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A
Amaral, I. F., Neiva, I., Ferreira Da Silva, F., Sousa, S. R., et al. (2013). Endothelialization of chitosan porous conduits via immobilization of a recombinant fibronectin fragment (rhFNIII7-10). Acta Biomaterialia, 9(3), 5643 - 5652.
Amaral, M., Dias, A. G., Gomes, P. S., Lopes, M. A., et al. (2008). Nanocrystalline diamond: In vitro biocompatibility assessment by MG63 and human bone marrow cells cultures. Journal of Biomedical Materials Research - Part A, 87(1), 91 - 99.
Amaral, C., Cunha, S. C., Fernandes, J. O., Tavares Da Silva, E., et al. (2013). Development of a new gas chromatography-mass spectrometry (GC-MS) methodology for the evaluation of 5α-reductase activity. Talanta, 107, 154 - 161.
Amaral, I. F., Lamghari, M., Sousa, S. R., Sampaio, P., & Barbosa, M. A. (2005). Rat bone marrow stromal cell osteogenic differentiation and fibronectin adsorption on chitosan membranes: The effect of the degree of acetylation. Journal of Biomedical Materials Research - Part A, 75(2), 387 - 397.
Amaral, C., Varela, C., Azevedo, M., da Silva, E. T., et al. (2013). Effects of steroidal aromatase inhibitors on sensitive and resistant breast cancer cells: Aromatase inhibition and autophagy. Journal of Steroid Biochemistry and Molecular Biology.
Amaral, C., Borges, M., Melo, S., da Silva, E. T., et al. (2012). Apoptosis and autophagy in breast cancer cells following exemestane treatment. PLoS ONE, 7(8).
Amaral, A. F. S., Cymbron, T., Gärtner, F., Lima, M., & Rodrigues, A. S. (2009). Trace metals and over-expression of metallothioneins in bladder tumoral lesions: A case-control study. BMC Veterinary Research, 5.
Amaral, C., Varela, C., Borges, M., Tavares Da Silva, E., et al. (2013). Steroidal aromatase inhibitors inhibit growth of hormone-dependent breast cancer cells by inducing cell cycle arrest and apoptosis. Apoptosis, 18(11), 1426 - 1436.
Amaral, I. F., Cordeiro, A. L., Sampaio, P., & Barbosa, M. A. (2007). Attachment, spreading and short-term proliferation of human osteoblastic cells cultured on chitosan films with different degrees of acetylation. Journal of Biomaterials Science, Polymer Edition, 18(4), 469 - 485.
Amaral, C., Varela, C., Correia-da-Silva, G., Tavares Da Silva, E., et al. (2013). New steroidal 17β-carboxy derivatives present anti-5α-reductase activity and anti-proliferative effects in a human androgen-responsive prostate cancer cell line. Biochimie, 95(11), 2097 - 2106.
Amaral, I. F., Sampaio, P., & Barbosa, M. A. (2006). Three-dimensional culture of human osteoblastic cells in chitosan sponges: The effect of the degree of acetylation. Journal of Biomedical Materials Research - Part A, 76(2), 335 - 346.
Andersson, K. - E., Chapple, C. R., Cardozo, L., Cruz, F., et al. (2009). Pharmacological treatment of overactive bladder: Report from the International Consultation on Incontinence. Current Opinion in Urology, 19(4), 380 - 394.
Andrade, C. Jda Silva, Beato, J., Monteiro, A., Costa, Á., et al. (2016). Spectral-Domain Optical Coherence Tomography as a Potential Biomarker in Huntington's Disease. Movement Disorders, 31(3), 377 - 383.
Andrade, E. B., Alves, J., Madureira, P., Oliveira, L., et al. (2013). TLR2-induced IL-10 production impairs neutrophil recruitment to infected tissues during neonatal bacterial sepsis. Journal of Immunology, 191(9), 4759 - 4768.
Andrade, C., Beato, J., Monteiro, A., Costa, Á., et al. (2016). Reply to Letter: Spectral-domain optical coherence tomography as a potential biomarker in Huntington’s disease. Movement Disorders, 31(11), 1762 - 1763.
Anheim, M., Monga, B., Fleury, M., Charles, P., et al. (2009). Ataxia with oculomotor apraxia type 2: Clinical, biological and genotype/phenotype correlation study of a cohort of 90 patients. Brain, 132(10), 2688 - 2698.
Anjo, S. I., Figueiredo, F., Fernandes, R., Manadas, B., & Oliveira, M. (2017). A proteomic and ultrastructural characterization of Aspergillus fumigatus' conidia adaptation at different culture ages. Journal of Proteomics, 161, 47 - 56.
Antal, Z., Luz, L. L., Safronov, B. V., Antal, M., & Szücs, P. (2015). Neurons in the lateral part of the lumbar spinal cord show distinct novel axon trajectories and are excited by short propriospinal ascending inputs. Brain Structure and Function.
Antal, Z., Luz, L. L., Safronov, B. V., Antal, M., & Szucs, P. (2016). Neurons in the lateral part of the lumbar spinal cord show distinct novel axon trajectories and are excited by short propriospinal ascending inputs. Brain Structure and Function, 221(4), 2343 - 2360.
Antal, Z., Luz, L. L., Safronov, B. V., Antal, M., & Szucs, P. (2016). Erratum to: Neurons in the lateral part of the lumbar spinal cord show distinct novel axon trajectories and are excited by short propriospinal ascending inputs (Brain Struct Funct, 2016, 10.1007/s00429-015-1046-3). Brain Structure and Function, 221(4), 2399 - 2400.
Antal, Z., Luz, L. L., Safronov, B. V., Antal, M., & Szücs, P. (2015). Erratum to: Neurons in the lateral part of the lumbar spinal cord show distinct novel axon trajectories and are excited by short propriospinal ascending inputs. Brain Structure and Function.
Antón, N., Santos-Aberturas, J., Mendes, M. V., Guerra, S. M., et al. (2007). PimM, a PAS domain positive regulator of pimaricin biosynthesis in Streptomyces natalensis. Microbiology, 153(9), 3174 - 3183.
Antoniou, A. N., Santos, S. G., Campbell, E. C., Lynch, S., et al. (2007). ERp57 interacts with conserved cysteine residues in the MHC class I peptide-binding groove. FEBS Letters, 581(10), 1988 - 1992.
Antunes, R. F., Brandão, C., Carvalho, G., Girão, C., & Arosa, F. A. (2009). Red blood cells carry out T cell growth and survival bioactivities that are sensitive to cyclosporine A. Cellular and molecular life sciences : CMLS, 66(20), 3387 - 3398.
Antunes, R. F., Brandão, C., Maia, M., & Arosa, F. A. (2011). Red blood cells release factors with growth and survival bioactivities for normal and leukemic T cells. Immunology and Cell Biology, 89(1), 111 - 121.

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