Gene interactions and pathways from curated databases and text-mining

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BMP2 — BMPR1B

Pathways - manually collected, often from reviews:

Protein-Protein interactions - manually collected from original source literature:

Studies that report less than 10 interactions are marked with *

Text-mined interactions from Literome

Murali et al., Development 2005 : These studies provide direct genetic evidence that Bmpr1a and Bmpr1b play redundant roles during retinal development, and that different threshold levels of Bmp signaling regulate distinct developmental programs such as patterning, growth and differentiation of the retina
Yoon et al., Proc Natl Acad Sci U S A 2005 (Osteochondrodysplasias) : In summary, our study demonstrates that BMPR1A and BMPR1B are functionally redundant during early chondrogenesis and that BMP signaling is required for chondrocyte proliferation, survival, and differentiation in vivo
Miyoshi et al., Biol Reprod 2006 : Since overexpression of BMPR1A and BMPR1B , but not SMADs, significantly enhanced the BMP responses, these type I receptors were revealed to be limiting factors for BMP signaling in KGN cells
Inai et al., Dev Biol 2008 : Exogenous BMP-2 or constitutively active ( ca ) BMPR-1B ( ALK6 ) -virus treatments induced migration of the mesenchymal cells into the collagen gels, whereas noggin, an antagonist of BMPs, or dominant negative ( dn ) BMPR-1 B ( ALK6 ) -virus treatments reduced cell migration from the mesenchymal cell aggregates