Hutchinson-Gilford progeria syndrome (HGPS) is a rare autosomal dominant genetic disease that is caused by a silent mutation of the
Su-Jin Lee, Youn-Sang Jung, Min-Ho Yoon, So-mi Kang, Ah-Young Oh, Jee-Hyun Lee, So-Young Jun, Tae-Gyun Woo, Ho-Young Chun, Sang Kyum Kim, Kyu Jin Chung, Ho-Young Lee, Kyeong Lee, Guanghai Jin, Min-Kyun Na, Nam Chul Ha, Clea Bárcena, José M.P. Freije, Carlos López-Otín, Gyu Yong Song, Bum-Joon Park
Title and authors | Publication | Year |
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Lamin A and microtubules collaborate to maintain nuclear morphology
Z Tariq, H Zhang, A Chia-Liu, Y Shen, Y Gete, ZM Xiong, C Tocheny, L Campanello, D Wu, W Losert, K Cao |
Nucleus | 2017 |
Intermediate filament proteins of digestive organs: physiology and pathophysiology
MB Omary |
AJP Gastrointestinal and Liver Physiology | 2017 |
Protein sequestration at the nuclear periphery as a potential regulatory mechanism in premature aging
L Serebryannyy, T Misteli |
The Journal of Cell Biology | 2017 |
A lipodystrophy-causing lamin A mutant alters conformation and epigenetic regulation of the anti-adipogenic MIR335 locus
A Oldenburg, N Briand, AL Sørensen, I Cahyani, A Shah, JØ Moskaug, P Collas |
The Journal of Cell Biology | 2017 |