"Nuclear Lamina" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
A lattice of fibrils which covers the entire inner surface of the nuclear envelope and interlinks nuclear pores (NUCLEAR PORE).
Descriptor ID |
D034881
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MeSH Number(s) |
A11.284.149.165.630.500 A11.284.430.106.279.345.700.700 A11.284.430.106.279.692.314 A11.284.835.514.700.500
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Concept/Terms |
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Below are MeSH descriptors whose meaning is more general than "Nuclear Lamina".
Below are MeSH descriptors whose meaning is more specific than "Nuclear Lamina".
This graph shows the total number of publications written about "Nuclear Lamina" by people in this website by year, and whether "Nuclear Lamina" was a major or minor topic of these publications.
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Year | Major Topic | Minor Topic | Total |
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2008 | 1 | 0 | 1 |
2009 | 1 | 0 | 1 |
2011 | 0 | 1 | 1 |
2012 | 1 | 0 | 1 |
2013 | 1 | 0 | 1 |
2022 | 0 | 1 | 1 |
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Below are the most recent publications written about "Nuclear Lamina" by people in Profiles.
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The nuclear lamina binds the EBV genome during latency and regulates viral gene expression. PLoS Pathog. 2022 04; 18(4):e1010400.
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Nuclear lamin phosphorylation: an emerging role in gene regulation and pathogenesis of laminopathies. Nucleus. 2020 12; 11(1):299-314.
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Transcription-independent TFIIIC-bound sites cluster near heterochromatin boundaries within lamina-associated domains in C. elegans. Epigenetics Chromatin. 2020 01 09; 13(1):1.
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Centrosomal protein TRIM43 restricts herpesvirus infection by regulating nuclear lamina integrity. Nat Microbiol. 2019 01; 4(1):164-176.
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Comparative analysis of metazoan chromatin organization. Nature. 2014 Aug 28; 512(7515):449-52.
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Emerin in health and disease. Semin Cell Dev Biol. 2014 May; 29:95-106.
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DNA sequence-dependent compartmentalization and silencing of chromatin at the nuclear lamina. Cell. 2012 Jun 22; 149(7):1474-87.
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Gene expression, chromosome position and lamin A/C mutations. Nucleus. 2011 May-Jun; 2(3):162-7.
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Mutation of SYNE-1, encoding an essential component of the nuclear lamina, is responsible for autosomal recessive arthrogryposis. Hum Mol Genet. 2009 Sep 15; 18(18):3462-9.
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Emerin and the nuclear lamina in muscle and cardiac disease. Circ Res. 2008 Jul 03; 103(1):16-23.