Abstract:
Technologies are provided herein for multiple platform support in a computer system firmware. A firmware is built for each hardware platform to be supported. At built time of the firmware for each platform to be supported, an instance of platform specific information is extracted from the built firmware and stored. Once the platform specific information instances have been collected for each platform to be supported, the platform specific information instances are stored in a multi-platform firmware. At run-time of the multi-platform firmware, the particular hardware platform that the multi-platform firmware is executing upon is identified. Once the platform has been identified, the particular instance of platform specific information corresponding to the identified platform is selected. The selected instance of platform specific information is then loaded and exposed for consumption by other programs.
Abstract:
A composition including a peptide sequence of the formula βX1-X2, the peptide sequence corresponding to an amino acid sequence of a fibrin beta chain fragment of a Bbeta chain of fibrinogen, wherein X1 represents an N-terminal end of the peptide sequence, and X2 represents a C-terminal end of the peptide sequence, wherein the peptide sequence includes additional amino acids between X1 and X2, wherein the peptide sequence may contain a non-naturally occurring amino acid residue, wherein the peptide sequence is other than a wild-type β15-42 monomer sequence per se, and wherein the peptide sequence is other than (β15-66) 2 dimer having two chains with each chain limited to wild type amino acids β15-65 and each chain further including a non-naturally occurring Gly at position 66 of each chain. Methods for treatment and pharmaceutical combinations may include a polypeptide agent such as Thymosin beta 4. In such methods and combinations, a dimer of the peptide sequence may include amino acids 15-66 of the fibrin beta chain.
Abstract:
The invention provides a method of treating inflammation, comprising administering to a subject in need thereof a therapeutically effective amount of an agent that inhibits binding of fibrin to Very Low Density Lipoprotein Receptor (VLDLR) or combination of this agent with agents inhibiting binding of fibrin to VE- cahherin (vascular endothelial cadherin).
Abstract:
A composition including a peptide sequence of the formula ßX1-X2, the peptide sequence corresponding to an amino acid sequence of a fibrin beta chain fragment of a Bbeta chain of fibrinogen, wherein X1 represents an N-terminal end of the peptide sequence, and X2 represents a C-terminal end of the peptide sequence, wherein the peptide sequence includes additional amino acids between X1 and X2, wherein the peptide sequence may contain a non-naturally occurring amino acid residue, wherein the peptide sequence is other than a wild-type ß15-42 monomer sequence per se, and wherein the peptide sequence is other than (ß15-66)2 dimer having two chains with each chain limited to wild type amino acids ß15-65 and each chain further including a non-naturally occurring Gly at position 66 of each chain. Methods for treatment and pharmaceutical combinations may include a polypeptide agent such as Thymosin beta 4. In such methods and combinations, a dimer of the peptide sequence may include amino acids 15-66 of the fibrin beta chain.