| 出版应用/物种/样品/稀释 | 参考文献 |
|---|
| O Grady G, Best H, Sztal T, Schartner V, Sanjuan Vazquez M, Donkervoort S, et al. Variants in the Oxidoreductase PYROXD1 Cause Early-Onset Myopathy with Internalized Nuclei and Myofibrillar Disorganization. Am J Hum Genet. 2016;99:1086-1105 pubmed 出版商 |
- 免疫细胞化学; 人类; 1:500; 图 2
- 免疫印迹; 人类; 1:500; 图 9
| Eisch V, Lu X, Gabriel D, Djabali K. Progerin impairs chromosome maintenance by depleting CENP-F from metaphase kinetochores in Hutchinson-Gilford progeria fibroblasts. Oncotarget. 2016;7:24700-18 pubmed 出版商 |
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| Tapia O, Fong L, Huber M, Young S, Gerace L. Nuclear envelope protein Lem2 is required for mouse development and regulates MAP and AKT kinases. PLoS ONE. 2015;10:e0116196 pubmed 出版商 |
| Jung H, Tatar A, Tu Y, Nobumori C, Yang S, Goulbourne C, et al. An absence of nuclear lamins in keratinocytes leads to ichthyosis, defective epidermal barrier function, and intrusion of nuclear membranes and endoplasmic reticulum into the nuclear chromatin. Mol Cell Biol. 2014;34:4534-44 pubmed 出版商 |
| Vaajanen A, Kalesnykas G, Vapaatalo H, Uusitalo H. The expression of Mas-receptor of the renin-angiotensin system in the human eye. Graefes Arch Clin Exp Ophthalmol. 2015;253:1053-9 pubmed 出版商 |
| Ho C, Jaalouk D, Vartiainen M, Lammerding J. Lamin A/C and emerin regulate MKL1-SRF activity by modulating actin dynamics. Nature. 2013;497:507-11 pubmed 出版商 |
| Boudreau E, Labib S, Bertrand A, Decostre V, Bolongo P, Sylvius N, et al. Lamin A/C mutants disturb sumo1 localization and sumoylation in vitro and in vivo. PLoS ONE. 2012;7:e45918 pubmed 出版商 |
| Mewborn S, Puckelwartz M, Abuisneineh F, Fahrenbach J, Zhang Y, MacLeod H, et al. Altered chromosomal positioning, compaction, and gene expression with a lamin A/C gene mutation. PLoS ONE. 2010;5:e14342 pubmed 出版商 |
| Verstraeten V, Caputo S, van Steensel M, Duband Goulet I, Zinn Justin S, Kamps M, et al. The R439C mutation in LMNA causes lamin oligomerization and susceptibility to oxidative stress. J Cell Mol Med. 2009;13:959-71 pubmed 出版商 |
