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anti-Human BMPR2 Antikörper:
anti-Mouse (Murine) BMPR2 Antikörper:
anti-Rat (Rattus) BMPR2 Antikörper:
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Human Polyclonal BMPR2 Primary Antibody für FACS, IHC (p) - ABIN388741
Pouliot, Blais, Labrie: Overexpression of a dominant negative type II bone morphogenetic protein receptor inhibits the growth of human breast cancer cells. in Cancer research 2003
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Human Polyclonal BMPR2 Primary Antibody für FACS, IHC - ABIN4899942
Huse, Bakkebø, Oksvold, Forfang, Hilden, Stokke, Smeland, Myklebust: Bone morphogenetic proteins inhibit CD40L/IL-21-induced Ig production in human B cells: differential effects of BMP-6 and BMP-7. in European journal of immunology 2011
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Human Monoclonal BMPR2 Primary Antibody für IF, WB - ABIN968806
, Lane, Machado, Pauciulo, Thomson, Phillips, Loyd, Nichols, Trembath: Heterozygous germline mutations in BMPR2, encoding a TGF-beta receptor, cause familial primary pulmonary hypertension. in Nature genetics 2000
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Human Polyclonal BMPR2 Primary Antibody für CyTOF, FACS - ABIN4899943
He, Dong, Wang, Xu, Dai, Ma, Zhu: Bone morphogenetic protein receptor IB as a marker for enrichment of osteogenic precursor-like cells in human dermis. in Archives of dermatological research 2011
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Human Monoclonal BMPR2 Primary Antibody für ICC, IHC - ABIN968988
Rosenzweig, Morse, Knowles, Chada, Khan, Roberts, McElroy, Juskiw, Mallory, Rich, Diamond, Barst: Clinical implications of determining BMPR2 mutation status in a large cohort of children and adults with pulmonary arterial hypertension. in The Journal of heart and lung transplantation : the official publication of the International Society for Heart Transplantation 2008
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Human Monoclonal BMPR2 Primary Antibody für IHC, ELISA - ABIN965686
Phillips, Poling, Phillips, Stanton, Austin, Cogan, Wheeler, Yu, Newman, Dietz, Loyd: Synergistic heterozygosity for TGFbeta1 SNPs and BMPR2 mutations modulates the age at diagnosis and penetrance of familial pulmonary arterial hypertension. in Genetics in medicine : official journal of the American College of Medical Genetics 2008
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bmpr2b mediates BMP signaling and is required to establish left-right asymmetry.
Studying the methylation pattern of the BMPR2 promoter region in pulmonary arterial hypertension patients and controls revealed a a CpG island, suitable for methylation, in the BMPR2 promoter region, in addition to NIT-2, sex-determining region Y, and heat shock factor transcription factor binding sites.No evidence of methylation was detected in this region in patients and controls.
Mutations in the bone morphogenetic protein receptor type-2 gene (BMPR2) have been identified in patients with pulmonary arterial hypertension.
Affected mutation carriers with heritable pulmonary hypertension have hypermethylation of the BMPR2 promotor compared with their unaffected relatives.
increased BMPR2 signal transduction is linked to fragile X (zeige FMR1 Antikörper) syndrome (FXS) and that the BMPR2-LIMK1 (zeige LIMK1 Antikörper) pathway is a putative therapeutic target in patients with FXS and possibly other forms of autism
A burden of rare variants in BMPR2 significantly contributed to the risk of pulmonary arterial hypertension. In the remaining one family, the patient carried a pathogenic variant in a member of potassium channels, KCNK3 (zeige KCNK3 Antikörper), which was the first replicative finding of channelopathy in an Asian population.
The SMYD2 may promote BMP signaling by directly methylating BMPR2, which, in turn, stimulates BMPR2 kinase activity and activation of the BMP pathway.
This review focuses on recent advances in rescuing BMPRII expression, function or signaling to prevent and reverse pulmonary vascular remodeling in pulmonary arterial hypertension and its feasibility for clinical translation. Furthermore, it summarizes the role of described miRNAs that directly target the BMPR2 gene in blood vessels. [review]
Endothelial BMPR2 signaling in pulmonary arterial hypertension is impaired by deletion of Vegfr3 (zeige FLT4 Antikörper).
