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The bone morphogenetic protein (BMP) receptors are a family of transmembrane serine/threonine kinases that include the type I receptors BMPR1A and BMPR1B and the type II receptor BMPR2. Additionally we are shipping BMPR1A Kits (42) and BMPR1A Proteins (38) and many more products for this protein.
Showing 10 out of 182 products:
Human Polyclonal BMPR1A Primary Antibody for EIA, WB - ABIN357376
Waite, Eng: BMP2 exposure results in decreased PTEN protein degradation and increased PTEN levels. in Human molecular genetics 2003
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Human Polyclonal BMPR1A Primary Antibody for EIA, IHC (p) - ABIN357372
Zhou, Woodford-Richens, Lehtonen, Kurose, Aldred, Hampel, Launonen, Virta, Pilarski, Salovaara, Bodmer, Conrad, Dunlop, Hodgson, Iwama, Järvinen, Kellokumpu, Kim, Leggett, Markie, Mecklin, Neale et al.: Germline mutations in BMPR1A/ALK3 cause a subset of cases of juvenile polyposis syndrome and of Cowden and Bannayan-Riley-Ruvalcaba syndromes. ... in American journal of human genetics 2001
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Human Polyclonal BMPR1A Primary Antibody for EIA, WB - ABIN357377
Aström, Jin, Imamura, Röijer, Rosenzweig, Miyazono, ten Dijke, Stenman: Chromosomal localization of three human genes encoding bone morphogenetic protein receptors. in Mammalian genome : official journal of the International Mammalian Genome Society 1999
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Human Polyclonal BMPR1A Primary Antibody for IHC (p), WB - ABIN388732
Kan, Liu, McGuire, Berger, Awatramani, Dymecki, Kessler: Dysregulation of local stem/progenitor cells as a common cellular mechanism for heterotopic ossification. in Stem cells (Dayton, Ohio) 2009
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Human Polyclonal BMPR1A Primary Antibody for EIA, IHC (p) - ABIN357374
Howe, Bair, Sayed, Anderson, Mitros, Petersen, Velculescu, Traverso, Vogelstein: Germline mutations of the gene encoding bone morphogenetic protein receptor 1A in juvenile polyposis. in Nature genetics 2001
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Human Polyclonal BMPR1A Primary Antibody for EIA, IHC (p) - ABIN357375
ten Dijke, Ichijo, Franzén, Schulz, Saras, Toyoshima, Heldin, Miyazono: Activin receptor-like kinases: a novel subclass of cell-surface receptors with predicted serine/threonine kinase activity. in Oncogene 1993
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Human Polyclonal BMPR1A Primary Antibody for FACS, WB - ABIN388737
Tominaga, Abe, Ueda, Goto, Nakahara, Murakami, Matsubara, Mima, Nagai, Araoka, Kishi, Fukushima, Jishage, Doi: Activation of bone morphogenetic protein 4 signaling leads to glomerulosclerosis that mimics diabetic nephropathy. in The Journal of biological chemistry 2011
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Report temporal regulation of BMPR1a mRNA expression in the oocyte, granulosa and theca cells of developing preovulatory follicles in the pig.
These results suggest that Pax8 (show PAX8 Antibodies) maybe the downstream molecule of ALK3, it mediates the murine heart development via cellular senescence, which may serve as a mechanism that compensates for the cell loss via apoptosis in heart development.
study suggested that Bmpr-Ia and Bmpr-Ib (show BMPR1B Antibodies) signaling regulates tooth formation via miR (show MLXIP Antibodies)-135a.
integrin alpha1beta1/BMPR IA may block BMP-2 (show BMP2 Antibodies)/BMPR IA complex information and interfere with the BMP-2 (show BMP2 Antibodies) signalling pathway in cells
signaling via activin (show Actbeta Antibodies)-like kinase 3 (ALK3/BMPR1A), a BMP type 1 receptor, is necessary for blastocyst attachment.
Interactions between mechanical loading and BMP signaling through BMPR1A.
Myo (show SYNPO2 Antibodies)-endothelial progenitors with functioning Bmpr1a signalling demonstrate myogenic potential, but their main function in vivo is to inhibit intramuscular adipogenesis, both through a cell-autonomous and a cell-cell interaction mechanism.
Bmpr1a is critical for the development and growth of the mandibular condyle via its effect on proliferation of prechondroblasts and chondrocyte differentiation
BMP-Smad4 (show SMAD4 Antibodies) signaling is required for precartilaginous mesenchymal condensation independent of Sox9 (show SOX9 Antibodies) in the mouse.
An essential role of finely tuned BMPRIA mediated signaling in temporomandibular joint development.
Alk3 mediated Bmp signaling is important in the cascade of events that regulate the contribution of EPDCs to the AV sulcus, annulus fibrosus, and the parietal leaflets of the AV valve
ALK3 and ALK6 (show BMPR1B Antibodies) both contribute to the gene regulatory network that regulates dorso-ventral patterning.
Data show that USP15 (show USP15 Antibodies) enhances BMP-induced phosphorylation of SMAD1 (show SMAD1 Antibodies) by interacting with and deubiquitylating ALK3.
Data show that protein kinase (show CDK7 Antibodies) LKB1 (show STK11 Antibodies) physically interacts with BMP type I receptors and requires Smad7 (show SMAD7 Antibodies) protein to promote downregulation of the receptor.
BMPR1A(+) ASCs show an enhanced ability for adipogenesis in vitro, as shown by gene expression and histological staining.
Duplication of 10q22.3-q23.3 encompassing BMPR1A gene is associated with congenital heart disease, microcephaly, and mild intellectual disability
Authors analyzed human databases from TCGA and survival data from microarrays to confirm BMPR1a tumor promoting functions, and found that high BMPR1a gene expression correlates with decreased survival regardless of molecular breast cancer subtype.
About half of BMPR1A-related polyps displayed loss of heterozygosity, predominantly in the epithelial compartment, compatible with BMPR1A acting as a tumour suppressor gene.
Results support a novel role for miR (show MLXIP Antibodies)-885-3p in tumor angiogenesis by targeting BMPR1A, which regulates a proangiogenic factor.
Decreased expression of BMPR1A was associated malignant gallbladder lesions.
High BMPR1A expression is associated with glioma tumorigenesis.
Data show that USP15 (show USP15 Antibodies) enhances BMP-induced phosphorylation of SMAD1 (show GARS Antibodies) by interacting with and deubiquitylating ALK3.
This is the first case report to document coding exon 3 duplication in the BMPR1A gene in a patient with juvenile polyposis syndrome.
The bone morphogenetic protein (BMP) receptors are a family of transmembrane serine/threonine kinases that include the type I receptors BMPR1A and BMPR1B and the type II receptor BMPR2. These receptors are also closely related to the activin receptors, ACVR1 and ACVR2. The ligands of these receptors are members of the TGF-beta superfamily. TGF-betas and activins transduce their signals through the formation of heteromeric complexes with 2 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.
bone morphogenetic protein receptor, type IA
, bone morphogenetic protein receptor type-1A
, bone morphogenetic protein receptor type-1A-like
, BMP type-1A receptor
, BMP-2/BMP-4 receptor
, activin receptor-like kinase 3
, serine/threonine-protein kinase receptor R5
, BMP receptor
, activin A receptor, type II-like kinase 3
, bone morphogenetic protein 4 receptor
, bone morphogenetic protein receptor, type 1A
, bone morphogenetic protein receptor type IA
, bone morphogenetic protein receptor IA
, BMP receptor 1
, bone morphogenic protein receptor 1
, protein kinase