Miguel Luz Soares

Luz Soares, Miguel

 

Miguel Luz Soares, Ph.D.
Responsible Investigator

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Phone: 22 042 6779

 

Research areas:

 

 

Publications

  • Luz Soares, M. & Torres-Padilla, M (2009). Electroporation and Sonoporation in Developmental Biology, chapter 17, pages 179-200. [More] 
  • Luz Soares, M., Torres-Padilla, M. & Zernicka-Goetz, M. (2008). Bone morphogenetic protein 4 signaling regulates development of the anterior visceral endoderm in the mouse embryo. Dev Growth Differ, 50(7), 615-621. [More] 
  • Luz Soares, M., Haraguchi, S., Torres-Padilla, M., Kalmar, T., Carpenter, L., Bell, G. et al. (2005). Functional studies of signaling pathways in peri-implantation development of the mouse embryo by RNAi. BMC Dev Biol, 28(5), 28. [More] 
  • Luz Soares, M., Coelho, T., Sousa, A., Batalov, S., Conceição, I., Sales-Luís, M. et al. (2005). Susceptibility and modifier genes in Portuguese transthyretin V30M amyloid polyneuropathy: complexity in a single-gene disease. Hum Mol Genet, 14(4), 543-553. [More] 
  • Luz Soares, M., Coelho, T., Sousa, A., Holmgren, G., Saraiva, M., Kastner, D. et al. (2004). Haplotypes and DNA sequence variation within and surrounding the transthyretin gene: genotype-phenotype correlations in familial amyloid polyneuropathy (V30M) in Portugal and Sweden. Eur J Hum Genet, 12(3), 225-237. [More] 
  • Luz Soares, M., Centola, M., Chae, J., Saraiva, M. & Kastner, D. (2003). Human transthyretin intronic open reading frames are not independently expressed in vivo or part of functional transcripts. Biochim Biophys Acta, 1626(1-3), 65-74. [More] 
  • Aksentijevich, I., Galon, J., Luz Soares, M., Mansfield, E., Hull, K., Oh, H. H. et al. (2001). The tumor-necrosis-factor receptor-associated periodic syndrome: new mutations in TNFRSF1A, ancestral origins, genotype-phenotype studies, and evidence for further genetic heterogeneity of periodic fevers. Am J Hum Genet, 69(2), 301-314. [More] 
  • Luz Soares, M., Buxbaum, J., Sirugo, G., Coelho, T., Sousa, A., Kastner, D. et al. (1999). Genetic anticipation in Portuguese kindreds with familial amyloidotic polyneuropathy is unlikely to be caused by triplet repeat expansions. Hum Genet, 104(6), 480-485. [More] 
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