Journal Article (72)

21.
Journal Article
Selevsek, N.; Caiment, F.; Nudischer, R.; Gmuender, H.; Agarkova, I.; Atkinson, F. L.; Bachmann, I.; Baier, V.; Barel, G.; Bauer, C. et al.; Boerno, S.; Bosc, N.; Clayton, O.; Cordes, H.; Deeb, S.; Gotta, S.; Guye, P.; Hersey, A.; Hunter, F. M. I.; Kunz, L.; Lewalle, A.; Lienhard, M.; Merken, J.; Minguet, J.; Oliveira, B.; Pluess, C.; Sarkans, U.; Schrooders, Y.; Schuchhardt, J.; Smit, I.; Thiel, C.; Timmermann, B.; Verheijen, M.; Wittenberger, T.; Wolski, W.; Zerck, A.; Heymans, S.; Kuepfer, L.; Roth, A.; Schlapbach, R.; Niederer, S.; Herwig, R.; Kleinjans, J.: Network integration and modelling of dynamic drug responses at multi-omics levels. Communications Biology 3, 573 (2020)
22.
Journal Article
Real, F. M.; Haas, S. A.; Franchini, P.; Xiong, P.; Simakov, O.; Kuhl, H.; Schöpflin, R.; Heller, D.; Moeinzadeh, M. H.; Heinrich, V. et al.; Krannich , T.; Bressin, A.; Hartmann, M. F.; Wudy, S. A.; Dechmann, D. K. N.; Hurtado, A.; Barrionuevo, F. J.; Schindler, M.; Harabula, I.; Osterwalder, M.; Hiller, M.; Wittler, L.; Visel, A.; Timmermann, B.; Meyer, A.; Vingron, M.; Jiménez, R.; Mundlos, S.; Lupiáñez, D. G.: The mole genome reveals regulatory rearrangements associated with adaptive intersexuality. Science 370 (6513), pp. 208 - 214 (2020)
23.
Journal Article
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 2020, 15587 (2020)
24.
Journal Article
Key, J.; Sen, N. E.; Arsović , A.; Krämer, S.; Hülse, R.; Khan, N. N.; Meierhofer, D.; Gispert, S.; Koepf, G.; Auburger, G.: Systematic Surveys of Iron Homeostasis Mechanisms Reveal Ferritin Superfamily and Nucleotide Surveillance Regulation to be Modified by PINK1 Absence. Cells 9 (10), 2229 (2020)
25.
Journal Article
Aparicio-Soto, M.; Riedel, F.; Leddermann, M.; Bacher, P.; Scheffold, A.; Kuhl, H.; Timmermann, B.; Chudakov, D. M.; Molin, S.; Worm, M. et al.; Heine, G.; Thierse, H.-J.; Luch, A.; Siewert, K.: TCRs with segment TRAV9-2 or a CDR3 histidine are overrepresented among nickel-specific CD4+ T cells. Allergy 75 (10), pp. 2574 - 2586 (2020)
26.
Journal Article
Espindola-Hernandez, P.; Mueller, J. C.; Carrete, M.; Boerno, S.; Kempenaers, B.: Genomic evidence for sensorial adaptations to a nocturnal predatory lifestyle in owls. Genome Biology and Evolution 12 (10), pp. 1895 - 1908 (2020)
27.
Journal Article
Grozdanov, P. N.; Masoumzadeh, E.; Kalscheuer, V. M.; Bienvenu, T.; Billuart, P.; Delrue, M.-A.; Latham, M. P.; MacDonald, C. C.: A missense mutation in the CSTF2 gene that impairs the function of the RNA recognition motif and causes defects in 3' end processing is associated with intellectual disability in humans. Nucleic Acids Research (London) 48 (17), pp. 9804 - 9821 (2020)
28.
