Our publications listed in the Puplication Repository of the Max Planck Society (PuRe)

Journal Article (128)

81.
Journal Article
Hendrickx, D. M.; Aerts, H. J. W. L.; Caiment, F.; Clark, D.; Ebbels, T. M. D.; Evelo, C. T.; Gmuender, H.; Hebels, D. G. A. J.; Herwig, R.; Hescheler, J. et al.; Jennen, D. G. J.; Jetten, M. J. A.; Kanterakis, S.; Keun, H. C.; Matser, V.; Overington, J. P.; Pilicheva, E.; Sarkans, U.; Segura-Lepe, M. P.; Sotiriadou, I.; Wittenberger, T.; Wittwehr, C.; Zanzi, A.; Kleinjans, J. C. S.: diXa: a data infrastructure for chemical safety assessment. Bioinformatics 31 (9), pp. 1505 - 1507 (2015)
82.
Journal Article
Hoffmann, F.; Singer, T.; Steinbeis, N.: Children's increased emotional egocentricity compared to adults is mediated by age-related differences in conflict processing. Child Development 86 (3), pp. 765 - 780 (2015)
83.
Journal Article
Laurent, A.; Calabrese, M.; Warnatz, H. J.; Yaspo, M. L.; Tkachuk, V.; Torres, M.; Blasi, F.; Penkov, D.: ChIP-Seq and RNA-Seq analyses identify components of the Wnt and Fgf signaling pathways as Prep1 target genes in mouse embryonic stem cells. PLoS One 10 (4), e0122518 (2015)
84.
Journal Article
Laurent, A.; Calabrese, M.; Warnatz, H. J.; Yaspo-Lehrach, M.-L.; Tkachuk, V.; Torres, M.; Blasi, F.; Penkov, D.: ChIP-Seq and RNA-Seq Analyses Identify Components of the Wnt and Fgf Signaling Pathways as Prep1 Target Genes in Mouse Embryonic Stem Cells. PLoS One (2015)
85.
Journal Article
van der Sluis, E. O.; Bauerschmitt, H.; Becker, T.; Mielke, T.; Frauenfeld, J.; Berninghausen, O.; Neupert, W.; Herrmann, J. M.; Beckmann, R.: Parallel Structural Evolution of Mitochondrial Ribosomes and OXPHOS Complexes. Genome biology and evolution 7 (5), pp. 1235 - 1251 (2015)
86.
Journal Article
Absmeier, E.; Rosenberger, L.; Apelt, L.; Becke, C.; Santos, K. F.; Stelzl, U.; Wahl, M. C.: A noncanonical PWI domain in the N-terminal helicase-associated region of the spliceosomal Brr2 protein. Acta Crystallographica Section D-Biological Crystallography 71 (Pt 4), pp. 762 - 771 (2015)
87.
Journal Article
Degenkolbe, E.; Schwarz, C.; Ott, C. E.; Konig, J.; Schmidt-Bleek, K.; Ellinghaus, A.; Schmidt, T.; Lienau, J.; Ploger, F.; Mundlos, S. et al.; Duda, G. N.; Willie, B. M.; Seemann, P.: Improved bone defect healing by a superagonistic GDF5 variant derived from a patient with multiple synostoses syndrome. Bone 73, pp. 111 - 119 (2015)
88.
Journal Article
Ito, H.; Shiwaku, H.; Yoshida, C.; Homma, H.; Luo, H.; Chen, X.; Fujita, K.; Musante, L.; Fischer, U.; Frints, S. G. et al.; Romano, C.; Ikeuchi, Y.; Shimamura, T.; Imoto, S.; Miyano, S.; Muramatsu, S. I.; Kawauchi, T.; Hoshino, M.; Sudol, M.; Arumughan, A.; Wanker, E. E.; Rich, T.; Schwartz, C.; Matsuzaki, F.; Bonni, A.; Kalscheuer, V. M.; Okazawa, H.: In utero gene therapy rescues microcephaly caused by Pqbp1-hypofunction in neural stem progenitor cells. Molecular Psychiatry 20 (4), pp. 459 - 471 (2015)
89.
Journal Article
Parianen Lesemann, F. H.; Reuter, E.-M.; Godde, B.: Tactile stimulation interventions: Influence of stimulation parameters on sensorimotor behavior and neurophysiological correlates in healthy and clinical samples. Neuroscience and Biobehavioral Reviews 51, pp. 126 - 137 (2015)
90.
Journal Article
Sheinman, M.; Massip, F.; Arndt, P. F.: Statistical properties of pairwise distances between leaves on a random Yule tree. PLoS One 10 (3), e0120206 (2015)
91.
