Florence J. Van Tienen

Maastricht, LI 6229ER, Netherlands

Last Updated: 09/26/2026

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Found 19 publications

Fusion Between Control Mesoangioblasts and mtDNA-Mutant Myotubes Preserves Myotube Morphology and Mitochondrial Network Organization.

Fusion Between Control Mesoangioblasts and mtDNA-Mutant Myotubes Preserves Myotube Morphology and Mitochondrial Network Organization.

Journal: International journal of molecular sciences

Published: December 19, 2025

Intra-arterial transplantation of autologous mesoangioblasts in m.3243A>G mutation carriers is safe: First phase 1/2 human clinical study.

Intra-arterial transplantation of autologous mesoangioblasts in m.3243A>G mutation carriers is safe: First phase 1/2 human clinical study.

Journal: Molecular therapy : the journal of the American Society of Gene Therapy

Published: December 23, 2024

Spinning Disk Confocal Microscopy for Optimized and Quantified Live Imaging of 3D Mitochondrial Network.

Spinning Disk Confocal Microscopy for Optimized and Quantified Live Imaging of 3D Mitochondrial Network.

Journal: International journal of molecular sciences

Published: March 24, 2024

Mitochondrial DNA D-loop variants correlate with a primary open-angle glaucoma subgroup.

Mitochondrial DNA D-loop variants correlate with a primary open-angle glaucoma subgroup.

Journal: Frontiers in ophthalmology

Published: October 08, 2023

One-pot, degradable, silica nanocarriers with encapsulated oligonucleotides for mitochondrial specific targeting.

One-pot, degradable, silica nanocarriers with encapsulated oligonucleotides for mitochondrial specific targeting.

Journal: Discover nano

Published: August 03, 2023

Low mitochondrial DNA copy number in buffy coat DNA of primary open-angle glaucoma patients.

Low mitochondrial DNA copy number in buffy coat DNA of primary open-angle glaucoma patients.

Journal: Experimental eye research

Published: February 02, 2023

Fusion of Wild-Type Mesoangioblasts with Myotubes of mtDNA Mutation Carriers Leads to a Proportional Reduction in mtDNA Mutation Load.

Fusion of Wild-Type Mesoangioblasts with Myotubes of mtDNA Mutation Carriers Leads to a Proportional Reduction in mtDNA Mutation Load.

Journal: International journal of molecular sciences

Published: December 14, 2022

Natural history, outcome measures and trial readiness in LAMA2-related muscular dystrophy and SELENON-related myopathy in children and adults: protocol of the LAST STRONG study.

Natural history, outcome measures and trial readiness in LAMA2-related muscular dystrophy and SELENON-related myopathy in children and adults: protocol of the LAST STRONG study.

Journal: BMC neurology

Published: June 23, 2021

Myogenic Cell Transplantation in Genetic and Acquired Diseases of Skeletal Muscle.

Myogenic Cell Transplantation in Genetic and Acquired Diseases of Skeletal Muscle.

Journal: Frontiers in genetics

Published: April 29, 2021

Blood biomarkers for assessment of mitochondrial dysfunction: An expert review.

Blood biomarkers for assessment of mitochondrial dysfunction: An expert review.

Journal: Mitochondrion

Published: April 13, 2021

Pathogenic SLIRP variants as a novel cause of autosomal recessive mitochondrial encephalomyopathy with complex I and IV deficiency.

Pathogenic SLIRP variants as a novel cause of autosomal recessive mitochondrial encephalomyopathy with complex I and IV deficiency.

Journal: European journal of human genetics : EJHG

Published: December 08, 2020

Tfam Knockdown Results in Reduction of mtDNA Copy Number, OXPHOS Deficiency and Abnormalities in Zebrafish Embryos.

Tfam Knockdown Results in Reduction of mtDNA Copy Number, OXPHOS Deficiency and Abnormalities in Zebrafish Embryos.

Journal: Frontiers in cell and developmental biology

Published: December 19, 2019

Showing 1-12 of 19

Last Updated: 09/26/2026