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PROP1 encodes a paired-like homeodomain transcription factor in the developing pituitary gland. Zusätzlich bieten wir Ihnen PROP1 Antikörper (30) und viele weitere Produktgruppen zu diesem Protein an.
Showing 9 out of 9 products:
Human PROP1 Protein expressed in HEK-293 Cells - ABIN2729760
Bando, Iguchi, Fukuoka, Yamamoto, Hidaka-Takeno, Okimura, Matsumoto, Suda, Nishizawa, Takahashi, Tojo, Takahashi: Involvement of PIT-1-reactive cytotoxic T lymphocytes in anti-PIT-1 antibody syndrome. in The Journal of clinical endocrinology and metabolism 2014
Genomic profiling reveals that PROP1 binds to genes expressed in epithelial cells like Claudin 23 (zeige CLDN23 Proteine), and to epithelial-mesenchymal transition inducer genes like Zeb2 (zeige ZEB2 Proteine), Notch2 (zeige NOTCH2 Proteine) and Gli2. Zeb2 (zeige ZEB2 Proteine) activation appears to be a key step in the epithelial-mesenchymal transition process.
SOX2 (zeige SOX2 Proteine) is a regulatory factor of Prop1 expression
Data show that human paired like homeodomain factor 1 (PROP1) can substitute functionally for mouse Prop1.
endocochlear potential and KCNJ10 (zeige KCNJ10 Proteine) immunostaining in the stria vascularis are indistinguishable from wild type, and no differences in neurofilament or synaptophysin (zeige SYP Proteine) staining are evident in Prop1(df) mutants
Data report the spatial and temporal regulation of Otx2 (zeige OTX2 Proteine) in normal mice and Prop1 mutant.
Several components of the main GH-signaling pathways exhibit enhanced sensitivity to the hormone in liver and muscle of Ames dwarf mice.
Studies suggest that TLE1 (zeige TLE1 Proteine) and TLE3 might also play roles independent of HESX1 (zeige HESX1 Proteine) by interacting with other transcription factors like PROP1.
Lhx4 (zeige LHX4 Proteine) and Prop1 have critical, but mechanistically different roles in specification and expansion of specialized anterior pituitary cells
Tcf4 (zeige TCF4 Proteine) and Aes (zeige AES Proteine) influence pituitary growth and development, and place Tcf4 (zeige TCF4 Proteine) and Tle3 in the genetic hierarchy with Prop1
PROP1 has a role in pituitary gland growth
PROP1 mutations are a prevalent cause of congenital CPHD with OPP, and therefore, PROP1 sequencing must be the first step of molecular investigation in patients with CPHD and OPP, especially in populations with a high frequency of PROP1 mutations.
Deletion in the PROP1 gene is associated with Combined pituitary hormone (zeige CGA Proteine) deficiency.
The anterior pituitary gland comprised specialized cell-types that arise from stem cells expressing SOX2 (zeige SOX2 Proteine) and PROP1, which is necessary to establish the stem cell pool and promote an epithelial to mesenchymal-like transition, releasing progenitors from the niche. [review]
GH replacement successfully corrects the growth deficit in children with Growth Hormone Deficiency . While the genetic aetiology remains undefined in most cases of Isolated Growth Hormone Deficiency , PROP1 mutations constitute a major cause for Multiple Pituitary Hormone Deficiencies. Persistence of Growth Hormone Deficiency into adulthood is related to abnormal pituitary morphology.
The present study reports on screening of POU1F1 (zeige POU1F1 Proteine), PROP1, and HESX1 (zeige HESX1 Proteine) in combined pituitary hormone (zeige CGA Proteine) deficiency patients and the novel variations identified.
A compound heterozygosity in the PROP1 gene has been identified for both probands. The first change represents a mutational hot spot (c.150delA, p.R53fsX164), whereas the second is a novel alteration (p.R112X) that leads to protein disruption. The resulting clinical phenotype was surprisingly distinct compared to most patients with genetic alterations in PROP1.
the most frequent variants in the PROP1 gene are not a consequence of variant hot spots as previously assumed, but are founder variants.
A novel heterozygous mutation in the HESX1 (zeige HESX1 Proteine) gene and a novel homozygous mutation in the PROP1 gene were detected in 2 pedigrees with combined pituitary hormone (zeige CGA Proteine) deficiency
The c.301_302delAG homozygous genotype had a high frequency of 38%, reaching 100% in group with familial cases of multiple pituitary hormone (zeige CGA Proteine) deficiency and 16% in group with sporadic forms of MPHD.
Data suggest that formation of a heterodimer between HESX1 (zeige HESX1 Proteine) and PROP1 allows HESX1 (zeige HESX1 Proteine) to become active, and that PROP1 then replaces HESX1 (zeige HESX1 Proteine) to advance to the middle stage of pituitary development.
Prop-1 participates in the regulation of FSHbeta gene
Prop-1 might be involved in development of gonadotropes and hormone production
Dimeric binding of PROP1 is able to recognize diverse palindromic TAAT sequences separated by 3 nucleotides and to exhibit its transcriptional activity.
The H173R mutation in PROP1 can be considered as a DNA marker for selecting individuals with superior growth traits, thereby contributing to research on breeding and genetics in the beef industry.
This gene encodes a paired-like homeodomain transcription factor in the developing pituitary gland. Expression occurs prior to and is required for expression of pou domain transcription factor 1, which is responsible for pituitary development and hormone expression. Mutations in this gene have been associated with combined pituitary hormone deficiency-2 as well as deficiencies in luteinizing hormone, follicle-stimulating hormone, growth hormone, prolactin, and thyroid-stimulating hormone.
, homeobox protein prophet of Pit-1
, pituitary specific homeodomain factor
, pituitary-specific homeodomain factor
, prophet of Pit-1
, PROP paired-like homeobox 1
, prophet of Pit1, paired-like homeodomain transcription factor
, paired like homeodomain factor 1
, prophet of Pit1 paired-like homeodomain transcription factor