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Human Molecular Genetics|April 23, 2019
Postnatal development of mice with combined genetic depletions of lamin A/C, emerin and lamina-associated polypeptide 1Yuexia Wang, Ji-Yeon Shin, Koki Nakanishi, et al.
Journal of Cell Science|April 2, 2016
A mutation abolishing the ZMPSTE24 cleavage site in prelamin A causes a progeroid disorderYuexia Wang, Uta Lichter-Konecki, Kwame Anyane-Yeboa, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 24, 2022
Abolishing the prelamin A ZMPSTE24 cleavage site leads to progeroid phenotypes with near-normal longevity in miceYuexia Wang, Khurts Shilagardi, Trunee Hsu, et al.
The Journal of Cell Biology|March 1, 2017
TorsinA controls TAN line assembly and the retrograde flow of dorsal perinuclear actin cables during rearward nuclear movementCosmo A Saunders, Nathan J Harris, Patrick T Willey, et al.
Plos One|August 21, 2012
Cardiomyocyte-specific expression of lamin a improves cardiac function in Lmna-/- miceRichard L Frock, Steven C Chen, Dao-Fu Da, et al.
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