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N. Arous

French Institute of Health and Medical Research

68

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Role of COMMD1 and CSN5 in transcriptional regulation of the CFTR gene

2009 Journal of Cystic Fibrosis
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COMMD1 promotes CFTR trafficking through inhibition of ubiquitination

2009 Journal of Cystic Fibrosis
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Misprocessing of the CFTR protein leads to mild cystic fibrosis phenotype.

2005 Human Mutation
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Resveratrol, a natural dietary phytoalexin, possesses similar properties to hydroxyurea towards erythroid differentiation

2001 British Journal of Haematology
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Two Mild Cystic Fibrosis-associated Mutations Result in Severe Cystic Fibrosis When Combined in Cis and Reveal a Residue Important for Cystic Fibrosis Transmembrane Conductance Regulator Processing and Function

2001 Journal of Biological Chemistry
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Haemoglobin J-Biskra: a new mildly unstable α1 gene variant with a deletion of eight residues (α50–57, α51–58 or α52–59) including the distal histidine

1998 British Journal of Haematology
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A recombinant bisphosphoglycerate mutase variant with acid phosphatase homology degrades 2,3-diphosphoglycerate

1994 Proceedings of the National Academy of Sciences of the United States of America
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Hemoglobin Saint Mandé [β102 (G4) Asn→Tyr]

1990 FEBS Journal
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Human bisphosphoglycerate mutase. Expression in Escherichia coli and use of site-directed mutagenesis in the evaluation of the role of the carboxyl-terminal region in the enzymatic mechanism.

1989 Journal of Biological Chemistry
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Hemoglobin Koln occurring in association with a beta zero thalassemia: hematologic and functional consequences

1989 Blood
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