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Anzahl der Publikationen: 24
Zeitschriftenartikel
Schluessel, Sabine 
ORCID: https://orcid.org/0000-0002-2485-8859; Zhang, Wei; Nowotny, Hanna; Bidlingmaier, Martin ORCID: https://orcid.org/0000-0002-4681-6668; Hintze, Stefan; Kunz, Sonja; Martini, Sebastian; Mehaffey, Stefan; Meinke, Peter; Neuerburg, Carl ORCID: https://orcid.org/0000-0002-1373-093X; Schmidmaier, Ralf; Schoser, Benedikt ORCID: https://orcid.org/0000-0002-2757-8131; Reisch, Nicole und Drey, Michael
(2023):
11-beta-hydroxysteroid dehydrogenase type 1 (HSD11B1) gene expression in muscle is linked to reduced skeletal muscle index in sarcopenic patients.
In: Aging Clinical and Experimental Research, Bd. 35, Nr. 12: S. 3073-3083
[PDF, 947kB]
ORCID: https://orcid.org/0000-0002-2485-8859; Zhang, Wei; Nowotny, Hanna; Bidlingmaier, Martin ORCID: https://orcid.org/0000-0002-4681-6668; Hintze, Stefan; Kunz, Sonja; Martini, Sebastian; Mehaffey, Stefan; Meinke, Peter; Neuerburg, Carl ORCID: https://orcid.org/0000-0002-1373-093X; Schmidmaier, Ralf; Schoser, Benedikt ORCID: https://orcid.org/0000-0002-2757-8131; Reisch, Nicole und Drey, Michael
(2023):
11-beta-hydroxysteroid dehydrogenase type 1 (HSD11B1) gene expression in muscle is linked to reduced skeletal muscle index in sarcopenic patients.
In: Aging Clinical and Experimental Research, Bd. 35, Nr. 12: S. 3073-3083
[PDF, 947kB]
Hintze, Stefan; Baber, Lisa; Hofmeister, Fabian; Jarmusch, Stefanie; Todorow, Vanessa; Mehaffey, Stefan; Tanganelli, Fabiana; Ferrari, Uta; Neuerburg, Carl; Teupser, Daniel; Bidlingmaier, Martin; Marques, Jair Gonzalez; Koletzko, Berthold; Schoser, Benedikt; Drey, Michael und Meinke, Peter
(2022):
Exploration of mitochondrial defects in sarcopenic hip fracture patients.
In: Heliyon, Bd. 8, Nr. 10, e11143
de las Heras, Jose I.; Todorow, Vanessa; Krecinic-Balic, Lejla; Hintze, Stefan; Czapiewski, Rafal; Webb, Shaun; Schoser, Benedikt; Meinke, Peter und Schirmer, Eric C.
(2022):
Metabolic, fibrotic and splicing pathways are all altered in Emery-Dreifuss muscular dystrophy spectrum patients to differing degrees.
In: Human Molecular Genetics, Bd. 32, Nr. 6: S. 1010-1031
Bork, Konrad; Wulff, Karin; Witzke, Guenther; Hardt, Jochen und Meinke, Peter
(2022):
Inheritance Pattern of Hereditary Angioedema Indicates Mutation-Dependent Selective Effects During Early Embryonic Development.
In: Journal of Allergy and Clinical Immunology / in Practice, Bd. 10, Nr. 4: S. 1029-1037
Carrasco-Rozas, Ana; Fernandez-Simon, Esther; Suarez-Calvet, Xavier; Pinol-Jurado, Patricia; Alonso-Perez, Jorge; de Luna, Noemi; Schoser, Benedikt; Meinke, Peter; Dominguez-Gonzalez, Cristina; Hernandez-Lain, Aurelio; Paradas, Carmen; Rivas, Eloy; Illa, Isabel; Olive, Montse; Gallardo, Eduard und Diaz-Manera, Jordi
(2022):
BNIP3 Is Involved in Muscle Fiber Atrophy in Late-Onset Pompe Disease Patients.
In: American Journal of Pathology, Bd. 192, Nr. 8: S. 1151-1166
Donandt, Tina; Hintze, Stefan; Krause, Sabine; Wolf, Eckhard; Schoser, Benedikt; Walter, Maggie C. und Meinke, Peter
(2022):
Isolation and Characterization of Primary DMD Pig Muscle Cells as an In Vitro Model for Preclinical Research on Duchenne Muscular Dystrophy.
