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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.

Author: Chung, Kun Sung, Park, Howard H., Ting, Kang, Takita, Hiroko, Apte, Suneel S., Kuboki, Yoshinori, Nishimura, Ichiro
Publisher: Elsevier B.V.
Publication Name: Developmental Biology
Subject: Biological sciences
ISSN: 0012-1606
Year: 1995
Collagen, Cartilage

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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.

Author: Barni, Tullio, Maggi, Mario, Fantoni, Guido, Serio, Mario, Tollaro, Isabella, Gloria, Luciana, Vannelli, Gabriella B.
Publisher: Elsevier B.V.
Publication Name: Developmental Biology
Subject: Biological sciences
ISSN: 0012-1606
Year: 1995
Endothelin

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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.

Author: Bucan, Maja, Nagle, Deborah L., Hough, Richard B., Chapman, Verne M., Lo, Cecilia W.
Publisher: Elsevier B.V.
Publication Name: Developmental Biology
Subject: Biological sciences
ISSN: 0012-1606
Year: 1995
Analysis, Chromosome mapping, Mutation (Biology), Mutation

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Subjects list: Research, Mandible, Mice, Mice (Rodents)
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