The following publications were published exclusively under the affiliation of the Max Planck Society. For publications by the principal investigator outside of the Max Planck Society, see the links on the lower left.

Journal Article (168)

Journal Article
Schwecke,, T.; Göttling, K.; Durek, P.; Dueñas, I.; Käufer, N. F.; Zock-Emmenthal, S.; Staub, E.; Neuhof, T.; Dieckmann, R.; von Döhren, H.: Nonribosomal peptide synthesis in S. pombe and the architecture of ferrichrome-type siderophore synthetases in fungi. ChemBioChem: A European Journal of Chemical Biology 7 (4), pp. 612 - 622 (2006)
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Yan, K.-L.; Zhang, X.-J.; Wang, Z.-M.; Yang, S.; Zhang, G.-L.; Wang, J.; Xiao, F.-L.; Gao, M.; Cui, Y.; Chen, J.-J. et al.; Fan, X.; Sun, L.-D.; Xia, Q.; Zhang, K.-Y.; Niu, Z.-M.; Xu, S.-J.; Tzschach, A.; Ropers, H.-H.; Huang, W.; Liu, J.-J.: A novel MGST2 non-synonymous mutation in a Chinese pedigree with psoriasis vulgaris. The Journal of Investigative Dermatology: Official Journal of the Society for Investigative Dermatology and the European Society for Dermatological Research 126 (5), pp. 1003 - 1005 (2006)
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Cossée, M.; Demeer, B.; Blanchet, P.; Echenne, B.; Singh, D.; Hagens, O.; Antin, M.; Finck, S.; Vallee, L.; Dollfus, H. et al.; Hegde, S.; Springell, K.; Thelma, B. K. ..; Woods, G.; Kalscheuer, V. M.; Mandel, J.-L.: Exonic microdeletions in the X-linked PQBP1 gene in mentally retarded patients: a pathogenic mutation and in-frame deletions of uncertain effect. European Journal of Human Genetics: the Official Journal of the European Society of Human Genetics 14 (4), pp. 418 - 425 (2006)
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Goyal, R.; Reinhardt, R.; Jeltsch, A.: Accuracy of DNA methylation pattern preservation by the Dnmt1 methyltransferase. Nucleic Acids Research. 34 (4), pp. 1182 - 1188 (2006)
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De-Zolt, S.; Schnütgen, F.; Seisenberger, C.; Hansen, J.; Hollatz, M.; Floss, T.; Ruiz, P.; Wurst, W.; von Melchner, H.: High-throughput trapping of secretory pathway genes in mouse embryonic stem cells. Nucleic Acids Research (London) 34 (3), p. e25 - e25 (2006)
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Schubbert, S.; Zenker, M.; Rowe, S. L. ..; Böll, S.; Klein, C.; Bollag, G.; van der Burgt, I.; Musante, L.; Kalscheuer, V. M.; Wehner, L.-E. et al.; Nguyen, H.; West, B.; Zhang, K. Y. J.; Sistermans, E.; Rauch, A.; Niemeyer, C. M.; Shannon, K.; Kratz, C. P.: Germline KRAS mutations cause Noonan syndrome. Nature Genetics 38 (3), pp. 331 - 336 (2006)
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Bækvad-Hansen, M.; Tümer, Z.; Delicado, A.; Erdogan, F.; Tommerup, N.; Larsen, L. A.: Delineation of a 2.2 Mb microdeletion at 5q35 associated with microcephaly and congenital heart disease. American Journal of Medical Genetics Part A 140 (5), pp. 427 - 33 (2006)
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Tzschach, A.; Krause-Plonka, I.; Menzel, C.; Kalscheuer, V. M.; Toennies, H.; Scherthan, H.; Knoblauch, A.; Radke, M.; Ropes, H.-H.; Hoeltzenbein, M.: Molecular cytogenetic analysis of a de novo interstitial deletion 5q23.3q31.2 and its phenotypic consequences. American Journal of Medical Genetics 140 (5), pp. 496 - 502 (2006)
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Booms, P.; Ney, A.; Barthel, F.; Moroy, G.; Counsell, D.; Gille, C.; Guo, G.; Pregla, R.; Mundlos, S.; Alix, A. J. P. et al.; Robinson, P. N.: A fibrillin-1-fragment containing the elastin-binding-protein GxxPG consensus sequence upregulates matrix metalloproteinase-1: biochemical and computational analysis. Journal of Molecular and Cellular Cardiology (London) 40 (2), pp. 234 - 246 (2006)
