S. Bitam

发表

2D QSAR studies on a series of (4S,5R)-5-[3,5-bis(trifluoromethyl)phenyl]-4-methyl-1,3-oxazolidin-2-one as CETP inhibitors

M. Hamadache, S. Bitam, H. Salah, 2020, SAR and QSAR in environmental research.

Prediction of therapeutic potency of tacrine derivatives as BuChE inhibitors from quantitative structure–activity relationship modelling

S. Hanini, M. Hamadache, S. Bitam, 2018, SAR and QSAR in environmental research.

In silico model of the human ClC-Kb chloride channel: pore mapping, biostructural pathology and drug screening

B. Villoutreix, M. Miteva, D. Lagorce, 2017, Scientific Reports.

Keratin 8 is a scaffolding and regulatory protein of ERAD complexes

J. Irving, D. Lomas, G. Lukács, 2022, Cellular and Molecular Life Sciences.

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

J. Mornon, I. Sermet-Gaudelus, I. Callebaut, 2018, Human mutation.

Discovery of novel potent ΔF508-CFTR correctors that target the nucleotide binding domain

Piotr Zielenkiewicz, Grzegorz Wieczorek, Michal Dadlez, 2013, EMBO molecular medicine.

Study of new macroamorcors and grafted copolymers by ozonisation of poly(vinyliden fluoride)

S. Bitam, A. Djebaili, A. Serdani, 2010 .

Rattlesnake Phospholipase A2 Increases CFTR-Chloride Channel Current and Corrects ∆F508CFTR Dysfunction: Impact in Cystic Fibrosis.

P. Corringer, G. Lukács, F. Saul, 2016, Journal of molecular biology.

New insights into structure and function of bis-phosphinic acid derivatives and implications for CFTR modulation

J. Mornon, I. Sermet-Gaudelus, I. Callebaut, 2021, Scientific Reports.

Disruption of cytokeratin-8 interaction with F508del-CFTR corrects its functional defect.

G. Lukács, I. Guerrera, I. Sermet-Gaudelus, 2012, Human molecular genetics.

QSAR model for prediction of the therapeutic potency of N-benzylpiperidine derivatives as AChE inhibitors

S. Hanini, M. Hamadache, S. Bitam, 2017, SAR and QSAR in environmental research.

An unexpected effect of TNF-α on F508del-CFTR maturation and function

I. Sermet-Gaudelus, N. Servel, A. Edelman, 2015, F1000Research.

Analysis of CLCNKB mutations at dimer‐interface, calcium‐binding site, and pore reveals a variety of functional alterations in ClC‐Kb channel leading to Bartter syndrome

M. Paulais, M. Keck, J. Teulon, 2019, Human mutation.

Rattlesnake Phospholipase A2 Increases CFTR-Chloride Channel Current and Corrects ∆F508CFTR Dysfunction: Impact in Cystic Fibrosis.

P. Corringer, G. Lukács, F. Saul, 2016, Journal of molecular biology.

An unexpected effect of TNF-α on F508del-CFTR maturation and function.

I. Sermet-Gaudelus, N. Servel, A. Edelman, 2015, F1000Research.

M. Paulais, M. Keck, J. Teulon, 2020 .