Annika Zink

Duesseldorf, NW, Germany

Last Updated: 09/26/2026

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Found 21 publications

Generation of an iPSC line IUFi004-A-13 with homozygous NDUFS1 mutation for the study of Leigh syndrome.

Generation of an iPSC line IUFi004-A-13 with homozygous NDUFS1 mutation for the study of Leigh syndrome.

Journal: Stem cell research

Published: February 07, 2026

Canonical autophagy remains inactive in induced pluripotent stem cells and neuronal progenitor cells following DNA damage induced by BPDE or etoposide.

Canonical autophagy remains inactive in induced pluripotent stem cells and neuronal progenitor cells following DNA damage induced by BPDE or etoposide.

Journal: Scientific reports

Published: September 26, 2025

Pluripotent stem-cell-based screening uncovers sildenafil as a mitochondrial disease therapy.

Pluripotent stem-cell-based screening uncovers sildenafil as a mitochondrial disease therapy.

Journal: Cell

Published: April 14, 2025

CRISPR/Cas9-mediated editing of COQ4 in induced pluripotent stem cells: A model for investigating COQ4-associated human coenzyme Q10 deficiency.

CRISPR/Cas9-mediated editing of COQ4 in induced pluripotent stem cells: A model for investigating COQ4-associated human coenzyme Q10 deficiency.

Journal: Stem cell research

Published: January 20, 2025

Patients with Allan-Herndon-Dudley Syndrome (MCT8 Deficiency) Display Symptoms of Parkinsonism in Childhood and Respond to Levodopa/Carbidopa Treatment.

Patients with Allan-Herndon-Dudley Syndrome (MCT8 Deficiency) Display Symptoms of Parkinsonism in Childhood and Respond to Levodopa/Carbidopa Treatment.

Journal: Movement disorders : official journal of the Movement Disorder Society

Published: September 04, 2024

Generation of two mother-child pairs of iPSCs from maternally inherited Leigh syndrome patients with m.8993 T > G and m.9176 T > G MT-ATP6 mutations.

Generation of two mother-child pairs of iPSCs from maternally inherited Leigh syndrome patients with m.8993 T > G and m.9176 T > G MT-ATP6 mutations.

Journal: Stem cell research

Published: December 22, 2022

A Novel Gene Controls a New Structure: PiggyBac Transposable Element-Derived 1, Unique to Mammals, Controls Mammal-Specific Neuronal Paraspeckles.

A Novel Gene Controls a New Structure: PiggyBac Transposable Element-Derived 1, Unique to Mammals, Controls Mammal-Specific Neuronal Paraspeckles.

Journal: Molecular biology and evolution

Published: October 07, 2022

Teriflunomide as a therapeutic means for myelin repair.

Teriflunomide as a therapeutic means for myelin repair.

Journal: Journal of neuroinflammation

Published: September 16, 2022

RNA-based generation of iPSCs from a boy carrying the mutation m.9185 T>C in the mitochondrial gene MT-ATP6 and from his healthy mother.

RNA-based generation of iPSCs from a boy carrying the mutation m.9185 T>C in the mitochondrial gene MT-ATP6 and from his healthy mother.

Journal: Stem cell research

Published: August 26, 2022

High-content analysis of neuronal morphology in human iPSC-derived neurons.

High-content analysis of neuronal morphology in human iPSC-derived neurons.

Journal: STAR protocols

Published: August 22, 2022

High-content screening of mitochondrial polarization in neural cells derived from human pluripotent stem cells.

High-content screening of mitochondrial polarization in neural cells derived from human pluripotent stem cells.

Journal: STAR protocols

Published: August 12, 2022

Generation of four iPSC lines from four patients with Leigh syndrome carrying homoplasmic mutations m.8993T > G or m.8993T > C in the mitochondrial gene MT-ATP6.

Generation of four iPSC lines from four patients with Leigh syndrome carrying homoplasmic mutations m.8993T > G or m.8993T > C in the mitochondrial gene MT-ATP6.

Journal: Stem cell research

Published: February 06, 2022

Showing 1-12 of 21

Last Updated: 09/26/2026