Publikationen von Susann Schweiger

Krauß, S.; So, J.; Hambrock, M.; Köhler, A.; Kunath, M.; Scharff, C.; Wessling, M.; Grzeschik, K.-H.; Schneider, R.; Schweiger, S.: Point mutations in GLI3 lead to misregulation of its subcellular localization. PLoS ONE 4, S. e7471 - e7471 (2009)

Aranda-Orgillés, B.; Aigner, J.; Kunath, M.; Lurz, R.; Schneider, R.; Schweiger, S.: Active transport of the ubiquitin ligase MID1 along the microtubules is regulated by protein phosphatase 2A. PLoS One 3 (10), S. e3507 - e3507 (2008)

Aranda-Orgillés, B.; Aigner, J.; Kunath, M.; Lurz, R.; Schneider, R.; Schweiger, S.: Active transport of the ubiquitin ligase MID1 along the microtubules is regulated by protein phosphatase 2A. PLoS One 3 (10), S. e3507 - e3507 (2008)

Winter, J.; Roepcke, S.; Krause, S.; Müller, E.-C.; Otto, A.; Vingron, M.; Schweiger, S.: Comparative 3’UTR analysis allows identification of regulatory clusters that drive Eph/ephrin expression in cancer cell lines. PLoS One 3 (7), S. e2780 - e2780 (2008)

Krauß, S.; Foerster, J.; Schneider, R.; Schweiger, S.: Protein Phosphatase 2A and Rapamycin regulate the nuclear localization and activity of the transcription factor GLI3. Cancer Research 68 (12), S. 4658 - 4665 (2008)

Aranda-Orgillés, B.; Trockenbacher, A.; Winter, J.; Aigner, J.; Köhler, A.; Jastrzebska, E.; Stahl, J.; Müller, E.-C.; Otto, A.; Wanker, E. E. et al.; Schneider, R.; Schweiger, S.: The Opitz syndrome gene product MID1 assembles a microtubule-associated ribonucleoprotein complex. Human Genetics 123 (2), S. 163 - 176 (2008)

So, J.; Müller, I.; Kunath, M.; Herrmann, S.; Ullmann, R.; Schweiger, S.: Diagnosis of a terminal deletion of 4p with duplication of Xp22.31 in a patient with findings of Opitz G/BBB syndrome and Wolf-Hirschhorn syndrome. American Journal of Medical Genetics Part A 146A (1), S. 103 - 109 (2008)

Winter, J.; Kunath, M.; Roepcke, S.; Krause, S.; Schneider, R.; Schweiger, S.: Alternative polyadenylation signals and promoters act in concert to control tissue-specific expression of the Opitz Syndrome gene MID1. BMC Molecular Biology [Elektronische Ressource] 8 (1), S. 105 - 133 (2007)

So, J.; Suckow, V.; Kijas, Z.; Kalscheuer, V.; Moser, B.; Winter, J.; Baars, M.; Firth, H.; Lunt, P.; Hamel, B. et al.; Meinecke, P.; Moraine, C.; Odent, S.; Schinzel, A.; van der Smagt, J.J.; Devriendt, K.; Albrecht, B.; Gillessen-Kaesbach, G.; van der Burgt, I.; Petrij, F.; Faivre, L.; McGaughran, J.; McKenzie, F.; Opitz, J. M.; Cox, T.; Schweiger, S.: Mild phenotypes in a series of patients with Opitz GBBB syndrome with MID1 mutations. American Journal of Medical Genetics Part A 132A (1), S. 1 - 7 (2006)

So, J.; Suckow, V.; Kijas, Z.; Kalscheuer, V.; Moser, B.; Winter, J.; Baars, M.; Firth, H.; Lunt, P.; Hamel, B. et al.; Meinecke, P.; Moraine, C.; Odent, S.; Schinzel, A.; van der Smagt, J.J.; Devriendt, K.; Albrecht, B.; Gillessen-Kaesbach, G.; van der Burgt, I.; Petrij, F.; Faivre, L.; McGaughran, J.; McKenzie, F.; Opitz, J. M.; Cox, T.; Schweiger, S.: Mild phenotypes in a series of patients with Opitz GBBB syndrome with MID1 mutations. American Journal of Medical Genetics Part A 132A (1), S. 1 - 7 (2006)

Hagens, O.; Minina, E.; Schweiger, S.; Ropers, H.-H.; Kalscheuer, V. M.: Characterization of FBX25, encoding a novel brain-expressed F-box protein. Biochimica et Biophysica Acta (BBA) - General Subjects 1760 (1), S. 110 - 118 (2006)

Shoichet, S. A.; Duprez, L.; Hagens, O.; Waetzig, V.; Menzel, C.; Herdegen, T.; Schweiger, S.; Dan, B.; Vamos, E.; Ropers, H.-H. et al.; Kalscheuer, V. M.: Truncation of the CNS-expressed JNK3 in a patient with a severe developmental epileptic encephalopathy. Human Genetics 118 (5), S. 559 - 567 (2006)

