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Molecular analysis of SLC26A4 gene in patients with nonsyndromic hearing loss and EVA: Identification of two novel mutations in Brazilian patients
(Elsevier Ireland LtdClareIrlanda, 2013)
SLC2A4 gene: a promising target for pharmacogenomics of insulin resistance
(Ashley PublicationsLondres, 2013-06)
Molecular genetic case-control women investigation from the first Brazilian high-risk study on functional psychosis
(Associação Brasileira de Psiquiatria - ABP, 2008)
OBJECTIVE: Data from epidemiological studies have demonstrated that genetics is an important risk factor for psychosis. The present study is part of a larger project, pioneer in Brazil, which has been conducted by other ...
Avaliação demográfica, clinico-laboratorial e genética de indivíduos com lupus eritematoso sistêmico e artrite reumatóide residentes em região tropical
(Universidade Federal do Rio Grande do NorteBRUFRNPrograma de Pós-Graduação em BioquímicaBioquímica; Biologia Molecular, 2006-10-03)
The aetiology of autoimmunes disease is multifactorial and involves interactions among environmental, hormonal and genetic factors. Many different genes may contribute to autoimmunes disease susceptibility. The major ...
Diseño y construcción de vectores para suprimir la expresión de los genes Lrrc8d, Slc4a3, Slc4a4 mediante la técnica shRNA
(Universidad Nacional de TrujilloPE, 2019)
La calidad de vida para muchos se ve afectada por una hipofunción de las glándulas salivales, al ser grave esta afección no cuenta con tratamientos que permitan revertirla. La saliva, está controlada por el SNA y los centros ...
A novel splicing mutation in the SLC9A3R1 gene in tumors from ovarian cancer patients
(Spandidos Publications, 2015-12)
The aim of the present study was to investigate novel molecular markers that could improve the diagnosis of ovarian cancer patients or be of predictive value. The sequence of the sodium‑hydrogen antiporter 3 regulator 1 ...
Determining mutations in G6PC and SLC37A4 genes in a sample of Brazilian patients with glycogen storage disease types Ia and Ib
(Soc Brasil GeneticaRibeirao PretBrasil, 2013)