Directional Next-Generation RNA Sequencing and Examination of Premature Termination Codon Mutations in Endoglin/Hereditary Haemorrhagic Telangiectasia

Por Govani, F.S., Giess, A., Mollet, I.G., Begbie, M.E., Jones, M.D., Game, L., Shovlin, C.L.
Publicado em 2013

Modulation of microRNA-375 expression alters voltage-gated Na(+) channel properties and exocytosis in insulin-secreting cells

Por Salunkhe, V A, Esguerra, J L S, Ofori, J K, Mollet, I G, Braun, M, Stoffel, M, Wendt, A, Eliasson, L
Publicado no Acta Physiol (Oxf) (2015)

Unconstrained mining of transcript data reveals increased alternative splicing complexity in the human transcriptome

Por Mollet, I. G., Ben-Dov, Claudia, Felício-Silva, Daniel, Grosso, A. R., Eleutério, Pedro, Alves, Ruben, Staller, Ray, Silva, Tito Santos, Carmo-Fonseca, Maria
Publicado em 2010