Zeitschriftenartikel (81)

41.
Zeitschriftenartikel
Aretz, I.; Hardt, C.; Wittig, I.; Meierhofer, D.: An impaired respiratory electron chain triggers down-regulation of the energy metabolism and de-ubiquitination of solute carrier amino acid transporters. Molecular and Cellular Proteomics 15 (5), S. 1526 - 1538 (2016)
42.
Zeitschriftenartikel
Broecker, F.; Hardt, C.; Herwig, R.; Timmermann, B.; Kerick, M.; Wunderlich, A.; Schweiger, M. R.; Borsig, L.; Heikenwalder, M.; Lehrach, H. et al.; Moelling, K.: Transcriptional signature induced by a metastasis-promoting c-Src mutant in a human breast cell line. The FEBS Journal 283 (9), S. 1669 - 1688 (2016)
43.
Zeitschriftenartikel
Meierhofer, D.; Halbach, M.; Şen, N. E.; Gispert, S.; Auburger, G.: Atxn2-Knock-Out mice show branched chain amino acids and fatty acids pathway alterations. Molecular and Cellular Proteomics 15 (5), S. 1728 - 1739 (2016)
44.
Zeitschriftenartikel
Spielmann, M.; Marx, S.; Barbi, G.; Flottmann, R.; Kehrer-Sawatzki, H.; Konig, R.; Horn, D.; Mundlos, S.; Nader, S.; Borck, G.: Femoral facial syndrome associated with a de novo complex chromosome 2q37 rearrangement. American Journal of Medical Genetics Part A 170A (5), S. 1202 - 1207 (2016)
45.
Zeitschriftenartikel
Aretz, I.; Meierhofer, D.: Advantages and Pitfalls of Mass Spectrometry Based Metabolome Profiling in Systems Biology. International Journal of Molecular Sciences 17 (5), pii: E632 (2016)
46.
Zeitschriftenartikel
Vij, S.; Kuhl, H.; Kuznetsova, I. S.; Komissarov, A.; Yurchenko, A. A.; Van Heusden, P.; Singh, S.; et al: Chromosomal-Level Assembly of the Asian Seabass Genome Using Long Sequence Reads and Multi-layered Scaffolding. PLoS Genetics 12 (4), e1005954 (2016)
47.
Zeitschriftenartikel
Hardt, C.; Beber, M. E.; Rasche, A.; Kamburov, A.; Hebels, D. G.; Kleinjans, J. C.; Herwig, R.: ToxDB: pathway-level interpretation of drug-treatment data. Database (Oxford) 2016, baw052 (2016)
48.
Zeitschriftenartikel
Cui, H.; Schlesinger, J.; Schoenhals, S.; Tönjes, M.; Dunkel, I.; Meierhofer, D.; Cano, E.; Schulz, K.; Berger, M. F.; Haack, T. et al.; Abdelilah-Seyfried, S.; Bulyk, M. L.; Sauer, S.; Sperling, S. R.: Phosphorylation of the chromatin remodeling factor DPF3a induces cardiac hypertrophy through releasing HEY repressors from DNA. Nucleic Acids Research (London) 46 (6), S. 2538 - 2553 (2016)
49.
Zeitschriftenartikel
Conrad, T.; Albrecht, A.-S.; Rodrigues de Melo Costa, V.; Sauer, S.; Meierhofer, D.; Ørom, U. A.: Serial interactome capture of the human cell nucleus. Nature Communications 7, 7:11212 (2016)
50.
Zeitschriftenartikel
Lupiáñez, D. G.; Spielmann, M.; Mundlos, S.: Breaking TADs: How Alterations of Chromatin Domains Result in Disease. Trends in Genetics 32 (4), S. 225 - 237 (2016)
51.
Zeitschriftenartikel
Mackenroth, L.; Fischer-Zirnsak, B.; Egerer, J.; Hecht, J.; Kallinich, T.; Stenzel, W.; Spors, B.; von Moers, A.; Mundlos, S.; Kornak, U. et al.; Gerhold, K.; Horn, D.: An overlapping phenotype of Osteogenesis imperfecta and Ehlers-Danlos syndrome due to a heterozygous mutation in COL1A1 and biallelic missense variants in TNXB identified by whole exome sequencing. American Journal of Medical Genetics Part A 170A (4), S. 1080 - 1085 (2016)
52.
