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Items: 13

1.
Plectin isoform 1b mediates mitochondrion–intermediate filament network linkage and controls organelle shape
Lilli Winter, Christina Abrahamsberg, Gerhard Wiche
J Cell Biol. 2008 Jun 16; 181(6): 903–911. doi: 10.1083/jcb.200710151
PMCID:
PMC2426950
AbstractArticlePDF–2.5M
2.
Plectin 1f scaffolding at the sarcolemma of dystrophic (mdx) muscle fibers through multiple interactions with β-dystroglycan
Günther A. Rezniczek, Patryk Konieczny, Branislav Nikolic, Siegfried Reipert, Doris Schneller, Christina Abrahamsberg, Kay E. Davies, Steve J. Winder, Gerhard Wiche
J Cell Biol. 2007 Mar 26; 176(7): 965–977. doi: 10.1083/jcb.200604179
PMCID:
PMC2064082
AbstractArticlePDF–3.9M
3.
A homozygous nonsense mutation in the PLEC1 gene in patients with epidermolysis bullosa simplex with muscular dystrophy.
S Chavanas, L Pulkkinen, Y Gache, F J Smith, W H McLean, J Uitto, J P Ortonne, G Meneguzzi
J Clin Invest. 1996 Nov 15; 98(10): 2196–2200. doi: 10.1172/JCI119028
PMCID:
PMC507667
SummaryPDF–170K
4.
Defective expression of plectin/HD1 in epidermolysis bullosa simplex with muscular dystrophy.
Y Gache, S Chavanas, J P Lacour, G Wiche, K Owaribe, G Meneguzzi, J P Ortonne
J Clin Invest. 1996 May 15; 97(10): 2289–2298. doi: 10.1172/JCI118671
PMCID:
PMC507309
SummaryPDF–1.1M
5.
Multiple Variable First Exons: A Mechanism for Cell- and Tissue-Specific Gene Regulation
Theresa Zhang, Peter Haws, Qiang Wu
Genome Res. 2004 Jan; 14(1): 79–89. doi: 10.1101/gr.1225204
PMCID:
PMC314283
AbstractArticlePDF–421K
6.
Human plectin: organization of the gene, sequence analysis, and chromosome localization (8q24).
C G Liu, C Maercker, M J Castañon, R Hauptmann, G Wiche
Proc Natl Acad Sci U S A. 1996 Apr 30; 93(9): 4278–4283. doi: 10.1073/pnas.93.9.4278
PMCID:
PMC39526
SummaryPage BrowsePDF–1.3M
7.
No major role for rare plectin variants in arrhythmogenic right ventricular cardiomyopathy
Edgar T. Hoorntje, Anna Posafalvi, Petros Syrris, K. Joeri van der Velde, Marieke C. Bolling, Alexandros Protonotarios, Ludolf G. Boven, Nuria Amat-Codina, Judith A. Groeneweg, Arthur A. Wilde, Nara Sobreira, Hugh Calkins, Richard N. W. Hauer, Marcel F. Jonkman, William J. McKenna, Perry M. Elliott, Richard J. Sinke, Maarten P. van den Berg, Stephen P. Chelko, Cynthia A. James, J. Peter van Tintelen, Daniel P. Judge, Jan D. H. Jongbloed
PLoS One. 2018; 13(8): e0203078. Published online 2018 Aug 30. doi: 10.1371/journal.pone.0203078
PMCID:
PMC6117038
AbstractArticlePDF–2.6M
8.
Epidermolysis bullosa simplex in sibling Eurasier dogs is caused by a PLEC non-sense variant
Elizabeth A. Mauldin, Ping Wang, Thierry Olivry, Paula S. Henthorn, Margret L. Casal
Vet Dermatol. Author manuscript; available in PMC 2017 Feb 24.
Published in final edited form as: Vet Dermatol. 2017 Feb; 28(1): 10–e3. Published online 2016 Nov 7. doi: 10.1111/vde.12394
PMCID:
PMC5324056
AbstractArticlePDF–2.9M
9.
Epidermolysis bullosa simplex with muscular dystrophy associated with PLEC deletion mutation
Valeria Carolina Alvarez, Sini Tellervo Penttilä, Valeria Luján Salutto, Bjarne Udd, Claudio Gabriel Mazia
Neurol Genet. 2016 Dec; 2(6): e109. Published online 2016 Oct 11. doi: 10.1212/NXG.0000000000000109
PMCID:
PMC5061415
ArticlePDF–94K
10.
Effects of Plectin Depletion on Keratin Network Dynamics and Organization
Marcin Moch, Reinhard Windoffer, Nicole Schwarz, Raphaela Pohl, Andreas Omenzetter, Uwe Schnakenberg, Fabian Herb, Kraisorn Chaisaowong, Dorit Merhof, Lena Ramms, Gloria Fabris, Bernd Hoffmann, Rudolf Merkel, Rudolf E. Leube
PLoS One. 2016; 11(3): e0149106. Published online 2016 Mar 23. doi: 10.1371/journal.pone.0149106
PMCID:
PMC4805305
AbstractArticlePDF–13M
11.
A common promoter hypomethylation signature in invasive breast, liver and prostate cancer cell lines reveals novel targets involved in cancer invasiveness
David Cheishvili, Barbara Stefanska, Cao Yi, Chen Chen Li, Patricia Yu, Ani Arakelian, Imrana Tanvir, Haseeb Ahmed Khan, Shafaat Rabbani, Moshe Szyf
Oncotarget. 2015 Oct 20; 6(32): 33253–33268. Published online 2015 Sep 22. doi: 10.18632/oncotarget.5291
PMCID:
PMC4741763
AbstractArticlePDF–4.8M
12.
Phosphorylation of serine 4642 in the C-terminus of plectin by MNK2 and PKA modulates its interaction with intermediate filaments
Jamal-Eddine Bouameur, Yann Schneider, Nadja Begré, Ryan P. Hobbs, Prakash Lingasamy, Lionel Fontao, Kathleen J. Green, Bertrand Favre, Luca Borradori
J Cell Sci. 2013 Sep 15; 126(18): 4195–4207. doi: 10.1242/jcs.127779
PMCID:
PMC3772390
AbstractArticle
13.
Alternatively Spliced Genes as Biomarkers for Schizophrenia, Bipolar Disorder and Psychosis: A Blood-Based Spliceome-Profiling Exploratory Study
S.J. Glatt, S.D. Chandler, C.A. Bousman, G. Chana, G.R. Lucero, E. Tatro, T. May, J.B. Lohr, W.S. Kremen, I.P. Everall, M.T. Tsuang
Curr Pharmacogenomics Person Med. Author manuscript; available in PMC 2011 Apr 28.
Published in final edited form as: Curr Pharmacogenomics Person Med. 2009 Sep; 7(3): 164–188. doi: 10.2174/1875692110907030164
PMCID:
PMC3083864
AbstractArticlePDF–514K

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