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KDM5A (zeige KDM5A Proteine)-mediated H3K4me3 modification participated in the etiology of osteoporosis and may provide new strategies to improve the clinical efficacy of BMP2 (zeige BMP2 Proteine) in osteoporotic conditions.
Kdm5a (zeige KDM5A Proteine) associates with p50 (zeige LSP1 Proteine) and binds to the Socs1 (zeige SOCS1 Proteine) promoter region in resting natural killer cells.
The present study was designed to detect the expression of Histone H3 (zeige HIST3H3 Proteine) lysine 4 methylation and its demethylases LSD1 (zeige KDM1A Proteine), RBP2 and SMCX (zeige KDM5C Proteine) in 21-, 40- and 60-day-old mouse testes.
Maintenance of gene silencing by the coordinate action of the H3K9 methyltransferase G9a/KMT1C (zeige EHMT2 Proteine) and the H3K4 demethylase (zeige MBD2 Proteine) Jarid1a/KDM5A (zeige KDM5A Proteine).
In terminally differentiated cells, common KDM5A (zeige KDM5A Proteine) and E2F4 (zeige E2F4 Proteine) gene targets were bound by the pRB (zeige PGR Proteine)-related protein p130, a DREAM complex component.
genetic ablation of Rbp2 decreases tumor formation and prolongs survival in Rb1(+/-) mice and Men1-defective mice.
Study reports that RBP2 is a demethylase (zeige MBD2 Proteine) that specifically catalyzes demethylation on histone H3 (zeige HIST3H3 Proteine) lysine 4, whose methylation is normally associated with transcriptionally active genes.
JARID1a (zeige KDM5A Proteine) formed a complex with CLOCK-BMAL1 (zeige ARNTL Proteine) which was recruited to Per2 (zeige PER2 Proteine) promoter;it increased histone acetylation by inhibiting histone deacetylase 1 (zeige HDAC1 Proteine) function and enhanced transcription by CLOCK-BMAL1 (zeige ARNTL Proteine); JARID1a (zeige KDM5A Proteine) depletion shortened period of circadian rhythms
KDM5A (zeige KDM5A Proteine) interacts physically with RBP-J (zeige RBPJ Proteine)
mutation can downregulate cardiac cell proliferation by repressing cyclin D1 (zeige CCND1 Proteine) expression in the same way as jumonji (zeige JARID2 Proteine)
Ectopic overexpression of RBP2 (zeige KDM5A Proteine) can induce cancer stem cell-like (CSC) phenotypes through epithelial to mesenchymal transition in renal cell carcinoma (zeige MOK Proteine) cells by converting them to a more mesenchymal phenotype.
miR (zeige MLXIP Proteine)-34a promotes the osteogenic differentiation of human adipose-derived stem cells via the RBP2 (zeige KDM5A Proteine)/NOTCH1 (zeige NOTCH1 Proteine)/CYCLIN D1 (zeige CCND1 Proteine) coregulatory network.
Domain-swapped dimers of RBP2 (zeige KDM5A Proteine) provides evidence for ordered folding intermediates.
promotes overexpression and activation of BCL2 (zeige BCL2 Proteine) in acute lymphoblastic leukemia development and progression
RBP2 (zeige KDM5A Proteine) could induce epithelial-mesenchymal transition in esophageal cancer cells and exert a greater effect on the expression of E-cadherin (zeige CDH1 Proteine) in lung squamous cells than in esophageal squamous cells.
RBP2 (zeige KDM5A Proteine) promotes HIF-1alpha (zeige HIF1A Proteine)-VEGF (zeige VEGFA Proteine)-induced angiogenesis of non-small cell lung cancer via the Akt (zeige AKT1 Proteine) pathway.
The structure of retinal-bound human CRBPII and the structure of retinol-bound CRBPII with retinol fully occupying the binding pocket are reported.
Data show that CRBPI (zeige RBP1 Proteine) and CRBPII bind 9-cis-retinol and 9-cis-retinal with high affinities, albeit with affinities somewhat lower than for all-trans-retinol and all-trans-retinal.
retinoic acid responsiveness of the human CRBP II promoter is mediated by an indirect mechanism and that this mechanism is associated with enterocyte differentiation.
We report here the X-ray structures of human apo (zeige C9orf3 Proteine) and holo CRBP II solved at 1.2 A resolution and compare the two structures between them and with the structures of zebrafish and rat CRBP II.
RBP2 is an abundant protein present in the small intestinal epithelium. It is thought to participate in the uptake and/or intracellular metabolism of vitamin A. Vitamin A is a fat-soluble vitamin necessary for growth, reproduction, differentiation of epithelial tissues, and vision. RBP2 may also modulate the supply of retinoic acid to the nuclei of endometrial cells during the menstrual cycle.
retinol-binding protein 2
, retinol binding protein 2, cellular
, histone demethylase JARID1A
, jumonji, AT rich interactive domain 1A (Rbp2 like)
, jumonji/ARID domain-containing protein 1A
, lysine-specific demethylase 5A
, retinoblastoma binding protein 2
, retinoblastoma-binding protein 2
, cellular retinol-binding protein II
, retinol-binding protein 2, cellular
, Retinol-binding protein 2 cellular
, Retinol-binding protein 2, cellular