Items where authors include "Lawless, D"

Article

Lawless, D, Allen, HL, Thaventhiran, JED et al. (7 more authors) (2023) Prevalence of CFTR variants in PID patients with bronchiectasis - an important modifying co-factor. Journal of Allergy and Clinical Immunology, 152 (1). pp. 257-265. ISSN 0091-6749

Wu, B, Rice, L, Shrimpton, J et al. (9 more authors) (2021) Biallelic mutations in calcium release activated channel regulator 2A (CRACR2A) cause a primary immunodeficiency disorder. eLife, 10. e72559. ISSN 2050-084X

Stremenova Spegarova, J, Lawless, D orcid.org/0000-0001-8496-3725, Mohamad, SMB et al. (24 more authors) (2020) Germline TET2 loss of function causes childhood immunodeficiency and lymphoma. Blood, 136 (9). pp. 1055-1066. ISSN 0006-4971

Abolhassani, H, El-Sherbiny, YM orcid.org/0000-0003-4791-3475, Arumugakani, G et al. (12 more authors) (2020) Expanding Clinical Phenotype and Novel Insights into the Pathogenesis of ICOS Deficiency. Journal of Clinical Immunology, 40. pp. 277-288. ISSN 0271-9142

Lawless, D orcid.org/0000-0001-8496-3725, Lango Allen, H, Thaventhiran, J et al. (6 more authors) (2019) Predicting the Occurrence of Variants in RAG1 and RAG2. Journal of Clinical Immunology, 39 (7). pp. 688-701. ISSN 0271-9142

Thwaites, DT orcid.org/0000-0002-1504-7712, Carter, C, Lawless, D orcid.org/0000-0001-8496-3725 et al. (2 more authors) (2019) A novel RAG1 mutation reveals a critical in vivo role for HMGB1/2 during V(D)J recombination. Blood, 133 (8). pp. 820-829. ISSN 0006-4971

Lawless, D, Pathak, S, Scambler, TE et al. (3 more authors) (2018) A Case of Adult-Onset Still’s Disease Caused by a Novel Splicing Mutation in TNFAIP3 Successfully Treated With Tocilizumab. frontiers in Immunology, 9. ARTN 1527. ISSN 1664-3224

Lawless, D, Geier, CB, Farmer, JR et al. (43 more authors) (2018) Prevalence and clinical challenges among adults with primary immunodeficiency and recombination-activating gene deficiency. Journal of Allergy and Clinical Immunology, 141 (6). pp. 2303-2306. ISSN 0091-6749

Lawless, D orcid.org/0000-0001-8496-3725, Mistry, A, Wood, PM et al. (7 more authors) (2017) Bialellic Mutations in Tetratricopeptide Repeat Domain 7A (TTC7A) Cause Common Variable Immunodeficiency-Like Phenotype with Enteropathy. Journal of Clinical Immunology, 37 (7). pp. 617-622. ISSN 0271-9142

Masters, SL, Lagou, V, Jeru, I et al. (29 more authors) (2016) Familial autoinflammation with neutrophilic dermatosis reveals a regulatory mechanism of pyrin activation. Science Translational Medicine, 8 (322). RA45. ISSN 1946-6234