"Proto-Oncogene 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.
Products of proto-oncogenes. Normally they do not have oncogenic or transforming properties, but are involved in the regulation or differentiation of cell growth. They often have protein kinase activity.
Descriptor ID |
D011518
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MeSH Number(s) |
D12.776.624.664.700
|
Concept/Terms |
Proto-Oncogene Proteins- Proto-Oncogene Proteins
- Proto Oncogene Proteins
- Proto-Oncogene Products, Cellular
- Cellular Proto-Oncogene Products
- Proto Oncogene Products, Cellular
- Proto Oncogene Proteins, Cellular
- c-onc Proteins
- c onc Proteins
- Cellular Proto-Oncogene Proteins
- Cellular Proto Oncogene Proteins
- Proto-Oncogene Proteins, Cellular
|
Below are MeSH descriptors whose meaning is more general than "Proto-Oncogene Proteins".
Below are MeSH descriptors whose meaning is more specific than "Proto-Oncogene Proteins".
This graph shows the total number of publications written about "Proto-Oncogene Proteins" by people in this website by year, and whether "Proto-Oncogene 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 | 4 | 2 | 6 |
1995 | 6 | 1 | 7 |
1996 | 16 | 2 | 18 |
1997 | 10 | 4 | 14 |
1998 | 10 | 3 | 13 |
1999 | 7 | 4 | 11 |
2000 | 8 | 10 | 18 |
2001 | 9 | 7 | 16 |
2002 | 9 | 6 | 15 |
2003 | 29 | 12 | 41 |
2004 | 19 | 13 | 32 |
2005 | 19 | 9 | 28 |
2006 | 4 | 1 | 5 |
2007 | 2 | 1 | 3 |
2008 | 5 | 0 | 5 |
2009 | 5 | 3 | 8 |
2010 | 0 | 3 | 3 |
2011 | 1 | 1 | 2 |
2012 | 7 | 1 | 8 |
2013 | 5 | 3 | 8 |
2014 | 4 | 5 | 9 |
2015 | 0 | 2 | 2 |
2016 | 2 | 0 | 2 |
2017 | 2 | 0 | 2 |
2018 | 3 | 0 | 3 |
2019 | 2 | 0 | 2 |
2020 | 1 | 0 | 1 |
2021 | 2 | 1 | 3 |
2022 | 0 | 3 | 3 |
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Below are the most recent publications written about "Proto-Oncogene Proteins" by people in Profiles.
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Sfrp4 expression in thyroxine treated calvarial cells. Life Sci. 2022 Dec 15; 311(Pt A):121158.
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Long non-coding RNA LINC00926 regulates WNT10B signaling pathway thereby altering inflammatory gene expression in PTSD. Transl Psychiatry. 2022 05 12; 12(1):200.
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Cigarette smoking is a secondary cause of folliculin loss. Thorax. 2023 Apr; 78(4):402-408.
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Structure-activity and mechanistic studies of non-peptidic inhibitors of the PLK1 polo box domain identified through REPLACE. Eur J Med Chem. 2022 Jan 05; 227:113926.
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Autocrine signaling by receptor tyrosine kinases in urothelial carcinoma of the bladder. PLoS One. 2021; 16(7):e0241766.
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Nonpeptidic, Polo-Box Domain-Targeted Inhibitors of PLK1 Block Kinase Activity, Induce Its Degradation and Target-Resistant Cells. J Med Chem. 2021 07 22; 64(14):9916-9925.
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Peptidomimetic Polo-Box-Targeted Inhibitors that Engage PLK1 in Tumor Cells and Are Selective against the PLK3 Tumor Suppressor. ChemMedChem. 2020 06 17; 15(12):1058-1066.
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Polo-like kinase 1 (Plk1) inhibition synergizes with taxanes in triple negative breast cancer. PLoS One. 2019; 14(11):e0224420.
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Isomorphic diffuse glioma is a morphologically and molecularly distinct tumour entity with recurrent gene fusions of MYBL1 or MYB and a benign disease course. Acta Neuropathol. 2020 01; 139(1):193-209.
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The Meisenheimer Complex as a Paradigm in Drug Discovery: Reversible Covalent Inhibition through C67 of the ATP Binding Site of PLK1. Cell Chem Biol. 2018 09 20; 25(9):1107-1116.e4.