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Lista de resultados: 1-10 de um total de 24 resultados (tempo de pesquisa: 0.0 segundos).
DataTítuloAutor(es)TipoAcesso
11-Jul-2016Does the Interplay Between Aging and Neuroinflammation Modulate Alzheimer's Disease Clinical Phenotypes? A Clinico-Pathological Perspective.Taipa, Ricardo Jorge Ferreira; Sousa, Ana Luísa; Pires, Manuel Melo; Sousa, NunoArtigoAcesso aberto
2008Analysis of highly conserved regions of the 3'UTR of MECP2 gene in patients with clinical diagnosis of Rett syndrome and other disorders associated with mental retardationSantos, Mónica; Yan, Jin; Temudo, Teresa; Oliveira, Guiomar; Vieira, José Pedro; Fen, Jinong; Sommer, Steve; Maciel, P.ArtigoAcesso restrito UMinho
2017Mild Left Ventricular Hypertrophy Unravels a Novel Nonsense Mutation of the GLA Gene Associated with the Classical Phenotype of Fabry DiseaseAzevedo, Olga; Gago, Miguel; Miltenberger-Miltenyi, Gabriel; Gaspar, Paulo; Sousa, Nuno; Cunha, DamiãoArtigoAcesso restrito autor
2019p16Ink4a deletion in cells of the intervertebral disc affects their matrix homeostasis and senescence associated secretory phenotype without altering onset of senescenceNovais, Emanuel J.; Diekman, Brian O.; Shapiro, Irving M.; Risbud, Makarand V.ArtigoAcesso restrito UMinho
Jan-2009Mutations in the MECP2 gene are not a major cause of Rett syndrome-like or related neurodevelopmental phenotype in male patientsSantos, Mónica; Temudo, Teresa; Kay, Teresa; Carrilho, Inês; Medeira, Ana; Cabral, Helena; Gomes, Roseli; Lourenço, Maria Teresa; Venâncio, Margarida; Calado, Eulália; Moreira, Ana; Oliveira, Guiomar; Maciel, P.ArtigoAcesso aberto
2007Expression of p120-catenin isoforms correlates with genomic and transcriptional phenotype of breast cancer cell linesParedes, Joana; Correia, Ana Luísa; Ribeiro, Ana Sofia; Schmitt, FernandoArtigoAcesso restrito UMinho
2010P-cadherin, vimentin and CK14 for identification of basal-like phenotype in breast carcinomas: an immunohistochemical studySousa, Bárbara; Paredes, Joana; Milanezi, Fernanda; Lopes, Nair; Martins, Diana; Dufloth, Rozany; Vieira, Daniella; Albergaria, André; Veronese, Luiz; Carneiro, Vitor; Carvalho, Sílvia; Costa, José Luis; Zeferino, Luiz; Schmitt, FernandoArtigoAcesso restrito autor
19-Dez-2009Developmental disturbances associated with agenesis of the permanent maxillary lateral incisorPinho, T.; Maciel, P.; Pollmann, C.ArtigoAcesso aberto
2005Deletion of the Caenorhabditis elegans homologues of the CLN3 gene, involved in human juvenile neuronal ceroid lipofuscinosis, causes a mild progeric phenotypeVoer, G. de; Bent, P. van der; Rodrigues, Ana João; Ommen, G.-J. B. van; Peters, D. J. M.; Taschner, P E MArtigoAcesso restrito UMinho
Nov-2005The molecular genetics of breast cancer: the contribution of comparative genomic hybridizationReis-Filho, Jorge S.; Simpson, Peter T.; Gale, Theodora; Lakhani, Sunil R.ArtigoAcesso restrito UMinho
1-10 de um total de 24 resultados (tempo de pesquisa: 0.0 segundos).

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