Transcriptome Analysis of CD4+ T Cells in Coeliac Disease Reveals Imprint of BACH2 and IFNγ Regulation

por Quinn, Emma M., Coleman, Ciara, Molloy, Ben, Dominguez Castro, Patricia, Cormican, Paul, Trimble, Valerie, Mahmud, Nasir, McManus, Ross
Publicado 2015

Heterozygous and homozygous variants in STX1A cause a neurodevelopmental disorder with or without epilepsy

por Luppe, Johannes, Sticht, Heinrich, Lecoquierre, François, Goldenberg, Alice, Gorman, Kathleen M., Molloy, Ben, Agolini, Emanuele, Novelli, Antonio, Briuglia, Silvana, Kuismin, Outi, Marcelis, Carlo, Vitobello, Antonio, Denommé-Pichon, Anne-Sophie, Julia, Sophie, Lemke, Johannes R., Abou Jamra, Rami, Platzer, Konrad
Publicado 2022