Bradley Peter
R&D, AstraZeneca
Goeteborg, O, Sweden
Goeteborg, O, Sweden
Last Updated: 09/26/2026
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Found 17 publications
Development of novel high-throughput biochemical competition assays to identify ligands of human asialoglycoprotein receptor 1.
Journal: SLAS discovery : advancing life sciences R & D
Published: July 02, 2025
The disease-causing mutation p.F907I reveals a novel pathogenic mechanism for POLγ-related diseases.
The disease-causing mutation p.F907I reveals a novel pathogenic mechanism for POLγ-related diseases.
Journal: Biochimica et biophysica acta. Molecular basis of disease
Published: March 23, 2023
Disease causing mutation (P178L) in mitochondrial transcription factor A results in impaired mitochondrial transcription initiation.
Journal: Biochimica et biophysica acta. Molecular basis of disease
Published: March 13, 2022
Non-coding 7S RNA inhibits transcription via mitochondrial RNA polymerase dimerization.
Journal: Cell
Published: October 29, 2021
Correction to 'DNA polymerase gamma mutations that impair holoenzyme stability cause catalytic subunit depletion'.
Journal: Nucleic acids research
Published: September 14, 2021
Ribonucleotides embedded in template DNA impair mitochondrial RNA polymerase progression.
Journal: Nucleic acids research
Published: April 23, 2021
DNA polymerase gamma mutations that impair holoenzyme stability cause catalytic subunit depletion.
Journal: Nucleic acids research
Published: December 15, 2020
Functional analysis of a novel POLγA mutation associated with a severe perinatal mitochondrial encephalomyopathy.
Journal: Neuromuscular disorders : NMD
Published: October 12, 2020
POLRMT mutations impair mitochondrial transcription causing neurological disease.
Journal: Nature communications
Published: May 13, 2020
TWINKLE and Other Human Mitochondrial DNA Helicases: Structure, Function and Disease.
Journal: Genes
Published: March 23, 2020
Small-molecule inhibitors of human mitochondrial DNA transcription.
Journal: Nature
Published: May 30, 2019
Last Updated: 09/26/2026