A. Pajak

发表

A functional peptidyl-tRNA hydrolase, ICT1, has been recruited into the human mitochondrial ribosome

Hans J C T Wessels, M. Huynen, R. Lightowlers, 2010, The EMBO journal.

Intra-mitochondrial Methylation Deficiency Due to Mutations in SLC25A26

Y. Okazaki, P. Govaert, B. Loeys, 2015, American journal of human genetics.

Scalable and robust SARS-CoV-2 testing in an academic center

Robert L. Goldstone, James M. A. Turner, J. Ule, 2020, Nature Biotechnology.

Resolving chaperone-assisted protein folding on the ribosome at the peptide level

T. Wales, Steven A. Howell, S. Kjær, 2022, bioRxiv.

Estimating the effectiveness of routine asymptomatic PCR testing at different frequencies for the detection of SARS-CoV-2 infections

Robert L. Goldstone, Naomi R. Waterlow, Quentin J. Leclerc, 2020, BMC Medicine.

Chorea, psychosis, acanthocytosis, and prolonged survival associated with ELAC2 mutations

P. Svenningsson, I. Savitcheva, A. Pajak, 2018, Neurology.

Defects of mitochondrial RNA turnover lead to the accumulation of double-stranded RNA in vivo

A. Pajak, A. Dhir, R. Wibom, 2019, PLoS genetics.

Characterisation of human mtRF1 and C12orf65 : what are their roles in mitochondrial protein synthesis?

A. Pajak, A. Pająk, 2013 .

Termination of Protein Synthesis in Mammalian Mitochondria*

Z. Chrzanowska-Lightowlers, R. Lightowlers, A. Pajak, 2011, The Journal of Biological Chemistry.

Pandemic peak SARS-CoV-2 infection and seroconversion rates in London frontline health-care workers

Robert L. Goldstone, James M. A. Turner, J. Ule, 2020, The Lancet.

Modulation of mtDNA copy number ameliorates the pathological consequences of a heteroplasmic mtDNA mutation in the mouse

A. Pajak, N. Larsson, R. Wibom, 2019, Science Advances.

Adult Onset Leigh Syndrome in the Intensive Care Setting: A Novel Presentation of a C12orf65 Related Mitochondrial Disease

Robert W. Taylor, P. Chinnery, R. Lightowlers, 2015, Journal of neuromuscular diseases.