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Showing results 10 to 16 of 16

Loss of hnRNPLL-dependent splicing of Ptprc has no impact on B-cell development, activation and terminal differentiation into antibody-secreting cells

Author(s)Yabas, Mehmet; Yazicioglu, Furkan; Hoyne, Gerard E., et al
TypeJournal article
Date Published2021
Date Created-

A multimorphic mutation in IRF4 causes human autosomal dominant combined immunodeficiency

Author(s)Fornes, Oriol; Jia, Alicia; Kuehn, Hye Sun, et al
TypeJournal article
Date Published20-Jan-2023
Date Created-

Mutations of the gene FNIP1 associated with a syndromic autosomal recessive immunodeficiency with cardiomyopathy and pre-excitation syndrome

Author(s)Niehues, Tim; Özgür, Tuba Turul; Bickes, Marie, et al
TypeJournal article
Date Published2020
Date Created-

A point mutation in IKAROS ZF1 causes a B cell deficiency in mice

Author(s)Boast, Brigette; Miosge, Lisa; Kuehn, Hye Sun, et al
TypeJournal article
Date Published2021
Date Created-
Structural determinants.pdf.jpg

Structural determinants of the IRF4/DNA homodimeric complex

Author(s)sundararaj, Srinivasan; Seneviratne, Sandali; Williams, Simon, et al
TypeJournal article
Date Published2021
Date Created-

A three-stage intrathymic development pathway for the mucosal-associated invariant T cell lineage

Author(s)Koay, Hui-Fern; Gherardin, Nicholas A; Enders, Anselm, et al
TypeJournal article
Date PublishedNov-2016
Date Created-

Up-regulation of LFA-1 allows liver-resident memory T cells to patrol and remain in the hepatic sinusoids

Author(s)McNamara, Hayley; Cai, Yeping; Wagle, Mayura, et al
TypeJournal article
Date Published2017
Date Created-

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