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Osr1/Osr2 normally repress bmp4 (zeige BMP4 Proteine) expression in the lateral plate mesoderm prior to respiratory specification.
nephrogenic transcription factors (osr1, osr2, hnf1b (zeige HNF1B Proteine), lhx1 (zeige LHX1 Proteine), pax8 (zeige PAX8 Proteine))play important role in nephrogenesis but have no pronephros induction potential upon overexpression; they activate transcription cascades reflecting activation by activin A (zeige INHBA Proteine), retinoic acid
Odd-skipped related 1 (OSR1) downregulated the activity of the Wnt (zeige WNT2 Proteine) signaling pathway by suppressing the expression of sex-determining region Y (zeige SRY Proteine)-box 9 (SOX9 (zeige SOX9 Proteine)) and beta-catenin (zeige CTNNB1 Proteine).
OSR1 (zeige OXSR1 Proteine) was downregulated in RCC (zeige XRCC1 Proteine) cells by promoter methylation. OSR1 (zeige OXSR1 Proteine) can function as a tumor suppressor via inhibition of invasion and proliferation in RCC (zeige XRCC1 Proteine) cells, possibly via upregulating tumor suppressor genes and downregulating oncogenes.
OSR1 (zeige OXSR1 Proteine) was sequenced in 186 children with primary vesicoureteric reflux, and 17 have single nucleotide polymorphisms
In summary, our study implicated a gene network involving Tbx5 (zeige TBX5 Proteine), Osr1 (zeige OXSR1 Proteine) and Pcsk6 interaction in second heart field for atrial septation, providing a molecular framework for understanding the role of Tbx5 (zeige TBX5 Proteine) in congenital heart disease ontogeny.
The findings of the present study showed, for the first time, the role of the OSR1 (zeige OXSR1 Proteine) rs12329305 polymorphism in the development of congenital malformations in cases of stillborn/neonatal death.
OSR1 (zeige OXSR1 Proteine) acts as a functional tumour suppressor in gastric cancer
OSR1 is expressed in human mesenchymal stem cells, the blastemal component of Wilms tumors and CD24+/CD133+ progenitor cells isolated from the mature kidney.
first report on molecular cloning and characterization of human OSR1 (zeige OXSR1 Proteine)
Transcriptome and functional analyses reveal that Osr1(+) cells provide a critical pro-myogenic niche via the production of muscle connective tissue specific extracellular matrix components and secreted signaling factors.
Hypothalamic OSR1 expression is suppressed by enhanced postnatal (maternal) care, but elevated by inflammatory microglia.
In contrast to H2A-interacting proteins, the H2A.Z (zeige H2AFZ Proteine)-interacting proteins are involved in transcriptional regulation. We found that the transcription factor Osr1 interacts with H2A.Z (zeige H2AFZ Proteine) both in vitro and in vivo. It also mediates H2A.Z (zeige H2AFZ Proteine) incorporation to a large number of target sites and regulates gene expression
These results indicate that OSR1 and SPAK (zeige STK39 Proteine) cooperatively regulate NKCC1 (zeige SLC12A2 Proteine)-dependent spermatogenesis in a SC-restricted manner.
Osr1 is a candidate gene implicated in the pathogenesis of vesicoureteric reflux and congenital abnormalities of the kidney and urinary tract in mice
Our data reveal that together SPAK (zeige STK39 Proteine) and OSR1 play essential roles in the pathway along the distal convoluted tubules that responds to fluctuations in plasma potassium
These results indicate that Osr1 and Wt1 (zeige WT1 Proteine) act synergistically to regulate nephron endowment by controlling metanephric mesenchyme specification during early nephrogenesis.
Tbx5 (zeige TBX5 Proteine) and Osr1 interact to regulate posterior second heart field cell cycle progression for cardiac septation.
odd-skipped related 1 is involved in regulation of mammalian kidney development
ROMK1 (zeige KCNJ1 Proteine) protein abundance and activity are down-regulated by SPAK (zeige STK39 Proteine) and OSR1
hand2 (zeige HAND2 Proteine) and the co-expressed zinc-finger transcription factor osr1 have functionally antagonistic influences on kidney development. Together, our data suggest that hand2 (zeige HAND2 Proteine) functions in opposition to osr1 to balance the formation of kidney and vein progenitors by regulating cell fate decisions at the lateral boundary of the Iintermediate mesoderm
findings identify osr1 as a Nodal-induced, negative feedback regulator of Nodal signaling that acts at the earliest stages of endoderm differentiation to limit the number of endoderm progenitors.
Our results place osr1 in a framework of transcriptional regulators that control the expression of podocin and nephrin (zeige NPHS1 Proteine) and thereby mediate podocyte differentiation.
The Osr1 and Osr2 genes act in the pronephric anlage downstream of retinoic acid signaling and upstream of Wnt2b (zeige WNT2B Proteine) to maintain pectoral fin development.
osr1 reveals a novel role for endoderm in regulating kidney versus vascular cell fate.
Transcription factor that plays a role in the regulation of embryonic heart and urogenital development (By similarity).
odd-skipped related 1 (Drosophila)
, protein odd-skipped-related 1
, zinc finger transcription factor
, odd-skipped homolog
, oxidative-stress responsive 1