Download The Molecular Basis of Skeletogenesis No. 232 by Gail Cardew, Jamie A. Goode, PDF
By Gail Cardew, Jamie A. Goode,
Brings jointly a cross-fertilization of rules among human molecular genetics, develeopmental biology, tissue biology and the biochemistry of mobile signalling pathways, in an effort to create new insights into the mechanisms of ordinary and irregular skeletogenesis.
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Additional info for The Molecular Basis of Skeletogenesis No. 232
Although the extracellular matrix is de-emphasized in this conference, I think it has an important role in putting molecules or constellations of molecules in the right place at the right time during morphogenesis. Bard: Whoever, for example, would have predicted that extracellular matrix molecules such as heperan sulfate could act as low affinity co-receptors for signals? Reddi: The availability of the ligand to the receptor is further modulated both by the extracellular matrix, and specific binding proteins such as Noggin and Corrin.
Nat Cell Biol 1:125—126 LIMB PATTERNING AND CHONDROGENESIS 43 Solursh M 1984 Cell and matrix interactions during limb chondrogenesis invitro. In: Trelstad RL (ed) The role of extracellular matrix in development. Alan R Liss, New York Weston AD, Rosen V, Chandraratnas RAS, Underhill TM 2000 Regulation of skeletal progenitor differentiation by the BMP and retinoid signaling pathways. J Cell Biol 148:679-690 General discussion I Meikle: All the genes that are involved in patterning the vertebrate limb are also involved in patterning the teeth.
If you just put in BMP beads without removing anything, this will not induce ectopic cartilage formation but more cell death. The system seems to be already a little biased in the sense that there are things in the interdigit region that seem to be able to respond to BMPs only as transducing a cell death signal. My other point has to do with the still unpublished work by Richard Maas on theMsx1/Msx2 double knockout. BMPs are expressed in the ectoderm and in the mesenchyme. Expression in the ectoderm may regulate expression in the mesenchyme.