Journal Article
Schlegel, A.; Muller, X.; Mueller, M.; Stepanova, A.; Kron, P.; de Rougemont, O.; Muiesan, P.; Clavien, P.-A.; Galkin, A.; Meierhofer, D. et al.; Dutkowski, P.: Hypothermic oxygenated perfusion protects from mitochondrial injury before liver transplantation. EBioMedicine 60, 103014 (2020)
29.
Journal Article
Beheshtian, M.; Akhtarkhavari, T.; Mehvari, S.; Mohseni, M.; Fattahi, Z.; Abedini, S. S.; Arzhangi , S.; Fadaee, M.; Jamali , P.; Najafipour, R. et al.; Kalscheuer, V. M.; Hu, H.; Ropers, H.-H.; Najmabadi, H.; Kahrizi, K.: Comprehensive genotype‐phenotype correlation in AP‐4 deficiency syndrome; Adding data from a large cohort of Iranian patients. Clinical Genetics: an international journal of genetics in medicine 2020, pp. 1 - 6 (2020)
30.
Journal Article
Bornhauser, B.; Cario, G.; Rinaldi, A.; Risch, T.; Rodriguez Martinez, V.; Schütte, M.; Warnatz, H.-J.; Scheidegger, N.; Mirkowska, P.; Temperli, M. et al.; Möller, C.; Schumich, A.; Dworzak, M.; Attarbaschi, A.; Brüggemann, M.; Ritgen, M.; Mejstrikova, E.; Hofmann, A.; Buldini, B.; Scarparo, P.; Basso, G.; Maglia, O.; Gaipa, G.; Skoblyn, T.-L.; te Kronnie, G.; Vendramini, E.; Panzer-Grümayer, R.; Barz, M. J.; Marovca, B.; Hauri-Hohl, M.; Niggli, F.; Eckert, C.; Schrappe, M.; Stanulla, M.; Zimmermann, M.; Wollscheid, B.; Yaspo, M.-L.; Bourquin, J.-P.: The hematopoietic stem cell marker VNN2 is associated with chemoresistance in pediatric B-cell precursor ALL. Blood Advances 17 (4), pp. 4052 - 4064 (2020)
31.
Journal Article
Suter , A.-A.; Santos-Simarro , F.; Mathiesen Toerring, P.; Abad Perez , A.; Ramos-Mejia, R.; Heath, K. E.; Huckstadt , V.; Parrón-Pajares, M.; Atta Mensah, M.; Hülsemann, W. et al.; Holtgrewe, M.; Mundlos, S.; Kornak, U.; Bartsch, O.; Ehmke, N.: Variable pulmonary manifestations in Chitayat syndrome: Six additional affected individuals. American Journal of Medical Genetics Part A 182 (9), pp. 2068 - 2076 (2020)
32.
Journal Article
Thibaut, F.; Hoehe, M. R.: Cannabinoids: for better and for worse. Dialogues in Clinical Neuroscience 22 (3), pp. 201 - 204 (2020)
33.
Journal Article
Hiepen, C.; Mendez, P.-L.; Knaus, P.: It Takes Two to Tango: Endothelial TGFβ/BMP Signaling Crosstalk with Mechanobiology. Cells 9 (9), 1965 (2020)
34.
Journal Article
Rieke, J. M.; Zhang, R.; Braun, D.; Yilmaz, Ö.; Japp, A. S.; Lopes, F. M.; Pleschka, M.; Hilger, A. C.; Schneider, S.; Newman, W. G. et al.; Beaman, G. M.; Nordenskjöld, A.; Ebert, A.-K.; Promm, M.; Roesch, W. H.; Stein, R.; Hirsch, K.; Schäfer, F.-M.; Schmiedeke, E.; Boemers, T. M.; Lacher, M.; Kluth, D.; Gosemann, J.-H.; Anderberg, M.; Barker, G.; Holmdahl, G.; Läckgren, G.; Keene, D.; Cervellione, R. M.; Giorgio, E.; Di Grazia, M.; Wouter, F. F. J.; Marcelis, C. L. M.; Van Rooij, I. A. L. M.; Bökenkamp, A.; Beckers, G. M. A.; Keegan, C. E.; Sharma, A.; Chand Dakal, T.; Wittler, L.; Grote, P.; Zwink, N.; Jenetzky, E.; Brusco, A.; Thiele, H.; Ludwig, M.; Schweizer, U.; Woolf, A. S.; Odermatt, B.; Reutter, H.: SLC20A1 Is Involved in Urinary Tract and Urorectal Development. Frontiers in Cell and Developmental Biology 8, 567 (2020)
35.
