Author

N. Aulner

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

Click to filter author papers

Immunology· 2 Cell Biology· 1 Microbiology· 1

Signature Assays, Organisms & Methods

Click to filter · or open tag

Approach:experimental assay· 4 Organism:human· 3 Assay:bulk RNA-seq· 2 Research Focus:cell type annotation· 2 Research Focus:host-pathogen & immune response· 2 Assay:proteomics· 2 Research Focus:chromatin & epigenetic regulation· 1 Research Focus:drug response / drug discovery· 1

Frequent Co-Authors

E. Prina· 2 shared G. F. Spaeth· 2 shared H. Lecoeur· 2 shared H. Varet· 2 shared A. Chansard· 1 shared A. Danckaert· 1 shared A. Giraud-Gatineau· 1 shared A. Mai· 1 shared

Activity by Year

2019-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 16 mutual co-author links

Click any collaborator node to inspect or filter shared papers

Focal author (center)Selected co-authorORCID co-authorUnlinked name

Curved chords = mutual co-authorship

2 shared papersImmunology

E. Prina

Mutual co-authors in cluster

Author profile →

4 papers

Recent·Most cited

An oxadiazole-based compound potentiates anti- tuberculosis treatment by increasing host resistance via zinc poisoning

A. Maure, E. Lawaree, F. Fiorentino, A. Pawlik, S. Gona, A. Giraud-Gatineau, M. J. G. Eldridge, A. Danckaert, D. Hardy, W. Frigui, C. Keck, N. Aulner, A. Mai, M. Hamon, L. B. Barreiro, , L. Tailleux

The paper identifies oxadiazole-based compounds that enhance anti-tuberculosis treatment by increasing host resistance through zinc poisoning of Mycobacterium tuberculosis.

bioRxiv · Jul 21, 2023 · PreprintMicrobiology

The m6A reader IGF2BP2 directs immune-metabolic reprogramming in Leishmania amazonensis-infected macrophages

S. Zhang, H. Lecoeur, H. Varet, R. Legendre, N. Mahtal, C. Proux, N. Aulner, S. Short, C. Grandjean, P. Bousso, E. Prina, G. F. Spaeth

This study identifies IGF2BP2 as an m6A reader that stabilizes glycolytic transcripts in Leishmania-infected macrophages, promoting HIF-1-independent glycolysis and immune-metabolic reprogramming.

bioRxiv · Sep 8, 2022 · PreprintImmunology

Unveiling the inter individual variability of human fibroblasts innate immune response using robust cell-based protocols

B. David-Watine, A. Chansard, M. Poujol de Molliens, N. Dubrulle, P. B. Falanga, T. Stephen, M. Hasan, G. van Zandbergen, N. Aulner, S. L. Shorte, Milieu interieur Consortium

This study develops standardized in vitro protocols to quantify inter-individual variability in human fibroblast innate immune responses using primary cells from a clinical cohort.

bioRxiv · Jun 4, 2020Immunology

Leishmania targets the macrophage epigenome and dampens the NF-κB/NLRP3- mediated inflammatory response

H. Lecoeur, E. Prina, T. Rosazza, K. Kokou, P. N'Diaye, N. Aulner, G. Bussotti, H. Varet, R. Weil, Y. Xing, G. X. Meng, G. F. Spaeth

This study shows Leishmania amazonensis modulates macrophage epigenetics to suppress NF-κB and NLRP3 inflammasome activation, aiding parasite survival.

bioRxiv · May 24, 2019 · PreprintCell Biology