Callebaut I - Search Results

1

CFTR: New insights into structure and function and implications for modulation by small molecules.

Kleizen B, Hunt JF, Callebaut I, Hwang TC, Sermet-Gaudelus I, Hafkemeyer S, Sheppard DN. Kleizen B, et al. Among authors: callebaut i. J Cyst Fibros. 2020 Mar;19 Suppl 1:S19-S24. doi: 10.1016/j.jcf.2019.10.021. Epub 2019 Nov 21. J Cyst Fibros. 2020. PMID: 31759907 Free article.

2

Nucleotide binding domains of human CFTR: a structural classification of critical residues and disease-causing mutations.

Eudes R, Lehn P, Férec C, Mornon JP, Callebaut I. Eudes R, et al. Among authors: callebaut i. Cell Mol Life Sci. 2005 Sep;62(18):2112-23. doi: 10.1007/s00018-005-5224-y. Cell Mol Life Sci. 2005. PMID: 16132229

3

CFTR: effect of ICL2 and ICL4 amino acids in close spatial proximity on the current properties of the channel.

Billet A, Mornon JP, Jollivet M, Lehn P, Callebaut I, Becq F. Billet A, et al. Among authors: callebaut i. J Cyst Fibros. 2013 Dec;12(6):737-45. doi: 10.1016/j.jcf.2013.02.002. Epub 2013 Mar 9. J Cyst Fibros. 2013. PMID: 23478129 Free article.

4

Function, pharmacological correction and maturation of new Indian CFTR gene mutations.

Sharma H, Jollivet Souchet M, Callebaut I, Prasad R, Becq F. Sharma H, et al. Among authors: callebaut i. J Cyst Fibros. 2015 Jan;14(1):34-41. doi: 10.1016/j.jcf.2014.06.008. Epub 2014 Jul 16. J Cyst Fibros. 2015. PMID: 25042876 Free article.

5

Full-open and closed CFTR channels, with lateral tunnels from the cytoplasm and an alternative position of the F508 region, as revealed by molecular dynamics.

Mornon JP, Hoffmann B, Jonic S, Lehn P, Callebaut I. Mornon JP, et al. Among authors: callebaut i. Cell Mol Life Sci. 2015 Apr;72(7):1377-403. doi: 10.1007/s00018-014-1749-2. Epub 2014 Oct 7. Cell Mol Life Sci. 2015. PMID: 25287046

6

Impact of the F508del mutation on ovine CFTR, a Cl- channel with enhanced conductance and ATP-dependent gating.

Cai Z, Palmai-Pallag T, Khuituan P, Mutolo MJ, Boinot C, Liu B, Scott-Ward TS, Callebaut I, Harris A, Sheppard DN. Cai Z, et al. Among authors: callebaut i. J Physiol. 2015 Jun 1;593(11):2427-46. doi: 10.1113/JP270227. Epub 2015 Apr 9. J Physiol. 2015. PMID: 25763566 Free PMC article.

7

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.

8

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.

9

The implications of CFTR structural studies for cystic fibrosis drug development.

Callebaut I, Hoffmann B, Mornon JP. Callebaut I, et al. Curr Opin Pharmacol. 2017 Jun;34:112-118. doi: 10.1016/j.coph.2017.09.006. Epub 2017 Nov 5. Curr Opin Pharmacol. 2017. PMID: 29096277 Review.

10

Cis variants identified in F508del complex alleles modulate CFTR channel rescue by small molecules.

Baatallah N, Bitam S, Martin N, Servel N, Costes B, Mekki C, Chevalier B, Pranke I, Simonin J, Girodon E, Hoffmann B, Mornon JP, Callebaut I, Sermet-Gaudelus I, Fanen P, Edelman A, Hinzpeter A. Baatallah N, et al. Among authors: callebaut i. Hum Mutat. 2018 Apr;39(4):506-514. doi: 10.1002/humu.23389. Epub 2018 Jan 16. Hum Mutat. 2018. PMID: 29271547

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