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The proximity of the expression of dax1 to 5th branchial arch and numerous known tooth markers led us to hypothesize that dax1 is involved in pharyngeal tooth development in the zebrafish.
Nonsense mutation in the DAX-1 gene is associated with precocious puberty and late-onset hypogonadotropic hypogonadism.
These findings suggested that the mutation of NR0B1 in X-linked adrenal hypoplasia congenita and hypogonadotropic hypogonadism enhanced the function of DAX1 to repress SF-1 (show NR5A1 ELISA Kits) activation, while DAX1 is expected to have additional roles in the pathological mechanism.
DAX1 and SF1 (show NR5A1 ELISA Kits) expression positively correlated in pediatric adrenocortical tumors, suggesting that these transcription factors might cooperate in adrenocortical tumorigenesis.
This novel mutation (p. V385L) of DAX-1 is the first to be identified in association with secretory azoospermia, thereby highlighting the important role of DAX-1 in spermatogenesis.
DAX-1 is less specific than Ap2beta (show AP2B1 ELISA Kits), however it is a sensitive marker for translocation positive ARMS and can be helpful in their diagnosis if used in combination with Ap2beta (show AP2B1 ELISA Kits)
DAX1 mutations were associated with X-linked adrenal hypoplasia congenita and hypogonadotropic hypogonadism.
Case Report: novel mutation in the NR0B1 (DAX1) gene in a large family with two boys affected by congenital adrenal hypoplasia.
DAX-1 protein is necessary to maintain normal spermatogenesis. In humans, male fertility has been studied in few patients carrying DAX-1 mutations. Review.
results suggest a previously unknown DAX-1/beta-Catenin (show CTNNB1 ELISA Kits) molecular network controlling HCC (show FAM126A ELISA Kits) development
Two Taiwanese patients with adrenal hypoplasia congenita were detected to have novel mutations of the DAX1 (NR0B1) gene.
Sf1 (show SF1 ELISA Kits) SUMOylation and Dax1 have roles in the physiological cessation of FAdE-mediated Sf1 (show SF1 ELISA Kits) expression and the resultant regression of the postnatal fetal cortex (X-zone)
Findings indicate that the Gata6 (show GATA6 ELISA Kits) promoter is activated by Esrrb (show ESRRB ELISA Kits) in association with Ncoa3 (show NCOA3 ELISA Kits), and Dax1 inhibited activities of Esrrb (show ESRRB ELISA Kits) and Ncoa3 (show NCOA3 ELISA Kits), resulting maintenance of the undifferentiated status of embryonic stem (ES) cells.
Data indicate that nuclear receptor subfamily 0 group B member 1 (Nr0b1) interacted with androgen receptor (AR (show AR ELISA Kits)) in Sertoli cells (SCs (show TWIST1 ELISA Kits)).
Nr0b1 is a negative regulator of Zscan4c in mouse embryonic stem cells
Dax1 and Nanog have roles in stabilizing mouse embryonic stem cells and induced pluripotency
Here we review the current knowledge on properties, functions and mechanisms of DAX1 action.
Insulin (show INS ELISA Kits)-mediated induction of DAX-1 in Leydig cells of testis may be a key regulatory step of serum sex hormone level in insulin (show INS ELISA Kits)-resistant states.
Dax1 functions as a negative regulator of Esrrb (show ESRRB ELISA Kits) and Oct3/4 (show POU5F1 ELISA Kits), and these molecules form a regulatory loop for controlling the pluripotency and self-renewal capacity of embryonic stem cells.
Transcriptional differences between mouse embryonic and epiblast stem cells is mediated through a Sox2 (show SOX2 ELISA Kits)/Esrrb (show ESRRB ELISA Kits) heterodimer regulating Nr0b1.
Excess DAX1 leads to XY ovotesticular disorder of sex development (DSD (show FADS1 ELISA Kits)) in mice by inhibiting steroidogenic factor-1 (SF1 (show NR5A1 ELISA Kits)) activation of the testis enhancer of SRY-box-9 (Sox9 (show SOX9 ELISA Kits)).
Involvement of Ad4BP/SF-1 (show NR5A1 ELISA Kits), DAX-1, and COUP-TFII (show NR2F2 ELISA Kits) transcription factor on steroid production and luteinization in ovarian theca cells.
the decrease of Dax-1 transcription factor and the increase in histone H3 (show HIST3H3 ELISA Kits) acetylation may play important roles in progesterone synthesis in luteinizing granulosa cells.
This gene encodes a protein that contains a DNA-binding domain. The encoded protein acts as a dominant-negative regulator of transcription which is mediated by the retinoic acid receptor. This protein also functions as an anti-testis gene by acting antagonistically to Sry. Mutations in this gene result in both X-linked congenital adrenal hypoplasia and hypogonadotropic hypogonadism.
, nuclear receptor subfamily 0 group B member 1
, nuclear receptor subfamily 0, group B, member 1
, orphan nuclear receptor DAX-1
, DSS-AHC critical region on the X chromosome, gene 1
, DSS-AHC critical region on the X chromosome protein 1
, nuclear hormone receptor
, nuclear receptor DAX-1
, nuclear receptor DAX1
, adrenal hyoplasia protein DAX1
, adrenal hypoplasia congenital
, adrenal hypoplasia congenita-like protein
, adrenal hypoplasia, congenital homolog