CUL7 gene

Known as: CULLIN 7, KIAA0076, CUL7 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

2005-2018
01220052018

Papers overview

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2018
2018
Colorectal cancer (CRC) is one of the most common cancers and a major cause of mortality. The present study aimed to identify… (More)
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2018
2018
Cullin (CUL)-RING E3 ubiquitin ligases (CRLs) are attractive therapeutic targets as they regulate diverse biological processes… (More)
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2016
2016
3-M syndrome (OMIM #273750) is a rare autosomal recessive growth disorder characterized by severe pre- and post-natal growth… (More)
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2014
2014
Dysfunctional regulation of signaling pathways downstream of the insulin receptor plays a pivotal role in the pathogenesis of… (More)
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2013
2013
3-M syndrome is an autosomal recessive disorder characterised by pre- and post-natal growth restriction, facial dysmorphism… (More)
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2013
2013
Paradis et al describe the work in which they identified CUL7 as a unique target gene in metabolic syndrome-related… (More)
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2010
2010
Germ line mutations of the ubiquitin ligase cullin 7 (CUL7) are linked to 3-M syndrome and Yakuts short stature syndrome, both of… (More)
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2010
2010
Intra-uterine growth restriction (IUGR) is defined by a restriction of fetal growth during gestation. It is a prevalent… (More)
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2006
2006
Cullins are a family of evolutionarily conserved proteins that bind to the small RING finger protein, ROC1, to constitute… (More)
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Highly Cited
2005
Highly Cited
2005
Intrauterine growth retardation is caused by maternal, fetal or placental factors that result in impaired endovascular… (More)
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