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Orphanet Journal of Rare Diseases|January 13, 2017
FOXN1 deficient nude severe combined immunodeficiencyIoanna A Rota, Fatima DhallaJournal of Visualized Experiments : Jove|October 3, 2013
Isolation of myeloid dendritic cells and epithelial cells from human thymusChristina Stoeckle, Ioanna A Rota, Eva Tolosa, et al.The Journal of Biological Chemistry|January 9, 2020
The crystal structure of human forkhead box N1 in complex with DNA reveals the structural basis for forkhead box family specificityJoseph A Newman, Hazel Aitkenhead, Angeline E Gavard, et al.Blood Advances|January 4, 2018
Cadherin 17 mutation associated with leaky severe combined immune deficiency is corrected by HSCTAngela R Smith, Ioanna A Rota, Stefano Maio, et al.Frontiers in Cell and Developmental Biology|March 25, 2021
Mechanistic Drivers of Müllerian Duct Development and Differentiation Into the OviductLaura Santana Gonzalez, Ioanna A Rota, Mara Artibani, et al.Nature Communications|June 21, 2013
Exploring the MHC-peptide matrix of central tolerance in the human thymusEleni Adamopoulou, Stefan Tenzer, Nina Hillen, et al.Communications Biology|June 4, 2021
The chaperonin CCT8 controls proteostasis essential for T cell maturation, selection, and functionBergithe E Oftedal, Stefano Maio, Adam E Handel, et al.Nature Immunology|April 20, 2023
Orthogonal cytokine engineering enables novel synthetic effector states escaping canonical exhaustion in tumor-rejecting CD8+ T cellsJesus Corria-Osorio, Santiago J Carmona, Evangelos Stefanidis, et al.Journal of Clinical Immunology|January 19, 2021
Expanding the Nude SCID/CID Phenotype Associated with FOXN1 Homozygous, Compound Heterozygous, or Heterozygous MutationsGiuliana Giardino, Svetlana O Sharapova, Peter Ciznar, et al.Science Advances|December 3, 2021
FOXN1 forms higher-order nuclear condensates displaced by mutations causing immunodeficiencyIoanna A Rota, Adam E Handel, Stefano Maio, et al.Pageof 2