"Cell Cycle 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 control the CELL DIVISION CYCLE. This family of proteins includes a wide variety of classes, including CYCLIN-DEPENDENT KINASES, mitogen-activated kinases, CYCLINS, and PHOSPHOPROTEIN PHOSPHATASES as well as their putative substrates such as chromatin-associated proteins, CYTOSKELETAL PROTEINS, and TRANSCRIPTION FACTORS.
Descriptor ID |
D018797
|
MeSH Number(s) |
D12.776.167
|
Concept/Terms |
Cell Cycle Proteins- Cell Cycle Proteins
- Cell Division Cycle Proteins
- Cell-Cycle Regulatory Proteins
- Cell Cycle Regulatory Proteins
- cdc Proteins
|
Below are MeSH descriptors whose meaning is more general than "Cell Cycle Proteins".
Below are MeSH descriptors whose meaning is more specific than "Cell Cycle Proteins".
This graph shows the total number of publications written about "Cell Cycle Proteins" by people in this website by year, and whether "Cell Cycle Proteins" was a major or minor topic of these publications.
To see the data from this visualization as text,
click here.
Year | Major Topic | Minor Topic | Total |
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1994 | 12 | 3 | 15 |
1995 | 14 | 3 | 17 |
1996 | 12 | 2 | 14 |
1997 | 19 | 7 | 26 |
1998 | 27 | 10 | 37 |
1999 | 33 | 10 | 43 |
2000 | 28 | 10 | 38 |
2001 | 40 | 17 | 57 |
2002 | 29 | 26 | 55 |
2003 | 33 | 28 | 61 |
2004 | 30 | 45 | 75 |
2005 | 39 | 35 | 74 |
2006 | 26 | 22 | 48 |
2007 | 21 | 28 | 49 |
2008 | 38 | 19 | 57 |
2009 | 20 | 34 | 54 |
2010 | 21 | 37 | 58 |
2011 | 25 | 35 | 60 |
2012 | 28 | 24 | 52 |
2013 | 15 | 20 | 35 |
2014 | 11 | 29 | 40 |
2015 | 13 | 26 | 39 |
2016 | 13 | 19 | 32 |
2017 | 18 | 15 | 33 |
2018 | 13 | 19 | 32 |
2019 | 25 | 13 | 38 |
2020 | 25 | 12 | 37 |
2021 | 25 | 6 | 31 |
2022 | 5 | 15 | 20 |
2023 | 4 | 15 | 19 |
2024 | 3 | 7 | 10 |
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Below are the most recent publications written about "Cell Cycle Proteins" by people in Profiles.
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Biologic and Clinical Analysis of Childhood Gamma Delta T-ALL Identifies LMO2/STAG2 Rearrangements as Extremely High Risk. Cancer Discov. 2024 Oct 04; 14(10):1838-1859.
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Exploration of the tunability of BRD4 degradation by DCAF16 trans-labelling covalent glues. Eur J Med Chem. 2024 Dec 05; 279:116904.
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RAD21 promotes oncogenesis and lethal progression of prostate cancer. Proc Natl Acad Sci U S A. 2024 Sep 03; 121(36):e2405543121.
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The ICF syndrome protein CDCA7 harbors a unique DNA binding domain that recognizes a CpG dyad in the context of a non-B DNA. Sci Adv. 2024 Aug 23; 10(34):eadr0036.
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Treatment options for biliary tract cancer: unmet needs, new targets and opportunities from both physicians' and patients' perspectives. Future Oncol. 2024; 20(20):1435-1450.
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Brd4::Nutm1 fusion gene initiates NUT carcinoma in vivo. Life Sci Alliance. 2024 Jul; 7(7).
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AKAP12 Upregulation Associates With PDE8A to Accelerate Cardiac Dysfunction. Circ Res. 2024 Apr 12; 134(8):1006-1022.
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Role of chromosomal cohesion and separation in aneuploidy and tumorigenesis. Cell Mol Life Sci. 2024 Feb 22; 81(1):100.
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A Phase I/II Study of GSK525762 Combined with Fulvestrant in Patients with Hormone Receptor-positive/HER2-negative Advanced or Metastatic Breast Cancer. Clin Cancer Res. 2024 01 17; 30(2):334-343.
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Epigenetic regulation of asymmetric cell division by the LIBR-BRD4 axis. Nucleic Acids Res. 2024 Jan 11; 52(1):154-165.