| Muscular Dystrophy-Associated SUN1 and SUN2 Variants Disrupt Nuclear-Cytoskeletal Connections and Myonuclear Organization P Meinke, E Mattioli, F Haque, S Antoku, M Columbaro, KR Straatman, ... PLoS genetics 10 (9), e1004605, 2014 | 176 | 2014 |
| A novel mutation in the coagulation factor 12 gene in subjects with hereditary angioedema and normal C1-inhibitor K Bork, K Wulff, P Meinke, N Wagner, J Hardt, G Witzke Clinical Immunology 141 (1), 31-35, 2011 | 149 | 2011 |
| The LINC complex and human disease P Meinke, TD Nguyen, MS Wehnert Biochemical Society Transactions 39 (6), 1693-1697, 2011 | 112 | 2011 |
| Tissue specificity in the nuclear envelope supports its functional complexity JI de Las Heras, P Meinke, DG Batrakou, V Srsen, N Zuleger, ARW Kerr, ... Nucleus 4 (6), 460-477, 2013 | 96 | 2013 |
| Novel hereditary angioedema linked with a heparan sulfate 3-O-sulfotransferase 6 gene mutation K Bork, K Wulff, BS Möhl, L Steinmüller-Magin, G Witzke, J Hardt, ... Journal of Allergy and Clinical Immunology 148 (4), 1041-1048, 2021 | 93 | 2021 |
| LINC’ing form and function at the nuclear envelope P Meinke, EC Schirmer FEBS letters 589 (19), 2514-2521, 2015 | 75 | 2015 |
| LINC complex alterations in DMD and EDMD/CMT fibroblasts S Taranum, E Vaylann, P Meinke, S Abraham, L Yang, S Neumann, ... European journal of cell biology 91 (8), 614-628, 2012 | 74 | 2012 |
| New ZMPSTE24 (FACE1) mutations in patients affected with restrictive dermopathy or related progeroid syndromes and mutation update CL Navarro, V Esteves-Vieira, S Courrier, A Boyer, T Duong Nguyen, ... European Journal of Human Genetics 22 (8), 1002-1011, 2014 | 62 | 2014 |
| Sarcopenia–endocrinological and neurological aspects MK Stangl, W Böcker, V Chubanov, U Ferrari, M Fischereder, ... Experimental and Clinical Endocrinology & Diabetes 6 (01), 8-22, 2019 | 57 | 2019 |
| Myotonic dystrophy—A progeroid disease? P Meinke, S Hintze, S Limmer, B Schoser Frontiers in neurology 9, 375942, 2018 | 38 | 2018 |
| A multistage sequencing strategy pinpoints novel candidate alleles for Emery-Dreifuss muscular dystrophy and supports gene misregulation as its pathomechanism P Meinke, ARW Kerr, R Czapiewski, JI de Las Heras, CR Dixon, E Harris, ... EBioMedicine 51, 2020 | 32 | 2020 |
| Contribution of SUN 1 Mutations to the Pathomechanism in Muscular Dystrophies P Li, P Meinke, LTT Huong, M Wehnert, AA Noegel Human mutation 35 (4), 452-461, 2014 | 32 | 2014 |
| Type-2 muscle fiber atrophy is associated with sarcopenia in elderly men with hip fracture F Tanganelli, P Meinke, F Hofmeister, S Jarmusch, L Baber, S Mehaffey, ... Experimental Gerontology 144, 111171, 2021 | 28 | 2021 |
| NET23/STING promotes chromatin compaction from the nuclear envelope P Malik, N Zuleger, JI de las Heras, N Saiz-Ros, AA Makarov, V Lazou, ... PLoS One 9 (11), e111851, 2014 | 25 | 2014 |
| Telomere elongation through hTERT immortalization leads to chromosome repositioning in control cells and genomic instability in Hutchinson‐Gilford progeria syndrome fibroblasts … MU Bikkul, RGA Faragher, G Worthington, P Meinke, ARW Kerr, A Sammy, ... Genes, Chromosomes and Cancer 58 (6), 341-356, 2019 | 22 | 2019 |
| Abnormal proliferation and spontaneous differentiation of myoblasts from a symptomatic female carrier of X-linked Emery–Dreifuss muscular dystrophy P Meinke, P Schneiderat, V Srsen, N Korfali, P Lê Thành, GJM Cowan, ... Neuromuscular Disorders 25 (2), 127-136, 2015 | 22 | 2015 |
| Moss-derived human recombinant GAA provides an optimized enzyme uptake in differentiated human muscle cells of Pompe disease S Hintze, S Limmer, P Dabrowska-Schlepp, B Berg, N Krieghoff, A Busch, ... International Journal of Molecular Sciences 21 (7), 2642, 2020 | 21 | 2020 |
| Progeroid laminopathy with restrictive dermopathy-like features caused by an isodisomic LMNA mutation p. R435C S Starke, P Meinke, D Camozzi, E Mattioli, R Pfaeffle, M Siekmeyer, ... Aging (Albany NY) 5 (6), 445, 2013 | 20 | 2013 |
| Immunohistochemistry on a panel of Emery–Dreifuss muscular dystrophy samples reveals nuclear envelope proteins as inconsistent markers for pathology P Le Thanh, P Meinke, N Korfali, V Srsen, MI Robson, M Wehnert, ... Neuromuscular Disorders 27 (4), 338-351, 2017 | 19 | 2017 |
| The increasing relevance of nuclear envelope myopathies P Meinke, EC Schirmer Current opinion in neurology 29 (5), 651-661, 2016 | 19 | 2016 |
Alastair KerrCRUK: University of ManchesterGeverifieerd e-mailadres voor manchester.ac.uk
