Publikationen von P. Rehling
Alle Typen
Zeitschriftenartikel (69)
1.
Zeitschriftenartikel
10, e68213 (2021)
Defining the interactome of the human mitochondrial ribosome identifies SMIM4 and TMEM223 as respiratory chain assembly factors. eLife 2.
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184 (23), S. 5824 - 5837.e15 (2021)
An in vitro system to silence mitochondrial gene expression. Cell 3.
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12, 5715 (2021)
Mapping protein interactions in the active TOM-TIM23 supercomplex. Nature Communications 4.
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22 (4), e51635 (2021)
Monitoring mitochondrial translation in living cells. EMBO Reports 5.
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128 (6), S. e102 - e120 (2021)
Caveolin3 stabilizes McT1-mediated lactate/proton transport in cardiomyocytes. Circulation Research 6.
Zeitschriftenartikel
595 (2), S. 157 - 168 (2021)
Defining the architecture of the human TIM22 complex by chemical crosslinking. FEBS Letters 7.
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19 (7), S. 1161 - 1178 (2020)
A Cross-linking mass spectrometry approach defines protein interactions in yeast mitochondria. Molecular and Cellular Proteomics 8.
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COA6 facilitates cytochrome c oxidase biogenesis as thiol-reductase for copper metallochaperones in mitochondria. Journal of Molecular Biology, (in press) (2020)
9.
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From TOM to the TIM23 complex - handing over of a precursor. Biological Chemistry, (in press) (2020)
10.
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20 (19), e48833 (2019)
MITRAC15/COA1 promotes mitochondrial translation in a ND2 ribosome-nascent chain complex. EMBO Reports 11.
Zeitschriftenartikel
431 (15), S. 2835 - 2851 (2019)
A MICOS-TIM22 association promotes carrier import into human mitochondria. Journal of Molecular Biology 12.
Zeitschriftenartikel
11 (5), e9561 (2019)
Inhibition of proteasome rescues a pathogenic variant of respiratory chain assembly factor COA7. EMBO Molecular Medicine 13.
Zeitschriftenartikel
1865 (4), S. 810 - 821 (2019)
The role of mitochondrial cardiolipin in heart function and its implication in cardiac disease. Biochimica et Biophysica Acta 14.
Zeitschriftenartikel
22, 101152 (2019)
O2 affects mitochondrial functionality ex vivo. Redox Biology 15.
Zeitschriftenartikel
218 (2), 598 (2019)
ROMO1 is a constituent of the human presequence translocase required for YME1L protease import. The Journal of Cell Biology 16.
Zeitschriftenartikel
97 (2), S. 269 - 279 (2019)
Overexpression of branched-chain amino acid aminotransferases rescues the growth defects of cells lacking the Barth syndrome-related gene TAZ1. Journal of Molecular Medicine 17.
Zeitschriftenartikel
568 (7758), S. 635 - 637 (2019)
Guarding the gate for mitochondrial entry. Nature 18.
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38 (15), e100871 (2019)
Redox signals at the ER-mitochondria interface control melanoma progression. The EMBO Journal 19.
Zeitschriftenartikel
27 (23), S. 4135 - 4144 (2018)
Mutations of the mitochondrial carrier translocase channel subunit TIM22 cause early-onset mitochondrial myopathy. Human Molecular Genetics 20.
Zeitschriftenartikel
8, 16913 (2018)
The codon sequences predict protein lifetimes and other parameters of the protein life cycle in the mouse brain. Scientific Reports