In: Life-Basel, Bd. 12, Nr. 10
[PDF, 3MB]
Duong, Nguyen Thuy; Dinh, Tran Huu; Möhl, Britta S.; Hintze, Stefan; Quynh, Do Hai; Ha, Duong Thi Thu; Ngoc, Ngo Diem; Dung, Vu Chi; Miyake, Noriko; Hai, Nong Van; Matsumoto, Naomichi und Meinke, Peter
(2022):
Cockayne syndrome without UV-sensitivity in Vietnamese siblings with novel ERCC8 variants.
In: Aging, Bd. 14, Nr. 13: S. 5299-5310
[PDF, 1MB]
Hintze, Stefan; Mensel, Raphaela; Knaier, Lisa; Schoser, Benedikt und Meinke, Peter
(28. Juni 2021):
CTG-Repeat Detection in Primary Human Myoblasts of Myotonic Dystrophy Type 1.
In: Frontiers in Neuroscience, Bd. 15, 686735
[PDF, 1MB]
Hofmeister, Fabian; Baber, Lisa; Ferrari, Uta; Hintze, Stefan; Jarmusch, Stefanie; Krause, Sabine; Meinke, Peter; Mehaffey, Stefan; Neuerburg, Carl; Tangenelli, Fabiana; Schoser, Benedikt ORCID: https://orcid.org/0000-0002-2757-8131 und Drey, Michael
(2021):
Late-onset neuromuscular disorders in the differential diagnosis of sarcopenia.
In: BMC neurology, Bd. 21, Nr. 1, 241
[PDF, 1MB]
ORCID: https://orcid.org/0000-0002-2757-8131 und Drey, Michael
(2021):
Late-onset neuromuscular disorders in the differential diagnosis of sarcopenia.
In: BMC neurology, Bd. 21, Nr. 1, 241
[PDF, 1MB]
Jarmusch, Stefanie; Baber, Lisa; Bidlingmaier, Martin ORCID: https://orcid.org/0000-0002-4681-6668; Ferrari, Uta; Hofmeister, Fabian; Hintze, Stefan; Mehaffey, Stefan; Meinke, Peter; Neuerburg, Carl; Schoser, Benedikt ORCID: https://orcid.org/0000-0002-2757-8131; Tanganelli, Fabiana und Drey, Michael
(2021):
Influence of IGF-I serum concentration on muscular regeneration capacity in patients with sarcopenia.
In: BMC musculoskeletal disorders, Bd. 22, Nr. 1, 807
[PDF, 830kB]
ORCID: https://orcid.org/0000-0002-4681-6668; Ferrari, Uta; Hofmeister, Fabian; Hintze, Stefan; Mehaffey, Stefan; Meinke, Peter; Neuerburg, Carl; Schoser, Benedikt ORCID: https://orcid.org/0000-0002-2757-8131; Tanganelli, Fabiana und Drey, Michael
(2021):
Influence of IGF-I serum concentration on muscular regeneration capacity in patients with sarcopenia.
In: BMC musculoskeletal disorders, Bd. 22, Nr. 1, 807
[PDF, 830kB]
Bork, Konrad; Wulff, Karin; Moehl, Britta S.; Steinmueller-Magin, Lars; Witzke, Gunther; Hardt, Jochen und Meinke, Peter
(2021):
Novel hereditary angioedema linked with a heparan sulfate 3-O-sulfotransferase 6 gene mutation.
In: Journal of Allergy and Clinical Immunology, Bd. 148, Nr. 4: S. 1041-1048
Hofmeister, Fabian; Baber, Lisa; Ferrari, Uta; Hintze, Stefan; Jarmusch, Stefanie; Krause, Sabine; Meinke, Peter; Mehaffey, Stefan; Neuerburg, Carl; Tangenelli, Fabiana; Schoser, Benedikt und Drey, Michael
(2021):
Late-onset neuromuscular disorders in the differential diagnosis of sarcopenia.
In: BMC Neurology, Bd. 21, Nr. 1, 241
Jarmusch, Stefanie; Baber, Lisa; Bidlingmaier, Martin; Ferrari, Uta; Hofmeister, Fabian; Hintze, Stefan; Mehaffey, Stefan; Meinke, Peter; Neuerburg, Carl; Schoser, Benedikt; Tanganelli, Fabiana und Drey, Michael
(2021):
Influence of IGF-I serum concentration on muscular regeneration capacity in patients with sarcopenia.
In: BMC Musculoskeletal Disorders, Bd. 22, Nr. 1, 807
Tanganelli, Fabiana; Meinke, Peter; Hofmeister, Fabian; Jarmusch, Stefanie; Baber, Lisa; Mehaffey, Stefan; Hintze, Stefan; Ferrari, Uta; Neuerburg, Carl; Kammerlander, Christian; Schoser, Benedikt und Drey, Michael
(2021):
Type-2 muscle fiber atrophy is associated with sarcopenia in elderly men with hip fracture.
