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Anna Maria Haschke

Establishment and Characterization of hTERT Immortalized Hutchinson–Gilford Progeria Fibroblast Cell Lines
2022 · Haihuan Lin, Juliane Mensch, et al. · Cells · 11
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Characterization of two iPSC lines from patients with maternally inherited leigh (MILS) and neuropathy, ataxia, and retinitis pigmentosa (NARP) syndrome carrying the MT-ATP6 m.8993 T>G mutation at different degrees of heteroplasmy
2024 · Anna Maria Haschke, Sebastian Diecke, et al. · Stem Cell Research · 1
3.74eP Biallelic MCUR1 nonsense mutation associated with vacuolar myopathy and altered mitochondrial calcium signalling
2026 · Anna Maria Haschke, Anja von Renesse, et al. · Neuromuscular Disorders
Biallelic MCUR1 nonsense mutation associated with vacuolar myopathy and altered mitochondrial calcium signaling
2026 · Anna Maria Haschke, Anja von Renesse, et al. · Acta Neuropathologica Communications
Additional file 2 of Biallelic MCUR1 nonsense mutation associated with vacuolar myopathy and altered mitochondrial calcium signaling
2026 · Haschke, Anna Maria, von Renesse, Anja, et al. · Figshare
Additional file 1 of Biallelic MCUR1 nonsense mutation associated with vacuolar myopathy and altered mitochondrial calcium signaling
2026 · Haschke, Anna Maria, von Renesse, Anja, et al. · Figshare
Reprogramming of two induced pluripotent stem cell clones from a patient with a novel MT-ATP6/8 mutation (m.8570 T > C)
2025 · Anna Maria Haschke, Sebastian Diecke, et al. · Stem Cell Research
Works count: 7
Citation count: 12
H-index: 1
I10-index: 1
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