Publikationen von T. Zemojtel

H. Hu, S. A. Haas, J. Chelly, H. Van Esch, M. Raynaud, A. P. M. de Brouwer, S. Weinert, G. Froyen, S. G. M. Frints, F. Laumonnier, T. Zemojtel, M. I. Love, H. Richard, A.-K. Emde, M. Bienek, C. Jensen, M. Hambrock, U. Fischer, C. Langnick, M. Feldkamp, W. Wissink-Lindhout, N. Lebrun, L. Castelnau, J. Rucci, R. Montjean, O. Dorseuil, P. Billuart, T. Stuhlmann, M. Shaw, M. A. Corbett, A. Gardner, S. Willis-Owen, C. Tan, K. L. Friend, S. Belet, K. E. P. van Roozendaal, M. Jimenez-Pocquet, M.-P. Moizard, N. Ronce, R. Sun, S. O'Keeffe, R. Chenna, A. van Bömmel, J. Göke, A. Hackett, M. Field, L. Christie, J. Boyle, E. Haan, J. Nelson, G. Turner, G. Baynam, G. Gillessen-Kaesbach, U. Müller, D. Steinberger, B. Budny, M. Badura-Stronka, A. Latos-Bieleńska, L. B. Ousager, P. Wieacker, G. Rodríguez Criado, M.-L. Bondeson, G. Annerén, A. Dufke, M. Cohen, L. Van Maldergem, C. Vincent-Delorme, B. Echenne, B. Simon-Bouy, T. Kleefstra, M. Willemsen, J.-P. Fryns, K. Devriendt, R. Ullmann, M. Vingron, K. Wrogemann, T. F. Wienker, A. Tzschach, H. van Bokhoven, J. Gecz, T. J. Jentsch, W. Chen, H.-H. Ropers, and V. M. Kalscheuer, "X-exome sequencing of 405 unresolved families identifies seven novel intellectual disability genes," Molecular Psychiatry 21 (1), 133-148 (2016).

Denise Emmerich, Tomasz Zemojtel, Jochen Hecht, Peter Krawitz, Malte Spielmann, Jirko Kühnisch, Karolina Kobus, Monika Oßwald, Verena Heinrich, Peter Berlien, Ute Müller, Victor-F. Mautner, Katharina Wimmer, Peter N. Robinson, Martin Vingron, Sigrid Tinschert, Stefan Mundlos, and Mateusz Kolanczyk, "Somatic neurofibromatosis type 1 (NF1) inactivation events in cutaneous neurofibromas of a single NF1 patient," European journal of human genetics 23 (6), 1870-1873 (2015).

Tomasz Zemojtel and Martin Vingron, "p53 binding sites in transposons," Frontiers in Genetics 3, 40 (2012).

Ruping Sun, Michael Love, Tomas Zemojtel, Anne-Katrin Emde, Ho-Ryun Chung, Martin Vingron, and Stefan Haas, "Breakpointer: using local mapping artifacts to support sequence breakpoint discovery from single-end reads," Bioinformatics 28 (7), 1024-1025 (2012).

M. Kolanczyk, V. Mautner, N. Kossler, R. Nguyen, J. Kuhnisch, T. Zemojtel, A. Jamsheer, E. Wegener, B. Thurisch, S. Tinschert, N. Holtkamp, S. J. Park, P. Birch, D. Kendler, A. Harder, S. Mundlos, and L. Kluwe, "MIA is a potential biomarker for tumour load in neurofibromatosis type 1," BMC Med 9, 82 (2011).

S. Lin, S. Haas, T. Zemojtel, P. Xiao, M. Vingron, and R. Li, "Genome-wide comparison of cyanobacterial transposable elements, potential genetic diversity indicators," Gene 473 (2), 139-49 (2011).

H. Najmabadi, H. Hu, M. Garshasbi, T. Zemojtel, S. S. Abedini, W. Chen, M. Hosseini, F. Behjati, S. Haas, P. Jamali, A. Zecha, M. Mohseni, L. Puttmann, L. N. Vahid, C. Jensen, L. A. Moheb, M. Bienek, F. Larti, I. Mueller, R. Weissmann, H. Darvish, K. Wrogemann, V. Hadavi, B. Lipkowitz, S. Esmaeeli-Nieh, D. Wieczorek, R. Kariminejad, S. G. Firouzabadi, M. Cohen, Z. Fattahi, I. Rost, F. Mojahedi, C. Hertzberg, A. Dehghan, A. Rajab, M. J. Banavandi, J. Hoffer, M. Falah, L. Musante, V. Kalscheuer, R. Ullmann, A. W. Kuss, A. Tzschach, K. Kahrizi, and H. H. Ropers, "Deep sequencing reveals 50 novel genes for recessive cognitive disorders," Nature 478 (7367), 57-63 (2011).

