Signal transducer and activator of transcription 5B deficiency due to a novel missense mutation in the coiled-coil domain by Acres, Meghan J., Gothe, Florian, Grainger, Angela, Skelton, Andrew J., Swan, David J., Willet, Joseph D.P., Leech, Suzy, Galcheva, Sonya, Iotova, Violeta, Hambleton, Sophie, Engelhardt, Karin R.

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Renal allograft rejection: Examination of delayed differentiation of Treg and Th17 effector T cells by Pekalski, Marcin, Jenkinson, Sarah E, Willet, Joseph D.P, Poyner, Elizabeth F.M, Alhamidi, Abdulaziz H, Robertson, Helen, Ali, Simi, Kirby, John A

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Defective Leukocyte Adhesion and Chemotaxis Contributes to Combined Immunodeficiency in Humans with Autosomal Recessive MST1 Deficiency by Dang, Tarana Singh, Willet, Joseph DP, Griffin, Helen R, Morgan, Neil V, O’Boyle, Graeme, Arkwright, Peter D, Hughes, Stephen M, Abinun, Mario, Tee, Louise J, Barge, Dawn, Engelhardt, Karin R, Jackson, Michael, Cant, Andrew J, Maher, Eamonn R, Koref, Mauro Santibanez, Reynard, Louise N, Ali, Simi, Hambleton, Sophie

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Chemokine receptor CXCR3 agonist prevents human T-cell migration in a humanized model of arthritic inflammation by O'Boyle, Graeme, Fox, Christopher R. J, Walden, Hannah R, Willet, Joseph D. P, Mavin, Emily R, Hine, Dominic W, Palmer, Jeremy M, Barker, Catriona E, Lamb, Christopher A, Ali, Simi, Kirby, John A

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Identification of Heterozygous Single- and Multi-exon Deletions in IL7R by Whole Exome Sequencing by Engelhardt, Karin R., Xu, Yaobo, Grainger, Angela, Germani Batacchi, Mila G. C., Swan, David J., Willet, Joseph D. P., Abd Hamid, Intan J., Agyeman, Philipp, Barge, Dawn, Bibi, Shahnaz, Jenkins, Lucy, Flood, Terence J., Abinun, Mario, Slatter, Mary A., Gennery, Andrew R., Cant, Andrew J., Santibanez Koref, Mauro, Gilmour, Kimberly, Hambleton, Sophie

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NUDCD3 deficiency disrupts V(D)J recombination to cause SCID and Omenn syndrome by Chen, Rui, Lukianova, Elena, van der Loeff, Ina Schim, Spegarova, Jarmila Stremenova, Willet, Joseph D P, James, Kieran D, Ryder, Edward J, Griffin, Helen, IJspeert, Hanna, Gajbhiye, Akshada, Lamoliatte, Frederic, Marin-Rubio, Jose L, Woodbine, Lisa, Lemos, Henrique, Swan, David J, Pintar, Valeria, Sayes, Kamal, Ruiz-Morales, Elias R, Eastham, Simon, Dixon, David, Prete, Martin, Prigmore, Elena, Jeggo, Penny, Boyes, Joan, Mellor, Andrew, Huang, Lei, van der Burg, Mirjam, Engelhardt, Karin R, Stray-Pedersen, Asbjørg, Erichsen, Hans Christian, Gennery, Andrew R, Trost, Matthias, Adams, David J, Anderson, Graham, Lorenc, Anna, Trynka, Gosia, Hambleton, Sophie

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Erratum to: Defective Leukocyte Adhesion and Chemotaxis Contributes to Combined Immunodeficiency in Humans with Autosomal Recessive MST1 Deficiency by Dang, Tarana Singh, Willet, Joseph D. P., Griffin, Helen R., Morgan, Neil V., O’Boyle, Graeme, Arkwright, Peter D., Hughes, Stephen M., Abinun, Mario, Tee, Louise J., Barge, Dawn, Engelhardt, Karin R., Jackson, Michael, Cant, Andrew J., Maher, Eamonn R., Koref, Mauro Santibanez, Reynard, Louise N., Ali, Simi, Hambleton, Sophie

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