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Compound heterozygous mutations in the kinase domain of IKKα lead to immunodeficiency and immune dysregulation.
medRxiv [Preprint]. 2024 May 17:2024.05.17.24307356. doi: 10.1101/2024.05.17.24307356.
medRxiv. 2024.
PMID: 38798321
Free PMC article.
Preprint.
A large deletion in a non-coding regulatory region leads to NFKB1 haploinsufficiency in two adult siblings.
Fusaro M, Coustal C, Barnabei L, Riller Q, Heller M, Ho Nhat D, Fourrage C, Rivière S, Rieux-Laucat F, Maria ATJ, Picard C.
Fusaro M, et al. Among authors: ho nhat d.
Clin Immunol. 2024 Apr;261:110165. doi: 10.1016/j.clim.2024.110165. Epub 2024 Feb 27.
Clin Immunol. 2024.
PMID: 38423196
Free article.
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Targeting a lineage-specific PI3Kɣ-Akt signaling module in acute myeloid leukemia using a heterobifunctional degrader molecule.
Kelly LM, Rutter JC, Lin KH, Ling F, Duchmann M, Latour E, Arang N, Pasquer H, Ho Nhat D, Charles J, Killarney ST, Ang HX, Namor F, Culeux C, Lombard B, Loew D, Swaney DL, Krogan NJ, Brunel L, Carretero É, Verdié P, Amblard M, Fodil S, Huynh T, Sebert M, Adès L, Raffoux E, Fenouille N, Itzykson R, Lobry C, Benajiba L, Forget A, Martin AR, Wood KC, Puissant A.
Kelly LM, et al. Among authors: ho nhat d.
Nat Cancer. 2024 Jul;5(7):1082-1101. doi: 10.1038/s43018-024-00782-5. Epub 2024 May 30.
Nat Cancer. 2024.
PMID: 38816660
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