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Page 1
CXCR4 Antagonist in HPV5-Associated Perianal Squamous-Cell Carcinoma.
Marin-Esteban V, Molet L, Laganà M, Ciocan D, Dominguez-Lafage C, Alouche N, Nguyen J, Gallego C, Mercier-Nomé F, Jaracz-Ros A, Beaupain B, Bouligand J, Proust A, Habib C, Bonnin RA, Girlich D, Fouyssac F, Schmutz JL, Bursztejn AC, Bellanné-Chantelot C, Bourrat E, Herfs M, Espéli M, Balabanian K, Schlecht-Louf G, Donadieu J, Bachelerie F, Deback C. Marin-Esteban V, et al. Among authors: beaupain b. N Engl J Med. 2024 Apr 11;390(14):1339-1341. doi: 10.1056/NEJMc2213180. N Engl J Med. 2024. PMID: 38598804 No abstract available.
CXCR4 WHIM syndrome is a cancer predisposition condition for virus-induced malignancies.
Moulin C, Beaupain B, Suarez F, Bertrand Y, Beaussant SC, Fischer A, Durin J, Ranta D, Espéli M, Bachelerie F, Bellanné-Chantelot C, Molina T, Emile JF, Balabanian K, Deback C, Donadieu J. Moulin C, et al. Among authors: beaupain b. Br J Haematol. 2024 Apr;204(4):1383-1392. doi: 10.1111/bjh.19373. Epub 2024 Mar 5. Br J Haematol. 2024. PMID: 38442908
Epidemiology of congenital neutropenia.
Donadieu J, Beaupain B, Mahlaoui N, Bellanné-Chantelot C. Donadieu J, et al. Among authors: beaupain b. Hematol Oncol Clin North Am. 2013 Feb;27(1):1-17, vii. doi: 10.1016/j.hoc.2012.11.003. Hematol Oncol Clin North Am. 2013. PMID: 23351985 Review.
Biallelic CXCR2 loss-of-function mutations define a distinct congenital neutropenia entity.
Marin-Esteban V, Youn J, Beaupain B, Jaracz-Ros A, Barlogis V, Fenneteau O, Leblanc T, Bellanger F, Pellet P, Buratti J, Lapillonne H, Bachelerie F, Donadieu J, Bellanné-Chantelot C. Marin-Esteban V, et al. Among authors: beaupain b. Haematologica. 2022 Mar 1;107(3):765-769. doi: 10.3324/haematol.2021.279254. Haematologica. 2022. PMID: 34854278 Free PMC article. No abstract available.
Description and outcome of a cohort of 8 patients with WHIM syndrome from the French Severe Chronic Neutropenia Registry.
Beaussant Cohen S, Fenneteau O, Plouvier E, Rohrlich PS, Daltroff G, Plantier I, Dupuy A, Kerob D, Beaupain B, Bordigoni P, Fouyssac F, Delezoide AL, Devouassoux G, Nicolas JF, Bensaid P, Bertrand Y, Balabanian K, Chantelot CB, Bachelerie F, Donadieu J. Beaussant Cohen S, et al. Among authors: beaupain b. Orphanet J Rare Dis. 2012 Sep 25;7:71. doi: 10.1186/1750-1172-7-71. Orphanet J Rare Dis. 2012. PMID: 23009155 Free PMC article.
High frequency of GATA2 mutations in patients with mild chronic neutropenia evolving to MonoMac syndrome, myelodysplasia, and acute myeloid leukemia.
Pasquet M, Bellanné-Chantelot C, Tavitian S, Prade N, Beaupain B, Larochelle O, Petit A, Rohrlich P, Ferrand C, Van Den Neste E, Poirel HA, Lamy T, Ouachée-Chardin M, Mansat-De Mas V, Corre J, Récher C, Plat G, Bachelerie F, Donadieu J, Delabesse E. Pasquet M, et al. Among authors: beaupain b. Blood. 2013 Jan 31;121(5):822-9. doi: 10.1182/blood-2012-08-447367. Epub 2012 Dec 6. Blood. 2013. PMID: 23223431 Free PMC article. Clinical Trial.
34 results