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NOMPB is required for the assembly of sensory cilia but not for the extension or function of the sperm flagellum.
Tg737 regulates a Wnt (show WNT2 ELISA Kits)/beta-catenin (show CTNNB1 ELISA Kits)/Snail (show SNAI1 ELISA Kits)-HNF4alpha (show HNF4A ELISA Kits) negative feedback circuit, thereby blocking EMT (show ITK ELISA Kits) and the malignant transformation of liver stem cells to liver cancer stem cells.
genetically ablated Kif3a (show KIF3A ELISA Kits), Ift88, and Ttc21b (show TTC21B ELISA Kits) in a series of specific spatiotemporal domains. The resulting phenotypes allow us to draw several conclusions. First, we conclude that the Ttc21b (show TTC21B ELISA Kits) cortical phenotype is not due to the activity of Ttc21b (show TTC21B ELISA Kits) within the brain itself
In order to evaluate the function of IFT88 in regulating craniofacial development, we generated Wnt1 (show WNT1 ELISA Kits)-Cre;Ift88fl/fl mice to eliminate Ift88 specifically in cranial neural crest (CNC) cells. Wnt1 (show WNT1 ELISA Kits)-Cre;Ift88fl/flpups died at birth due to severe craniofacial defects including bilateral cleft lip and palate and tongue agenesis, following the loss of the primary cilia in the CNC-derived palatal mesenchyme
IFT88 influences chondrocyte actin organization and biomechanics.
These data indicate that TGF-beta (show TGFB1 ELISA Kits) regulates Ift88 gene expression at least in part via posttrascriptional manner.
Results suggest that EGF (show EGF ELISA Kits) exerts mitogenic effects in the orpk cilia (-) cells via activation of growth-associated amiloride-sensitive NHEs and ERK (show EPHB2 ELISA Kits).
We propose that Ift88 and primary cilia regulate expression of Sfrp5 (show SFRP5 ELISA Kits) and Wnt (show WNT2 ELISA Kits) signaling pathways in growth plate via regulation of Ihh (show IHH ELISA Kits) signaling.
Knockout of Bbs7 combined with a hypomorphic Ift88 allele (orpk as a model for Shh (show SHH ELISA Kits) dysfuction) results in embryonic lethality with e12.5 embryos having exencephaly, pericardial edema, cleft palate and abnormal limb development.
Data show that IFT88 is present in the Golgi of spermatids, that the microtubule-associated golgin GMAP210 (show TRIP11 ELISA Kits) and IFT88 participate in acrosome, HTCA, and tail biogenesis.
Epidermal cilia function was analyzed using conditional alleles of the ciliogenic genes Ift88 and Kif3a (show KIF3A ELISA Kits).
multivariate Cox (show COX8A ELISA Kits) regression analyses demonstrated that Tg737 expression was an independent factor for predicting the overall survival of hepatocellular carcinoma patients
MiR (show MLXIP ELISA Kits)-548a-5p negatively regulates the tumor inhibitor gene Tg737 and promotes tumorigenesis in vitro and in vivo, indicating its potential as a novel therapeutic target for hepatocellular carcinoma.
subtle regulation of IFT and associated cilia structure, tunes the wnt (show WNT2 ELISA Kits) response controlling stem cell differentiation.
this work suggests that Tg737 is involved in the invasion and migration of hepatoma cells under hypoxia, with the involvement of the polycystin-1 (show PKD1 ELISA Kits), IL-8 (show IL8 ELISA Kits), and TGF-beta1 (show TGFB1 ELISA Kits) signaling pathway
A mutation in IFT88 causes a hitherto unknown human ciliopathy.
Data show that IFT88 depletion induces mitotic defects in human cultured cells, in kidney cells from the IFT88 mouse mutant Tg737(orpk) and in zebrafish embryos.
The results indicate that loss of heterozygosity of the tumor suppressor gene Tg737 may play an important role in the carcinogenetic mechanism of liver cancer stem cells.
IFT88 is a centrosomal protein regulating G1-S transition in non-ciliated cells.
This gene encodes a member of the tetratrico peptide repeat (TPR) family. Mutations of a similar gene in mouse can cause polycystic kidney disease. Two transcript variants encoding distinct isoforms have been identified for this gene.
intraflagellar transport protein 88 homolog
, intraflagellar transport 88 homolog (Chlamydomonas)
, TPR repeat protein 10
, intraflagellar transport 88 homolog
, recessive polycystic kidney disease protein Tg737
, tetratricopeptide repeat domain 10
, tetratricopeptide repeat protein 10
, transgene insert site 737, insertional mutation, polycystic kidney disease
, polaris homolog
, probe hTg737 (polycystic kidney disease, autosomal recessive)
, recessive polycystic kidney disease protein Tg737 homolog