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2007
Stevanin, G., Santorelli, F. M., Azzedine, H., Coutinho, P., et al. (2007). Mutations in SPG11, encoding spatacsin, are a major cause of spastic paraplegia with thin corpus callosum. Nature Genetics, 39(3), 366 - 372.
Stevanin, G., Santorelli, F. M., Azzedine, H., Coutinho, P., et al. (2007). Mutations in SPG11, encoding spatacsin, are a major cause of spastic paraplegia with thin corpus callosum. Nature Genetics, 39(3), 366 - 372.
Stevanin, G., Santorelli, F. M., Azzedine, H., Coutinho, P., et al. (2007). Mutations in SPG11, encoding spatacsin, are a major cause of spastic paraplegia with thin corpus callosum. Nature Genetics, 39(3), 366 - 372.
Stevanin, G., Santorelli, F. M., Azzedine, H., Coutinho, P., et al. (2007). Mutations in SPG11, encoding spatacsin, are a major cause of spastic paraplegia with thin corpus callosum. Nature Genetics, 39(3), 366 - 372.
Stevanin, G., Santorelli, F. M., Azzedine, H., Coutinho, P., et al. (2007). Mutations in SPG11, encoding spatacsin, are a major cause of spastic paraplegia with thin corpus callosum. Nature Genetics, 39(3), 366 - 372.
Ferro, A., Carvalho, A. L., Teixeira-Castro, A., Almeida, C., et al. (2007). NEDD8: A new ataxin-3 interactor. Biochimica et Biophysica Acta - Molecular Cell Research, 1773(11), 1619 - 1627.
Ferro, A., Carvalho, A. L., Teixeira-Castro, A., Almeida, C., et al. (2007). NEDD8: A new ataxin-3 interactor. Biochimica et Biophysica Acta - Molecular Cell Research, 1773(11), 1619 - 1627.
Botelho, A. S., Teixeira, L., Correia-da-Costa, J. M., Faustino, A. M. R., et al. (2007). Neospora caninum: High susceptibility to the parasite in C57BL/10ScCr mice. Experimental Parasitology, 115(1), 68 - 75.
Botelho, A. S., Teixeira, L., Correia-da-Costa, J. M., Faustino, A. M. R., et al. (2007). Neospora caninum: High susceptibility to the parasite in C57BL/10ScCr mice. Experimental Parasitology, 115(1), 68 - 75.
Baiou, D., Santha, P., Avelino, A., Charrua, A., et al. (2007). Neurochemical characterization of insulin receptor-expressing primary sensory neurons in wild-type and vanilloid type 1 transient receptor potential receptor knockout mice. Journal of Comparative Neurology, 503(2), 334 - 347.
Baiou, D., Santha, P., Avelino, A., Charrua, A., et al. (2007). Neurochemical characterization of insulin receptor-expressing primary sensory neurons in wild-type and vanilloid type 1 transient receptor potential receptor knockout mice. Journal of Comparative Neurology, 503(2), 334 - 347.
Stevanin, G., Paternotte, C., Coutinho, P., Klebe, S., et al. (2007). A new locus for autosomal recessive spastic paraplegia (SPG32) on chromosome 14q12-q21. Neurology, 68(21), 1837 - 1840.
Stevanin, G., Paternotte, C., Coutinho, P., Klebe, S., et al. (2007). A new locus for autosomal recessive spastic paraplegia (SPG32) on chromosome 14q12-q21. Neurology, 68(21), 1837 - 1840.
Couto, A. R., Bruges-Armas, J., Peach, C. A., Chapman, K., et al. (2007). A novel LEMD3 mutation common to patients with osteopoikilosis with and without melorheostosis. Calcified Tissue International, 81(2), 81 - 84.
Couto, A. R., Bruges-Armas, J., Peach, C. A., Chapman, K., et al. (2007). A novel LEMD3 mutation common to patients with osteopoikilosis with and without melorheostosis. Calcified Tissue International, 81(2), 81 - 84.
Tena, J. J., Neto, A., De La Calle-Mustienes, E., Bras-Pereira, C., et al. (2007). Odd-skipped genes encode repressors that control kidney development. Developmental Biology, 301(2), 518 - 531.
Reis, F., Rocha-Pereira, P., Teixeira de Lemos, E., Parada, B., et al. (2007). Oxidative Stress in Cyclosporine-Induced Hypertension: Evidence of Beneficial Effects or Tolerance Development With Nitrate Therapy. Transplantation Proceedings, 39(8), 2494 - 2500.
Costa, C., & Vendeira, P. (2007). The penis and endothelium. Extragenital aspects of erectile dysfunction. O pénis e o endotélio. Aspectos extra genitais da disfunção eréctilRevista Internacional de Andrologia, 5(1), 50 - 58.
Stendel, C., Roos, A., Deconinck, T., Pereira, J., et al. (2007). Peripheral nerve demyelination caused by a mutant Rho GTPase guanine nucleotide exchange factor, frabin/FGD4. American Journal of Human Genetics, 81(1), 158 - 164.
Morales-Hojas, R., Cheke, R. A., & Post, R. J. (2007). A preliminary analysis of the population genetics and molecular phylogenetics of Onchocerca volvulus (Nematoda: Filarioidea) using nuclear ribosomal second internal transcribed spacer sequences. Memorias do Instituto Oswaldo Cruz, 102(7), 879 - 882.
Beubler, E., Eisenberg, E., Castro-Lopes, J., & Rhodin, A. (2007). Prescribing policies of opioids for chronic pain. Journal of Pain and Palliative Care Pharmacotherapy, 21(2), 53 - 55.
Westermark, P., Benson, M. D., Buxbaum, J. N., Cohen, A. S., et al. (2007). A primer of amyloid nomenclature. Amyloid, 14(3), 179 - 183.
Costa, V., Quintanilha, A., & Moradas-Ferreira, P. (2007). Protein oxidation, repair mechanisms and proteolysis in Saccharomyces cerevisiae. IUBMB Life, 59(4-5), 293 - 298.
Paneque, H. M., Prieto, A. L., Reynaldo, R. R., Cruz, M. T., et al. (2007). Psychological aspects of presymptomatic diagnosis of spinocerebellar ataxia type 2 in Cuba. Community Genetics, 10(3), 132 - 139.
Vieira, J., Cardoso, C. S., Pinto, J., Patil, K., et al. (2007). A putative gene located at the MHC class I region around the D6S105 marker contributes to the setting of CD8+ T-lymphocyte numbers in humans. International Journal of Immunogenetics, 34(5), 359 - 367.

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