T. Zemojtel, S. M. Kielbasa, P. F. Arndt, S. Behrens, G. Bourque, and M. Vingron, "CpG deamination creates transcription factor-binding sites with high efficiency," Genome Biol Evol 3, 1304-11 (2011).

Anne S. Jürgens, Mateusz Kolanczyk, Dietrich C. C. Moebest, Tomasz Zemojtel, Urs Lichtenauer, Marlena Duchniewicz, Melanie P. Gantert, Jochen Hecht, Uwe Hattenhorst, Stefan Burdach, Annette Dorn, Mark P. Kamps, Felix Beuschlein, Daniel Räpple, and Jürgen S. Scheele, "PBX1 is dispensable for neural commitment of RA-treated murine ES cells," In Vitro Cellular & Developmental Biology - Animal 45 (5-6), 252-263 (2009).

Jürgen S. Scheele, Mateusz Kolanczyk, Melanie Gantert, Tomasz Zemojtel, Annette Dorn, David B. Sykes, Dietrich C. C. Möbest, Mark P. Kamps, and Daniel Räpple, "The Spt-Ada-Gcn5-acetyltransferase complex interaction motif of E2a is essential for a subset of transcriptional and oncogenic properties of E2a-Pbx1," Leukemia & Lymphoma 50 (5), 816-828 (2009).

Tomasz Zemojtel, Szymon M. Kielbasa, Peter F. Arndt, Ho-Ryun Chung, and Martin Vingron, "Methylation and deamination of CpGs generate p53-binding sites on a genomic scale.," Trends in Genetics 25 (2), 63-66 (2009).

Tomasz Zemojtel, Tobias Penzkofer, Jörg Schultz, Thomas Dandekar, Richard Badge, and Martin Vingron, "Exonization of active mouse L1s: a driver of transcriptome evolution?," BMC Genomics 8, e392-e392 (2007).

Urs D. Lichtenauer, Marlena Duchniewicz, Mateusz Kolanczyk, Andreas Hoeflich, Stephanie Hahner, Tobias Else, Andrew B. Bicknell, Tomasz Zemojtel, Nancy R. Stallings, Dominik M. Schulte, Mark P. Kamps, Gary D. Hammer, Jürgen S. Scheele, and Felix Beuschlein, "Pre-B-cell transcription factor 1 and steroidogenic factor 1 synergistically regulate adrenocortical growth and steroidogenesis.," Endocrinology: Official Journal of the Endocrine Society 148 (2), 693-704 (2007).

Urs D. Lichtenauer, Marlena Duchniewicz, Mateusz Kolanczyk, Andreas Hoeflich, Stephanie Hahner, Tobias Else, Andrew B. Bicknell, Tomasz Zemojtel, Nancy R. Stallings, Dominik M. Schulte, Mark P. Kamps, Gary D. Hammer, Jürgen S. Scheele, and Felix Beuschlein, "Pre-B-cell transcription factor 1 and steroidogenic factor 1 synergistically regulate adrenocortical growth and steroidogenesis.," Endocrinology: Official Journal of the Endocrine Society 148 (2), 693-704 (2007).

Tomasz Zemojtel, Andreas Fröhlich, M. Cristina Palmieri, Mateusz Kolanczyk, Ivan Mikula, Lucjan S. Wyrwicz, Erich E. Wanker, Stefan Mundlos, Martin Vingron, Pavel Martasek, and Jörg Durner, "Plant nitric oxide synthase: a never-ending story?," Trends in Plant Science 11 (11), 524-525 (2006).

Tomasz Zemojtel, Mateusz Kolanczyk, Nadine Kossler, Sigmar Stricker, Rudi Lurz, Ivan Mikula, Marlena Duchniewicz, Markus Schuelke, Pedram Ghafourifar, Pavel Martasek, Marrtin Vingron, and Stefan Mundlos, "Mammalian mitochondrial nitric oxide synthase: Characterization of a novel candidate.," FEBS Letters 580 (2), 455-462 (2006).

Marlena Duchniewicz, Tomasz Zemojtel, Mateusz Kolanczyk, Steffen Grossmann, Jürgen S. Scheele, and Fried J. T. Zwartkruis, "Rap1A-deficient T and B cells show impaired integrin-mediated cell adhesion," Molecular and Cellular Biology 26 (2), 643-653 (2006).

Tomasz Zemojtel, T. Penzkofer, M. Duchniewicz, and F. J. T . Zwartkruis, "hRap1B-retro: a novel human processed Rap1B gene blurs the picture?," Leukemia 20 (1), 145-146 (2006).

Tobias Penzkofer, Thomas Dandekar, and Tomasz Zemojtel, "L1Base: from functional annotation to prediction of active LINE-1 elements," Database Issue , D498-D500 (2005).

Krzysztof Ginalsk and Tomasz Zemojtel, "ECEPE proteins: a novel family of eukaryotic cysteine proteinases," Trends in Biochemical Sciences: TIBS / International Union of Biochemistry and Molecular Biology 29 (10), 524-526 (2004).