Uwe Richter

发表

Quality control of mitochondrial protein synthesis is required for membrane integrity and cell fitness

P. Marttinen, Uwe Richter, Taina Lahtinen, 2015, The Journal of cell biology.

Translation of MT-ATP6 pathogenic variants reveals distinct regulatory consequences from the co-translational quality control of mitochondrial protein synthesis

S. Seneca, Kah Ying Ng, Uwe Richter, 2021, Human molecular genetics.

Why translation counts for mitochondria – retrograde signalling links mitochondrial protein synthesis to mitochondrial biogenesis and cell proliferation

Uwe Richter, B. Battersby, 2013, Journal of Cell Science.

A Mitochondrial Ribosomal and RNA Decay Pathway Blocks Cell Proliferation

D. Greco, H. Jacobs, T. Nyman, 2013, Current Biology.

Fibroblast Growth Factor 21 Drives Dynamics of Local and Systemic Stress Responses in Mitochondrial Myopathy with mtDNA Deletions.

V. Velagapudi, H. Liljenbäck, A. Suomalainen, 2019, Cell metabolism.

Defective mitochondrial RNA processing due to PNPT1 variants causes Leigh syndrome

A. Paetau, A. Suomalainen, Sanna Matilainen, 2017, Human molecular genetics.

Coibamide A Targets Sec61 to Prevent Biogenesis of Secretory and Membrane Proteins

W. Vogel, S. Oishi, K. McPhail, 2019, ACS chemical biology.

Phage-Type RNA Polymerase RPOTmp Performs Gene-Specific Transcription in Mitochondria of Arabidopsis thaliana[W][OA]

A. Millar, J. Whelan, I. Small, 2009, The Plant Cell Online.

Evolution of plant phage-type RNA polymerases: the genome of the basal angiosperm Nuphar advena encodes two mitochondrial and one plastid phage-type RNA polymerases

T. Börner, Chang-fa Yin, A. Weihe, 2010, BMC Evolutionary Biology.

Evolution of plant phage-type RNA polymerases

T. Börner, Chang-fa Yin, A. Weihe, 2022 .

Translation of MT-ATP6 pathogenic variants reveals distinct regulatory consequences from the co-translational quality control of mitochondrial protein synthesis

S. Seneca, Kah Ying Ng, Uwe Richter, 2021, bioRxiv.

Mitochondrial stress response triggered by defects in protein synthesis quality control

Robert W. Taylor, S. Seneca, T. Nyman, 2019, Life Science Alliance.

Mechanism of membrane-tethered mitochondrial protein synthesis

R. Best, A. Amunts, Austin Choi, 2021, Science.

Nonstop mRNAs generate a ground state of mitochondrial gene expression noise

L. Paulin, Cory D. Dunn, O. Safronov, 2022, Science advances.

RNA modification landscape of the human mitochondrial tRNALys regulates protein synthesis

E. Shoubridge, T. Pan, M. Evans, 2018, Nature Communications.

The molecular pathology of pathogenic mitochondrial tRNA variants

Robert W. Taylor, R. Mcfarland, Uwe Richter, 2021, FEBS letters.

A novel mitochondrial ATP6 frameshift mutation causing isolated complex V deficiency, ataxia and encephalomyopathy.

A. Schaller, C. Jackson, D. Hahn, 2017, European journal of medical genetics.

Convergent evolution of mevalonate pathway in Inonotus obliquus and Betula pendula

P. Auvinen, J. Salojärvi, L. Paulin, 2021, bioRxiv.

Whole-exome sequencing identifies a mutation in the mitochondrial ribosome protein MRPL44 to underlie mitochondrial infantile cardiomyopathy

A. Paetau, A. Suomalainen, H. Pihko, 2013, Journal of Medical Genetics.

Mice harbouring a SCA28 patient mutation in AFG3L2 develop late-onset ataxia associated with enhanced mitochondrial proteotoxicity

F. Tempia, S. Geuna, E. Donetti, 2018, Neurobiology of Disease.

A mitochondrial rRNA dimethyladenosine methyltransferase in Arabidopsis

A. Brennicke, T. Börner, A. Weihe, 2010, The Plant journal : for cell and molecular biology.

Mitochondrial nascent chain quality control determines organelle form and function.

O. Safronov, Uwe Richter, B. Battersby, 2019, ACS chemical biology.

Evolution of Phage-Type RNA Polymerases in Higher Plants: Characterization of the Single Phage-Type RNA Polymerase Gene from Selaginella moellendorffii

T. Börner, Chang-fa Yin, A. Weihe, 2009, Journal of Molecular Evolution.

Two RpoT genes of Physcomitrella patens encode phage-type RNA polymerases with dual targeting to mitochondria and plastids.

R. Reski, E. Decker, T. Börner, 2002, Gene.

Splicing Defect in Mitochondrial Seryl‐tRNA Synthetase Gene Causes Progressive Spastic Paresis Instead of HUPRA Syndrome

T. Linnankivi, P. Isohanni, H. Tyynismaa, 2016, Human mutation.

A variant in MRPS14 (uS14m) causes perinatal hypertrophic cardiomyopathy with neonatal lactic acidosis, growth retardation, dysmorphic features and neurological involvement

F. Martin, A. Schaller, M. Huemer, 2018, Human molecular genetics.

Splicing Defect in Mitochondrial Seryl‐tRNA Synthetase Gene Causes Progressive Spastic Paresis Instead of HUPRA Syndrome

T. Linnankivi, P. Isohanni, H. Tyynismaa, 2016, Human mutation.

Mice harbouring a SCA28 patient mutation in AFG3L2 develop late-onset ataxia associated with enhanced mitochondrial proteotoxicity

F. Tempia, S. Geuna, E. Donetti, 2019, Neurobiology of Disease.

Phage-Type RNA Polymerase RPOTmp Performs Gene-Specific Transcription in Mitochondria of Arabidopsis thaliana[W][OA]

A. Millar, I. Small, T. Börner, 2009, The Plant Cell Online.

A third mitochondrial RNA polymerase in the moss Physcomitrella patens

T. Börner, A. Weihe, Uwe Richter, 2013, Current Genetics.