Modulated expression of type X collagen in the Meckel's cartilage with different developmental fates
Article Abstract:
Type X collagen does not appear to be associated with hypertrophic cartilage matrix formation in the distal part of Meckel's cartilage. However, a role in endochondral ossification is indicated by the spatial distribution of type X collagen only in the caudal region of Meckel's cartilage. The study also suggests that the molecular mechanism of type X collagen expression is related to differential development in Meckel's cartilage. Type X collagen's presence or absence may be a key to understanding the regulation of phenotypic transformation in Meckel's cartilage and the molecular basis of mandible evolution from non-mammalian to mammalian species.
Publication Name: Developmental Biology
Subject: Biological sciences
ISSN: 0012-1606
Year: 1995
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Identification and localization of endothelin-1 and its receptors in human fetal jaws
Article Abstract:
A study was conducted to examine the role of the endothelin-1 (ET-1) gene and its receptors in the development of human fetal craniofacial tissues of nine- to 12-week old fetuses. Radioligand binding studies revealed localization of ET-1 in the epithelial cells of the oral cavity and showed high concentrations of its receptors in the membranes of the fetal jaws. Autoradiography revealed localization of binding sites in the embryonic mandibular process of the oral cavity. This suggests that ET-1 contributes in the formation of the human mandible.
Publication Name: Developmental Biology
Subject: Biological sciences
ISSN: 0012-1606
Year: 1995
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Lethality of Rw\Rw mouse embryos during early postimplantation development
Article Abstract:
Genetic and physical mapping studies prove that the rump white (Rw) mutation in the mouse is associated with a large chromosomal inversion, based on segregation analysis of the mutant phenotype in heterozygous mice. Three mutations on mouse chromosome 5, white spotting (W), patch (Ph), and Rw produce pigmentation disorders. The W phenotype results from a mutation altering the c-kit protooncogene and Ph with the deletion of Pdgfra.
Publication Name: Developmental Biology
Subject: Biological sciences
ISSN: 0012-1606
Year: 1995
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