Matches in SemOpenAlex for { <https://semopenalex.org/work/W2106704887> ?p ?o ?g. }
- W2106704887 endingPage "116R" @default.
- W2106704887 startingPage "107R" @default.
- W2106704887 abstract "Small leucine-rich proteoglycans (SLRPs) are extracellular molecules that bind to TGFbetas and collagens and other matrix molecules. In vitro, SLRPs were shown to regulate collagen fibrillogenesis, a process essential in development, tissue repair, and metastasis. To better understand their functions in vivo, mice deficient in one or two of the four most prominent and widely expressed SLRPs (biglycan, decorin, fibromodulin, and lumican) were recently generated. All four SLRP deficiencies result in the formation of abnormal collagen fibrils. Taken together, the collagen phenotypes demonstrate a cooperative, sequential, timely orchestrated action of the SLRPs that altogether shape the architecture and mechanical properties of the collagen matrix. In addition, SLRP-deficient mice develop a wide array of diseases (osteoporosis, osteoarthritis, muscular dystrophy, Ehlers-Danlos syndrome, and corneal diseases), most of them resulting primarily from an abnormal collagen fibrillogenesis. The development of these diseases by SLRP-deficient mice suggests that mutations in SLRPs may be part of undiagnosed predisposing genetic factors for these diseases. Although the distinct phenotypes developed by the different singly deficient mice point to distinct in vivo function for each SLRP, the analysis of the double-deficient mice also demonstrates the existence of rescuing/compensation mechanisms, indicating some functional overlap within the SLRP family." @default.
- W2106704887 created "2016-06-24" @default.
- W2106704887 creator A5050123695 @default.
- W2106704887 creator A5089377430 @default.
- W2106704887 date "2002-09-01" @default.
- W2106704887 modified "2023-10-17" @default.
- W2106704887 title "Mice deficient in small leucine-rich proteoglycans: novel in vivo models for osteoporosis, osteoarthritis, Ehlers-Danlos syndrome, muscular dystrophy, and corneal diseases" @default.
- W2106704887 cites W1481976779 @default.
- W2106704887 cites W1491950503 @default.
- W2106704887 cites W1500193811 @default.
- W2106704887 cites W1515550479 @default.
- W2106704887 cites W1520651346 @default.
- W2106704887 cites W1543315777 @default.
- W2106704887 cites W1544527238 @default.
- W2106704887 cites W1591638778 @default.
- W2106704887 cites W1599843882 @default.
- W2106704887 cites W1603078285 @default.
- W2106704887 cites W1967014829 @default.
- W2106704887 cites W1971249148 @default.
- W2106704887 cites W1972041825 @default.
- W2106704887 cites W1972571287 @default.
- W2106704887 cites W1972574335 @default.
- W2106704887 cites W197569723 @default.
- W2106704887 cites W1976976492 @default.
- W2106704887 cites W1977494019 @default.
- W2106704887 cites W1980534733 @default.
- W2106704887 cites W1984143412 @default.
- W2106704887 cites W1984155123 @default.
- W2106704887 cites W1984452766 @default.
- W2106704887 cites W1991388845 @default.
- W2106704887 cites W1992492704 @default.
- W2106704887 cites W1995839201 @default.
- W2106704887 cites W1996764985 @default.
- W2106704887 cites W1998487818 @default.
- W2106704887 cites W2002509647 @default.
- W2106704887 cites W2003969011 @default.
- W2106704887 cites W2004897012 @default.
- W2106704887 cites W2007834031 @default.
- W2106704887 cites W2009212790 @default.
- W2106704887 cites W2016005410 @default.
- W2106704887 cites W2017096535 @default.
- W2106704887 cites W2019365102 @default.
- W2106704887 cites W2023494944 @default.
- W2106704887 cites W2023707289 @default.
- W2106704887 cites W2030320259 @default.
- W2106704887 cites W2030777510 @default.
- W2106704887 cites W2034364425 @default.
- W2106704887 cites W2036341761 @default.
- W2106704887 cites W2041345827 @default.
- W2106704887 cites W2042573371 @default.
- W2106704887 cites W2044614528 @default.
- W2106704887 cites W2044859814 @default.
- W2106704887 cites W2051107672 @default.
- W2106704887 cites W2052577034 @default.
- W2106704887 cites W2053597586 @default.
- W2106704887 cites W2054482368 @default.
- W2106704887 cites W2055070923 @default.
- W2106704887 cites W2056246779 @default.
- W2106704887 cites W2061509321 @default.
- W2106704887 cites W2064332824 @default.
- W2106704887 cites W2070013317 @default.
- W2106704887 cites W2070086097 @default.
- W2106704887 cites W2071430673 @default.
- W2106704887 cites W2073764175 @default.
- W2106704887 cites W2075073611 @default.
- W2106704887 cites W2077002479 @default.
- W2106704887 cites W2082255168 @default.
- W2106704887 cites W2082340092 @default.
- W2106704887 cites W2085050040 @default.
- W2106704887 cites W2087282233 @default.
- W2106704887 cites W2089179152 @default.
- W2106704887 cites W2090206992 @default.
- W2106704887 cites W2090603283 @default.
- W2106704887 cites W2093498304 @default.
- W2106704887 cites W2093526323 @default.
- W2106704887 cites W2101896709 @default.
- W2106704887 cites W2107283165 @default.
- W2106704887 cites W2110799319 @default.
- W2106704887 cites W2120347833 @default.
- W2106704887 cites W2121094033 @default.
- W2106704887 cites W2121555787 @default.
- W2106704887 cites W2129591536 @default.
- W2106704887 cites W2131244812 @default.
- W2106704887 cites W2134259286 @default.
- W2106704887 cites W2136547055 @default.
- W2106704887 cites W2141877739 @default.
- W2106704887 cites W2142335737 @default.
- W2106704887 cites W2144816848 @default.
- W2106704887 cites W2156854226 @default.
- W2106704887 cites W2159058635 @default.
- W2106704887 cites W2160038542 @default.
- W2106704887 cites W2163692671 @default.
- W2106704887 cites W4239494812 @default.
- W2106704887 cites W4296927411 @default.
- W2106704887 doi "https://doi.org/10.1093/glycob/cwf065" @default.
- W2106704887 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/12213783" @default.
- W2106704887 hasPublicationYear "2002" @default.
- W2106704887 type Work @default.