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BMP1 encodes a protein that is capable of inducing formation of cartilage in vivo. Additionally we are shipping BMP1 Antibodies (64) and BMP1 Proteins (12) and many more products for this protein.
Showing 10 out of 46 products:
Studies indicate crosstalk between Notch receptor and Wnt protein, Hedgehog protein, hypoxia and transforming growth factor beta (TGFbeta)/bone morphogenetic protein (BMP) pathways.
study thus highlights the severe and progressive nature of BMP1-associated OI in adults and broadens insights into the functional consequences of BMP1/mTLD-deficiency on ECM (show MMRN1 ELISA Kits) organization.
Data indicate that BMP-1 can simultaneously trigger matrix assembly and boost the synthesis of matrix proteins via a direct effect on growth factors in the contexts of development, growth and tissue repair. [review]
Two novel variants in the BMP1 gene: c.808A>G and c.1297G>T care associated with osteogenesis imperfecta (show COL1A2 ELISA Kits).
Frequent bone fracture in children is cause by BMP1-1 deficiency.
mutations of the DSP-PP P4 to P4' cleavage site can block, impair or accelerate dentin sialoprotein phosphophoryn cleavage, and suggest that its Bone morphogenic protein 1 cleavage site is conserved in order to regulate its cleavage efficiency
High BMP1 expression is associated with type-1 diabetes.
Loss of bone morphogenetic protein is associated with prostate cancer.
miR (show MLXIP ELISA Kits)-194 suppresses metastasis of non-small cell lung cancer through regulating expression of BMP1 and p27kip1 (show CDKN1B ELISA Kits)
Sequence analysis of BMP1 genes did not reveal any putative mutations for hyperostosis cranialis interna to chromosome 8p21
The presented data demonstrate Bmp1/Tll1 (show TLL1 ELISA Kits) products to be of profound importance to bone growth and modeling.
Bone morphogenetic protein-1 processes insulin-like growth factor-binding protein 3 (show IGFBP3 ELISA Kits).
during endochondral ossification, BMP and TGFbeta (show TGFB1 ELISA Kits) signaling can have antagonistic effects on chondrocyte proliferation and differentiation in vivo
BMP-1 protein was expressed in type I and IIa but not in IIb muscle fibers. BMP-1 mRNA levels were unaffected by either food deprivation or hindlimb suspension.
periostin (show POSTN ELISA Kits) supported BMP-1-mediated proteolytic activation of LOX (show LOX ELISA Kits) on the extracellular matrix, which promoted collagen cross-linking.
products of Bmp1 and Tll1 (show TLL1 ELISA Kits) are responsible for in vivo cleavage of Chordin (show CHRD ELISA Kits) in mammals
processing of the prodomain of OGN (show OGN ELISA Kits) by BMP-1 potentiates the ability of OGN (show OGN ELISA Kits) to modulate the formation of collagen fibrils
BMP1 cleaves LTBP1 (show LTBP1 ELISA Kits) at two specific sites, liberating the large latent complex from the extracellular matrix and resulting in consequent activation of TGFbeta1 (show TGFB1 ELISA Kits) via cleavage of its prodomain, latency-associated peptide (show TGFB1 ELISA Kits), by non-BMP1-like proteinases.
BMP signaling promotes the generation of astrocytes and mature, myelinating oligodendrocytes in vivo but does not affect oligodendrocyte precursor development, thus suggesting tight regulation of BMP signaling to ensure proper gliogenesis
Bmp1 processes prl (show PRL ELISA Kits) to a 17-kDa anti-angiogenic factor (show VEGFA ELISA Kits).
Sizzled is unique among secreted frizzled-related proteins for its ability to specifically inhibit bone morphogenetic protein-1 (BMP-1)/tolloid-like (show TLL1 ELISA Kits) proteinases
Crescent (show SFRP5 ELISA Kits) is a new component of the dorsal-ventral patterning pathway, which functions as the dorsal counterpart of Sizzled, through the regulation of chordinases of the Tolloid family.
This gene encodes a protein that is capable of inducing formation of cartilage in vivo. Although other bone morphogenetic proteins are members of the TGF-beta superfamily, this gene encodes a protein that is not closely related to other known growth factors. This gene is expressed as alternatively spliced variants that share an N-terminal protease domain but differ in their C-terminal region.
bone morphogenetic protein 1
, Bone morphogenetic protein 1
, bone morphogenetic protein 1-like
, mammalian tolloid protein
, procollagen C-endopeptidase
, procollagen C-proteinase
, bone morphogenetic protein 1a