Download Ciba Foundation Symposium 205 - Dental Enamel by CIBA Foundation Symposium PDF

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The molecular mechanisms and protein species linked to the mineralization of mature dental tooth are energetic components of study. This publication makes a speciality of particular components of study together with the structural chemistry, protein biochemistry and genetics of tooth improvement.


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Extra resources for Ciba Foundation Symposium 205 - Dental Enamel

Sample text

References Boyde A 1978 Cutting teeth in the SEM. Scanning 1:157-165 Boyde A 1990 Physical effects of clinical procedures on the hard dental tissues. In: Elderton RJ (ed) The dentition and dental care. Heinemann, London, p 49-73 Greenberg G, Bringas P, Slavkin HC 1983 The epithelial genotype controls the pattern of extracellular enamel prism formation. Differentiation 25:32-43 Rosser H, Boyde A, Stewart ADG 1967 Preliminary observations of the calciumconcentration in developing enamel by scanning electron probe X-rayemission microanalysis.

In this regard, CaATPase expression is not found in the proximal portions of secretory ameloblasts (Borke et al 1995). The calcium-CaBP complexes would then move towards the distal cytoplasm and, after release from CaBPs, calcium ions may be extruded towards the enamel matrix by the Ca-ATPase in the Tomes’ process membranes. However, based on its localization, calbindin-D 28 kDa has been postulated to be involved in the regulation of intracellular calcium homeostasis, signalling and cytoskeletal maintenance rather than the active transport system (Berdal et al 1991).

In the latter case, however, there is a second class of orientation change where one set ends obliquely head-on to the sides of the other, or sets clash obliquely head-on. A third aspect prevails where there is little, if any, differencein the orientation of adjacent domains, but their different developmental timing and location determines that there is a locally Werent packing density: the concentration of protein in the orientation discontinuity plane does not differ at the initial secretory step, but increases during the maturational history of the tissue.

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