Paul T. Sharpe – författare
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4 produkter
4 produkter
E-bok
Engelska, 20081 268 kr
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Most people have some interest in embryos; this probably results, in part, from their interest in understanding the biological origins of themselves and their offspring and, increasingly, concerns about how environmental change such as pollution might affect human development. Obviously, et- cal considerations preclude experimental studies of human embryos and, c- sequently, the developmental biologist has turned to other species to examine this process. Fortunately, the most significant conclusion to be drawn from the experimental embryology of the last two decades is the manner in which orthologous or closely related molecules are deployed to mediate similar - velopmental processes in both vertebrates and invertebrates. The molecular mechanisms regulating processes fundamental to most animals, such as axial patterning or axon guidance, are frequently conserved during evolution. (It is now widely believed that the differences between phyla and classes are the result of new genes, arising mostly by duplication and divergence of extant sequences, regulating the appearance of derived characters. ) Other vertebrates are obviously most likely to use the same devel- mental mechanisms as humans and, within the vertebrate subphylum, the - parent degree of conservation of developmental mechanism is considerable. It has long been recognized that particular vertebrate species offer either d- tinct advantages in investigating particular stages of development or are - pecially amenable to particular manipulations. No single animal can provide all the answers because not all types of experiments can be carried out on a single species.
Häftad, Engelska, 2019
249 kr
Skickas inom 5-8 vardagar
E-bok
PDF, Engelska, 2013708 kr
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Häftad, Engelska, 2014
565 kr
Skickas inom 10-15 vardagar
The osteoclasts in Paget's disease are abnormal both in num- ber and size and show nuclear inclusions as well as cytoplasmic inclusions that suggest a viral etiology for Paget's disease. Use of in vitro model systems for examining osteoclast physiology in Paget's disease has shown that these cells have an increased rate of formation, express high levels of IL-6, IL-6 receptor, and NF-IL-6, as well as most recently, the c-FOS protooncogene. 31 The precur- sors for these pagetic osteoclasts have several abnormalities includ- ing hyperresponsivity to 1,25-dihydroxyvitamin D , presence of 3 measles virus nucleocapsid transcripts, and hyperresponsivity to the marrow microenvironment. In addition, the marrow microenviron- ment is also abnormal in Paget's disease. These data suggest that the initial pathologic event that occurs in Paget's disease affects the osteoclast precursor, as well as the mature osteoclast.The per- sistence of Paget's disease as a highly localized lesion(s) in patients following diagnosis may be due to the abnormalities in the mar- row microenvironment that induce abnormal circulating osteoclast precursors to "home" to the sites of previous disease and induce increased osteoclast formation in these areas. In areas of normal bone, the normal marrow microenvironment does not induce en- hanced osteoclast formation, but allows these cells to differentiate toward the monocyte macrophage lineage in the form of mature monocytes.