Items where authors include "Werner, A"

Article

Ferrada, MA, Savic, S orcid.org/0000-0001-7910-0554, Ospina Cardona, D et al. (29 more authors) (2022) Translation of cytoplasmic UBA1 contributes to VEXAS syndrome pathogenesis. Blood, 140 (13). pp. 1496-1506. ISSN 0006-4971

Poulter, JA orcid.org/0000-0003-2048-5693, Collins, JC, Cargo, C et al. (12 more authors) (2021) Novel somatic mutations in UBA1 as a cause of VEXAS syndrome. Blood. ISSN 0006-4971

Klionsky, DJ, Abdel-Aziz, AK, Abdelfatah, S et al. (2926 more authors) (2021) Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition). Autophagy, 17 (1). pp. 1-382. ISSN 1554-8627

Beck, DB, Ferrada, MA, Sikora, KA et al. (59 more authors) (2020) Somatic Mutations in UBA1 and Severe Adult-Onset Autoinflammatory Disease. New England Journal of Medicine. NEJMoa2026834. ISSN 0028-4793

Jesson, CP, Pearce, CM, Simon, H et al. (6 more authors) (2017) H₂O₂ Enables Convenient Removal of RAFT End-Groups from Block Copolymer Nano-Objects Prepared via Polymerization-Induced Self-Assembly in Water. Macromolecules, 50 (1). pp. 182-191. ISSN 0024-9297

Conference or Workshop Item

Beck, D, Ferrada, M, Sikora, K et al. (19 more authors) (2020) Somatic Mutations in a Single Residue of UBA1 Cause VEXAS, a Severe Adult-Onset Rheumatic Disease Presenting as Relapsing Polychondritis, Polyarteritis Nodosa, or Giant Cell Arteritis. In: ACR Convergence 2020, 05-09 Nov 2020, Online.