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Browsing by Author Jordan, Peter

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Issue DateTitleAuthor(s)
Apr-2012Stimulation of Rac1 signalling enhances apical retention of chemically corrected F508del-CFTR in human airway cells.Matos, Paulo; Moniz, Sónia; Moraes, Bruno; Mendes, Ana Isabel; Amaral, Margarida D.; Jordan, Peter
Nov-2011The contribution of CK2 and spleen tyrosine kinase (SYK) to CFTR trafficking and PKA-induced activityLuz, Simão; Kongsuphol, Patthara; Mendes, Ana Isabel; Romeiras, Francisco; Sousa, Marisa; Schreiber, Rainer; Matos, Paulo; Jordan, Peter; Mehta, Anil; Amaral, Margarida D.; Kunzelmann, Karl; Farinha, Carlos M.
2011The deleterious effect of missense mutations on pre-mRNA splicingGonçalves, Vânia; Jordan, Peter
29-Nov-2012The role of Rac1-modulated gene transcription in tumorigenesisJordan, Peter; Costa, Júlia; Barros, Patrícia
Aug-2012Three-way translocation (X;20;16)(p11;q13;q23) in essential thrombocythemia implicates NFATC2 in dysregulation of CSF2 expression and megakaryocyte proliferationVieira, Luis; Vaz, Andreia; Matos, Paulo; Ambrósio, Ana Paula; Nogueira, Manel; Marques, Bárbara; Pereira, AM; Jordan, Peter; da Silva, Maria Gomes
Jan-2012Transcriptional regulation by antagonistic promoter binding of BCL-6 or Stat5 is modulated by Rac1 SignalingBarros, Patrícia; Jordan, Peter; Matos, Paulo
Jun-2012Transcription initiation arising from E-cadherin/CDH1 intron2: a novel protein isoform that increases gastric cancer cell invasion and angiogenesisPinheiro, Hugo; Carvalho, Joana; Oliveira, Patrícia; Ferreira, Daniel; Teixeira Pinto, Marta; Osório, Hugo; Licastro, Danilo; Bordeira-Carriço, Renata; Jordan, Peter; Lazarevic, Dejan; Sanges, Remo; Stupka, Elia; Huntsman, David; Seruca, Raquel; Oliveira, Carla
Oct-2013Unverricht-Lundborg disease: development of splicing therapeutic approaches for a patient with an homozygous mutation in the cystatin B gene9th Annual Meeting of the Oligonucleotide Therapeutics Society; Matos, Liliana; Duarte, Ana Joana; Jordan, Peter; Prata, Maria João; Chaves, João; Amaral, Olga; Alves, Sandra
Apr-2011A WNK4 gene variant relates to osteoporosis and not to hypertension in the Portuguese populationMendes, Ana Isabel; Mascarenhas, Mário Rui; Matos, Sónia; Sousa, Inês; Ferreira, Joana; Barbosa, Ana Paula; Bicho, Manuel; Jordan, Peter
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