Journal Article (167)

121.
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)
122.
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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)
123.
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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)
124.
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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)
125.
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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)
126.
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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)
127.
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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)
128.
Journal Article
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)
129.
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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)
130.
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)
131.
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)
132.
Journal Article
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)
133.
Journal Article
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)
134.
Journal Article
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)
135.
Journal Article
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)
136.
Journal Article
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)
137.
Journal Article
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)
138.
Journal Article
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)
139.
Journal Article
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)
140.
Journal Article
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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