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Cycling hypoxia could induce significant changes in CLDN1 (zeige CLDN1 Antikörper) and CLDN7 expression in nasopharyngeal cancer cells, indirectly regulation P18 (zeige CDKN2C Antikörper) expression and affecting cell invasion/proliferation.
These results identify EpCAM (zeige EPCAM Antikörper) as a substrate of matriptase (zeige ST14 Antikörper) and link HAI-2 (zeige SPINT2 Antikörper), matriptase (zeige ST14 Antikörper), EpCAM (zeige EPCAM Antikörper), and claudin-7 in a functionally important pathway that causes disease when it is dysregulated.
84/118, 64/118, 52/118 reaction with claudin-1, claudin-3 (zeige CLDN3 Antikörper) and claudin-4 (zeige CLDN4 Antikörper) in cancer and colon polyps had a membrane localization, respectively.Mislocalization claudin-3 (zeige CLDN3 Antikörper) to nucleus in colon cancer and mislocalization claudin-4 (zeige CLDN4 Antikörper) to nucleus in adenomas of the colon were detected for the first time.
suggest that the reduction of CLDN5 (zeige CLDN5 Antikörper), 7, and 18 expression loses the suppressive ability of interaction between PDK1 (zeige PDK1 Antikörper) and Akt (zeige AKT1 Antikörper) and causes sustained phosphorylation of Akt (zeige AKT1 Antikörper), resulting in the disordered proliferation in lung squamous carcinoma cells
These results suggested that increase of Cldn4 (zeige CLDN4 Antikörper)-expression may be involved in early molecular events during carcinogenesis of adenocarcinoma, whereas increase of Cldn7-expression may be associated with tumor invasion or progression.
that the dysregulated expression of these miRNAs, in conjunction with the high claudin 1 levels, could serve as a useful biomarker that identifies a subset of tumors within the poorly characterized basal-like subtype of breast cancer
localization of Cldn3 (zeige CLDN3 Antikörper), Cldn7 and Cldn10 (zeige CLDN10 Antikörper) proteins in the different compartments of murine endometrium up to day 8.5 of pregnancy (dpc) as well as in human endometrium and first trimester decidua
The expression of claudin-7 has no obviously difference between cervical carcinoma tissues and adjacent non-neoplastic tissues.
We identified hepatocyte nuclear factor 4alpha as a regulatory factor that bound endogenous CLDN7 promoter in differentiating intestinal epithelial cells and stimulated CLDN7 promoter activity.
claudin 1 and claudin 4 (zeige CLDN4 Antikörper) are differentially involved in atopic dermatitis pathogenesis
Intestinal Cldn7 deletion initiated inflammation and hyperplasia in mice.
Data show that claudin-4 (zeige CLDN4 Antikörper) and claudin-7 were observed in hepatocytes of severely damaged mouse and human livers.
The intestine-specific Cldn7 deficiency caused colonic inflammation, even though TJ structures were still present due to other claudins.
Salmonella targets the tight junction protein (zeige OCLN Antikörper) claudin-2 (zeige CLDN2 Antikörper) to facilitate bacterial invasion.
In mice, claudin-7 has non-TJ functions, including maintenance of epithelial cell-matrix interactions and intestinal homeostasis.
TSLP (zeige TSLP Antikörper) induces expression of tight junction protein (zeige OCLN Antikörper) claudin-7 in dendritic cells via NF-kappaB (zeige NFKB1 Antikörper) as well as via TLRs and may control tight junctions of DCs to preserve the epithelial barrier during allergic inflammation
Claudin-7 is essential for NaCl homeostasis in distal nephrons, and the paracellular ion transport pathway plays indispensable roles in keeping ionic balance in kidneys.
claudin-7 was found in the same nephron segments as claudin-8 (zeige CLDN8 Antikörper), but it was expressed primarily at the basolateral membrane
Tumor necrosis factor-alpha (zeige TNF Antikörper) increases claudin-1 (zeige CLDN1 Antikörper), 4, and 7 expression in renal tubular cells, altering permeability and transepithelial electrical resistance.
the effect of claudin-7 overexpression in LLC-PK1 cells on paracellular transport is mediated through a concurrent decrease in the paracellular conductance to Cl(-) and an increase in the paracellular conductance to Na(+).
These findings indicate that claudin-4 (zeige CLDN4 Antikörper) and -7 may play a role in the gingiva junctional epithelium even in the absence of tight junctions.
This gene encodes a member of the claudin family. Claudins are integral membrane proteins and components of tight junction strands. Tight junction strands serve as a physical barrier to prevent solutes and water from passing freely through the paracellular space between epithelial or endothelial cell sheets, and also play critical roles in maintaining cell polarity and signal transductions. Differential expression of this gene has been observed in different types of malignancies, including breast cancer, ovarian cancer, hepatocellular carcinomas, urinary tumors, prostate cancer, lung cancer, head and neck cancers, thyroid carcinomas, etc.. Alternatively spliced transcript variants encoding different isoforms have been found.
, claudin-like protein ZF4A22
, clostridium perfringens enterotoxin receptor-like 2