Zeitschriftenartikel
Louro, B.; Kuhl, H.; Tine, M.; de Koning, D.-J.; Batargias, C.; Volckaert, F. A. M.; Reinhardt, R.; Canario, A. V. M.; Power, D. M.: Characterization and refinement of growth related quantitative trait loci in European sea bass (Dicentrarchus labrax) using a comparative approach. Aquaculture 455, S. 8 - 21 (2016)
53.
Zeitschriftenartikel
Sprink, T.; Ramrath, D. J. F.; Yamamoto, H.; Yamamoto, K.; Loerke, J.; Ismer, J.; Hildebrand, P. W.; Scheerer, P.; Bürger, J.; Mielke, T. et al.; Spahn, C. M. T.: Structures of ribosome-bound initiation factor 2 reveal mechanism of subunit association. Science Advances 2 (3), e1501502 (2016)
54.
Zeitschriftenartikel
Knierim, E.; Hirata, H.; Wolf, N. I.; Morales-Gonzalez, S.; Schottmann, G.; Tanaka, Y.; Rudnik-Schöneborn, S.; Orgeur, M.; Zerres, K.; Vogt, S. et al.; van Riesen, A.; Gill, E.; Seifert, F.; Zwirner, A.; Kirschner, J.; Goebel, H. H.; Hübner, C.; Stricker, S.; Meierhofer, D.; Stenzel, W.; Schuelke, M.: Mutations in Subunits of the Activating Signal Cointegrator 1 Complex Are Associated with Prenatal Spinal Muscular Atrophy and Congenital Bone Fractures. The American Journal of Human Genetics 98, S. 1 - 17 (2016)
55.
Zeitschriftenartikel
Ibrahim, D.; Tayebi, N.; Knaus, A.; Stiege, A. C.; Sahebzamani, A.; Hecht, J.; Mundlos, S.; Spielmann, M.: A homozygous HOXD13 missense mutation causes a severe form of synpolydactyly with metacarpal to carpal transformation. American Journal of Medical Genetics Part A 170 (3), S. 615 - 621 (2016)
56.
Zeitschriftenartikel
Iqbal, Z.; Püttmann, L.; Musante, L.; Razzaq, A.; Zahoor, M. Y.; Hu, H.; Wienker, T. F.; Garshasbi, M.; Fattahi, Z.; Gilissen, C. et al.; Vissers, L. E.; de Brouwer, A. P.; Veltman, J. A.; Pfundt, R.; Najmabadi, H.; Ropers, H. H.; Riazuddin, S.; Kahrizi, K.; van Bokhoven, H.: Missense variants in AIMP1 gene are implicated in autosomal recessive intellectual disability without neurodegeneration. European journal of human genetics 24 (3), S. 392 - 399 (2016)
57.
Zeitschriftenartikel
Mueller, J. C.; Kuhl, H.; Timmermann, B.; Kempenaers, B.: Characterization of the genome and transcriptome of the blue tit Cyanistes caeruleus: polymorphisms, sex-biased expression and selection signals. Molecular Ecology Resources 16 (2), S. 549 - 561 (2016)
58.
Zeitschriftenartikel
Olech, E. M.; Zemojtel, T.; Sowinska-Seidler, A.; Mundlos, S.; Robinson, P. N.; Karczewski, M.; Jamsheer, A.: Identification of a molecular defect in a stillborn fetus with perinatal lethal hypophosphatasia using a disease-associated genome sequencing approach. Polish Journal of Pathology 67 (1), S. 78 - 83 (2016)
59.
Zeitschriftenartikel
Smith, Z. D.; Sindhu, C.; Meissner, A.: Molecular features of cellular reprogramming and development. Nature Reviews Molecular Cell Biology 17 (3), S. 139 - 154 (2016)
60.
Zeitschriftenartikel
Veenvliet, J. V.: Studying Mesodiencephalic Dopaminergic Neuron Development In Vivo to Improve Stem Cell Therapy in Parkinson’s Disease. The Journal of Neuroscience 36 (6), S. 1794 - 1796 (2016)
Zur Redakteursansicht