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Cited by 231

The DOI matches its Crossref record; 11 of the 11 references it cites were found in a registry or an index.

Nuclear lamin functions and disease

Open access
Butin-Israeli, Veronika, Adam, Stephen A., Goldman, Anne E., Goldman, Robert D.·2012·Trends in Genetics

Abstract

Recent studies have shown that premature cellular senescence and normal organ development and function depend on the type V intermediate filament proteins, the lamins, which are major structural proteins of the nucleus. This review presents an up-to-date summary of the literature describing new findings on lamin functions in various cellular processes and emphasizes the relationship between the lamins and devastating diseases ranging from premature aging to cancer. Recent insights into the structure and function of the A- and B- type lamins in normal cells and their dysfunctions in diseased cells are providing novel targets for the development of new diagnostic procedures and disease intervention. We summarize these recent findings, focusing on data from mice and humans, and highlight the expanding knowledge of these proteins in both healthy and diseased cells.

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Crossref · 10.1016/j.tig.2012.06.001

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Metadata

Authors
Butin-Israeli, V., Adam, S. A., Goldman, A. E., & Goldman, R. D.
Venue
Trends in Genetics
Publisher
Elsevier BV
Published
2012-09
Volume
28
Issue
9
Pages
464-471
ISSN
0168-9525 (ISSN-L)
OpenAlex
W2136835005
Cited by
231
References
11
FWCI
1.44
Type
journal article
Language
en
Open access
green

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CoChat. (2026). Citation check: Nuclear lamin functions and disease. https://app.cochat.ai/papers/10.1016/j.tig.2012.06.001
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Butin-Israeli, V., Adam, S. A., Goldman, A. E., & Goldman, R. D. (2012). Nuclear lamin functions and disease. Trends in Genetics. https://doi.org/10.1016/j.tig.2012.06.001

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.