Zeitschriftenartikel (1347)

641.
Zeitschriftenartikel
Kauppila, J. H. K.; Baines, H. L.; Bratic, A.; Simard, M.-L.; Freyer, C.; Mourier, A.; Stamp, C.; Filograna, R.; Larsson, N.G.; Greaves, L. C. et al.; Stewart, J. B.: A Phenotype-Driven Approach to Generate Mouse Models with Pathogenic mtDNA Mutations Causing Mitochondrial Disease. Cell Rep 16 (11), S. 2980 - 90 (2016)
642.
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Lalić, J.; Posavec Marjanović, M.; Palazzo, L.; Perina, D.; Sabljić, I.; Žaja, R.; Colby, T.; Pleše, B.; Halasz, M.; Jankevicius, G. et al.; Bucca, G.; Ahel, M.; Matić, I.; Ćetković, H.; Luić, M.; Mikoč, A.; Ahel, I.: Disruption of Macrodomain Protein SCO6735 Increases Antibiotic Production in Streptomyces coelicolor. J Biol Chem 291 (44), S. 23175 - 23187 (2016)
643.
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Djuardi, Y.; Supali, T.; Wibowo, H.; Heijmans, B. T.; Deelen, J.; Slagboom, P. E.; Houwing-Duistermaat, J. J.; Sartono, E.; Yazdanbakhsh, M.: Maternal and child cytokine relationship in early life is not altered by cytokine gene polymorphisms. Genes Immun 17 (7), S. 380 - 385 (2016)
644.
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Cross, B. C.; Lawo, S.; Archer, C. R.; Hunt, J. R.; Yarker, J. L.; Riccombeni, A.; Little, A. S.; McCarthy, N. J.; Moore, J. D.: Increasing the performance of pooled CRISPR-Cas9 drop-out screening. Sci Rep 6, S. 31782 (2016)
645.
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Perez-Perez, R.; Lobo-Jarne, T.; Milenkovic, D.; Mourier, A.; Bratic, A.; Garcia-Bartolome, A.; Fernandez-Vizarra, E.; Cadenas, S.; Delmiro, A.; Garcia-Consuegra, I. et al.; Arenas, J.; Martin, M. A.; Larsson, N.G.; Ugalde, C.: COX7A2L Is a Mitochondrial Complex III Binding Protein that Stabilizes the III2+IV Supercomplex without Affecting Respirasome Formation. Cell Rep 16 (9), S. 2387 - 98 (2016)
646.
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Tatsuta, T.; Langer, T.: Intramitochondrial phospholipid trafficking. Biochim Biophys Acta 1862 (1), S. 81 - 89 (2016)
647.
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Noordam, R.; Oudt, C. H.; Deelen, J.; Slagboom, P. E.; Beekman, M.; van Heemst, D.: Assessment of the contribution of APOE gene variants to metabolic phenotypes associated with familial longevity at middle age. Aging (Albany NY) 8 (8), S. 1790 - 801 (2016)
648.
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Kühl, I.; Miranda, M.; Posse, V.; Milenkovic, D.; Mourier, A.; Siira, S. J.; Bonekamp, N.; Neumann, U.; Filipovska, A.; Polosa, P. L. et al.; Gustafsson, C. M.; Larsson, N.G.: POLRMT regulates the switch between replication primer formation and gene expression of mammalian mtDNA. Sci Adv 2 (8), S. e1600963 (2016)
649.
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von Schimmelmann, M.; Feinberg, P. A.; Sullivan, J. M.; Ku, S. M.; Badimon, A.; Duff, M. K.; Wang, Z.; Lachmann, A.; Dewell, S.; Ma'ayan, A. et al.; Han, M. H.; Tarakhovsky, A.; Schaefer, A.: Polycomb repressive complex 2 (PRC2) silences genes responsible for neurodegeneration. Nat Neurosci 19 (10), S. 1321 - 30 (2016)
650.
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Hartmann, B.; Wai, T.; Hu, H.; MacVicar, T.; Musante, L.; Fischer-Zirnsak, B.; Stenzel, W.; Graf, R.; van den Heuvel, L.; Ropers, H. H. et al.; Wienker, T. F.; Hubner, C.; Langer, T.; Kaindl, A. M.: Homozygous YME1L1 mutation causes mitochondriopathy with optic atrophy and mitochondrial network fragmentation. Elife 5 (2016)
651.
