Lindsey Van Haute

Cambridge, ENG, United Kingdom

Last Updated: 09/26/2026

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Found 26 publications

Biallelic NSUN3 Variants Cause Diverse Phenotypic Spectrum Disease: From Isolated Optic Atrophy to Severe Early-Onset Mitochondrial Disorder.

Biallelic NSUN3 Variants Cause Diverse Phenotypic Spectrum Disease: From Isolated Optic Atrophy to Severe Early-Onset Mitochondrial Disorder.

Journal: Investigative ophthalmology & visual science

Published: June 04, 2025

Clinically translatable mitochondrial gene therapy in muscle using tandem mtZFN architecture.

Clinically translatable mitochondrial gene therapy in muscle using tandem mtZFN architecture.

Journal: EMBO molecular medicine

Published: October 08, 2024

The catalytic activity of methyltransferase METTL15 is dispensable for its role in mitochondrial ribosome biogenesis.

The catalytic activity of methyltransferase METTL15 is dispensable for its role in mitochondrial ribosome biogenesis.

Journal: RNA biology

Published: June 24, 2024

Pathogenic PDE12 variants impair mitochondrial RNA processing causing neonatal mitochondrial disease.

Pathogenic PDE12 variants impair mitochondrial RNA processing causing neonatal mitochondrial disease.

Journal: EMBO molecular medicine

Published: April 05, 2024

Transcriptome Sequencing Reveals the Mechanism behind Chemically Induced Oral Mucositis in a 3D Cell Culture Model.

Transcriptome Sequencing Reveals the Mechanism behind Chemically Induced Oral Mucositis in a 3D Cell Culture Model.

Journal: International journal of molecular sciences

Published: January 29, 2023

A library of base editors for the precise ablation of all protein-coding genes in the mouse mitochondrial genome.

A library of base editors for the precise ablation of all protein-coding genes in the mouse mitochondrial genome.

Journal: Nature biomedical engineering

Published: June 01, 2022

TEFM variants impair mitochondrial transcription causing childhood-onset neurological disease.

TEFM variants impair mitochondrial transcription causing childhood-onset neurological disease.

Journal: Nature communications

Published: September 30, 2021

In vivo mitochondrial base editing via adeno-associated viral delivery to mouse post-mitotic tissue.

In vivo mitochondrial base editing via adeno-associated viral delivery to mouse post-mitotic tissue.

Journal: Nature communications

Published: September 14, 2021

A late-stage assembly checkpoint of the human mitochondrial ribosome large subunit.

A late-stage assembly checkpoint of the human mitochondrial ribosome large subunit.

Journal: Nature communications

Published: July 27, 2021

The FASTK family proteins fine-tune mitochondrial RNA processing.

The FASTK family proteins fine-tune mitochondrial RNA processing.

Journal: PLoS genetics

Published: May 04, 2021

Quantitative density gradient analysis by mass spectrometry (qDGMS) and complexome profiling analysis (ComPrAn) R package for the study of macromolecular complexes.

Quantitative density gradient analysis by mass spectrometry (qDGMS) and complexome profiling analysis (ComPrAn) R package for the study of macromolecular complexes.

Journal: Biochimica et biophysica acta. Bioenergetics

Published: December 07, 2020

Detection of 5-formylcytosine in Mitochondrial Transcriptome.

Detection of 5-formylcytosine in Mitochondrial Transcriptome.

Journal: Methods in molecular biology (Clifton, N.J.)

Published: November 24, 2020

Showing 1-12 of 26

Last Updated: 09/26/2026