzi , G.; Gruber-Sedlmayr, U.; Guex, N.; Heron, D.; Holla, Ø. L.; Hurst, A. C. E.; Juusola, J.; Kronn, D.; Lavrov, A.; Lee, C.; Lorrain, S.; Merckoll, E.; Mikhaleva, A.; Norman, J.; Pradervand, S.; Prchalová, D.; Rhodes, L.; Sanders , V. R.; Sedláček, Z.; Seebacher , H. A.; Sellars, E. A.; Sirchia, F.; Takenouchi, T.; Tanaka, A. J.; Taska-Tench, H.; Tønne, E.; Tveten, K.; Vitiello, G.; Vlčková , M.; Uehara, T.; Nava, C.; Yalcin, B.; Kosaki, K.; Donnai, D.; Mundlos, S.; Brunetti-Pierri, N.; Chung, W. K.; Reymond, A.: Variants in the degron of AFF3 are associated with intellectual disability, mesomelic dysplasia, horseshoe kidney, and epileptic encephalopathy. The American Journal of Human Genetics 108 (5), S. 857 - 873 (2021)

Hübschmann, D.; Kleinheinz, K.; Wagener, R.; Bernhart, S. H.; López, C.; Toprak, U. H.; Sungalee, S.; Ishaque, N.; Kretzmer, H.; Kreuz, M. et al.; Waszak, S. M.; Paramasivam, N.; Ammerpohl, O.; Aukema, S. M.; Beekman, R.; Bergmann, A. K.; Bieg, M.; Binder, H.; Borkhardt, A.; Borst, C.; Brors, B.; Bruns, P.; de Santa Pau, E. C.; Claviez, A.; Doose, G.; Haake, A.; Karsch, D.; Haas, S.; Hansmann, M.-L.; Hoell, J. I.; Hovestadt, V.; Huang, B.; Hummel, M.; Jäger-Schmidt, C.; Kerssemakers, J. N. A.; Korbel, J. O.; Kube, D.; Lawerenz, C.; Lenze, D.; Martens, J. H. A.; Ott, G.; Radlwimmer, B.; Reisinger, E.; Richter, J.; Rico, D.; Rosenstiel, P.; Rosenwald, A.; Schillhabel, M.; Stilgenbauer, S.; Stadler, P. F.; Martín-Subero, J. I.; Szczepanowski, M.; Warsow, G.; Weniger, M. A.; Zapatka, M.; Valencia, A.; Stunnenberg, H. G.; Lichter, P.; Möller, P.; Loeffler, M.; Eils, R.; Klapper, W.; Hoffmann, S.; Trümper, L.; ICGC MMML-Seq consortium; ICGC DE-Mining consortium; BLUEPRINT consortium; Küppers, R.; Schlesner, M.; Siebert, R.: Mutational mechanisms shaping the coding and noncoding genome of germinal center derived B-cell lymphomas. Leukemia: the Journal of Normal and Malignant Hemopoiese ; Official Journal of the Leukemia Research Fund U.K. 35 (7), S. 2002 - 2016 (2021)

Roch, T.; Giesecke-Thiel, C.; Blazquez-Navarro, A.; Wehler, P.; Thieme, C. J.; Juelke, K.; Grütz, G.; Hörstrup, J.; Witzke, O.; Dittmer, U. et al.; Stervbo, U.; Reinke, P.; Westhoff, T. H.; Babel, N.: Generation of HBsAg-reactive T- and B-cells following HBV vaccination in serological non-responders under hemodialysis treatment. European Journal of Immunology 51 (5), S. 1278 - 1281 (2021)

Pivovarova-Ramich, O.; Loske, J.; Hornemann, S.; Markova, M.; Seebeck, N.; Rosenthal, A.; Klauschen, F.; Castro, J. P.; Buschow, R.; Grune, T. et al.; Lange, V.; Rudovich, N.; Ouwens, D. M.: Hepatic Wnt1 Inducible Signaling Pathway Protein 1 (WISP-1/CCN4) Associates with Markers of Liver Fibrosis in Severe Obesity. Cells 10, 1048 (2021)

Azouz, N. P.; Klingler, A. M.; Callahan, V.; Akhrymuk, I. V.; Elez, K.; Raich, L.; Henry, B. M.; Benoit, J. L.; Benoit, S. W.; Noé, F. et al.; Kehn-Hall, K.; Rothenberg, M. E.: Alpha 1 Antitrypsin is an Inhibitor of the SARS-CoV-2–Priming Protease TMPRSS2. Pathogens and Immunity 6 (6), S. 55 - 74 (2021)

Genolet, O.; Monaco, A. A.; Dunkel, I.; Boettcher, M.; Schulz, E. G.: Identification of X-chromosomal genes that drive sex differences in embryonic stem cells through a hierarchical CRISPR screening approach. Genome Biology 22, 110 (2021)

