"CREB-Binding Protein" 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 member of the p300-CBP transcription factor family that was initially identified as a binding partner for CAMP RESPONSE ELEMENT-BINDING PROTEIN. Mutations in CREB-binding protein are associated with RUBINSTEIN-TAYBI SYNDROME.
MeSH Number(s)
D08.811.913.050.134.440.249
Concept/Terms
CREB-Binding Protein- CREB-Binding Protein
- CREB Binding Protein
- Nuclear Protein CBP
- CBP, Nuclear Protein
- Phospho-CREB-Binding Protein
- Phospho CREB Binding Protein
Below are MeSH descriptors whose meaning is more general than "CREB-Binding Protein".
Below are MeSH descriptors whose meaning is more specific than "CREB-Binding Protein".
This graph shows the total number of publications written about "CREB-Binding Protein" by people in Harvard Catalyst Profiles by year, and whether "CREB-Binding Protein" was a major or minor topic of these publication.
To see the data from this visualization as text,
click here.
Year | Major Topic | Minor Topic | Total |
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1996 | 0 | 2 | 2 |
1997 | 0 | 4 | 4 |
1998 | 0 | 7 | 7 |
1999 | 0 | 9 | 9 |
2000 | 0 | 13 | 13 |
2001 | 0 | 11 | 11 |
2002 | 0 | 5 | 5 |
2003 | 0 | 4 | 4 |
2004 | 0 | 5 | 5 |
2005 | 2 | 3 | 5 |
2006 | 1 | 1 | 2 |
2008 | 0 | 2 | 2 |
2009 | 3 | 5 | 8 |
2010 | 1 | 4 | 5 |
2011 | 5 | 1 | 6 |
2012 | 0 | 2 | 2 |
2013 | 0 | 2 | 2 |
2014 | 1 | 2 | 3 |
2015 | 2 | 1 | 3 |
2016 | 3 | 1 | 4 |
2017 | 2 | 1 | 3 |
2018 | 1 | 0 | 1 |
2019 | 0 | 1 | 1 |
2020 | 1 | 0 | 1 |
2021 | 2 | 0 | 2 |
Below are the most recent publications written about "CREB-Binding Protein" by people in Profiles.
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NF-?B suppression synergizes with E7386, an inhibitor of CBP/ß-catenin interaction, to block proliferation of patient-derived colon cancer spheroids. Biochem Biophys Res Commun. 2022 01 01; 586:93-99.
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Discovery of spirohydantoins as selective, orally bioavailable inhibitors of p300/CBP histone acetyltransferases. Bioorg Med Chem Lett. 2021 05 01; 39:127854.
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Targeted degradation of the enhancer lysine acetyltransferases CBP and p300. Cell Chem Biol. 2021 04 15; 28(4):503-514.e12.
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SATB2 drives glioblastoma growth by recruiting CBP to promote FOXM1 expression in glioma stem cells. EMBO Mol Med. 2020 12 07; 12(12):e12291.
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Structure-based drug optimization and biological evaluation of tetrahydroquinolin derivatives as selective and potent CBP bromodomain inhibitors. Bioorg Med Chem Lett. 2020 11 15; 30(22):127480.
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Design, synthesis, and biological evaluation of tetrahydroquinolin derivatives as potent inhibitors of CBP bromodomain. Bioorg Chem. 2020 08; 101:103991.
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Interaction between the scaffold proteins CBP by IQGAP1 provides an interface between gene expression and cytoskeletal activity. Sci Rep. 2020 04 01; 10(1):5753.
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Pharmacological Modulation of the Wnt/ß-Catenin Pathway Inhibits Proliferation and Promotes Differentiation of Long-Lived Memory CD4+ T Cells in Antiretroviral Therapy-Suppressed Simian Immunodeficiency Virus-Infected Macaques. J Virol. 2019 12 12; 94(1).
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Preferential sensitivity to HDAC inhibitors in tumors with CREBBP mutation. Cancer Gene Ther. 2020 05; 27(5):294-300.
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Mocetinostat for patients with previously treated, locally advanced/metastatic urothelial carcinoma and inactivating alterations of acetyltransferase genes. Cancer. 2019 02 15; 125(4):533-540.