Mitochondrial Gene Expression – Seite 3

20. Juli 2020

Novel Secondary Ion Mass Spectrometry Methods for the Examination of Metabolic Effects at the Cellular and Subcellular Levels

Bonnin EA, Rizzoli SO

22. Juli 2020

Local translation in synaptic mitochondria influences synaptic transmission

Yousefi R, Fornasiero EF, Cyganek L, Jakobs S, Rizzoli SO, Rehling P, Pacheu-Grau D

29. Juli 2020

Developmental GABA polarity switch and neuronal plasticity in Bioengineered Neuronal Organoids

Zafeiriou MP, Bao G, Hudson J, Halder R, Blenkle A, Schreiber MK, Fischer A, Schild D, Zimmermann WH

11. August 2020

Multicolor 3D MINFLUX nanoscopy of mitochondrial MICOS proteins

Pape JK, Stephan T, Balzarotti F, Büchner R, Lange F, Riedel D, Jakobs S, Hell SW

28. August 2020

Premature aging disorders: A clinical and genetic compendium

Schnabel F, Kornak U, Wollnik B

7. Oktober 2020

Heterozygous truncating variants in SUFU cause congenital ocular motor apraxia

Schröder S, Li Y, Yigit G, Altmüller J, Bader I, Bevot A, Biskup S, Dreha-Kulaczewski S, Christoph Korenke G, Kottke R, Mayr JA, Preisel M, Toelle SP, Wente-Schulz S, Wortmann SB, Hahn H, Boltshauser E, Uhmann A, Wollnik B, Brockmann K

28. Oktober 2020

Mechanism of SARS-CoV-2 polymerase inhibition by remdesivir

Kokic G, Hillen HS, Tegunov D, Dienemann C, Seitz F, Schmitzova J, Farnung L, Siewert A, Hoebartner C, Cramer P

30. November 2020

Structural basis of nucleosome transcription mediated by Chd1 and FACT

Farnung L, Ochmann M, Engeholm M, Cramer P

2. Dezember 2020

Dual function of GTPBP6 in biogenesis and recycling of human mitochondrial ribosomes

Lavdovskaia E, Denks K, Nadler F, Steube E, Linden A, Urlaub H, Rodnina MV, Richter-Dennerlein R

7. Dezember 2020

Aplasia cutis congenita in a CDC42-related developmental phenotype

Schnabel F, Kamphausen SB, Funke R, Kaulfuß S, Wollnik B, Zenker M

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