Peter Meinke

Affiliations: 
Maximillian Ludwig University - Munich 
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"Peter Meinke"
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Li C, Warren DT, Zhou C, et al. (2024) Nesprin-2 is a novel scaffold protein for telethonin and FHL-2 in the cardiomyocyte sarcomere. The Journal of Biological Chemistry. 107254
Schluessel S, Zhang W, Nowotny H, et al. (2023) 11-beta-hydroxysteroid dehydrogenase type 1 (HSD11B1) gene expression in muscle is linked to reduced skeletal muscle index in sarcopenic patients. Aging Clinical and Experimental Research
Donandt T, Todorow V, Hintze S, et al. (2023) Nuclear Small Dystrophin Isoforms during Muscle Differentiation. Life (Basel, Switzerland). 13
Todorow V, Hintze S, Schoser B, et al. (2023) Nuclear envelope transmembrane proteins involved in genome organization are misregulated in myotonic dystrophy type 1 muscle. Frontiers in Cell and Developmental Biology. 10: 1007331
Hintze S, Baber L, Hofmeister F, et al. (2022) Exploration of mitochondrial defects in sarcopenic hip fracture patients. Heliyon. 8: e11143
de Las Heras JI, Todorow V, Krečinić-Balić L, et al. (2022) Metabolic, fibrotic, and splicing pathways are all altered in Emery-Dreifuss muscular dystrophy Spectrum patients to differing degrees. Human Molecular Genetics
Todorow V, Hintze S, Kerr ARW, et al. (2021) Transcriptome Analysis in a Primary Human Muscle Cell Differentiation Model for Myotonic Dystrophy Type 1. International Journal of Molecular Sciences. 22
Meinke P, Kerr ARW, Czapiewski R, et al. (2019) A multistage sequencing strategy pinpoints novel candidate alleles for Emery-Dreifuss muscular dystrophy and supports gene misregulation as its pathomechanism. Ebiomedicine
Duan J, Navarro-Dorado J, Clark JH, et al. (2019) The cell-wide web coordinates cellular processes by directing site-specific Ca flux across cytoplasmic nanocourses. Nature Communications. 10: 2299
Bikkul MU, Faragher RGA, Worthington G, et al. (2018) Telomere elongation through hTERT immortalisation leads to chromosome repositioning in control cells and genomic instability in Hutchinson-Gilford Progeria syndrome fibroblasts, expressing a novel SUN1 isoform. Genes, Chromosomes & Cancer
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