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Mostrando ítems 81-90 de 106
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 ...
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 ...
Expressão de miRNAs relacionados com a proliferação de precursores neuronais durante desenvolvimento cerebelar
(Universidade Federal de São Paulo (UNIFESP), 2019-02-28)
The cerebellum is an important organ to study development in the central nervous system. When matured, the cerebellum presents a well-defined three-layered cortex. Its development initiates during the embryonic period and ...
Characterization of Ectonucleotidases in Human Medulloblastoma Cell Lines: ecto-5 ' NT/CD73 in Metastasis as Potential Prognostic Factor
(PUBLIC LIBRARY SCIENCESAN FRANCISCO, 2012)
Medulloblastoma (MB) is the most common malignant brain tumor in children and occurs mainly in the cerebellum. Important intracellular signaling molecules, such those present in the Sonic Hedgehog and Wnt pathways, are ...
The CK1 gene family: Expression patterning in zebrafish development
(Society of Biology of Chile, 2007)
Protein kinase CK1 is a ser/thr protein kinase family which has been identified in the cytosol cell fraction, associated with membranes as well as in the nucleus. Several isoforms of this gene family have been described ...
Homozygous mutation in CEP19, a gene mutated in morbid obesity, in Bardet-Biedl syndrome with predominant postaxial polydactyly
(2018)
Background Bardet-Biedl syndrome (BBS) is a ciliopathy with extensive phenotypic variability and genetic heterogeneity. We aimed to discover the gene mutated in a consanguineous kindred with multiple cases of a BBS phenotype. ...