Ioanna A. Rota
Oxford, ENG, United Kingdom
Last Updated: 09/26/2026
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Found 9 publications
FOXN1 forms higher-order nuclear condensates displaced by mutations causing immunodeficiency.
Journal: Science advances
Published: December 03, 2021
Mechanistic Drivers of Müllerian Duct Development and Differentiation Into the Oviduct.
Journal: Frontiers in cell and developmental biology
Published: September 11, 2020
The chaperonin CCT8 controls proteostasis essential for T cell maturation, selection, and function.
Journal: Communications biology
Published: August 17, 2020
Expanding the Nude SCID/CID Phenotype Associated with FOXN1 Homozygous, Compound Heterozygous, or Heterozygous Mutations.
Journal: Journal of clinical immunology
Published: July 21, 2020
The crystal structure of human forkhead box N1 in complex with DNA reveals the structural basis for forkhead box family specificity.
Journal: The Journal of biological chemistry
Published: July 25, 2019
Keratinocyte growth factor impairs human thymic recovery from lymphopenia.
Journal: JCI insight
Published: May 08, 2019
Cadherin 17 mutation associated with leaky severe combined immune deficiency is corrected by HSCT.
Journal: Blood advances
Published: August 16, 2017
FOXN1 deficient nude severe combined immunodeficiency.
Journal: Orphanet journal of rare diseases
Published: October 06, 2016
Showing 1-9 of 9
Last Updated: 09/26/2026