Journal Article
Grosswendt, S.; Kretzmer, H.; Smith, Z. D.; Sampath Kumar, A.; Hetzel, S.; Wittler, L.; Klages, S.; Timmermann, B.; Mukherji, S.; Meissner, A.: Epigenetic regulator function through mouse gastrulation. Nature 584, pp. 102 - 108 (2020)
36.
Journal Article
Charlton, J.; Jung, E. J.; Mattei, A. L.; Bailly, N.; Liao, J.; Martin, E. J.; Gießelmann, P.; Brändl, B.; Stamenova, E. K.; Müller, F.-J. et al.; Kiskinis, E.; Gnirke, A.; Smith, Z. D.; Meissner, A.: TETs compete with DNMT3 activity in pluripotent cells at thousands of methylated somatic enhancers. Nature Genetics 52 (8), pp. 819 - 827 (2020)
37.
Journal Article
Chua, R. L.; Lukassen, S.; Trump, S.; Hennig, B. P.; Wendisch, D.; Pott, F.; Debnath, O.; Thürmann, L.; Kurth, F.; Völker, M. T. et al.; Kazmierski, J.; Timmermann, B.; Twardziok, S.; Schneider, S.; Machleidt, F.; Müller-Redetzky, H.; Maier, M.; Krannich, A.; Schmidt, S.; Balzer, F.; Liebig, J.; Loske, J.; Suttorp, N.; Eils, J.; Ishaque, N.; Liebert, U. G.; von Kalle, C.; Hocke, A.; Witzenrath, M.; Goffinet, C.; Drosten, C.; Laudi, S.; Lehmann, I.; Conrad, C.; Sander, L.-E.; Eils, R.: COVID-19 severity correlates with airway epithelium-immune cell interactions identified by single-cell analysis. Nature Biotechnology 38 (8), pp. 970 - 979 (2020)
38.
Journal Article
Barel, G.; Herwig, R.: NetCore: a network propagation approach using node coreness. Nucleic Acids Research 48 (17), e98 (2020)
39.
Journal Article
The ENCODE Project Consortium; Snyder, M. P.; Gingeras, T. R.; Moore, J. E.; Weng, Z.; Gerstein, M. B.; Ren, B.; Hardison, R. C.; Stamatoyannopoulos, J. A.; Graveley, B. R. et al.; Feingold, E. A.; Pazin, M. J.; Pagan, M.; Gilchrist, D. A.; Hitz, B. C.; Cherry, J. M.; Bernstein, B. E.; Mendenhall, E. M.; Zerbino, D. R.; Frankish, A.; Flicek, P.; Myers , R. M.; Meissner, A.: Perspectives on ENCODE. Nature 583, pp. 693 - 698 (2020)
40.
Journal Article
Mehvari, S.; Larti, F.; Hu, H.; Fattahi, Z.; Beheshtian, M.; Abedini, S. S.; Arzhangi, S.; Ropers, H.-H.; Kalscheuer, V. M.; Auld, D. et al.; Kahrizi, K.; Riazalhosseini, Y.; Najmabadi, H.: Whole genome sequencing identifies a duplicated region encompassing Xq13.2q13.3 in a large Iranian family with intellectual disability. Molecular Genetics & Genomic Medicine 8 (10), e1418 (2020)
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