Lange, B. M. H.: Protein complexes and their function in cell division pathways in health and disease. Cell News 36, pp. 28 - 31 (2010)

Lange, B. M. H.: Der virtuelle Patient - Systembiologie ist die Chance für die individuelle Medizin. GenomXPress 1/2010, pp. 6 - 8 (2010)

Laumet, G.; Chouraki, V.; Grenier-Boley, B.; Legry, V.; Heath, S.; Zelenika, D.; Fievet, N.; Hannequin, D.; Delepine, M.; Pasquier, F. et al.; Hanon, O.; Brice, A.; Epelbaum, J.; Berr, C.; Dartigues, J. F.; Tzourio, C.; Campion, D.; Lathrop, M.; Bertram, L.; Amouyel, P.; Lambert, J. C.: Systematic analysis of candidate genes for Alzheimer's disease in a French, genome-wide association study. Journal of Alzheimer's Disease 20 (4), pp. 1181 - 1188 (2010)

Lebedeva, E.; Stingl, J. C.; Thal, D. R.; Ghebremedhin, E.; Strauss, J.; Özer, E.; Bertram, L.; von Einem, B.; Tumani, H.; Otto, M. et al.; Riepe, M. W.; Högel, J.; Ludolph, A. C.; von Arnim, C. A.: Genetic variants in PSEN2 and correlation to CSF beta-amyloid42 levels in AD. Neurobiology of Aging (2010)

Liska, F.; Snajdr, P.; Stricker, S.; Gosele, C.; Krenova, D.; Mundlos, S.; Hubner, N.: Impairment of Sox9 expression in limb buds of rats homozygous for hypodactyly mutation. Folia Biologica 56 (2), pp. 58 - 65 (2010)

Lunshof, J.E.; Bobe, J.; Aach, J.; Angrist, M.; Thakuria, J.V.; Vorhaus, D.B.; Hoehe, M.R.; Church, G.M.: Personal genomes in progress: from the human genome project to the personal genome project. Dialogues in Clinical Neurosciences 12 (1), pp. 47 - 60 (2010)

May, P.; Kreuchwig, A.; Steinke, T.; Koch, I.: PTGL: a database for secondary structure-based protein topologies. Nucleic Acids Research 38 (Database issue), pp. D326 - 30 (2010)

Meng, G.; Mosig, A.; Vingron, M.: A computational evaluation of over-representation of regulatory motifs in the promoter regions of differentially expressed genes. BMC Bioinformatics 11, p. 11:267 - 11:267 (2010)

Musante, L.; Kunde, S.-A.; Sulistio, T. O.; Frints, S. G.M.; Schwartz, C. E.; Martínez, F.; Romano, C.; Ropers, H.-H.; Kalscheuer, V. M.; Fischer, U. et al.; Grimme, A.: Common pathological mutations in PQBP1 induce nonsense-mediated mRNA decay and enhance exclusion of the mutant exon. Human Mutation 31 (1), pp. 90 - 98 (2010)

Negrisolo, E.; Kuhl, H.; Forcato, C.; Vitulo, N.; Reinhardt, R.; Patarnello, T.; Bargelloni, L.: Different phylogenomic approaches to resolve the evolutionary relationships among model fish species. Molecular Biology and Evolution 27 (12), pp. 2757 - 2774 (2010)

Polak, P.; Querfurth, R.; Arndt, P. F.: The evolution of transcription-associated biases of mutations across vertebrates. BMC Evolutionary Biology 10, p. 10:187 - 10:187 (2010)

Prigione, A.; Adjaye, J.: Modulation of mitochondrial biogenesis and bioenergetic metabolism upon in vitro and in vivo differentiation of human ES and iPS cells. International Journal of Developmental Biology 54 (11/12), pp. 1729 - 1741 (2010)

Rocha, P. P.; Bleiss, W.; Schrewe, H.: Mosaic Expression of Med12 in Female Mice Leads to Exencephaly, Spina Bifida, and Craniorachischisis. Birth Defects Research Part A: Clinical and Molecular Teratology 88 (8), pp. 626 - 632 (2010)

Rödelsperger, C.; Dieterich, C.: CYNTENATOR: progressive gene order alignment of 17 vertebrate genomes. PLoS ONE 5 (1), p. e8861 - e8861 (2010)

Ropers, H.-H.: Single gene disorders come into focus – again. Dialogues. Dialogues in Clinical Neuroscience 12 (1), pp. 95 - 102 (2010)

Slezak, R.; Luczak, K.; Kalscheuer, V.; Neumann, T. E.; Sasiadek, M. M.: Noonan-like/multiple giant cell lesion syndrome in two adult patients with SOS1 gene mutations. Clin Dysmorphol 19 (3), pp. 157 - 60 (2010)

Tchatchou, S.; Riedel, A.; Lyer, S.; Schmutzhard, J.; Strobel-Freidekind, O.; Gronert-Sum, S.; Mietag, C.; D'Amato, M.; Schlehe, B.; Hemminki, K. et al.; Sutter, C.; Ditsch, N.; Blackburn, A.; Hill, L. Z.; Jerry, D. J.; Bugert, P.; Weber, B. H.; Niederacher, D.; Arnold, N.; Varon-Mateeva, R.; Wappenschmidt, B.; Schmutzler, R. K.; Engel, C.; Meindl, A.; Bartram, C. R.; Mollenhauer, J.; Burwinkel, B.: Identification of a DMBT1 polymorphism associated with increased breast cancer risk and decreased promoter activity. Human Mutations 31 (1), pp. 60 - 66 (2010)

Tzschach, A.; Bisgaard, A. M.; Kirchhoff, M.; Graul-Neumann, L. M.; Neitzel, H.; Page, S.; Ahmed, A.; Muller, I.; Erdogan, F.; Ropers, H. H. et al.; Kalscheuer, V. M.; Ullmann, R.: Chromosome aberrations involving 10q22: report of three overlapping interstitial deletions and a balanced translocation disrupting C10orf11. Eur J Hum Genet 18 (3), pp. 291 - 5 (2010)

Urcana, E.; Haertela, U.; Stylloua, M.; Hickel, R.; Scherthan, H.; Reich, F. X.: Real-time xCELLigence impedance analysis of the cytotoxicity of dental composite components on human gingival fibroblasts. Dental Materials: Official Publication of the Academy of Dental Materials 26 (1), pp. 51 - 58 (2010)

Wild, R.; Patil, S.; Popovi, M.; Zappi, M.; Dufreche, S.; Bajpai, R.: Lipids from Lipomyces starkeyi. Food Technology and Biotechnology 48 (3), pp. 329 - 335 (2010)