Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Ante S. Lundberg"'
Autor:
Yi Wang, Masha Fridkis-Hareli, Ante S. Lundberg, Nirmal K. Banda, Jeff Hunter, Michael Storek, Fang Sun, Gaurav Mehta, Richard Altman, Eran Or, Suresh Katti, Krista Johnson, Tao Peng, V. Michael Holers
Publikováno v:
Molecular Immunology. 105:150-164
Complement activation in human diseases is characterized by the local covalent deposition of the long-lived C3 fragments iC3b/C3dg/C3d. Previously, TT30, a complement alternative pathway (AP)-selective inhibitor, was designed as a fusion protein link
Autor:
Mark D. Fleming, Scott W Miller, William C. Hahn, Sheila A. Stewart, Brian Elenbaas, Kimberly A. Hartwell, John C. Olsen, Mary W. Brooks, Scott H. Randell, Robert A. Weinberg, Ante S. Lundberg
Publikováno v:
Oncogene. 21:4577-4586
One critical step in the development of a cancerous cell is its acquisition of an unlimited replicative lifespan, the process termed immortalization. Experimental model systems designed to study cellular transformation ex vivo have relied to date on
Publikováno v:
Current Opinion in Cell Biology. 12:705-709
Senescence is now understood to be the final phenotypic state adopted by a cell in response to several distinct cell physiological processes, including proliferation, oncogene activation and oxygen free radical toxicity. The role of telomere maintena
Autor:
Christopher M. Counter, Ante S. Lundberg, Roderick L. Beijersbergen, Robert A. Weinberg, Mary W. Brooks, William C. Hahn
Publikováno v:
Nature. 400:464-468
During malignant transformation, cancer cells acquire genetic mutations that override the normal mechanisms controlling cellular proliferation. Primary rodent cells are efficiently converted into tumorigenic cells by the coexpression of cooperating o
Autor:
Ante S. Lundberg, Robert A. Weinberg
Publikováno v:
Molecular and Cellular Biology. 18:753-761
The retinoblastoma protein (pRb) acts to constrain the G1-S transition in mammalian cells. Phosphorylation of pRb in G1 inactivates its growth-inhibitory function, allowing for cell cycle progression. Although several cyclins and associated cyclin-de
Autor:
Michael Mcdermott, Daniel L. Kastner, Christine Hsu, John D. Holloman, Gabriele Schmidt-Wolf, Ante S. Lundberg, Animesh A. Sinha, Hugh O. Mcdevitt, Patrick Cashin, Michael G. Molloy, Brian Mulcahy, Fergal O'Gara, Fiona I. Mcconnell, Claire Adams, Muhammad A. Khan, Frederick Wolfe, Laurence A. Rubin, Daniel O. Clegg, Dee Husebye, Christopher I. Amos, Ryk H. Ward
Publikováno v:
Arthritis & Rheumatism. 38:91-95
OBJECTIVE To evaluate the role of the T cell receptor beta chain locus (TCRB) in genetic susceptibility to rheumatoid arthritis (RA). METHODS Twenty-eight multiplex RA families were recruited from 3 rheumatology outpatient departments. All members we
Autor:
V. Michael Holers, Christopher J. Horvath, Antonio M. Risitano, Masha Fridkis-Hareli, Istvan Mazsaroff, Michael Storek, Ante S. Lundberg
Publikováno v:
Blood. 118(17)
To selectively modulate human complement alternative pathway (CAP) activity implicated in a wide range of acute and chronic inflammatory conditions and to provide local cell surface and tissue-based inhibition of complement-induced damage, we develop
Autor:
Hugh O. McDevitt, Ante S. Lundberg
Publikováno v:
Proceedings of the National Academy of Sciences. 89:6545-6549
The high degree of polymorphism seen at major histocompatibility complex (MHC) class II loci is a feature unique to the MHC. Most of the beta-chain polymorphism is localized in "hypervariable" regions (HVRs). HVR amino acid sequence similarity betwee
Publikováno v:
Biopharmaceuticsdrug disposition. 31(1)
The pharmacokinetics, bioavailability and effects on electrocardiographic (ECG) parameters of fludarabine phosphate (2F-ara-AMP) were evaluated in adult patients with B-cell chronic lymphocytic leukemia. Patients received single doses of intravenous
Autor:
Judith C. W. Marsh, Serena Marotta, Michael Storek, Antonio M. Risitano, Andrzej Hellmann, Austin G. Kulasekararaj, Ilene C. Weitz, Mittie K. Doyle, Modupe Elebute, Ante S. Lundberg, Leonardo Sahelijo, Casey O'Connell, Giridharan Ramsingh, Yang Dai
Publikováno v:
Blood. 126:2137-2137
TT30 is a novel, recombinant human fusion protein, linking the C3d-binding domain of human complement receptor 2 (CR2) with the complement regulatory domain of human factor H (fH). TT30 is designed to inhibit the complement alternative pathway (CAP)