CTNNBIP1: Difference between revisions

Jump to navigation Jump to search
m (Bot: HTTP→HTTPS (v475))
 
imported>Nemo bis
(Added free to read link in citations with OAbot #oabot)
 
Line 20: Line 20:
*{{cite journal  |vauthors=Kohler EM, Chandra SH, Behrens J, Schneikert J |title=Beta-catenin degradation mediated by the CID domain of APC provides a model for the selection of APC mutations in colorectal, desmoid and duodenal tumours. |journal=Hum. Mol. Genet. |volume=18 |issue= 2 |pages= 213–26 |year= 2009 |pmid= 18854359 |doi= 10.1093/hmg/ddn338 }}
*{{cite journal  |vauthors=Kohler EM, Chandra SH, Behrens J, Schneikert J |title=Beta-catenin degradation mediated by the CID domain of APC provides a model for the selection of APC mutations in colorectal, desmoid and duodenal tumours. |journal=Hum. Mol. Genet. |volume=18 |issue= 2 |pages= 213–26 |year= 2009 |pmid= 18854359 |doi= 10.1093/hmg/ddn338 }}
*{{cite journal  |vauthors=Seo E, Jho EH |title=Axin-independent phosphorylation of APC controls beta-catenin signaling via cytoplasmic retention of beta-catenin. |journal=Biochem. Biophys. Res. Commun. |volume=357 |issue= 1 |pages= 81–6 |year= 2007 |pmid= 17418091 |doi= 10.1016/j.bbrc.2007.03.117 }}
*{{cite journal  |vauthors=Seo E, Jho EH |title=Axin-independent phosphorylation of APC controls beta-catenin signaling via cytoplasmic retention of beta-catenin. |journal=Biochem. Biophys. Res. Commun. |volume=357 |issue= 1 |pages= 81–6 |year= 2007 |pmid= 17418091 |doi= 10.1016/j.bbrc.2007.03.117 }}
*{{cite journal  |vauthors=Ladeiro Y, Couchy G, Balabaud C |title=MicroRNA profiling in hepatocellular tumors is associated with clinical features and oncogene/tumor suppressor gene mutations. |journal=Hepatology |volume=47 |issue= 6 |pages= 1955–63 |year= 2008 |pmid= 18433021 |doi= 10.1002/hep.22256 |display-authors=etal}}
*{{cite journal  |vauthors=Ladeiro Y, Couchy G, Balabaud C |title=MicroRNA profiling in hepatocellular tumors is associated with clinical features and oncogene/tumor suppressor gene mutations. |journal=Hepatology |volume=47 |issue= 6 |pages= 1955–63 |year= 2008 |pmid= 18433021 |doi= 10.1002/hep.22256 |display-authors=etal|url=http://www.hal.inserm.fr/docs/00/32/95/10/PDF/HEP-07-1716R1.pdf }}
*{{cite journal  |vauthors=Zhang H, Xue Y |title=Wnt pathway is involved in advanced gastric carcinoma. |journal=Hepatogastroenterology |volume=55 |issue= 84 |pages= 1126–30 |year=  2008|pmid= 18705344 |doi=  }}
*{{cite journal  |vauthors=Zhang H, Xue Y |title=Wnt pathway is involved in advanced gastric carcinoma. |journal=Hepatogastroenterology |volume=55 |issue= 84 |pages= 1126–30 |year=  2008|pmid= 18705344 |doi=  }}
*{{cite journal  |vauthors=Wang HX, Tekpetey FR, Kidder GM |title=Identification of WNT/beta-CATENIN signaling pathway components in human cumulus cells. |journal=Mol. Hum. Reprod. |volume=15 |issue= 1 |pages= 11–7 |year= 2009 |pmid= 19038973 |doi= 10.1093/molehr/gan070 }}
*{{cite journal  |vauthors=Wang HX, Tekpetey FR, Kidder GM |title=Identification of WNT/beta-CATENIN signaling pathway components in human cumulus cells. |journal=Mol. Hum. Reprod. |volume=15 |issue= 1 |pages= 11–7 |year= 2009 |pmid= 19038973 |doi= 10.1093/molehr/gan070 }}

Latest revision as of 12:41, 4 November 2018

VALUE_ERROR (nil)
Identifiers
Aliases
External IDsGeneCards: [1]
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

n/a

n/a

RefSeq (protein)

n/a

n/a

Location (UCSC)n/an/a
PubMed searchn/an/a
Wikidata
View/Edit Human

Beta-catenin-interacting protein 1 is a protein that is encoded in humans by the CTNNBIP1 gene.[1][2]

Function

The protein encoded by this gene binds CTNNB1 and prevents interaction between CTNNB1 and TCF (T-cell transcription factor) family members. The encoded protein is a negative regulator of the Wnt signaling pathway.[1]

References

  1. 1.0 1.1 "Entrez Gene: catenin".
  2. Tago K, Nakamura T, Nishita M, Hyodo J, Nagai S, Murata Y, Adachi S, Ohwada S, Morishita Y, Shibuya H, Akiyama T (July 2000). "Inhibition of Wnt signaling by ICAT, a novel beta-catenin-interacting protein". Genes Dev. 14 (14): 1741–9. PMC 316784. PMID 10898789.

Further reading

External links

This article incorporates text from the United States National Library of Medicine, which is in the public domain.