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CIRH1A encodes a WD40-repeat-containing protein that is localized to the nucleolus. Additionally we are shipping CIRH1A Proteins (5) and many more products for this protein.
Showing 10 out of 28 products:
Human Polyclonal CIRH1A Primary Antibody for EIA, FACS - ABIN951532
Yu, Mitchell, Richter: Cirhin up-regulates a canonical NF-kappaB element through strong interaction with Cirip/HIVEP1. in Experimental cell research 2009
Show all 2 references for ABIN951532
Human Polyclonal CIRH1A Primary Antibody for ELISA, WB - ABIN566605
Freed, Prieto, McCann, McStay, Baserga: NOL11, implicated in the pathogenesis of North American Indian childhood cirrhosis, is required for pre-rRNA transcription and processing. in PLoS genetics 2012
data provide the first in vivo evidence of a role for Cirhin in biliary development, and support the hypothesis that congenital defects affecting ribosome biogenesis can activate a cellular stress response mediated by p53 (show TP53 Antibodies)
A missense mutation (R565W) in cirhin (FLJ14728) in North American Indian childhood cirrhosis
Cirhin is a nucleolar protein (show MCRS1 Antibodies) and the R565W mutation, for which all North American Indian childhood cirrhosis patients are homozygous, has no effect on subcellular localization.
Cirhin is a transcriptional regulatory factor of this NF-kappaB (show NFKB1 Antibodies) sequence and could be a participant in the regulation of other genes with NF-kappaB (show NFKB1 Antibodies) responsive elements.
This gene encodes a WD40-repeat-containing protein that is localized to the nucleolus. Mutation of this gene causes North American Indian childhood cirrhosis, a severe intrahepatic cholestasis that results in transient neonatal jaundice, and progresses to periportal fibrosis and cirrhosis in childhood and adolescence.
, testis-expressed gene 292
, cirrhosis, autosomal recessive 1A (cirhin)
, UTP4, small subunit (SSU) processome component, homolog
, testis expressed gene 292
, testis-expressed gene 292 protein