Nuclear Pore Complex Proteins
"Nuclear Pore Complex Proteins" 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.
Proteins that form the structure of the NUCLEAR PORE. They are involved in active, facilitated and passive transport of molecules in and out of the CELL NUCLEUS.
Descriptor ID |
D028861
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MeSH Number(s) |
D12.776.157.530.750.625 D12.776.543.585.750.625
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Concept/Terms |
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Below are MeSH descriptors whose meaning is more general than "Nuclear Pore Complex Proteins".
Below are MeSH descriptors whose meaning is more specific than "Nuclear Pore Complex Proteins".
This graph shows the total number of publications written about "Nuclear Pore Complex Proteins" by people in this website by year, and whether "Nuclear Pore Complex Proteins" was a major or minor topic of these publications.
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Year | Major Topic | Minor Topic | Total |
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2000 | 0 | 2 | 2 | 2005 | 0 | 1 | 1 | 2007 | 1 | 0 | 1 | 2010 | 1 | 0 | 1 | 2012 | 0 | 1 | 1 | 2013 | 0 | 1 | 1 | 2015 | 2 | 0 | 2 |
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Below are the most recent publications written about "Nuclear Pore Complex Proteins" by people in Profiles.
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Stuwe T, Bley CJ, Thierbach K, Petrovic S, Schilbach S, Mayo DJ, Perriches T, Rundlet EJ, Jeon YE, Collins LN, Huber FM, Lin DH, Paduch M, Koide A, Lu V, Fischer J, Hurt E, Koide S, Kossiakoff AA, Hoelz A. Architecture of the fungal nuclear pore inner ring complex. Science. 2015 Oct 02; 350(6256):56-64.
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Stuwe T, Correia AR, Lin DH, Paduch M, Lu VT, Kossiakoff AA, Hoelz A. Nuclear pores. Architecture of the nuclear pore complex coat. Science. 2015 Mar 06; 347(6226):1148-52.
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Ikegami K, Lieb JD. Integral nuclear pore proteins bind to Pol III-transcribed genes and are required for Pol III transcript processing in C. elegans. Mol Cell. 2013 Sep 26; 51(6):840-9.
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Rosebeck S, Rehman AO, Apel IJ, Kohrt D, Appert A, O'Donnell MA, Ting AT, Du MQ, Baens M, Lucas PC, McAllister-Lucas LM. The API2-MALT1 fusion exploits TNFR pathway-associated RIP1 ubiquitination to promote oncogenic NF-?B signaling. Oncogene. 2014 May 08; 33(19):2520-30.
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Narayan N, Lee IH, Borenstein R, Sun J, Wong R, Tong G, Fergusson MM, Liu J, Rovira II, Cheng HL, Wang G, Gucek M, Lombard D, Alt FW, Sack MN, Murphy E, Cao L, Finkel T. The NAD-dependent deacetylase SIRT2 is required for programmed necrosis. Nature. 2012 Dec 13; 492(7428):199-204.
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Ikegami K, Lieb JD. Nucleoporins and transcription: new connections, new questions. PLoS Genet. 2010 Feb 26; 6(2):e1000861.
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Qin K, Du X, Rich BH. An Alu-mediated rearrangement causing a 3.2kb deletion and a novel two base pair deletion in AAAS gene as the cause of triple A syndrome. Mol Genet Metab. 2007 Dec; 92(4):359-63.
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Connerly PL, Esaki M, Montegna EA, Strongin DE, Levi S, Soderholm J, Glick BS. Sec16 is a determinant of transitional ER organization. Curr Biol. 2005 Aug 23; 15(16):1439-47.
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Kobzev YN, Martinez-Climent J, Lee S, Chen J, Rowley JD. Analysis of translocations that involve the NUP98 gene in patients with 11p15 chromosomal rearrangements. Genes Chromosomes Cancer. 2004 Dec; 41(4):339-52.
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Hammond AT, Glick BS. Dynamics of transitional endoplasmic reticulum sites in vertebrate cells. Mol Biol Cell. 2000 Sep; 11(9):3013-30.
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