In: Experimental Gerontology, Bd. 144, 111171
Todorow, Vanessa; Hintze, Stefan; Kerr, Alastair R. W.; Hehr, Andreas; Schoser, Benedikt und Meinke, Peter
(2021):
Transcriptome Analysis in a Primary Human Muscle Cell Differentiation Model for Myotonic Dystrophy Type 1.
In: International Journal of Molecular Sciences, Bd. 22, Nr. 16, 8607
Hintze, Stefan; Limmer, Sarah; Dabrowska-Schlepp, Paulina; Berg, Birgit; Krieghoff, Nicola; Busch, Andreas; Schaaf, Andreas; Meinke, Peter und Schoser, Benedikt
(2020):
Moss-Derived Human Recombinant GAA Provides an Optimized Enzyme Uptake in Differentiated Human Muscle Cells of Pompe Disease.
In: International Journal of Molecular Sciences, Bd. 21, Nr. 7, 2642
Meinke, Peter; Kerr, Alastair R. W.; Czapiewski, Rafal; de Las Heras, Jose; Dixon, Charles R.; Harris, Elizabeth; Koelbel, Heike; Muntoni, Francesco; Schara, Ulrike; Straub, Volker; Schoser, Benedikt; Wehnert, Manfred und Schirmer, Eric C.
(2020):
A multistage sequencing strategy pinpoints novel candidate alleles for Emery-Dreifuss muscular dystrophy and supports gene misregulation as its pathomechanism.
In: Ebiomedicine, Bd. 51, 102587
Stangl, Michaela Katja; Böcker, Wolfgang; Chubanov, Vladimir; Ferrari, Uta; Fischereder, Michael; Gudermann, Thomas; Hesse, Eric; Meinke, Peter; Reincke, Martin; Reisch, Nicole; Saller, Maximilian M.; Seissler, Jochen; Schmidmaier, Ralf; Schoser, Benedikt; Then, Cornelia; Thorand, Barbara und Drey, Michael
(2019):
Sarcopenia - Endocrinological and Neurological Aspects.
In: Experimental and Clinical Endocrinology & Diabetes, Bd. 127, Nr. 1: S. 8-22
Bikkul, Mehmet U.; Faragher, Richard G. A.; Worthington, Gemma; Meinke, Peter; Kerr, Alastair R. W.; Sammy, Aakila; Riyahi, Kumars; Horton, Daniel; Schirmer, Eric C.; Hubank, Michael; Kill, Ian R.; Anderson, Rhona M.; Slijepcevic, Predrag; Makarov, Evgeny und Bridger, Joanna M.
(2019):
Telomere elongation through hTERT immortalization leads to chromosome repositioning in control cells and genomic instability in Hutchinson-Gilford progeria syndrome fibroblasts, expressing a novel SUN1 isoform.
In: Genes Chromosomes & Cancer, Bd. 58, Nr. 6: S. 341-356
Meinke, Peter; Limmer, Sarah; Hintze, Stefan und Schoser, Benedikt
(2019):
Assessing metabolic profiles in human myoblasts from patients with late-onset Pompe disease.
In: Annals of Translational Medicine, Bd. 7, Nr. 13, 277
Hintze, Stefan; Knaier, Lisa; Limmer, Sarah; Schoser, Benedikt und Meinke, Peter
(2018):
Nuclear Envelope Transmembrane Proteins in Myotonic Dystrophy Type 1.
In: Frontiers in Physiology, Bd. 9, 1532
[PDF, 1MB]
Meinke, Peter; Hintze, Stefan; Limmer, Sarah und Schoser, Benedikt
(2018):
Myotonic Dystrophy-A Progeroid Disease?
In: Frontiers in Neurology, Bd. 9, 601
[PDF, 1MB]
Thanh, Phu Le; Meinke, Peter; Korfali, Nadia; Srsen, Vlastimil; Robson, Michael I.; Wehnert, Manfred; Schoser, Benedikt; Sewry, Caroline A. und Schirmer, Eric C.
(2017):
Immunohistochemistry on a panel of Emery-Dreifuss muscular dystrophy samples reveals nuclear envelope proteins as inconsistent markers for pathology.
In: Neuromuscular Disorders, Bd. 27, Nr. 4: S. 338-351
Meinke, Peter und Schirmer, Eric C.
(2016):
The increasing relevance of nuclear envelope myopathies.
In: Current Opinion in Neurology, Bd. 29, Nr. 5: S. 651-661