Suchergebnisse

Morava, E.; Bartsch, O.; Czako, M.; Frensel, A.; Kalscheuer, V.; Karteszi, J.; Kosztolanyi, G.: Small inherited terminal duplication of 7q with hydrocephalus, cleft palate, joint contractures, and severe hypotonia. Clinical Dysmorphology 12 (2), S. 123 - 127 (2003)

Roberts, R. J.; Belfort, M.; Bestor, T.; Bhagwat, A. S.; Bickle, T. A.; Bitinaite, J.; Blumenthal, R. M.; Degtyarev, S. K.; Dryden, D. T. F.; Dybvig, K. et al.; Firman, K.; Gromova, E. S.; Gumport, R. I.; Halford, S. E.; Hattman, S.; Heitman, J.; Hornby, D. P.; Janulaitis, A.; Jeltsch, A.; Josephsen, J.; Kiss, A.; Klaenhammer, T. R.; Kobayashi, I.; Kong, H. M.; Kruger, D. H.; Lacks, S.; Marinus, M. G.; Miyahara, M.; Morgan, R. D.; Murray, N. E.; Nagaraja, V.; Piekarowicz, A.; Pingoud, A.; Raleigh, E.; Rao, D. N.; Reich, N.; Repin, V. E.; Selker, E. U.; Shaw, P.-C.; Stein, D. C.; Stoddard, B. L.; Szybalski, W.; Trautner, T. A.; Van Etten, J. L.; Vitor, J. M. B.; Wilson, G. G.; Xu, S.-Y.: A nomenclature for restriction enzymes, DNA methyltransferases, homing endonucleases and their genes. Nucleic Acids Research 31 (7), S. 1805 - 1812 (2003)

Schweiger, S.; Schneider, R.: The MID1/PP2A complex: a key to the pathogenesis of Opitz BBB/G syndrome. BioEssays 25 (4), S. 356 - 366 (2003)

Schwikowski, B.; Vingron, M.: Weighted sequence graphs: boosting iterated dynamic programming using locally suboptimal solutions. Discrete Applied Mathematics 127 (1), S. 95 - 117 (2003)

Schweiger, S.; Chaoui, R.; Tennstedt, C.; Lehmann, K.; Mundlos, S.; Tinschert, S.: Antenatal onset of cortical hyperostosis (Caffey disease): Case report and review. American Journal of Medical Genetics Part A 120A (4), S. 547 - 552 (2003)

Branson, R.; Potoczna, N.; Kral, J. G.; Lentes, K.-U.; Hoehe, M. R.; Horber, F. F.: Binge eating as a major phenotype of melanocortin 4 receptor gene mutations. New England Journal of Medicine 348 (12), S. 1096 - 1103 (2003)

Orlova, E. V.; Gowen, B.; Dröge, A.; Stiege, A.; Weise, F.; Lurz, R.; van Heel, M.; Tavares, P.: Structure of a viral DNA gatekeeper at 10 angstrom resolution by cryo-electron microscopy. EMBO Journal 22 (6), S. 1255 - 1262 (2003)

Horn, D.; Neitzel, H.; Tonnies, H.; Kalscheuer, V.; Kunze, J.; Hinkel, G. K.; Bartsch, O.: Familial MCA/MR syndrome due to inherited submicroscopic translocation t(18;21)(q22.1q21.3) with breakpoint at the Down syndrome critical region. American Journal of Medical Genetics Part A 117A (3), S. 236 - 244 (2003)

Nordhoff, E.; Schurenberg, M.; Thiele, G.; Luebbert, C.; Kloeppel, K.-D.; Theiss, D.; Lehrach, H.; Gobom, J.: Sample preparation protocols for MALDI-MS of peptides and oligonucleotides using prestructured sample supports. International Journal of Mass Spectrometry 226 (1), S. 163 - 180 (2003)

Pfeifer, C.; Scherthan, H.; Thomsen, P. D.: Sex-specific telomere redistribution and synapsis initiation in cattle oogenesis. Developmental Biology 255 (2), S. 206 - 215 (2003)

Aulehla, A.; Wehrle, C.; Brand-Saberi, B.; Kemler, R.; Gossler, A.; Kanzler, B.; Herrmann, B. G.: Wnt3a plays a major role in the segmentation clock controlling somitogenesis. Developmental Cell 4 (3), S. 395 - 406 (2003)

Berger, A.; Mayr, J. A.; Meierhofer, D.; Fötschl, U.; Bittner, R.; Budka, H.; Grethen, C.; Huemer, M.; Kofler, B.; Sperl, W.: Severe depletion of mitochondrial DNA in spinal muscular atrophy. Acta Neuropathologica 105 (3), S. 245 - 251 (2003)

Cahill, D. J.: Protein arrays: Potential diagnostic tool? The Journal of Gene Medicine 5 (3), S. S6 - S6 (2003)

de Graaf, K.; Buessow, K.; Becker, W.: Identification of a novel substrate of the kinase DYRK1A by solid-phase phosphorylation of an arrayed cDNA expression library. Naunyn-Schmiedebergs Archives of Pharmacology 367 (Suppl. 1), S. R58 - R58 (2003)

Dinos, G. P.; Connell, S. R.; Nierhaus, K. H.; Kalpaxis, D. L.: Erythromycin, roxithromycin, and clarithromycin: Use of slow-binding kinetics to compare their in vitro interaction with a bacterial ribosomal complex active in peptide bond formation. Molecular Pharmacology 63 (3), S. 617 - 623 (2003)

Frohme, M.; Flopp, J.; Schwarz, M.; Beissbarth, T.; Hoheisel, J.; Radeke, H. H.: Development of membrane and glass cDNA arrays for the analysis of genes involved in renal inflammatory migration. Naunyn-Schmiedebergs Archives of Pharmacology 367 (Suppl. Suppl. 1), S. R122 - R122 (2003)

Heinemann, U.; Buessow, K.; Mueller, U.; Umbach, P.: Facilities and methods for the high-throughput crystal structural analysis of human proteins. Accounts of Chemical Research 36 (3), S. 157 - 163 (2003)

Kodzius, R.; Rhyner, C.; Konthur, Z.; Buczek, D.; Lehrach, H.; Walter, G.; Crameri, R.: Rapid identification of allergen-encoding cDNA clones by phage display and high-density arrays. Combinatorial Chemistry & High Throughput Screening 6 (2), S. 147 - 154 (2003)

Kriventseva, E. V.; Koch, I.; Apweiler, R.; Vingron, M.; Bork, P.; Gelfand, M. S.; Sunyaev, S.: Increase of functional diversity by alternative splicing. Trends in Genetics 19 (3), S. 124 - 128 (2003)

Rock, R.; Vortkamp, A.; Gessler, M.: Characterization of the murine four-jointed x1 (fjx1) and its putative receptor. European Journal of Cell Biology 82 (Suppl. 53), S. 31 - 31 (2003)