Disrupting BMPR2 impairs TGFbeta1 (zeige TGFB1 Antikörper)- and BMP4 (zeige BMP4 Antikörper)-mediated elastic fiber assembly and is of pathophysiologic significance in pulmonary arterial hypertension.
Cav-1 (zeige CAV1 Antikörper) depletion, oxidative stress-mediated reduction in BMPRII expression, and enhanced TGF-beta (zeige TGFB1 Antikörper)-driven SMAD-2 (zeige SMAD2 Antikörper)/3 signaling promote pulmonary vascular remodeling in inflamed lungs.
Dual luciferase report assay verified that miR (zeige MLXIP Antikörper)-3065-5p could bind to the 3'UTR (zeige UTS2R Antikörper) of bone morphogenetic protein receptor type II (BMPR2), which dramatically increased in the beginning of odontoblastic differentiation but decreased in the terminal differentiation stage.
These results suggested that endogenous PTH enhanced BMPR2 expression by a cAMP/PKA/CREB pathway in osteoblasts, and increased RUNX2 expression through transduction of the BMP/pSMAD1/5/8 signaling pathway
BMPR2 gene transfer reduced TGF-beta (zeige TGFB1 Antikörper) effects on Smad2 (zeige SMAD2 Antikörper), Smad1 (zeige SMAD1 Antikörper)/5/8 and Erk1/2 (zeige MAPK1/3 Antikörper) phosphorylation in human pulmonary arterial smooth muscle cells
Deleting Bmpr2 in mouse skeletal progenitor cells impaired activin (zeige Actbeta Antikörper) signaling resulting in an increased bone formation rate and high bone mass.
The findings suggest that the mutant ALK2 (zeige ACRV1 Antikörper) related to Fibrodysplasia ossificans progressiva is enhanced by bone morphogenetic protein type II receptors via the T203-regulated phosphorylation of ALK2 (zeige ACRV1 Antikörper).
BMPR2 has tumor suppressive functions in the stroma by regulating inflammation.
Serotonin can increase ERalpha (zeige ESR1 Antikörper) expression in human pulmonary arterial smooth muscle cells and antagonism of oestrogen receptor alpha reverses serotonin-dependent PH in the mouse and increases bone morphogenetic protein receptor type 2 expression
Report temporal regulation of BMPR2 mRNA expression in the oocyte, granulosa and theca cells of developing preovulatory follicles in the pig.
Losartan therapy was associated with persistent overexpressions of ANG II (zeige AGT Antikörper), AT2 (zeige AGTR2 Antikörper), ET-1 (zeige EDN1 Antikörper), ETB (zeige EDNRB Antikörper), and angiopoietin-1 (zeige ANGPT1 Antikörper) and with a return to normal of the BMPR-2 expression.
the miR-17-92 cluster is involved in granulosa cell proliferation and differentiation by coordinately targeting the PTEN (zeige PTEN Antikörper) and BMPR2 genes.
Stimulation of BMPRII promotes normal pulmonary artery endothelial cell function by activating eNOS (zeige NOS3 Antikörper).
This gene encodes a member of the bone morphogenetic protein (BMP) receptor family of transmembrane serine/threonine kinases. The ligands of this receptor are BMPs, which are members of the TGF-beta superfamily. BMPs are involved in endochondral bone formation and embryogenesis. These proteins transduce their signals through the formation of heteromeric complexes of two different types of serine (threonine) kinase receptors: type I receptors of about 50-55 kD and type II receptors of about 70-80 kD. Type II receptors bind ligands in the absence of type I receptors, but they require their respective type I receptors for signaling, whereas type I receptors require their respective type II receptors for ligand binding. Mutations in this gene have been associated with primary pulmonary hypertension, both familial and fenfluramine-associated, and with pulmonary venoocclusive disease.
bone morphogenetic protein receptor type II
, bone morphogenetic protein receptor type-2
, bone morphogenetic protein receptor type II b
, BMP type II receptor
, BMP type-2 receptor
, type II activin receptor-like kinase
, type II receptor for bone morphogenetic protein-4
, bone morphogenic protein receptor, type II (serine/threonine kinase)
, bone morphogenic protein receptor type 2