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Page 1
Functional characterization of HNF4A gene variants identify promoter and cell line specific transactivation effects.
Kaci A, Solheim MH, Silgjerd T, Hjaltadottir J, Hornnes LH, Molnes J, Madsen A, Sjøholt G, Bellanné-Chantelot C, Caswell R, Sagen JV, Njølstad PR, Aukrust I, Bjørkhaug L. Kaci A, et al. Among authors: bellanne chantelot c. Hum Mol Genet. 2024 May 4;33(10):894-904. doi: 10.1093/hmg/ddae027. Hum Mol Genet. 2024. PMID: 38433330 Free PMC article.
Molecular mechanism of HNF-1A-mediated HNF4A gene regulation and promoter-driven HNF4A-MODY diabetes.
Kind L, Molnes J, Tjora E, Raasakka A, Myllykoski M, Colclough K, Saint-Martin C, Adelfalk C, Dusatkova P, Pruhova S, Valtonen-André C, Bellanné-Chantelot C, Arnesen T, Kursula P, Njølstad PR. Kind L, et al. Among authors: bellanne chantelot c. JCI Insight. 2024 Jun 10;9(11):e175278. doi: 10.1172/jci.insight.175278. JCI Insight. 2024. PMID: 38855865 Free PMC article.
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: bellanne chantelot c. 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: bellanne chantelot c. Br J Haematol. 2024 Apr;204(4):1383-1392. doi: 10.1111/bjh.19373. Epub 2024 Mar 5. Br J Haematol. 2024. PMID: 38442908
Somatic genetic alterations predict hematological progression in GATA2 deficiency.
Largeaud L, Collin M, Monselet N, Vergez F, Fregona V, Larcher L, Hirsch P, Duployez N, Bidet A, Luquet I, Bustamante J, Dufrechou S, Prade N, Nolla M, Hamelle C, Tavitian S, Habib C, Meynier M, Bellanne-Chantelot C, Donadieu J, De Fontbrune FS, Fieschi C, Ferster A, Delhommeau F, Delabesse E, Pasquet M. Largeaud L, et al. Among authors: bellanne chantelot c. Haematologica. 2023 Jun 1;108(6):1515-1529. doi: 10.3324/haematol.2022.282250. Haematologica. 2023. PMID: 36727400 Free PMC article.
Fertility and pregnancy outcomes in women with nonclassic 21-hydroxylase deficiency.
Carrière C, Nguyen LS, Courtillot C, Tejedor I, Chakhtoura Z, Bellanné-Chantelot C, Tardy V, Leban M, Touraine P, Bachelot A. Carrière C, et al. Among authors: bellanne chantelot c. Clin Endocrinol (Oxf). 2023 Mar;98(3):315-322. doi: 10.1111/cen.14842. Epub 2022 Nov 17. Clin Endocrinol (Oxf). 2023. PMID: 36325983
Variants influencing age at diagnosis of HNF1A-MODY.
Ludwig-Słomczyńska AH, Seweryn MT, Radkowski P, Kapusta P, Machlowska J, Pruhova S, Gasperikova D, Bellanne-Chantelot C, Hattersley A, Kandasamy B, Letourneau-Freiberg L, Philipson L, Doria A, Wołkow PP, Małecki MT, Klupa T. Ludwig-Słomczyńska AH, et al. Among authors: bellanne chantelot c. Mol Med. 2022 Sep 14;28(1):113. doi: 10.1186/s10020-022-00542-0. Mol Med. 2022. PMID: 36104811 Free PMC article.
200 results