Peter Meinke
Peter Meinke
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Citado por
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
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
The LINC complex and human disease
P Meinke, TD Nguyen, MS Wehnert
Biochemical Society Transactions 39 (6), 1693-1697, 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
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
LINC’ing form and function at the nuclear envelope
P Meinke, EC Schirmer
FEBS letters 589 (19), 2514-2521, 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
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
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
Myotonic dystrophy—A progeroid disease?
P Meinke, S Hintze, S Limmer, B Schoser
Frontiers in neurology 9, 601, 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
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
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
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
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
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
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
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
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
The increasing relevance of nuclear envelope myopathies
P Meinke, EC Schirmer
Current opinion in neurology 29 (5), 651-661, 2016
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Artículos 1–20