BACKGROUND: Small Ubiquitin-like MOdifier protein (SUMO) is a key regulator of nuclear functions but little is known regarding the role of the post-translational modification sumoylation outside of the nucleus, particularly in the Central Nervous System (CNS). METHODOLOGY/PRINCIPAL FINDINGS: Here, we report that the expression levels of...
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2012 (v1)Journal articleUploaded on: October 11, 2023
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January 2013 (v1)Journal article
BACKGROUND INFORMATION: Sumoylation is a key post-translational modification by which the Small Ubiquitin-like MOdifier (SUMO) polypeptide is covalently attached to specific lysine residues of substrate proteins through a specific enzymatic pathway. Although sumoylation participates in the regulation of nuclear homeostasis, the sumoylation...
Uploaded on: December 3, 2022 -
January 2011 (v1)Journal article
We investigated the possible functional- and physical protein-interactions between two airway Cl(-) channels, SLC26A9 and CFTR. Bronchial CFBE41o-cell lines expressing CFTR(WT) or CFTR(DeltaF508) were transduced with SLC26A9. Immunoblots identified a migrating band corresponding to SLC26A9 present in whole cell lysates as on apical membrane of...
Uploaded on: December 3, 2022 -
2012 (v1)Journal article
BACKGROUND: Small Ubiquitin-like MOdifier protein (SUMO) is a key regulator of nuclear functions but little is known regarding the role of the post-translational modification sumoylation outside of the nucleus, particularly in the Central Nervous System (CNS). METHODOLOGY/PRINCIPAL FINDINGS: Here, we report that the expression levels of...
Uploaded on: December 2, 2022 -
January 2013 (v1)Journal article
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March 16, 2012 (v1)Journal article
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January 2013 (v1)Journal article
BACKGROUND INFORMATION: Sumoylation is a key post-translational modification by which the Small Ubiquitin-like MOdifier (SUMO) polypeptide is covalently attached to specific lysine residues of substrate proteins through a specific enzymatic pathway. Although sumoylation participates in the regulation of nuclear homeostasis, the sumoylation...
Uploaded on: October 11, 2023 -
December 2014 (v1)Journal article
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December 2014 (v1)Journal article
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December 2014 (v1)Journal article
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August 5, 2011 (v1)Journal article
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February 22, 2018 (v1)Journal article
Fragile X syndrome (FXS) is the most frequent inherited cause of intellectual disability and the best-studied monogenic cause of autism. FXS results from the functional absence of the fragile X mental retardation protein (FMRP) leading to abnormal pruning and consequently to synaptic communication defects. Here we show that FMRP is a substrate...
Uploaded on: December 4, 2022 -
December 2018 (v1)Journal article
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December 2018 (v1)Journal article
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December 2018 (v1)Journal article
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Uploaded on: February 22, 2023 -
December 2018 (v1)Journal article
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Uploaded on: December 4, 2022