Results 281 to 290 of about 158,026 (312)
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Archives of Biochemistry and Biophysics, 1987
Dissected embryonic chick limbs release neutral metalloproteinases during endochondral bone development. These enzymes degrade cartilage proteoglycan and gelatin in culture medium. We found the enzymes active in the medium conditioned by explants of the region adjacent to the bone marrow cavity (cavity-surround). These enzymes degrade proteoglycan (PG)
Y, Mikuni-Takagaki, Y S, Cheng
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Dissected embryonic chick limbs release neutral metalloproteinases during endochondral bone development. These enzymes degrade cartilage proteoglycan and gelatin in culture medium. We found the enzymes active in the medium conditioned by explants of the region adjacent to the bone marrow cavity (cavity-surround). These enzymes degrade proteoglycan (PG)
Y, Mikuni-Takagaki, Y S, Cheng
openaire +2 more sources
Cardiovascular Pathology, 2006
Coxsackievirus B3 (CVB3) is the major causative agent of myocarditis in humans. In the mouse model, the inflammatory phase of myocarditis results in extensive damage to the heart and triggers profound extracellular matrix (ECM) remodeling, which may ultimately lead to dilated cardiomyopathy.
Caroline, Cheung +8 more
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Coxsackievirus B3 (CVB3) is the major causative agent of myocarditis in humans. In the mouse model, the inflammatory phase of myocarditis results in extensive damage to the heart and triggers profound extracellular matrix (ECM) remodeling, which may ultimately lead to dilated cardiomyopathy.
Caroline, Cheung +8 more
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Tissue Inhibitors of Metalloproteinases in Cancer
2002Our understanding of the biological function of tissue inhibitors of metalloproteinases (TIMP) has significantly evolved from an initial focus on the extracellular matrix (ECM) to a much broader function that includes a regulatory role on cell growth, survival and transformation. The bases for this larger role of TIMPs are several. 1.
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Tissue Inhibitor of Metalloproteinase
2017Marcello G. Masciantonio, Sean E. Gill
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