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CUL7 gene

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

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2016
2016
Changes in facial appearance from neonate to adult in 3-M syndrome patient with novel CUL7 gene mutations
Abstract 3-M syndrome (OMIM #273750, #612921, and #614205) is a rare autosomal recessive growth disorder that is characterized by… 
2015
2015
An adult with 3-M syndrome
3-M syndrome is a rare autosomal recessive disorder characterised by short stature, dysmorphic facial features and skeletal… 
2014
2014
Altered frequency of sequence variants in growth-related genes in children with short stature
1Centre for Paediatrics and Child Health, InsFtute of Human Development, Faculty of Medical and Human Sciences, University of… 
2013
2013
Abstract 330A: Differential expression of angiogenic genes in invasive high grade serous ovarian carcinomas.
Proceedings: AACR 104th Annual Meeting 2013; Apr 6-10, 2013; Washington, DC Our objective is to establish quantifiable and… 
2012
2012
A novel genetic marker of liver disease aetiology in hepatocellular carcinoma: culling the metabolic syndrome
Paradis et al 1 describe the work in which they identified CUL7 as a unique target gene in metabolic syndrome-related… 
2005
2005
Dimerization of CUL7 and PARC Is Not Required for All CUL7 Functions and Mouse Development
ABSTRACT CUL7, a recently identified member of the cullin family of E3 ubiquitin ligases, forms a unique SCF-like complex and is… 
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