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Genetic variants in folate and cobalamin metabolism-related genes in nonsyndromic cleft lip and/or Palate
(2015-11-01)
The aim of this study was to evaluate the association of the polymorphisms in TCN2 (rs1801198) gene and in MTRR (rs1801394) gene with nonsyndromic cleft lip and/or palate (NSCL/P) in a Brazilian population. Genomic DNA was ...
Fisuras orofaciales en Chile : asociación entre niveles de metilación global del ADN y variantes genéticas presentes MTHFR, SLC19A1 Y TCN2
(Universidad de Chile, 2020)
En la etiología de las fisuras orofaciales no sindrómicas (FOFNS) el metabolismo de los folatos
jugaría un importante rol, en donde se han reportado asociaciones con variantes
hipofuncionales de genes de este metabolismo ...
Genotyping and characterization of two polymorphic microsatellite markers located within introns 29 and 30 of the human thyroglobulin gene
(Mary Ann Liebert, 2002-09)
The purpose of the present work was to characterize two new polymorphic microsatellite markers in the thyroglobulin gene. TGrI29 and TGrI30 repeats are located within introns 29 and 30, respectively. Genetic studies were ...
Expression of human papillomavirus type 16 E7 oncoprotein alters keratinocytes expression profile in response to tumor necrosis factor-alpha
(OXFORD UNIV PRESS, 2010)
Acute expression of E7 oncogene from human papillomavirus (HPV) 16 or HPV18 is sufficient to overcome tumor necrosis factor (TNF)-alpha cytostatic effect on primary human keratinocytes. In the present study, we investigated ...