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Dlugaszewska, B.; Silahtaroglu, A.; Menzel, C.; Kübart, S.; Cohen, M.; Mundlos, S.; Tümer, Z.; Kjaer, K.; Friedrich, U.; Ropers, H.-H. et al.; Tommerup, N.; Neitzerl, H.; Kalscheuer, V. M.: Breakpoints around the HOXD cluster result in various limb malformations. Journal of Medical Genetics 43 (2), pp. 111 - 118 (2006)
Journal Article
Dlugaszewska, B.; Silahtaroglu, A.; Menzel, C.; Kübart, S.; Cohen, M.; Mundlos, S.; Tümer, Z.; Kjaer, K.; Friedrich, U.; Ropers, H.-H. et al.; Tommerup, N.; Neitzerl, H.; Kalscheuer, V. M.: Breakpoints around the HOXD cluster result in various limb malformations. Journal of Medical Genetics 43 (2), pp. 111 - 118 (2006)
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Garshasbi, M.; Motazacker, M. M.; Kahrizi, K.; Behjati, F.; Abedini, S. S.; Nieh, S. E.; Firouzabadi, S. G.; Becker, C.; Rüschendorf, F.; Nürnberg, P. et al.; Tzschach, A.; Vazifehmand, R.; Erdogan, F.; Ullmann, R.; Lenzner, S.; Kuss, A. W.; Ropers, H.-H.; Najmabadi, H.: SNP array-based homozygosity mapping reveals MCPH1 deletion in family with autosomal recessive mental retardation and mild microcephaly. Human Genetics 118 (6), pp. 708 - 715 (2006)
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Hultschig, C.; Kreutzberger, J.; Seitz, H.; Konthur, Z.; Büssow, K.; Lehrach, H.: Recent advances of protein microarrays. Current Opinion in Chemical Biology 10 (1), pp. 4 - 10 (2006)
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Lipatov1, M.; Arndt, P. F.; Hwa, T.; Petrov, D. A.: A novel method distinguishes between mutation rates and fixation biases in patterns of single-nucleotide substitution. Journal of Molecular Evolution: the Journal of the International Society of Molecular Evolution 62 (2), pp. 168 - 175 (2006)
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Lugtenberg, D.; Yntema, H. G.; Banning, M. J. G.; Oudakker, A. R.; Firth, H. V.; Willatt, L.; Raynaud, M.; Kleefstra, T.; Fryns, J.-P.; Ropers, H.-H. et al.; Chelly, J.; Moraine, C.; Gécz, J.; van Reeuwijk, J.; Nabuurs, S. B.; de Vries, B. B. A.; Hamel, B. C. J.; de Brouwer, A. P. M.; van Bokhoven, H.: ZNF674: a new KRAB-containing zinc finger gene involved in non-syndromic X-linked mental retardation. American Journal of Human Genetics: : AJHG / American Society of Human Genetics 78 (2), pp. 265 - 278 (2006)
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Meierhofer, D.; Ebner, S.; Mayr, J. A.; Jones, N. D.; Kofler, B.; Sperl, W.: Platelet transfusion can mimic somatic mtDNA mutations. Leukemia: the Journal of Normal and Malignant Hemopoiese ; Official Journal of the Leukemia Research Fund U.K. 20 (2), pp. 362 - 363 (2006)
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Seo, H.-S.; Abedin, S.; Kamp, D.; Wilson, D. N.; Nierhaus, K.; Cooperman, B. S.: EF-G-dependent GTPase on the ribosome: Conformational change and fusidic acid inhibition. Biochemistry 45 (8), pp. 2504 - 2514 (2006)
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Tzschach,, A.; Hoffmann, K.; Hoeltzenbein, M.; Bache, I.; Tommerup, N.; Bommer, C.; Körner, H.; Kalscheuer, V. M.; Ropers, H.-H.: Molecular characterization of a balanced chromosome translocation in psoriasis vulgaris. Clinical Genetics 69 (2), pp. 189 - 193 (2006)
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Zintzaras, E.; Brown, N. P.; Kowald, A.: Non-parametric classification of protein secondary structures. Computers in Biology and Medicine (Elmsford, NY) 36 (2), pp. 145 - 156 (2006)
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Meierhofer, D.; Mayr, J. A.; Fink, K.; Schmeller, N.; Kofler, B.; Sperl, W.: Mitochondrial DNA mutations in renal cell carcinomas revealed no general impact on energy metabolism. British Journal of Cancer 94 (2), pp. 268 - 274 (2006)
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