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

Year Number of Results
1991 2
1992 4
1993 4
1994 9
1995 2
1996 3
1997 7
1998 9
1999 5
2000 10
2001 12
2002 12
2003 10
2004 10
2005 12
2006 11
2007 8
2008 12
2009 6
2010 9
2011 8
2012 10
2013 13
2014 8
2015 8
2016 11
2017 19
2018 13
2019 9
2020 16
2021 18
2022 10
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Search Results

275 results
Results by year
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Page 1
CFTR structure.
Callebaut I, Chong PA, Forman-Kay JD. Callebaut I, et al. J Cyst Fibros. 2018 Mar;17(2S):S5-S8. doi: 10.1016/j.jcf.2017.08.008. Epub 2017 Aug 31. J Cyst Fibros. 2018. PMID: 28866450 Free article. Review.
Early-onset autoimmunity associated with SOCS1 haploinsufficiency.
Hadjadj J, Castro CN, Tusseau M, Stolzenberg MC, Mazerolles F, Aladjidi N, Armstrong M, Ashrafian H, Cutcutache I, Ebetsberger-Dachs G, Elliott KS, Durieu I, Fabien N, Fusaro M, Heeg M, Schmitt Y, Bras M, Knight JC, Lega JC, Lesca G, Mathieu AL, Moreews M, Moreira B, Nosbaum A, Page M, Picard C, Ronan Leahy T, Rouvet I, Ryan E, Sanlaville D, Schwarz K, Skelton A, Viallard JF, Viel S, Villard M, Callebaut I, Picard C, Walzer T, Ehl S, Fischer A, Neven B, Belot A, Rieux-Laucat F. Hadjadj J, et al. Among authors: callebaut i. Nat Commun. 2020 Oct 21;11(1):5341. doi: 10.1038/s41467-020-18925-4. Nat Commun. 2020. PMID: 33087723 Free PMC article.
Mutations in the SRP54 gene cause severe congenital neutropenia as well as Shwachman-Diamond-like syndrome.
Bellanné-Chantelot C, Schmaltz-Panneau B, Marty C, Fenneteau O, Callebaut I, Clauin S, Docet A, Damaj GL, Leblanc T, Pellier I, Stoven C, Souquere S, Antony-Debré I, Beaupain B, Aladjidi N, Barlogis V, Bauduer F, Bensaid P, Boespflug-Tanguy O, Berger C, Bertrand Y, Carausu L, Fieschi C, Galambrun C, Schmidt A, Journel H, Mazingue F, Nelken B, Quah TC, Oksenhendler E, Ouachée M, Pasquet M, Saada V, Suarez F, Pierron G, Vainchenker W, Plo I, Donadieu J. Bellanné-Chantelot C, et al. Among authors: callebaut i. Blood. 2018 Sep 20;132(12):1318-1331. doi: 10.1182/blood-2017-12-820308. Epub 2018 Jun 18. Blood. 2018. PMID: 29914977 Free PMC article.
Editorial: Hybrid Biomolecular Modeling.
Jonic S, Miyashita O, Callebaut I. Jonic S, et al. Among authors: callebaut i. Front Mol Biosci. 2018 Nov 9;5:98. doi: 10.3389/fmolb.2018.00098. eCollection 2018. Front Mol Biosci. 2018. PMID: 30474030 Free PMC article. No abstract available.
Structure-Based Understanding of ABCA3 Variants.
Onnée M, Fanen P, Callebaut I, de Becdelièvre A. Onnée M, et al. Among authors: callebaut i. Int J Mol Sci. 2021 Sep 24;22(19):10282. doi: 10.3390/ijms221910282. Int J Mol Sci. 2021. PMID: 34638622 Free PMC article.
Gain-of-function IKZF1 variants in humans cause immune dysregulation associated with abnormal T/B cell late differentiation.
Hoshino A, Boutboul D, Zhang Y, Kuehn HS, Hadjadj J, Özdemir N, Celkan T, Walz C, Picard C, Lenoir C, Mahlaoui N, Klein C, Peng X, Azar A, Reigh E, Cheminant M, Fischer A, Rieux-Laucat F, Callebaut I, Hauck F, Milner J, Rosenzweig SD, Latour S. Hoshino A, et al. Among authors: callebaut i. Sci Immunol. 2022 Mar 25;7(69):eabi7160. doi: 10.1126/sciimmunol.abi7160. Epub 2022 Mar 25. Sci Immunol. 2022. PMID: 35333544
Mechanism of MRX inhibition by Rif2 at telomeres.
Roisné-Hamelin F, Pobiega S, Jézéquel K, Miron S, Dépagne J, Veaute X, Busso D, Du ML, Callebaut I, Charbonnier JB, Cuniasse P, Zinn-Justin S, Marcand S. Roisné-Hamelin F, et al. Among authors: callebaut i. Nat Commun. 2021 May 12;12(1):2763. doi: 10.1038/s41467-021-23035-w. Nat Commun. 2021. PMID: 33980827 Free PMC article.
The uteroglobin fold.
Callebaut I, Poupon A, Bally R, Demaret JP, Housset D, Delettré J, Hossenlopp P, Mornon JP. Callebaut I, et al. Ann N Y Acad Sci. 2000;923:90-112. doi: 10.1111/j.1749-6632.2000.tb05522.x. Ann N Y Acad Sci. 2000. PMID: 11193783 Review.
Molecular modelling and molecular dynamics of CFTR.
Callebaut I, Hoffmann B, Lehn P, Mornon JP. Callebaut I, et al. Cell Mol Life Sci. 2017 Jan;74(1):3-22. doi: 10.1007/s00018-016-2385-9. Epub 2016 Oct 7. Cell Mol Life Sci. 2017. PMID: 27717958 Review.
Somatic genetic rescue of a germline ribosome assembly defect.
Tan S, Kermasson L, Hilcenko C, Kargas V, Traynor D, Boukerrou AZ, Escudero-Urquijo N, Faille A, Bertrand A, Rossmann M, Goyenechea B, Jin L, Moreil J, Alibeu O, Beaupain B, Bôle-Feysot C, Fumagalli S, Kaltenbach S, Martignoles JA, Masson C, Nitschké P, Parisot M, Pouliet A, Radford-Weiss I, Tores F, de Villartay JP, Zarhrate M, Koh AL, Phua KB, Reversade B, Bond PJ, Bellanné-Chantelot C, Callebaut I, Delhommeau F, Donadieu J, Warren AJ, Revy P. Tan S, et al. Among authors: callebaut i. Nat Commun. 2021 Aug 19;12(1):5044. doi: 10.1038/s41467-021-24999-5. Nat Commun. 2021. PMID: 34413298 Free PMC article.
275 results