"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 | 2 | 14 |
1995 | 12 | 2 | 14 |
1996 | 11 | 2 | 13 |
1997 | 17 | 9 | 26 |
1998 | 27 | 10 | 37 |
1999 | 34 | 10 | 44 |
2000 | 24 | 10 | 34 |
2001 | 33 | 15 | 48 |
2002 | 19 | 17 | 36 |
2003 | 33 | 28 | 61 |
2004 | 30 | 46 | 76 |
2005 | 39 | 36 | 75 |
2006 | 24 | 24 | 48 |
2007 | 20 | 26 | 46 |
2008 | 37 | 20 | 57 |
2009 | 20 | 33 | 53 |
2010 | 22 | 35 | 57 |
2011 | 26 | 36 | 62 |
2012 | 29 | 24 | 53 |
2013 | 15 | 19 | 34 |
2014 | 14 | 28 | 42 |
2015 | 14 | 27 | 41 |
2016 | 16 | 19 | 35 |
2017 | 18 | 15 | 33 |
2018 | 14 | 17 | 31 |
2019 | 26 | 16 | 42 |
2020 | 22 | 12 | 34 |
2021 | 23 | 6 | 29 |
2022 | 5 | 16 | 21 |
2023 | 4 | 14 | 18 |
2024 | 1 | 2 | 3 |
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Below are the most recent publications written about "Cell Cycle Proteins" by people in Profiles.
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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.
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Preclinical efficacy of targeting epigenetic mechanisms in AML with 3q26 lesions and EVI1 overexpression. Leukemia. 2024 Mar; 38(3):545-556.
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The BRD4-NUT Fusion Alone Drives Malignant Transformation of NUT Carcinoma. Cancer Res. 2023 12 01; 83(23):3846-3860.
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EZH2 Cooperates with BRD4-NUT to Drive NUT Carcinoma Growth by Silencing Key Tumor Suppressor Genes. Cancer Res. 2023 12 01; 83(23):3956-3973.
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Glial Cell Adhesion Molecule (GlialCAM) Determines Proliferative versus Invasive Cell States in Glioblastoma. J Neurosci. 2023 11 22; 43(47):8043-8057.
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Comparative Clinicopathologic and Genomic Analysis of Hepatocellular Neoplasm, Not Otherwise Specified, and Hepatoblastoma. Mod Pathol. 2024 Feb; 37(2):100385.
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Molecular Basis for SPINDOC-Spindlin1 Engagement and Its Role in Transcriptional Attenuation. J Mol Biol. 2024 Apr 01; 436(7):168371.
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Phase I Results of Bromodomain and Extra-Terminal Inhibitor PLX51107 in Combination with Azacitidine in Patients with Relapsed/Refractory Myeloid Malignancies. Clin Cancer Res. 2023 11 01; 29(21):4352-4360.