Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Annemarie H. Ralston"'
Publikováno v:
The FASEB Journal. 15:115-122
Several observations suggest the existence of potent endogenous suppressors of human immunodeficiency virus type 1 (HIV-1) production, and inhibitors of serine proteases may participate in this effect. Alpha-1-antitrypsin (AAT) is the most abundant c
Autor:
Carolyn L. Orthner, Annemarie H. Ralston, Dan Gee, Randy Kent, Billy Kolen, J.D. McGriff, William N. Drohan
Publikováno v:
Vox Sanguinis. 69:309-318
Autor:
Leland Shapiro, Philip E. Silkoff, Courtney L. Bryan, Edward D. Chan, Annemarie H. Ralston, Gregory B. Pott
Publikováno v:
Journal of leukocyte biology. 92(6)
Alpha-1-antitrypsin inhibits NO production, iNOS expression, and NFκB activation in murine macrophagic cells; exhaled NO is increased in AAT-deficient patients compared to controls. NO is an endogenously produced gas that regulates inflammation, vas
Publikováno v:
Chest. 120:S72-S74
Autor:
Thomas D. Sutliff, Kelli Benge, Masaaki Terashima, Ning Huang, Somen Nandi, Jianmin Huang, William N. Drohan, Liying Wu, Annemarie H. Ralston, Raymond L. Rodriguez
Publikováno v:
Biotechnology progress. 17(1)
Human alpha-1-antitrypsin (AAT), the most abundant protease inhibitor found in the blood, was expressed in rice embryonic tissue suspension cell culture. This was accomplished by cloning the codon-optimized AAT gene into a vector containing the rice
Autor:
J.D. McGriff, Randy Kent, Dan M. Gee, Annemarie H. Ralston, Carolyn L. Orthner, William N. Drohan, Billy L. Kolen
Publikováno v:
Vox sanguinis. 69(4)
Activated protein C (APC) is a highly specific serine proteinase which functions as an important naturally occurring antithrombotic enzyme. APC also has anti-inflammatory properties. We have developed a large-scale process for the production of APC f
Autor:
Dudley K. Strickland, Carolyn L. Orthner, John Tharakan, William H. Velander, Annemarie H. Ralston, W. N. Drohan, Rapti D. Madurawe
Publikováno v:
Biotechnology Progress. 5:119-125
Immunosorbents have been developed which utilize metal-dependent interactions between monoclonal antibody(s) (Mab) and human plasma Protein C and Factor IX, members of the vitamin K-dependent plasma protein family. In this report, we describe the pot