Journal Article
Bellander, M.; Bäckman, L.; Liu, T.; Schjeide, B.-M.; Bertram, L.; Schmiedek, F.; Lindenberger, U.; Lövdén, M.: Lower Baseline Performance but Greater Plasticity of Working Memory for Carriers of the Val Allele of the COMT Val(158)Met Polymorphism. Neuropsychology 29 (2), pp. 247 - 54 (2015)
92.
Journal Article
Grossmann, A.; Benlasfer, N.; Birth, P.; Hegele, A. K.; Wachsmuth, F.; Apelt, L.; Stelzl, U.: Phospho-tyrosine dependent protein-protein interaction network. Molecular Systems Biology 11 (3), 0794 (2015)
93.
Journal Article
Kobus, K.; Hartl, D.; Ott, C. E.; Osswald, M.; Huebner, A.; von der Hagen, M.; Emmerich, D.; Kühnisch, J.; Morreau, H.; Hes, F. J. et al.; Mautner, V. F.; Harder, A.; Tinschert, S.; Mundlos, S.; Kolanczyk, M.: Double NF1 inactivation affects adrenocortical function in NF1Prx1 mice and a human patient. PLoS One 10 (3), e0119030 (2015)
94.
Journal Article
Meierhofer, D.; Weidner, C.; Sauer, S.: Correction to "Integrative analysis of transcriptomics, proteomics and metabolomics data of white adipose and liver tissue of high-fat diet and rosiglitazone-treated insulin-resistant mice identified pathway alterations and molecular hubs". Journal of Proteome Research 14 (3), pp. 1643 - 1644 (2015)
95.
Journal Article
Iqbal, Z.; Willemsen, M. H.; Papon, M. A.; Musante, L.; Benevento, M.; Hu, H.; Venselaar, H.; Wissink-Lindhout, W. M.; Vulto-van Silfhout, A. T.; Vissers, L. E. et al.; de Brouwer, A. P.; Marouillat, S.; Wienker, T. F.; Ropers, H. H.; Kahrizi, K.; Nadif Kasri, N.; Najmabadi, H.; Laumonnier, F.; Kleefstra, T.; van Bokhoven, H.: Homozygous SLC6A17 mutations cause autosomal-recessive intellectual disability with progressive tremor, speech impairment, and behavioral problems. The American Journal of Human Genetics 96 (3), pp. 386 - 396 (2015)
96.
Journal Article
Bellander, M.; Bäckman, L.; Liu, T.; Schjeide, B.-M.; Bertram, L.; Schmiedek, F.; Lindenberger, U.; Lövdén, M.: Lower baseline performance but greater plasticity of working memory for carriers of the val allele of the COMT val158met polymorphism. Neuropsychology 29 (2), pp. 247 - 254 (2015)
97.
Journal Article
Bielmann, R.; Habann, M.; Eugster, M. R.; Lurz, R.; Calendar, R.; Klumpp, J.; Loessner, M. J.: Receptor binding proteins of Listeria monocytogenes bacteriophages A118 and P35 recognize serovar-specific teichoic acids. Virology 477, pp. 110 - 118 (2015)
98.
Journal Article
Larti, F.; Kahrizi, K.; Musante, L.; Hu, H.; Papari, E.; Fattahi, Z.; Bazazzadegan, N.; Liu, Z.; Banan, M.; Garshasbi, M. et al.; Wienker, T. F.; Ropers, H.-H.; Galjart, N.; Najmabadi, H.: A defect in the CLIP1 gene (CLIP-170) can cause autosomal recessive intellectual disability. European journal of human genetics 23 (3), pp. 331 - 336 (2015)
99.
Journal Article
Nalls, M. A.; Bras, J.; Hernandez, G. D.; Keller, M. F.; Majounie, E.; Renton, A. E.; Saad, M.; Jansen, I.; Guerreiro, R.; Lubbe, S. et al.; Plagnol, V.; Gibbs, R.; Schulte, C.; Pankratz, N.; Sutherland, M.; Bertram, L.; Lill, C. M.; DeStefano, A. L.; Faroud, T.; Eriksson, N.; Tung, J. Y.; Edsall, C.; Nichols, N.; Brooks, J.; Arepalli, S.; Pliner, H.; Letson, C.; Heutink, P.; Martinez, M.; Gasser, T.; Traynor, B. J.; Wood, N.; Hardy, J.; Singleton, A. B.: NeuroX, a fast and efficient genotyping platform for investigation of neurodegenerative diseases. Neurobiology of Aging 36 (3), pp. 1605.e7 - 1605.e12 (2015)
100.
Journal Article
Oladnabi, M.; Musante, L.; Larti, F.; Hu, H.; Abedini, S. S.; Wienker, T. F.; Ropers, H. H.; Kahrizi, K.; Najmabadi, H.: New evidence for the role of calpain 10 in autosomal recessive intellectual disability: identification of two novel nonsense variants by exome sequencing in Iranian families. Archives of Iranian Medicine 18 (3), pp. 179 - 184 (2015)
Go to Editor View