Zeitschriftenartikel (128)

81.
Zeitschriftenartikel
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), S. 1505 - 1507 (2015)
82.
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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), S. 765 - 780 (2015)
83.
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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.
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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.
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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), S. 1235 - 1251 (2015)
86.
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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), S. 762 - 771 (2015)
87.
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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, S. 111 - 119 (2015)
88.
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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), S. 459 - 471 (2015)
89.
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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, S. 126 - 137 (2015)
90.
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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.
Zeitschriftenartikel
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), S. 247 - 54 (2015)
92.
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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.
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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.
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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), S. 1643 - 1644 (2015)
95.
Zeitschriftenartikel
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), S. 386 - 396 (2015)
96.
Zeitschriftenartikel
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), S. 247 - 254 (2015)
97.
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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, S. 110 - 118 (2015)
98.
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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), S. 331 - 336 (2015)
99.
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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), S. 1605.e7 - 1605.e12 (2015)
100.
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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), S. 179 - 184 (2015)
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