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CIRH1A encodes a WD40-repeat-containing protein that is localized to the nucleolus. Additionally we are shipping CIRH1A Antibodies (30) and CIRH1A Proteins (5) and many more products for this protein.
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 ELISA Kits)
A missense mutation (R565W) in cirhin (FLJ14728) in North American Indian childhood cirrhosis
Cirhin is a nucleolar protein (show MCRS1 ELISA Kits) 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 ELISA Kits) sequence and could be a participant in the regulation of other genes with NF-kappaB (show NFKB1 ELISA Kits) 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