Meinke P - Search Results

1

A multistage sequencing strategy pinpoints novel candidate alleles for Emery-Dreifuss muscular dystrophy and supports gene misregulation as its pathomechanism.

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. Meinke P, et al. EBioMedicine. 2020 Jan;51:102587. doi: 10.1016/j.ebiom.2019.11.048. Epub 2019 Dec 17. EBioMedicine. 2020. PMID: 31862442 Free PMC article.

2

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.

3

LINC complex alterations in DMD and EDMD/CMT fibroblasts.

Taranum S, Vaylann E, Meinke P, Abraham S, Yang L, Neumann S, Karakesisoglou I, Wehnert M, Noegel AA. Taranum S, et al. Among authors: meinke p. Eur J Cell Biol. 2012 Aug;91(8):614-28. doi: 10.1016/j.ejcb.2012.03.003. Epub 2012 May 1. Eur J Cell Biol. 2012. PMID: 22555292 Free PMC article.

4

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.

5

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.

6

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

7

Muscular dystrophy-associated SUN1 and SUN2 variants disrupt nuclear-cytoskeletal connections and myonuclear organization.

Meinke P, Mattioli E, Haque F, Antoku S, Columbaro M, Straatman KR, Worman HJ, Gundersen GG, Lattanzi G, Wehnert M, Shackleton S. Meinke P, et al. PLoS Genet. 2014 Sep 11;10(9):e1004605. doi: 10.1371/journal.pgen.1004605. eCollection 2014 Sep. PLoS Genet. 2014. PMID: 25210889 Free PMC article.

8

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.

9

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.

10

LINC'ing form and function at the nuclear envelope.

Meinke P, Schirmer EC. Meinke P, et al. FEBS Lett. 2015 Sep 14;589(19 Pt A):2514-21. doi: 10.1016/j.febslet.2015.06.011. Epub 2015 Jun 19. FEBS Lett. 2015. PMID: 26096784 Free article. Review.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

135 results

Search Page