Buscar
Mostrando ítems 1-10 de 68
Contributions of PTCH gene variants to isolated cleft lip and palate
(SAGE Publications, 2020)
Eventos epigenéticos no ameloblastoma: um enfoque na metilação e transcrição de metaloproteinases da matriz e perda de heterozigosidade do gene PTCH
(Universidade Federal de Minas GeraisUFMG, 2012-05-25)
Ameloblastoma is a benign odontogenic neoplasm with an aggressive behavior and high recurrence rates. Some studies have been performed to elucidated molecular mechanisms and genetic alterations evolving tumor pathogenesis. ...
Immunohistochemical Analysis of Human Homologue of Drosophila Patched (PTCH) in Dental Follicles of Impacted Third Molars
(SOC CHILENA ANATOMIATEMUCO, 2012)
This study investigated the immunodetection of PTCH in epithelial components of dental follicles associated with impacted third molars without radiographic signs of pathosis. One hundred and five specimens of dental follicles ...
Immunohistochemical evaluation of Sonic Hedgehog signaling pathway proteins (Shh, Ptch1, Ptch2, Smo, Gli1, Gli2, and Gli3) in sporadic and syndromic odontogenic keratocysts
(2018-03-21)
Aims: The aim of this study was to compare the clinical and demographic features of 62 patients presenting sporadic odontogenic keratocysts (OKCs) or OKCs associated with nevoid basal cell carcinoma syndrome (NBCCS). In ...
PTCH1 gene mutations in exon 17 and loss of heterozygosity on D9S180 microsatellite in sporadic and inherited human basal cell carcinomas
(WILEY-BLACKWELL, 2011)
Background Basal cell carcinomas (BCCs) are the most frequent human cancer that results from malignant transformation of basal cells in the epidermis. Gorlin syndrome is a rare inherited autosomal dominant disease that ...
Schilbach–Rott syndrome associated with 9q22.32q22.33 duplication, involving the PTCH1 gene
(2019-08-01)
Schilbach–Rott syndrome (SRS, OMIM%164220) is a disorder of unknown aetiology that is characterised by hypotelorism, epichantal folds, cleft palate, dysmorphic face, hypospadia in males and mild mental retardation in some ...
Contributions of PTCH gene variants to isolated cleft lip and palate
(SAGE Publications, 2006)
No evidence for mutations in exons 1, 8 and 18 of the patched gene in sporadic skin lesions of Brazilian patients
(Associação Brasileira de Divulgação Científica, 2003)
Análise dos genes GL1 E PTCH1 em indivíduos com anomalias craniofaciais de linha média, olho e face
(Universidade Estadual Paulista (Unesp), 2012-07-01)
Classificada como a quarta anomalia congênita mais frequente em recém-nascidos, as anomalias craniofaciais constituem um grupo diverso e complexo, determinando, na maioria das vezes aos seus portadores, um prognóstico ...