Titlebook: Cartilage and Osteoarthritis; Massimo Sabatini,Philippe Pastoureau,Frédéric Ceun Book 2004 Humana Press 2004

昆蟲

Analysis of Chondrocyte Functional Markers and Pericellular Matrix Components by Flow Cytometry,ays considered include the insulin-like growth factor-1 (IGF-1)/IGF receptor I (IGFRI), and the transforming growth factor-β1 (TGF-β1)/TGF-β receptor II (TGF-βRII) cascades, as well as the interleukin-1α/β (IL-1α/β)/interleukin-1 receptors I and II (IL-1RI and II) systems. Catabolic enzymes that med

CRAB

A Simple and Reliable Assay of Proteoglycan Synthesis by Cultured Chondrocytes,hondrocytes, total proteoglycan synthesis (SP plus CAP) was increased 3.5-fold after the addition of 1.34 n. insulin-like growth factor-1 (IGF-1) compared with nonstimulated cells. Further addition of a fourfold molar ratio of IGF binding protein-3 completely abolished this effect. This method can b

degradation

LURE

Abominate

Molecular Biology Intelligence Units only one cell type in both normal and diseased conditions. However, care has to be taken not to over- and misinterpret results, and some major challenges must be overcome in order to utilize the potential of this technology properly in the field of osteoarthritis.

GAVEL

合唱隊

Book 2004ularly in the weight-bearing joints. It has a stronger prevalence in women, and its incidence increases with age. OA is a major and growing health concern in developed countries, owing to steadily increasing life expectancy and the demand for better quality of life. Because of its chronic nature and

Inertia

1543-1894 degeneration of articular cartilage, particularly in the weight-bearing joints. It has a stronger prevalence in women, and its incidence increases with age. OA is a major and growing health concern in developed countries, owing to steadily increasing life expectancy and the demand for better quality

perjury

偶像

Tom McMaster,David Wastell,Janice I. DeGross metalloproteinase and type II collagen gene expression from chondrocytes of human origin. Specific gene expression is revealed on an ethidium bromide-containing agarose gel on an ultraviolet plate and normalized to that of a housekeeping gene.