Related references
Note: Only part of the references are listed.The Structural Basis of ZMPSTE24-Dependent Laminopathies
Andrew Quigley et al.
SCIENCE (2013)
Structure of the Integral Membrane Protein CAAX Protease Ste24p
Edward E. Pryor et al.
SCIENCE (2013)
Human ZMPSTE24 disease mutations: residual proteolytic activity correlates with disease severity
Jemima Barrowman et al.
HUMAN MOLECULAR GENETICS (2012)
Progeria: Translational insights from cell biology
Leslie B. Gordon et al.
JOURNAL OF CELL BIOLOGY (2012)
Biogenesis of the Saccharomyces cerevisiae Pheromone a-Factor, from Yeast Mating to Human Disease
Susan Michaelis et al.
MICROBIOLOGY AND MOLECULAR BIOLOGY REVIEWS (2012)
The Posttranslational Processing of Prelamin A and Disease
Brandon S. J. Davies et al.
ANNUAL REVIEW OF GENOMICS AND HUMAN GENETICS (2009)
ZMPSTE24, an integral membrane zinc metalloprotease with a connection to progeroid disorders
Jemima Barrowman et al.
BIOLOGICAL CHEMISTRY (2009)
HIV protease inhibitors block the zinc metalloproteinase ZMPSTE24 and lead to an accumulation of prelamin A in cells
Catherine Coffinier et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2007)
Human laminopathies: nuclei gone genetically awry
Brian C. Capell et al.
NATURE REVIEWS GENETICS (2006)
Zmpste24 deficiency in mice causes spontaneous bone fractures, muscle weakness, and a prelamin A processing defect
MO Bergo et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2002)
Share Paper
