Gene interactions and pathways from curated databases and text-mining

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BMP2 — BMPR1A

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
Kano et al., Endocrinology 2005 : Furthermore, intracellular BMP signaling was markedly suppressed by dexamethasone treatment and the expression of ALK-2, ALK-3 , and BMPRII was significantly inhibited by dexamethasone
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
Huang et al., Proc Natl Acad Sci U S A 2009 : Overexpression of constitutively active BMP receptor ( CA ) -BMPr1A or CA-BMPr1B induces commitment in the absence of BMP2/4, whereas overexpression of a dominant negative receptor dominant-negative-BMPr1A suppresses commitment induced by BMP