Foerster, J.; Nolte, I.; Junge, J.; Bruinenberg, M.; Schweiger, S.; Spaar, K.; van der Steege, G.; Ehlert, C.; Mulder, M.; Kalscheuer, V.: Haplotype sharing analysis identifies a retroviral dUTPase as candidate susceptibility gene for psoriasis. The Journal of Investigative Dermatology: an International Journal for Research in Cutaneous Biology 124 (1), S. 99 - 102 (2005)

So, J.; Suckow, V.; Kijas, Z.; Kalscheuer, V. M.; Moser, B.; Winter, J.; Baars, M.; Firth, H.; Lunt, P.; Hamel, B. et al.; Meinecke, P.; Moraine, C.; Odent, S.; Schinzel, A.; van der Smagt, J.J.; Devriendt, K.; Albrecht, B.; Gillessen-Kaesbach, G.; van der Burgt, I.; Petrij, F.; Faivre, L.; McGaughran, J.; McKenzie, F.; Opitz, J. M.; Cox, T.; Schweiger, S.: Mild phenotypes in a series of patients with Opitz GBBB syndrome with MID1 mutations. American Journal of Medical Genetics: Part A 132 (1), S. 1 - 7 (2005)

So, J.; Suckow, V.; Kijas, Z.; Kalscheuer, V. M.; Moser, B.; Winter, J.; Baars, M.; Firth, H.; Lunt, P.; Hamel, B. et al.; Meinecke, P.; Moraine, C.; Odent, S.; Schinzel, A.; van der Smagt, J.J.; Devriendt, K.; Albrecht, B.; Gillessen-Kaesbach, G.; van der Burgt, I.; Petrij, F.; Faivre, L.; McGaughran, J.; McKenzie, F.; Opitz, J. M.; Cox, T.; Schweiger, S.: Mild phenotypes in a series of patients with Opitz GBBB syndrome with MID1 mutations. American Journal of Medical Genetics: Part A 132 (1), S. 1 - 7 (2005)

Winter, J.; Lehmann, T.; Krauß, S.; Trockenbacher, A.; Kijas, Z.; Foerster, J.; Suckow, V.; Yaspo, M.-L.; Kulozik, A.; Kalscheuer, V. M. et al.; Schneider, R.; Schweiger, S.: Regulation of the MID1 protein function is fine-tuned by a complex pattern of alternative splicing. Human Genetics 114 (6), S. 541 - 552 (2004)

Winter, J.; Lehmann, T.; Krauß, S.; Trockenbacher, A.; Kijas, Z.; Foerster, J.; Suckow, V.; Yaspo, M.-L.; Kulozik, A.; Kalscheuer, V. M. et al.; Schneider, R.; Schweiger, S.: Regulation of the MID1 protein function is fine-tuned by a complex pattern of alternative splicing. Human Genetics 114 (6), S. 541 - 552 (2004)

Foerster, J.; Nolte, I.; Schweiger, S.; Ehlert, C.; Bruinenberg, M.; Spaar, K.; van der Steege, G.; Mulder, M.; Kalscheuer, V. M.; Moser, B. et al.; Kijas, Z.; Seeman, P.; Ständer, M.; Sterry, W.; te Meerman, G.: Evaluation of the IRF-2 gene as a candidate for PSORS3. Journal of Investigative Dermatology 122 (1), S. 61 - 64 (2004)

Kalscheuer, V. M.; Freude, K.; Musante, L.; Jensen, L. R.; Yntema, H. G.; Gecz, J.; Sefiani, A.; Hoffmann, K.; Moser, B.; Haas, S. et al.; Gurok, U.; Haesler, S.; Aranda, B.; Nshedjan, A.; Tzschach, A.; Hartmann, N.; Roloff, T.-C.; Shoichet, S.; Hagens, O.; Tao, J.; van Bokhoven, H.; Turner, G.; Chelly, J.; Moraine, C.; Fryns, J.-P.; Nuber, U.; Hoeltzenbein, M.; Scharff, C.; Scherthan, H.; Lenzner, S.; Hamel, B. C. J.; Schweiger, S.; Ropers, H.-H.: Mutations in the polyglutamine binding protein 1 gene cause X-linked mental retardation. Nature Genetics 35 (4), S. 313 - 315 (2003)

Zeitz, C.; Scherthan, H.; Freier, S.; Feil, S.; Suckow, V.; Schweiger, S.; Berger, W.: NYX (Nyctalopin on chromosome X), the gene mutated in congenital stationary night blindness, encodes a cell surface protein. Investigative Ophthalmology & Visual Science 44 (10), S. 4184 - 4191 (2003)