A monoclonal antibody which recognises each of the nuclear lamin polypeptides in mammalian cells.
Author:
Publisher
Wiley
Subject
General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,Molecular Biology,General Neuroscience
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/j.1460-2075.1983.tb01431.x/fullpdf
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2. The R439C mutation inLMNAcauses lamin oligomerization and susceptibility to oxidative stress;Journal of Cellular and Molecular Medicine;2009-05
3. Application of 2-dimensional difference gel electrophoresis (2D-DIGE) to the study of thrombin-activated human platelet secretome;Platelets;2008-01
4. Compound heterozygosity for mutations in LMNA causes a progeria syndrome without prelamin A accumulation;Human Molecular Genetics;2006-06-16
5. Regulation of Microtubule-dependent Recycling at theTrans-Golgi Network by Rab6A and Rab6A';Molecular Biology of the Cell;2005-01
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