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BMP inhibition is sufficient for neural induction in vivo, and that in the absence of ventral BMPs, Spemann organizer signals are not required for brain formation.
Bmp7 gradients steer nerve growth cones by a balancing act of limk1 (zeige LIMK1 Proteine) and SSH on AD/cofilin (zeige CFL1 Proteine).
Bmp antagonists and morpholinos designed against Bmp4, Bmp2, and Bmp7 demonstrate that Bmp signaling is critical for ventral, but not dorsoanterior endoderm formation
these data support a model in which Tfap2a (zeige TFAP2A Proteine), acting through Bmp7a, modulates Fgf and Notch (zeige NOTCH1 Proteine) signaling to control the duration, amount and speed of SAG (zeige SAG Proteine) neural development.
Cloning and expression of a second zebrafish bmp7 homolog, bmp7b.
maternally supplied Smad5 (zeige SMAD5 Proteine) is already required to mediate ventral specification prior to zygotic Bmp2 (zeige BMP4 Proteine)/7 signaling to establish the initial dorsoventral asymmetry
Overexpression of truncated ALK5 (zeige TGFBR1 Proteine) in a B-cell line counteracted BMP-7-induced apoptosis, whereas overexpression of truncated ALK4 (zeige ACVR1B Proteine) had no effect.
study suggests that the common genetic polymorphisms of BMP7 gene are not major contributors to variations in Bone Mineral Density or osteoporotic fracture in postmenopausal Chinese women.
Patients with hereditary pulmonary arterial hypertension had significantly higher BMP7 concentrations than patients with idiopathic pulmonary arterial hypertension and control subjects.
Expression of bone morphogenetic protein 7 ligand was significantly increased in patients with abnormal uterine bleeding. Study demonstrates that bone morphogenetic protein 7 is a promising target for future investigation and pharmacologic treatment of abnormal uterine bleeding.
BMP-7 directly upregulates adhesion and migration of human monocytic cells via activation of beta 2 integrins, Akt (zeige AKT1 Proteine), and FAK (zeige PTK2 Proteine).
results showed that stimulation by BMP-7 leads to an increased osteogenic potential of Mesenchymal stem cells.
The disequilibrium between BMP-7 and TGF-beta (zeige TGFB1 Proteine) signals plays a relevant role in the LV remodelling response to haemodynamic stress in aortic stenosis patients with left ventricular hypertrophy/dysfunction.
BMP7 may partly mediate the antiproliferative effect of oridonin by activating p38 MAPK (zeige MAPK14 Proteine) in colon cancer cells.
Data show that interaction of fibrillin-1 (zeige FBN1 Proteine) with the bone morphogenetic protein 7 (BMP-7) complex results in a conformational change.
the role of BMP-7 and its downstream signals in the neuroprotective effects of oxygen-glucose deprivation preconditioning
BMP-7 therefore is an attractive candidate for tackling a multifaceted disease such as diabetes, since it not only reduces body fat, but also strengthens insulin (zeige INS Proteine) signaling, causing improved glucose uptake and ameliorating peripheral insulin (zeige INS Proteine) resistance.
Our studies indicate that BMP7 is an important factor during the process of implantation that contributes to healthy embryonic development.
Western blot analysis demonstrated that following BMP2 (zeige BMP2 Proteine) and BMP7 cotransfection of MC3T3E1 cells, the protein expression levels of BMP2 (zeige BMP2 Proteine), BMP4 (zeige BMP4 Proteine), BMP6 (zeige BMP6 Proteine), BMP7, BMP9 (zeige GDF2 Proteine) and Wnt3a (zeige WNT3A Proteine) were increased compared with control cells
The disequilibrium between BMP-7 and TGF-beta (zeige TGFB1 Proteine) signals plays a relevant role in the LV remodelling response to haemodynamic stress in mice subjected to transverse aortic constriction leading to left ventricular hypertrophy/dysfunction.
the in vivo inter-relationships between Bmp7 and Usag-1 (zeige SOSTDC1 Proteine), was examined.
only BMP7, not BMP2 (zeige BMP2 Proteine) or BMP4 (zeige BMP4 Proteine), is necessary for interdigital programmed cell death
odontoblast beta-catenin signaling may act through regulation of BMP signaling to maintain the integrity of HERS cells
BMP7 and FGF9 coordinately regulate AP-1 (zeige JUN Proteine) transcription to promote G1-S cell cycle progression and nephron progenitor cells proliferation.
Gdf-5 (zeige GDF5 Proteine) induced the expression of the alpha5 sub-unit, while Bmp-7 induced the expression of the alphaV sub-unit.
MiR (zeige MLXIP Proteine)-22 promotes the development of liver cirrhosis through BMP7 suppression.
Study detected a 5-bp insertion-deletion at 602 bp upstream from the transcription start site of the BMP7 gene promoter among 258 pigs of 3 breeds; based on correlation analysis, the 5-bp indel site does not significantly affect porcine reproductive traits.
These results suggest that g.35161T>C is a potential candidate gene locus for litter size traits and the BMP7 gene might be associated with the quantitative trait locus controlling the litter size.
the combined treatment with TGF-beta1 (zeige TGFB1 Proteine) and BMP-7 or treatment first with TGF-beta1 (zeige TGFB1 Proteine) followed by BMP-7 was more effective than other treatment groups in both chondrogenic differentiation and SZP (zeige PRG4 Proteine) secretion.
Some single nucleotide polymorphisms and haplotypes in BMP7 are associated with cattle growth traits.
Data report that BMP-7 suppresses granulosa cell apoptosis by inhibiting the release of caspase-activated DNase (CAD (zeige DFFB Proteine)) via a mechanism which does not appear to be associated with the mitochondrial pathway, whereas BMP-4 (zeige BMP4 Proteine) inhibits the release of CAD.
BMP7 enhances the effect of BMSCs on extracellular matrix remodeling in a rabbit model of intervertebral disc degeneration.
Data show that BMP-2 (zeige BMP2 Proteine), BMP-4 (zeige BMP4 Proteine), and BMP-7, noggin (zeige NOG Proteine), and chordin (zeige CHRD Proteine) were colocalized in rimming osteoblasts, osteoclasts, and chondrocytes.
The bone morphogenetic proteins (BMPs) are a family of secreted signaling molecules that can induce ectopic bone growth. Many BMPs are part of the transforming growth factor-beta (TGFB) superfamily. BMPs were originally identified by an ability of demineralized bone extract to induce endochondral osteogenesis in vivo in an extraskeletal site. Based on its expression early in embryogenesis, the BMP encoded by this gene has a proposed role in early development and possible bone inductive activity.
bone morphogenetic protein 7 (osteogenic protein 1)
, bone morphogenetic protein 7
, osteogenic protein 1
, bone moorphogenic protein-7