P. O'Brien | Semantic Scholar

Haplotyping suggests that the mutation in all five breeds of lean, heavily muscled swine has a common origin, and the development of a noninvasive diagnostic test will provide the basis for elimination of the MH gene or its controlled inclusion in swine breeding programs.

These data demonstrate for the first time that ApoA5 is a secreted protein present in human serum and is associated with specific lipoprotein particles, and indicate that the circulating concentration of human Apo A5 is very low compared with other apolipoproteins.

PAR1 is the predominant thrombin receptor expressed in HUVEC and cleavage of PAR1 is required for endothelial cell responses to throm bin; although PAR3 may be expressed, there is still no evidence that it mediatesThrombin responses; and transactivation of PAR2 by cleaved PAR1 can contribute to endothelialcell responses to Thrombin, particularly when signaling through PAR1 has been blocked.

This summary report of the workshop focuses on the major issues discussed during presentations and open forums and noted consensus achieved among the participants on topics from nomenclature to best practices.

This review focuses on recent information about the manner in which signaling through these receptors is initiated and terminated, including evidence for inter- as well as intramolecular modes of activation, and continuing efforts to identify additional, biologically-relevant proteases that can activate PAR family members.

The design of a 4,096 word one microsecond magnetic film store, presented at Western Electronics Show and Conference, Los Angeles, August 1962; Second International Conference on Information Processing (IFIP), Munich, Germany, August-September 1962.

PAR1 is the predominant thrombin receptor expressed in HUVEC and cleavage of PAR1 is required for endothelial cell responses toThrombin, and transactivation of PAR2 by cleaved PAR1 can contribute to endothelial cells responses to throm bin, particularly when signaling through PAR2 is blocked.

Retroviral vectors containing CD4 and an appropriate chemokine receptor were evaluated and were able to target HIV- and SIV-infected cell lines and monocyte-derived macrophages in a manner that corresponded to the specificity of the viral envelope glycoprotein for its CD4-chemokine receptors complex.