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SLC23A2-05 (rs4987219) and KRAS-LCS6 (rs61764370) polymorphisms in patients with squamous cell carcinoma of the head and neck
(Spandidos Publ LtdAthensGrécia, 2014)
Iodide handling disorders (NIS, TPO, TG, IYD)
(Elsevier, 2017-03)
Iodide Handling Disorders lead to defects of the biosynthesis of thyroid hormones (thyroid dyshormonogenesis, TD) and thereafter congenital hypothyroidism (CH), the most common endocrine disease characterized by low levels ...
Bases genéticas del autismoGenetic basis of autism
(Instituto Nacional de Pediatría, 2010)
Bases genéticas del autismoGenetic basis of autism
(Instituto Nacional de Pediatría, 2010)
Spatio-specific regulation of endocrine-responsive gene transcription by periovulatory endocrine profiles in the bovine reproductive tract
(Csiro Publishing, 2016-01-01)
In cattle, pro-oestrous oestradiol and dioestrous progesterone concentrations modulate endometrial gene expression and fertility. The aim was to compare the effects of different periovulatory endocrine profiles on the ...
The Na+/glucose cotransporters: from genes to therapy
(Associação Brasileira de Divulgação Científica, 2010)
Glucose enters eukaryotic cells via two types of membrane-associated carrier proteins, the Na+/glucose cotransporters (SGLT) and the facilitative glucose transporters (GLUT). The SGLT family consists of six members. Among ...
Polimorfismos dos genes SLC11A1 e DLA-DRB1 e susceptibilidade de cães à leishmaniose
(Universidade Estadual Paulista (Unesp), 2011)
The importance of visceral leishmaniasis in the context of public health has increased in the last decade. The manifestation of visceral leishmaniasis in dogs is variable and genetic studies and its relationship with ...
Downregulation of OCLN and GAS1 in clear cell renal cell carcinoma
(2017-03-01)
Clear cell renal cell carcinoma (ccRCC) is the most common histological subtype of kidney cancer. This carcinoma is histologically characterized by the presence of clear and abundant cytoplasm. In the present study, we ...
Haplotypes from the SLC45A2 gene are associated with the presence of freckles and eye, hair and skin pigmentation in Brazil
(2017-03-01)
The Solute Carrier Family 45, Member 2 (SLC45A2) gene encodes the Membrane-Associated Transporter Protein (MATP), which mediates melanin synthesis by tyrosinase trafficking and proton transportation to melanosomes. At least ...