Zeitschriftenartikel (1347)
641.
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16 (11), S. 2980 - 90 (2016)
A Phenotype-Driven Approach to Generate Mouse Models with Pathogenic mtDNA Mutations Causing Mitochondrial Disease. Cell Rep 642.
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291 (44), S. 23175 - 23187 (2016)
Disruption of Macrodomain Protein SCO6735 Increases Antibiotic Production in Streptomyces coelicolor. J Biol Chem 643.
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17 (7), S. 380 - 385 (2016)
Maternal and child cytokine relationship in early life is not altered by cytokine gene polymorphisms. Genes Immun 644.
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6, S. 31782 (2016)
Increasing the performance of pooled CRISPR-Cas9 drop-out screening. Sci Rep 645.
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16 (9), S. 2387 - 98 (2016)
COX7A2L Is a Mitochondrial Complex III Binding Protein that Stabilizes the III2+IV Supercomplex without Affecting Respirasome Formation. Cell Rep 646.
Zeitschriftenartikel
1862 (1), S. 81 - 89 (2016)
Intramitochondrial phospholipid trafficking. Biochim Biophys Acta 647.
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8 (8), S. 1790 - 801 (2016)
Assessment of the contribution of APOE gene variants to metabolic phenotypes associated with familial longevity at middle age. Aging (Albany NY) 648.
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2 (8), S. e1600963 (2016)
POLRMT regulates the switch between replication primer formation and gene expression of mammalian mtDNA. Sci Adv 649.
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19 (10), S. 1321 - 30 (2016)
Polycomb repressive complex 2 (PRC2) silences genes responsible for neurodegeneration. Nat Neurosci 650.
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5 (2016)
Homozygous YME1L1 mutation causes mitochondriopathy with optic atrophy and mitochondrial network fragmentation. Elife 651.
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16 (7), S. 1874 - 90 (2016)
Hierarchical RNA Processing Is Required for Mitochondrial Ribosome Assembly. Cell Rep 652.
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6, S. 30484 (2016)
Fibroblast growth factor 21 reflects liver fat accumulation and dysregulation of signalling pathways in the liver of C57BL/6J mice. Sci Rep 653.
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82, S. 166 - 74 (2016)
Employing biomarkers of healthy ageing for leveraging genetic studies into human longevity. Exp Gerontol 654.
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17 (1), S. 138 (2016)
Blood lipids influence DNA methylation in circulating cells. Genome Biol 655.
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7, S. 11884 (2016)
Loss of the RNA-binding protein TACO1 causes late-onset mitochondrial dysfunction in mice. Nat Commun 656.
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15 (5), S. 872 - 84 (2016)
Longer lifespan in male mice treated with a weakly estrogenic agonist, an antioxidant, an alpha-glucosidase inhibitor or a Nrf2-inducer. Aging Cell 657.
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213 (5), S. 525 - 34 (2016)
MICOS and phospholipid transfer by Ups2-Mdm35 organize membrane lipid synthesis in mitochondria. J Cell Biol 658.
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15 (7), S. 695 - 707 (2016)
Identification of additional risk loci for stroke and small vessel disease: a meta-analysis of genome-wide association studies. Lancet Neurol. 659.
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53 (10), S. 690 - 6 (2016)
Deficiency of HTRA2/Omi is associated with infantile neurodegeneration and 3-methylglutaconic aciduria. J Med Genet 660.
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129 (12), S. 2297 - 306 (2016)
OPA1 processing in cell death and disease - the long and short of it. J Cell Sci