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Rackham, O.; Busch, J. D.; Matic, S.; Siira, S. J.; Kuznetsova, I.; Atanassov, I.; Ermer, J. A.; Shearwood, A. M.; Richman, T. R.; Stewart, J. B. et al.; Mourier, A.; Milenkovic, D.; Larsson, N.G.; Filipovska, A.: Hierarchical RNA Processing Is Required for Mitochondrial Ribosome Assembly. Cell Rep 16 (7), S. 1874 - 90 (2016)
652.
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Rusli, F.; Deelen, J.; Andriyani, E.; Boekschoten, M. V.; Lute, C.; van den Akker, E. B.; Muller, M.; Beekman, M.; Steegenga, W. T.: Fibroblast growth factor 21 reflects liver fat accumulation and dysregulation of signalling pathways in the liver of C57BL/6J mice. Sci Rep 6, S. 30484 (2016)
653.
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Deelen, J.; van den Akker, E. B.; Trompet, S.; van Heemst, D.; Mooijaart, S. P.; Slagboom, P. E.; Beekman, M.: Employing biomarkers of healthy ageing for leveraging genetic studies into human longevity. Exp Gerontol 82, S. 166 - 74 (2016)
654.
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Dekkers, K. F.; van Iterson, M.; Slieker, R. C.; Moed, M. H.; Bonder, M. J.; van Galen, M.; Mei, H.; Zhernakova, D. V.; van den Berg, L. H.; Deelen, J. et al.; van Dongen, J.; van Heemst, D.; Hofman, A.; Hottenga, J. J.; van der Kallen, C. J.; Schalkwijk, C. G.; Stehouwer, C. D.; Tigchelaar, E. F.; Uitterlinden, A. G.; Willemsen, G.; Zhernakova, A.; Franke, L.; t Hoen, P. A.; Jansen, R.; van Meurs, J.; Boomsma, D. I.; van Duijn, C. M.; van Greevenbroek, M. M.; Veldink, J. H.; Wijmenga, C.; Consortium, B.; van Zwet, E. W.; Slagboom, P. E.; Jukema, J. W.; Heijmans, B. T.: Blood lipids influence DNA methylation in circulating cells. Genome Biol 17 (1), S. 138 (2016)
655.
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Richman, T. R.; Spahr, H.; Ermer, J. A.; Davies, S. M.; Viola, H. M.; Bates, K. A.; Papadimitriou, J.; Hool, L. C.; Rodger, J.; Larsson, N.G. et al.; Rackham, O.; Filipovska, A.: Loss of the RNA-binding protein TACO1 causes late-onset mitochondrial dysfunction in mice. Nat Commun 7, S. 11884 (2016)
656.
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Strong, R.; Miller, R. A.; Antebi, A.; Astle, C. M.; Bogue, M.; Denzel, M. S.; Fernandez, E.; Flurkey, K.; Hamilton, K. L.; Lamming, D. W. et al.; Javors, M. A.; de Magalhaes, J. P.; Martinez, P. A.; McCord, J. M.; Miller, B. F.; Muller, M.; Nelson, J. F.; Ndukum, J.; Rainger, G. E.; Richardson, A.; Sabatini, D. M.; Salmon, A. B.; Simpkins, J. W.; Steegenga, W. T.; Nadon, N. L.; Harrison, D. E.: Longer lifespan in male mice treated with a weakly estrogenic agonist, an antioxidant, an alpha-glucosidase inhibitor or a Nrf2-inducer. Aging Cell 15 (5), S. 872 - 84 (2016)
657.
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Aaltonen, M. J.; Friedman, J. R.; Osman, C.; Salin, B.; di Rago, J. P.; Nunnari, J.; Langer, T.; Tatsuta, T.: MICOS and phospholipid transfer by Ups2-Mdm35 organize membrane lipid synthesis in mitochondria. J Cell Biol 213 (5), S. 525 - 34 (2016)
658.
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Deelen, J.; Neurology Working Group of the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium; Stroke Genetics Network; International Stroke Genetics Consortium (ISGC): Identification of additional risk loci for stroke and small vessel disease: a meta-analysis of genome-wide association studies. Lancet Neurol. 15 (7), S. 695 - 707 (2016)
659.
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Mandel, H.; Saita, S.; Edvardson, S.; Jalas, C.; Shaag, A.; Goldsher, D.; Vlodavsky, E.; Langer, T.; Elpeleg, O.: Deficiency of HTRA2/Omi is associated with infantile neurodegeneration and 3-methylglutaconic aciduria. J Med Genet 53 (10), S. 690 - 6 (2016)
660.
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MacVicar, T.; Langer, T.: OPA1 processing in cell death and disease - the long and short of it. J Cell Sci 129 (12), S. 2297 - 306 (2016)
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