| Year |
Citation |
Score |
| 2023 |
Schluessel S, Zhang W, Nowotny H, Bidlingmaier M, Hintze S, Kunz S, Martini S, Mehaffey S, Meinke P, Neuerburg C, Schmidmaier R, Schoser B, Reisch N, Drey M. 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. PMID 37943405 DOI: 10.1007/s40520-023-02574-w |
0.3 |
|
| 2023 |
Donandt T, Todorow V, Hintze S, Graupner A, Schoser B, Walter MC, Meinke P. Nuclear Small Dystrophin Isoforms during Muscle Differentiation. Life (Basel, Switzerland). 13. PMID 37374149 DOI: 10.3390/life13061367 |
0.801 |
|
| 2023 |
Todorow V, Hintze S, Schoser B, Meinke P. Nuclear envelope transmembrane proteins involved in genome organization are misregulated in myotonic dystrophy type 1 muscle. Frontiers in Cell and Developmental Biology. 10: 1007331. PMID 36699009 DOI: 10.3389/fcell.2022.1007331 |
0.811 |
|
| 2022 |
Hintze S, Baber L, Hofmeister F, Jarmusch S, Todorow V, Mehaffey S, Tanganelli F, Ferrari U, Neuerburg C, Teupser D, Bidlingmaier M, Marques JG, Koletzko B, Schoser B, Drey M, ... Meinke P, et al. Exploration of mitochondrial defects in sarcopenic hip fracture patients. Heliyon. 8: e11143. PMID 36303924 DOI: 10.1016/j.heliyon.2022.e11143 |
0.765 |
|
| 2022 |
de Las Heras JI, Todorow V, Krečinić-Balić L, Hintze S, Czapiewski R, Webb S, Schoser B, Meinke P, Schirmer EC. Metabolic, fibrotic, and splicing pathways are all altered in Emery-Dreifuss muscular dystrophy Spectrum patients to differing degrees. Human Molecular Genetics. PMID 36282542 DOI: 10.1093/hmg/ddac264 |
0.74 |
|
| 2021 |
Todorow V, Hintze S, Kerr ARW, Hehr A, Schoser B, Meinke P. Transcriptome Analysis in a Primary Human Muscle Cell Differentiation Model for Myotonic Dystrophy Type 1. International Journal of Molecular Sciences. 22. PMID 34445314 DOI: 10.3390/ijms22168607 |
0.792 |
|
| 2019 |
Meinke P, Kerr ARW, Czapiewski R, de Las Heras JI, Dixon CR, Harris E, Kölbel H, Muntoni F, Schara U, Straub V, Schoser B, Wehnert M, Schirmer EC. A multistage sequencing strategy pinpoints novel candidate alleles for Emery-Dreifuss muscular dystrophy and supports gene misregulation as its pathomechanism. Ebiomedicine. PMID 31862442 DOI: 10.1016/J.Ebiom.2019.11.048 |
0.745 |
|
| 2019 |
Duan J, Navarro-Dorado J, Clark JH, Kinnear NP, Meinke P, Schirmer EC, Evans AM. The cell-wide web coordinates cellular processes by directing site-specific Ca flux across cytoplasmic nanocourses. Nature Communications. 10: 2299. PMID 31127110 DOI: 10.1038/S41467-019-10055-W |
0.585 |
|
| 2018 |
Bikkul MU, Faragher RGA, Worthington G, Meinke P, Kerr ARW, Sammy A, Riyahi K, Horton D, Schirmer EC, Hubank M, Kill IR, Anderson RM, Slijepcevic P, Makarov E, Bridger JM. 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. PMID 30474255 DOI: 10.1002/Gcc.22711 |
0.632 |
|
| 2018 |
Hintze S, Knaier L, Limmer S, Schoser B, Meinke P. Nuclear Envelope Transmembrane Proteins in Myotonic Dystrophy Type 1. Frontiers in Physiology. 9: 1532. PMID 30425655 DOI: 10.3389/fphys.2018.01532 |
0.395 |
|
| 2016 |
Le Thanh P, Meinke P, Korfali N, Srsen V, Robson MI, Wehnert M, Schoser B, Sewry CA, Schirmer EC. Immunohistochemistry on a panel of Emery-Dreifuss muscular dystrophy samples reveals nuclear envelope proteins as inconsistent markers for pathology. Neuromuscular Disorders : Nmd. PMID 28214269 DOI: 10.1016/J.Nmd.2016.12.003 |
0.773 |
|
| 2016 |
Meinke P, Schirmer EC. The increasing relevance of nuclear envelope myopathies. Current Opinion in Neurology. 29: 651-61. PMID 27389815 DOI: 10.1097/Wco.0000000000000359 |
0.635 |
|
| 2016 |
Makarov AA, Rizzotto A, Meinke P, Schirmer EC. Purification of Lamins and Soluble Fragments of NETs. Methods in Enzymology. 569: 79-100. PMID 26778554 DOI: 10.1016/Bs.Mie.2015.09.006 |
0.747 |
|
| 2015 |
Meinke P, Schirmer EC. LINC'ing form and function at the nuclear envelope. Febs Letters. 589: 2514-21. PMID 26096784 DOI: 10.1016/J.Febslet.2015.06.011 |
0.624 |
|
| 2015 |
Meinke P, Schneiderat P, Srsen V, Korfali N, Lê Thành P, Cowan GJ, Cavanagh DR, Wehnert M, Schirmer EC, Walter MC. Abnormal proliferation and spontaneous differentiation of myoblasts from a symptomatic female carrier of X-linked Emery-Dreifuss muscular dystrophy. Neuromuscular Disorders : Nmd. 25: 127-36. PMID 25454731 DOI: 10.1016/J.Nmd.2014.09.012 |
0.763 |
|
| 2014 |
Malik P, Zuleger N, de las Heras JI, Saiz-Ros N, Makarov AA, Lazou V, Meinke P, Waterfall M, Kelly DA, Schirmer EC. NET23/STING promotes chromatin compaction from the nuclear envelope. Plos One. 9: e111851. PMID 25386906 DOI: 10.1371/Journal.Pone.0111851 |
0.716 |
|
| 2014 |
Meinke P, Mattioli E, Haque F, Antoku S, Columbaro M, Straatman KR, Worman HJ, Gundersen GG, Lattanzi G, Wehnert M, Shackleton S. Muscular dystrophy-associated SUN1 and SUN2 variants disrupt nuclear-cytoskeletal connections and myonuclear organization. Plos Genetics. 10: e1004605. PMID 25210889 DOI: 10.1371/Journal.Pgen.1004605 |
0.434 |
|
| 2013 |
de Las Heras JI, Meinke P, Batrakou DG, Srsen V, Zuleger N, Kerr AR, Schirmer EC. Tissue specificity in the nuclear envelope supports its functional complexity. Nucleus (Austin, Tex.). 4: 460-77. PMID 24213376 DOI: 10.4161/Nucl.26872 |
0.743 |
|
| 2012 |
Taranum S, Vaylann E, Meinke P, Abraham S, Yang L, Neumann S, Karakesisoglou I, Wehnert M, Noegel AA. LINC complex alterations in DMD and EDMD/CMT fibroblasts. European Journal of Cell Biology. 91: 614-28. PMID 22555292 DOI: 10.1016/j.ejcb.2012.03.003 |
0.377 |
|
| 2011 |
Meinke P, Nguyen TD, Wehnert MS. The LINC complex and human disease. Biochemical Society Transactions. 39: 1693-7. PMID 22103509 DOI: 10.1042/BST20110658 |
0.362 |
|
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