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We conclude that PAX8 immunostain is negative in most cervical cell carcinomas and is less frequently expressed in endocervical adenocarcinomas as compared with the previously reported high sensitivity for ovarian and endometrial adenocarcinomas
Study postulated that both TTF-1 (show NKX2-1 ELISA Kits) and PAX-8 when co-expressed and have anti-proliferative and anti-tumorigenic properties up to a threshold expression level and beyond that, are able to induce pro-tumorigenic effects in thyroid carcinomas.
Direct sequencing of the PAX8 gene revealed a novel single nucleotide substitution (c.162 A>T) in exon 2 that resulted in the substitution of the normal serine 54 with a cysteine (S54C), which segregated with elevated serum TSH levels.
This is the first report of PAX8 aberrant transcript production in cervical cancer. Reported PAX8 isoforms possess differential transactivation properties; therefore, besides being a helpful marker for detection of cancer, PAX8 isoforms can plausibly exert differential regulation properties during carcinogenesis
PAX2 (show PAX2 ELISA Kits), PAX8, CDX2 (show CDX2 ELISA Kits) immunostains was preformed to the TMA slides.
Pax8 gene Rearrangement is associated with Breast Cancer.
PAX8 was negative in all cases of pulmonary neuroendocrine carcinoma (PNEC) while positive in 86.4% of thymic cases (TNEC). TTF-1 (show NKX2-1 ELISA Kits) positivity was associated with high sensitivity but low specificity for PNEC, and adding PAX8 negativity significantly increased the specificity. PAX8 positivity alone showed essentially 100% specificity and 86.4% sensitivity for TNEC.
Study suggested that PAX8 eQTLs SNPs (rs4848320 and rs1110839) located in lncRNA PAX8-AS1 might predict decreased risk of cervical cancer.
High Levels of mRNA of both PAX8 are associated with benign than in malignant thyroid lesions.
results indicate that presence of PAX8 immunoreactivity in an undifferentiated brain tumor lacking gliofibrillary acidic protein expression should prompt consideration of a metastatic tumor
Pax8 is required for cell proliferation of pronephric precursors and regulates the expression of hnf1b (show HNF1B ELISA Kits) and wnt (show WNT2 ELISA Kits) pathway genes in the kidney field.
nephrogenic transcription factors (osr1 (show OSR1 ELISA Kits), osr2, hnf1b (show HNF1B ELISA Kits), lhx1 (show LHX1 ELISA Kits), pax8)play important role in nephrogenesis but have no pronephros induction potential upon overexpression; they activate transcription cascades reflecting activation by activin A (show INHBA ELISA Kits), retinoic acid
These results suggest that Pax8 maybe the downstream molecule of ALK3 (show BMPR1A ELISA Kits), it mediates the murine heart development via cellular senescence, which may serve as a mechanism that compensates for the cell loss via apoptosis in heart development.
Mice lacking microRNAs in Pax8-expressing cells develop hypothyroidism and end-stage renal failure
PAX8 protein expression was associated with germinal layers in human and murine forebrain and hindbrain development.
Pax8 is essential for function and survival of adult thyroid cells.
a core regulatory subcircuit composed of Pax2 (show PAX2 ELISA Kits)/8, Gata3 (show GATA3 ELISA Kits) and Lim1 (show LHX1 ELISA Kits) turns on a deeper layer of transcriptional regulators while activating effector genes responsible for cell signaling and tissue organization.
The Pax8 promoter appears to be autoregulated, a feature that might be responsible for the haploinsufficiency displayed by this gene.
Inducible, Pax8-rtTA-based deletion of VHL (show VHL ELISA Kits) leads to organ-specific expression of epithelial HIF and erythropoietin (show EPO ELISA Kits) in liver and kidney without causing pathological changes.
study concludes that Cadherin-16 is a novel downstream target of the transcription factor Pax8, likely since the early steps of thyroid development, and that its expression is associated with the fully differentiated state of the thyroid cell
a thyroid-specific regulatory element in the 5' upstream region of the Pax8 gene
these data identify Pax2 (show PAX2 ELISA Kits) and Pax8 as critical regulators that specify the nephric lineage.
Pax2a and Pax8 regulate cell differentiation during sensory placode formation
pax8 works with related genes pax2a/pax2b to downregulate otic expression of foxi1 (show FOXI1 ELISA Kits), a necessary step for further otic development
evolutionary links between jaw and ear formation can be traced to Fgf-Foxi1 (show FOXI1 ELISA Kits)-Pax8 pathways
Pax2a and Pax8 are the main effectors downstream of Fgf signals in ear formation
pax8 is initially required for normal otic induction, and subsequently pax8, pax2a and pax2b act redundantly to maintain otic fate
This gene encodes a member of the paired box (PAX) family of transcription factors. Members of this gene family typically encode proteins that contain a paired box domain, an octapeptide, and a paired-type homeodomain. This nuclear protein is involved in thyroid follicular cell development and expression of thyroid-specific genes. Mutations in this gene have been associated with thyroid dysgenesis, thyroid follicular carcinomas and atypical follicular thyroid adenomas. Alternatively spliced transcript variants encoding different isoforms have been described.
paired box 8
, paired box gene 8
, paired box protein Pax-8
, paired domain gene 8
, Pax-8 protein
, Pax-8 DNA-binding transcription factor