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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2014 2
2015 5
2016 1
2017 2
2018 10
2019 8
2020 4
2021 9
2022 3
2023 4
2024 2

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43 results

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Page 1
Involvement of the JAK-STAT pathway in the molecular landscape of tyrosine kinase fusion-negative hypereosinophilic syndromes: A nationwide CEREO study.
Groh M, Fenwarth L, Labro M, Boudry A, Fournier E, Wemeau M, Marceau-Renaut A, Daltro de Oliveira R, Abraham J, Barry M, Blanche P, Bodard Q, Braun T, Chebrek S, Decamp M, Durel CA, Forcade E, Gerfaud-Valentin M, Golfier C, Gourguechon C, Grardel N, Kosmider O, Martis N, Melboucy Belkhir S, Merabet F, Michon A, Moreau S, Morice C, Néel A, Nicolini FE, Pascal L, Pasquier F, Pieragostini A, Roche-Lestienne C, Rousselot P, Terriou L, Thiebaut-Bertrand A, Viallard JF, Preudhomme C, Kahn JE, Lefevre G, Duployez N; CEREO Collaborators. Groh M, et al. Among authors: marceau renaut a. Am J Hematol. 2024 Apr 2. doi: 10.1002/ajh.27306. Online ahead of print. Am J Hematol. 2024. PMID: 38563187
Three UBA1 clones for a unique VEXAS syndrome.
Podvin B, Cleenewerck N, Nibourel O, Marceau-Renaut A, Roynard P, Preudhomme C, Duployez N, Terriou L. Podvin B, et al. Among authors: marceau renaut a. Rheumatology (Oxford). 2024 Feb 1;63(2):e48-e50. doi: 10.1093/rheumatology/kead472. Rheumatology (Oxford). 2024. PMID: 37698981 No abstract available.
Prognostic impact of RUNX1 mutations and deletions in pediatric acute myeloid leukemia: results from the French ELAM02 study group.
Lew-Derivry L, Marceau-Renaut A, Fenwarth L, Cuccuini W, Ballerini P, Ferreboeuf M, Guilmatre A, Petit A, Gandemer V, Rialland F, Schneider P, Michel G, Bertrand Y, Baruchel A, Preudhomme C, Leverger G, Lapillonne H. Lew-Derivry L, et al. Among authors: marceau renaut a. Leukemia. 2023 Aug;37(8):1723-1726. doi: 10.1038/s41375-023-01931-y. Epub 2023 Jun 16. Leukemia. 2023. PMID: 37328541 Free PMC article. No abstract available.
UBTF tandem duplications define a distinct subtype of adult de novo acute myeloid leukemia.
Duployez N, Vasseur L, Kim R, Largeaud L, Passet M, L'Haridon A, Lemaire P, Fenwarth L, Geffroy S, Helevaut N, Celli-Lebras K, Adès L, Lebon D, Berthon C, Marceau-Renaut A, Cheok M, Lambert J, Récher C, Raffoux E, Micol JB, Pigneux A, Gardin C, Delabesse E, Soulier J, Hunault M, Dombret H, Itzykson R, Clappier E, Preudhomme C. Duployez N, et al. Among authors: marceau renaut a. Leukemia. 2023 Jun;37(6):1245-1253. doi: 10.1038/s41375-023-01906-z. Epub 2023 Apr 21. Leukemia. 2023. PMID: 37085611 Free PMC article.
Leon's helmet.
Gonzalez H, Marceau-Renaut A, Spentchian M, Hassoun M, Guignedoux G. Gonzalez H, et al. Among authors: marceau renaut a. Haematologica. 2023 May 1;108(5):1450-1451. doi: 10.3324/haematol.2022.281125. Haematologica. 2023. PMID: 36226490 Free PMC article. No abstract available.
Molecular heterogeneity and measurable residual disease of rare NPM1 mutations in acute myeloid leukemia: a nationwide experience from the GBMHM study group.
Fournier E, Heiblig M, Lespinasse C, Flandrin-Gresta P, Geay A, Miguet L, Fenwarth L, Vallat L, Soubeyrand B, Marceau-Renaut A, Plesa A, Preudhomme C, Sujobert P, Hayette S, Duployez N, Huet S. Fournier E, et al. Among authors: marceau renaut a. Leukemia. 2022 May;36(5):1390-1400. doi: 10.1038/s41375-022-01534-z. Epub 2022 Mar 7. Leukemia. 2022. PMID: 35256762 No abstract available.
Biological Effects of BET Inhibition by OTX015 (MK-8628) and JQ1 in NPM1-Mutated (NPM1c) Acute Myeloid Leukemia (AML).
Djamai H, Berrou J, Dupont M, Coudé MM, Delord M, Clappier E, Marceau-Renaut A, Kaci A, Raffoux E, Itzykson R, Berthier C, Wu HC, Hleihel R, Bazarbachi A, de Thé H, Baruchel A, Gardin C, Dombret H, Braun T. Djamai H, et al. Among authors: marceau renaut a. Biomedicines. 2021 Nov 17;9(11):1704. doi: 10.3390/biomedicines9111704. Biomedicines. 2021. PMID: 34829934 Free PMC article.
43 results