Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Angus M Tester"'
Autor:
Angus M Tester, Jennifer H Cox, Andrea R Connor, Amanda E Starr, Richard A Dean, Xose S Puente, Carlos López-Otín, Christopher M Overall
Publikováno v:
PLoS ONE, Vol 2, Iss 3, p e312 (2007)
We identify matrix metalloproteinase (MMP)-8, the polymorphonuclear (PMN) leukocyte collagenase, as a critical mediator initiating lipopolysaccharide (LPS)-responsiveness in vivo. PMN infiltration towards LPS is abrogated in Mmp8-null mice. MMP-8 cle
Externí odkaz:
https://doaj.org/article/43867c694e834ccb82d6c92d53dbe95f
Autor:
Eugenia Diaconu, Michelle Lin, J. Edwin Blalock, Eric Pearlman, Patricia L. Jackson, Angus M. Tester, Christopher M. Overall
Publikováno v:
The American Journal of Pathology. 173:144-153
Matrix metalloproteinase (MMP)-8 and MMP-9 play several roles in inflammation, including degradation of extracellular matrix (ECM) components and regulation of cytokine activity. To determine the roles of MMP-8 and MMP-9 in a neutrophil-dependent inf
Autor:
Luca Mazzucchelli, Angus M. Tester, Christopher M. Overall, Marlene Wolf, Maddalena Lis, Lara Hasan, Mark Liebi, Robert E. Hunger
Publikováno v:
The Journal of Immunology. 176:6512-6522
Chemokine processing by proteases is emerging as an important regulatory mechanism of leukocyte functions and possibly also of cancer progression. We screened a large panel of chemokines for degradation by cathepsins B and D, two proteases involved i
Autor:
Milagros Balbín, Alberto M. Pendás, Carlos López-Otín, Christopher M. Overall, Aurora Astudillo, Ana S. Pitiot, Steven D. Shapiro, Antonio Fueyo, Angus M. Tester
Publikováno v:
Nature Genetics. 35:252-257
Matrix metalloproteinases (MMPs) have fundamental roles in tumor progression, but most clinical trials with MMP inhibitors have not shown improvements in individuals with cancer. This may be partly because broad-range inhibitors also reduce host-prot
Publikováno v:
Clinical and Experimental Metastasis. 18:553-560
We have investigated the gelatinase profiles and invasiveness of clonal tumour sublines derived from a spontaneously arising mammary tumour in a Balb/cfC3H mouse. The 67NR. 66c14 and 4T1.2 sublines have low, intermediate and high metastatic potential
Autor:
Christopher J. Handley, Wendy E. Cain, Gregory J. Checkley, Anne E. Cant, Ann D. Winter, Margaret A. Campbell, Geraldine L. Chow, Angus M. Tester
Publikováno v:
Archives of Biochemistry and Biophysics. 329:181-190
Bovine collateral ligament synthesized a 35S-labeled large proteoglycan species which eluted with a Kav of approximately 0.27 on Sepharose CL-2B and contained only chondroitin sulfate chains with a molecular mass of approximately 32 kDa. Fluorography
Autor:
Xose S. Puente, Jennifer H. Cox, Richard A. Dean, Angus M. Tester, Christopher M. Overall, Andrea R. Connor, Amanda E. Starr, Carlos López-Otín
Publikováno v:
PLoS ONE
PLoS ONE, Vol 2, Iss 3, p e312 (2007)
PLoS ONE, Vol 2, Iss 3, p e312 (2007)
We identify matrix metalloproteinase (MMP)-8, the polymorphonuclear (PMN) leukocyte collagenase, as a critical mediator initiating lipopolysaccharide (LPS)-responsiveness in vivo. PMN infiltration towards LPS is abrogated in Mmp8-null mice. MMP-8 cle
Autor:
Emma C. Walker, Mark Waltham, Marc E. Lippman, Erik W. Thompson, Margaret M. Bills, Angus M. Tester, Se Jeong Oh, Francis G. Kern, William G. Stetler-Stevenson, Seog Nyeon Bae
Publikováno v:
Cancer research. 64(2)
The ability to activate pro-matrix metalloproteinase (pro-MMP)-2 via membrane type-MMP is a hallmark of human breast cancer cell lines that show increased invasiveness, suggesting that MMP-2 contributes to human breast cancer progression. To investig
Publikováno v:
Clinicalexperimental metastasis. 19(5)
Orthotopic or intracardiac injection of human breast cancer cell lines into immunocompromised mice allows study of the molecular basis of breast cancer metastasis. We have established a quantitative real-time PCR approach to analyze metastatic spread
Publikováno v:
Matrix biology : journal of the International Society for Matrix Biology. 18(1)
In explant cultures of articular cartilage from cattle of different ages radiolabeled leucine was shown to be incorporated into link proteins 1, 2 and 3. The newly synthesized link proteins were incorporated into and lost from the cartilage extracell