Meinke P - Search Results

1

Nuclear Small Dystrophin Isoforms during Muscle Differentiation.

Donandt T, Todorow V, Hintze S, Graupner A, Schoser B, Walter MC, Meinke P. Donandt T, et al. Among authors: meinke p. Life (Basel). 2023 Jun 11;13(6):1367. doi: 10.3390/life13061367. Life (Basel). 2023. PMID: 37374149 Free PMC article.

2

Tissue specificity in the nuclear envelope supports its functional complexity.

de Las Heras JI, Meinke P, Batrakou DG, Srsen V, Zuleger N, Kerr AR, Schirmer EC. de Las Heras JI, et al. Among authors: meinke p. Nucleus. 2013 Nov-Dec;4(6):460-77. doi: 10.4161/nucl.26872. Epub 2013 Nov 8. Nucleus. 2013. PMID: 24213376 Free PMC article. Review.

3

NET23/STING promotes chromatin compaction from the nuclear envelope.

Malik P, Zuleger N, de las Heras JI, Saiz-Ros N, Makarov AA, Lazou V, Meinke P, Waterfall M, Kelly DA, Schirmer EC. Malik P, et al. Among authors: meinke p. PLoS One. 2014 Nov 11;9(11):e111851. doi: 10.1371/journal.pone.0111851. eCollection 2014. PLoS One. 2014. PMID: 25386906 Free PMC article.

4

The LINC complex and human disease.

Meinke P, Nguyen TD, Wehnert MS. Meinke P, et al. Biochem Soc Trans. 2011 Dec;39(6):1693-7. doi: 10.1042/BST20110658. Biochem Soc Trans. 2011. PMID: 22103509 Review.

5

Contribution of SUN1 mutations to the pathomechanism in muscular dystrophies.

Li P, Meinke P, Huong le TT, Wehnert M, Noegel AA. Li P, et al. Among authors: meinke p. Hum Mutat. 2014 Apr;35(4):452-61. doi: 10.1002/humu.22504. Epub 2014 Jan 13. Hum Mutat. 2014. PMID: 24375709

6

Progeroid laminopathy with restrictive dermopathy-like features caused by an isodisomic LMNA mutation p.R435C.

Starke S, Meinke P, Camozzi D, Mattioli E, Pfaeffle R, Siekmeyer M, Hirsch W, Horn LC, Paasch U, Mitter D, Lattanzi G, Wehnert M, Kiess W. Starke S, et al. Among authors: meinke p. Aging (Albany NY). 2013 Jun;5(6):445-59. doi: 10.18632/aging.100566. Aging (Albany NY). 2013. PMID: 23804595 Free PMC article.

7

Abnormal proliferation and spontaneous differentiation of myoblasts from a symptomatic female carrier of X-linked Emery-Dreifuss muscular dystrophy.

Meinke P, Schneiderat P, Srsen V, Korfali N, Lê Thành P, Cowan GJ, Cavanagh DR, Wehnert M, Schirmer EC, Walter MC. Meinke P, et al. Neuromuscul Disord. 2015 Feb;25(2):127-36. doi: 10.1016/j.nmd.2014.09.012. Epub 2014 Oct 6. Neuromuscul Disord. 2015. PMID: 25454731 Free PMC article.

8

Immunohistochemistry on a panel of Emery-Dreifuss muscular dystrophy samples reveals nuclear envelope proteins as inconsistent markers for pathology.

Le Thanh P, Meinke P, Korfali N, Srsen V, Robson MI, Wehnert M, Schoser B, Sewry CA, Schirmer EC. Le Thanh P, et al. Among authors: meinke p. Neuromuscul Disord. 2017 Apr;27(4):338-351. doi: 10.1016/j.nmd.2016.12.003. Epub 2016 Dec 21. Neuromuscul Disord. 2017. PMID: 28214269 Free PMC article.

9

Myotonic Dystrophy-A Progeroid Disease?

Meinke P, Hintze S, Limmer S, Schoser B. Meinke P, et al. Front Neurol. 2018 Jul 25;9:601. doi: 10.3389/fneur.2018.00601. eCollection 2018. Front Neurol. 2018. PMID: 30140252 Free PMC article.

10

Sarcopenia - Endocrinological and Neurological Aspects.

Stangl MK, Böcker W, Chubanov V, Ferrari U, Fischereder M, Gudermann T, Hesse E, Meinke P, Reincke M, Reisch N, Saller MM, Seissler J, Schmidmaier R, Schoser B, Then C, Thorand B, Drey M. Stangl MK, et al. Among authors: meinke p. Exp Clin Endocrinol Diabetes. 2019 Jan;127(1):8-22. doi: 10.1055/a-0672-1007. Epub 2018 Sep 10. Exp Clin Endocrinol Diabetes. 2019. PMID: 30199918 Review.

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