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Systems Analysis of the 22q11.2 Microdeletion Syndrome Converges on a Mitochondrial Interactome Necessary for Synapse Function and Behavior
(2019)
Neurodevelopmental disorders offer insight into synaptic mechanisms. To unbiasedly uncover these mechanisms, we studied the 22q11.2 syndrome, a recurrent copy number variant, which is the highest schizophrenia genetic risk ...
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)
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 ...