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HOXB13 encodes a transcription factor that belongs to the homeobox gene family. Additionally we are shipping HOXB13 Proteins (5) and many more products for this protein.
Showing 10 out of 70 products:
Guinea Pig Polyclonal HOXB13 Primary Antibody for WB - ABIN2779853
Kondrashov, Pusic, Stumpf, Shimizu, Hsieh, Xue, Ishijima, Shiroishi, Barna: Ribosome-mediated specificity in Hox mRNA translation and vertebrate tissue patterning. in Cell 2011
Human Polyclonal HOXB13 Primary Antibody for WB - ABIN374750
Zhao, Yamashita, Ishikawa: Regulation of tumor invasion by HOXB13 gene overexpressed in human endometrial cancer. in Oncology reports 2005
Guinea Pig Polyclonal HOXB13 Primary Antibody for WB - ABIN2779854
Albrecht, Kornak, Böddrich, Süring, Robinson, Stiege, Lurz, Stricker, Wanker, Mundlos: A molecular pathogenesis for transcription factor associated poly-alanine tract expansions. in Human molecular genetics 2004
Cdx (show CDX1 Antibodies) and Wnt (show WNT2 Antibodies) mutations and premature Hox13 (show HOXA5 Antibodies) expression also cause similar neural dysmorphology
Hoxb13 has a negative effect on skin wound repair
Data demonstrate that FOXA1 (show FOXA1 Antibodies) directly regulates HOXB13 in human prostate epithelial cells, and show that this prostate-specific (show KLK3 Antibodies) regulatory mechanism is conserved in mice.
results suggest a specific role for Hoxb13 in a differentiation pathway that gives the ventral prostate epithelium a unique identity, as well as a more general role in ventral prostate morphogenesis that is redundant with other Hox13 (show HOXA5 Antibodies) paralogs
Hoxb13 knockout mice exhibit enhanced cutaneous wound healing.
Epidermal HOXB13 signal was detected over the entire body surface, but surprisingly, essentially all of the signal was cytoplasmic in developing skin
An increase of the Ala repeat above a certain length (22 Ala)in the Hoxd13 (show HOXD13 Antibodies) sequence, resulting in synpolydactyly, is associated with a shift in the localization of Hox13 (show HOXA5 Antibodies) from nuclear to cytoplasmic and aggregation.
Hoxb13 cis (show CISH Antibodies)-regulatory elements provide a powerful tool to achieve androgen-independent transgene expression in the prostate and distal colon-specific expression in the gastrointestinal tract
This is the first study to investigate the HOXB13 G84E mutation in Danish men. The mutation was detected in 0.49% of controls and in 2.51% of cases, and was associated with 5.12-fold increased relative risk of being diagnosed with prostate cancer. In our RP cohort, HOXB13 mutation carriers were more likely to develop aggressive prostate cancer.
HOXB13 is a useful marker for prostate origin when doubt exists regarding the site of the primary of a metastatic lesion
Tumor-associated macrophage-secreted CXCL8 (show IL8 Antibodies) downregulated the ERalpha (show ESR1 Antibodies) expression of endometrial cancer cells via HOXB13, which may be associated with cancer invasion, metastasis and poor prognosis.
Study provides insights suggesting that HOXB13 plays an important role in prostate tumorigenesis and malignant progression via the regulation of both p21 (show CDKN1A Antibodies) and JNK (show MAPK8 Antibodies) signaling.
The Breast Cancer Index (BCI) is a continuous risk index model of two previously described biomarkers: molecular grade index (MGI) and HOXB13:IL17BR (H:I) ratio
Studies indicate that the germline homeo box B13 protein (HOXB13) p.Gly84Glu mutation is significantly increased the risk of cancers.
review the functions attributed to HOXB13, by highlighting the most recent findings supporting the hypothesis that HOXB13 might serve as a novel biomarker for the prognosis of prostate cancer
Recent studies have shown that HOXB13 is a strong candidate for familial Prostate cancer gene.
The strongest predictors are the BRCA2 (show BRCA2 Antibodies) mutations, and the highly penetrant G84E mutation in HOXB13
We showed for the first time that HOXB13 is a sensitive and specific marker for detection of prostatic origin in distant metastases.
This gene encodes a transcription factor that belongs to the homeobox gene family. Genes of this family are highly conserved among vertebrates and essential for vertebrate embryonic development. This gene has been implicated to play a role in fetal skin development and cutaneous regeneration. In mice, a similar gene was shown to exhibit temporal and spatial colinearity in the main body axis of the embryo, but was not expressed in the secondary axes, which suggests functions in body patterning along the axis. This gene and other HOXB genes form a gene cluster at chromosome the 17q21-22 region.
, homeo box B13
, homeobox protein Hox-B13