Schreyer, S.; Berndt, N.; Eckstein, J.; Mülleder, M.; Hemmati-Sadeghi, S.; Klein, C.; Abuelnor, B.; Panzel, A.; Meierhofer, D.; Spranger, J. et al.; Steiner, B.; Brachs, S.: Dietary-challenged mice with Alzheimer-like pathology show increased energy expenditure and reduced adipocyte hypertrophy and steatosis. Aging 13 (8), S. 10891 - 10919 (2021)

Knudsen, T. B.; Spielmann, M.; Megason, S. G.; Faustman, E. M.: Single-cell profiling for advancing birth defects research and prevention. Birth Defects Research 113 (7), S. 546 - 559 (2021)

Berndt, N.; Eckstein, J.; Heucke, N.; Wuensch, T.; Gajowski, R.; Stockmann, M.; Meierhofer, D.; Holzhütter, H.-G.: Metabolic Heterogeneity of Human Hepatocellular Carcinoma (HCC): Implications for Personalized Pharmacological Treatment. The FEBS Journal 288 (7), S. 2332 - 2346 (2021)

Inak, G.; Rybak-Wolf, A.; Lisowski, P.; Pentimalli, T. M.; Jüttner, R.; Glažar, P.; Uppal, K.; Bottani, E.; Brunetti, D.; Secker, C. et al.; Zink, A.; Meierhofer, D.; Henke , M.-T.; Dey, M.; Ciptasar, U.; Mlody, B.; Hahn, T.; Berruezo-Llacuna, M.; Karaiskos, N.; Di Virgilio, M.; Mayr, J. A.; Wortmann, S. B.; Priller , J.; Gotthardt, M.; Jones , D. P.; Mayatepek, E.; Stenzel, W.; Diecke, S.; Kühn, R.; Wanker , E. E.; Rajewsky, N.; Schuelke, M.; Prigione, A.: Defective metabolic programming impairs early neuronal morphogenesis in neural cultures and an organoid model of Leigh syndrome. Nature Communications 12, 1929 (2021)

Pooryasin, A.; Maglione, M.; Schubert, M.; Matkovic-Rachid, T.; Hasheminasab, S.-M.; Pech, U.; Fiala, A.; Mielke, T.; Sigrist, S. J.: Unc13A and Unc13B contribute to the decoding of distinct sensory information in Drosophila. Nature Communications (12), 1932 (2021)

Benner, P.: Computing Leapfrog Regularization Paths with Applications to Large-Scale K-mer Logistic Regression. Journal of Computational Biology 28 (6), S. 560 - 569 (2021)

Nikolay, R.; Hilal, T.; Schmidt, S.; Qin, B.; Schwefel, D.; Vieira-Vieira, C. H.; Mielke, T.; Bürger, J.: Snapshots of native pre-50S ribosomes reveal a biogenesis factor network and evolutionary specialization. Molecular Cell 81 (6), S. 1200 - 1215 (2021)

Annaldasula, S.; Gajos, M.; Mayer, A.: IsoTV: processing and visualizing functional features of translated transcript isoforms. Bioinformatics 37 (18), S. 3070 - 3072 (2021)

Allou, L.; Balzano, S.; Magg, A.; Quinodoz, M.; Royer-Bertrand, B.; Schöpflin, R.; Chan, W.-L.; Speck-Martins, C. E.; Rocha Carvalho, D.; Farage, L. et al.; Marques Lourenço, C.; Albuquerque, R.; Rajagopal, S.; Nampoothiri, S.; Campos-Xavier, B.; Chiesa, C.; Niel-Bütschi, F.; Wittler, L.; Timmermann, B.; Spielmann, M.; Robson, M.; Ringel, A.; Heinrich, V.; Cova, G.; Andrey , G.; Prada-Medina, C. A.; Pescini-Gobert, R.; Unger, S.; Bonafé, L.; Grote, P.; Rivolta, C.; Mundlos, S.; Superti-Furga, A.: Non-coding deletions identify Maenli lncRNA as a limb-specific En1 regulator. Nature 592 (7852), S. 93 - 98 (2021)

Panconesi, R.; Mauricio , F. C.; Mueller, M.; Meierhofer, D.; Dutkowski, P.; Muiesan, P.; Schlegel, A.: Viability Assessment in Liver Transplantation—What Is the Impact of Dynamic Organ Preservation? Biomedicines 9 (2), 161 (2021)

Amaral, A.; Herrmann, B. G.: RAC1 controls progressive movement and competitiveness of mammalian spermatozoa. PLoS Genetics 17 (2), e1009308 (2021)

Berndt, N.; Kolbe, E.; Gajowski, R.; Eckstein, J.; Ott, F.; Meierhofer, D.; Holzhütter, H. G.; Matz‐Soja, M.: Functional consequences of metabolic zonation in murine livers: New insights for an old story. Hepatology 73 (2), HEP-19-1360, S. 795 - 810 (2021)

Reichenbach, M.; Mendez, P.-L.; da Silva Madaleno, C.; Ugorets, V.; Rikeit, P.; Boerno, S.; Jatzlau, J.; Knaus, P.: Differential Impact of Fluid Shear Stress and YAP/TAZ on BMP/TGF-β Induced Osteogenic Target Genes. Advanced Biology 5 (2), 2000051 (2021)