Cullin 7 抗体
(Cullin 7 (CUL7))
The protein encoded by this gene is a component of an E3 ubiquitin-protein ligase complex. The encoded protein interacts with TP53, CUL9, and FBXW8 proteins. Defects in this gene are a cause of 3M syndrome type 1 (3M1). Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2009].
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Latest Publications for our Cullin 7 抗体
: "Cullin 7 and Fbxw 8 expression in trophoblastic cells is regulated via oxygen tension: implications for intrauterine growth restriction?" in: The journal of maternal-fetal & neonatal medicine, Vol. 25, Issue 11, pp. 2209-15, (2012) (PubMed).: "Selective cochlear degeneration in mice lacking the F-box protein, Fbx2, a glycoprotein-specific ubiquitin ligase subunit." in: The Journal of neuroscience : the official journal of the Society for Neuroscience, Vol. 27, Issue 19, pp. 5163-71, (2007) (PubMed).
: "Targeted disruption of p185/Cul7 gene results in abnormal vascular morphogenesis." in: Proceedings of the National Academy of Sciences of the United States of America, Vol. 100, Issue 17, pp. 9855-60, (2003) (PubMed).
: "CUL7: A DOC domain-containing cullin selectively binds Skp1.Fbx29 to form an SCF-like complex." in: Proceedings of the National Academy of Sciences of the United States of America, Vol. 99, Issue 26, pp. 16601-6, (2002) (PubMed).
Aliases for Cullin 7 抗体
cullin 7 (CUL7) 抗体cullin 7 (Cul7) 抗体
2510004L20Rik 抗体
AA409809 抗体
C230011P08Rik 抗体
CUL7 抗体
cullin-7 抗体
Cullin-7 抗体
dJ20C7.5 抗体
KIAA0076 抗体
p185 抗体
p193 抗体
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