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Characterization of pax1, pax9, and uncx sclerotomal genes during Xenopus laevis embryogenesis
(Wiley, 2013-03)
Background: The axial skeleton develops from the sclerotome, a mesenchymal cell population derived from somites. Sclerotomal cells migrate from somites to the perinotochordal and perineural space where they differentiate ...
Association between PAX-9 promoter polymorphisms and hypodontia in humans
(Elsevier B.V., 2005-10-01)
Hypodontia, the congenital absence of one or a few teeth, is one of the most common alterations of the human dentition. The most common permanent missing teeth are the third molars, second premolars, and maxitlary lateral ...
Association between PAX-9 promoter polymorphisms and hypodontia in humans
(Elsevier B.V., 2005-10-01)
Hypodontia, the congenital absence of one or a few teeth, is one of the most common alterations of the human dentition. The most common permanent missing teeth are the third molars, second premolars, and maxitlary lateral ...
Association between PAX-9 promoter polymorphisms and hypodontia in humans
(Elsevier B.V., 2014)
Absence of mutations in PAX8, NKX2.5, and TSH receptor genes in patients with thyroid dysgenesis
(SBEM-SOC BRASIL ENDOCRINOLOGIA & METABOLOGIARIO DE JANEIRO, RJ, 2013-08-02)
Objectives: To precisely classify the various forms of TD, and then to screen for mutations in transcription factor genes active in thyroid development. Subjects and methods: Patients underwent ultrasound, thyroid scan, ...