The Structural Basis of ZMPSTE24-Dependent Laminopathies-Reference-Cited by-同舟云学术

The Structural Basis of ZMPSTE24-Dependent Laminopathies

Published:2013-03-28 Issue:6127 Volume:339 Page:1604-1607
ISSN:0036-8075
Container-title:Science
language:en
Short-container-title:Science

Author:

Quigley A.,Dong Y. Y.,Pike A. C. W.,Dong L.,Shrestha L.,Berridge G.,Stansfeld P. J.,Sansom M. S. P.,Edwards A. M.,Bountra C.,von Delft F.,Bullock A. N.,Burgess-Brown N. A.,Carpenter E. P.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

Reference49 articles.

1. Nuclear Lamins

2. The lamin protein family

3. Zmpste24 deficiency in mice causes spontaneous bone fractures, muscle weakness, and a prelamin A processing defect

4. Loss of ZMPSTE24 (FACE-1) causes autosomal recessive restrictive dermopathy and accumulation of Lamin A precursors

5. ZMPSTE24, an integral membrane zinc metalloprotease with a connection to progeroid disorders

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