SKP Cullin F-Box Protein Ligases
"SKP Cullin F-Box Protein Ligases" 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 subset of ubiquitin protein ligases that are formed by the association of a SKP DOMAIN PROTEIN, a CULLIN DOMAIN PROTEIN and a F-BOX DOMAIN PROTEIN.
| Descriptor ID |
D044843
|
| MeSH Number(s) |
D08.811.464.938.750.750
|
| Concept/Terms |
SKP1-Cullin Ubiquitin Ligases- SKP1-Cullin Ubiquitin Ligases
- Ligases, SKP1-Cullin Ubiquitin
- SKP1 Cullin Ubiquitin Ligases
- Ubiquitin Ligases, SKP1-Cullin
- Skp1-Cullin-1-F-box Ubiquitin Ligase
- Ligase, Skp1-Cullin-1-F-box Ubiquitin
- Skp1 Cullin 1 F box Ubiquitin Ligase
- Ubiquitin Ligase, Skp1-Cullin-1-F-box
- Skp1-Cullin-F-Box Proteins
- Skp1 Cullin F Box Proteins
|
Below are MeSH descriptors whose meaning is more general than "SKP Cullin F-Box Protein Ligases".
Below are MeSH descriptors whose meaning is more specific than "SKP Cullin F-Box Protein Ligases".
This graph shows the total number of publications written about "SKP Cullin F-Box Protein Ligases" by people in this website by year, and whether "SKP Cullin F-Box Protein Ligases" 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 |
|---|
| 2000 | 0 | 1 | 1 |
| 2001 | 0 | 1 | 1 |
| 2002 | 0 | 1 | 1 |
| 2003 | 0 | 1 | 1 |
| 2005 | 0 | 2 | 2 |
| 2006 | 1 | 0 | 1 |
| 2007 | 1 | 1 | 2 |
| 2008 | 1 | 1 | 2 |
| 2010 | 2 | 2 | 4 |
| 2011 | 2 | 0 | 2 |
| 2012 | 1 | 3 | 4 |
| 2013 | 1 | 0 | 1 |
| 2014 | 2 | 1 | 3 |
| 2015 | 0 | 2 | 2 |
| 2017 | 0 | 2 | 2 |
| 2020 | 1 | 2 | 3 |
To return to the timeline,
click here.
Below are the most recent publications written about "SKP Cullin F-Box Protein Ligases" by people in Profiles.
-
FBXO28 causes developmental and epileptic encephalopathy with profound intellectual disability. Epilepsia. 2021 01; 62(1):e13-e21.
-
The GSK-3?-FBXL21 Axis Contributes to Circadian TCAP Degradation and Skeletal Muscle Function. Cell Rep. 2020 09 15; 32(11):108140.
-
Mechanisms Regulating Muscle Protein Synthesis in CKD. J Am Soc Nephrol. 2020 11; 31(11):2573-2587.
-
A novel FBXO28 frameshift mutation in a child with developmental delay, dysmorphic features, and intractable epilepsy: A second gene that may contribute to the 1q41-q42 deletion phenotype. Am J Med Genet A. 2018 07; 176(7):1549-1558.
-
Systemic inflammation is associated with exaggerated skeletal muscle protein catabolism in maintenance hemodialysis patients. JCI Insight. 2017 11 16; 2(22).
-
The nuclear phosphatase SCP4 regulates FoxO?transcription factors during muscle wasting?in chronic kidney disease. Kidney Int. 2017 08; 92(2):336-348.
-
Inhibition of Stat3 activation suppresses caspase-3 and the ubiquitin-proteasome system, leading to preservation of muscle mass in cancer cachexia. J Biol Chem. 2015 Apr 24; 290(17):11177-87.
-
The orphan nuclear receptor Nur77 is a determinant of myofiber size and muscle mass in mice. Mol Cell Biol. 2015 Apr; 35(7):1125-38.
-
CSN6 drives carcinogenesis by positively regulating Myc stability. Nat Commun. 2014 Nov 14; 5:5384.
-
MAFbx/Atrogin-1 is required for atrophic remodeling of the unloaded heart. J Mol Cell Cardiol. 2014 Jul; 72:168-76.