Bruno Costes

INSERM U955, Univ Paris Est Créteil
Creteil, 94010, France

Last Updated: 09/26/2026

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Found 17 publications

Low C4A copy numbers and higher HERV gene insertion contributes to increased risk of SLE, with absence of association with disease phenotype and disease activity.

Low C4A copy numbers and higher HERV gene insertion contributes to increased risk of SLE, with absence of association with disease phenotype and disease activity.

Journal: Immunologic research
Published: January 18, 2024

Peptide CIGB-552 has a synergistic effect on CFTR-F508del when combined with elexacaftor/tezacaftor/ivacaftor triple therapy for cystic fibrosis.

Peptide CIGB-552 has a synergistic effect on CFTR-F508del when combined with elexacaftor/tezacaftor/ivacaftor triple therapy for cystic fibrosis.

Journal: British journal of pharmacology
Published: December 30, 2023

Low peripheral mitochondrial DNA copy number during manic episodes of bipolar disorders is associated with disease severity and inflammation.

Low peripheral mitochondrial DNA copy number during manic episodes of bipolar disorders is associated with disease severity and inflammation.

Journal: Brain, behavior, and immunity
Published: July 18, 2021

Methylprednisolone pulse treatment improves ProSP-C trafficking in twins with SFTPC mutation: An isoform story?

Methylprednisolone pulse treatment improves ProSP-C trafficking in twins with SFTPC mutation: An isoform story?

Journal: British journal of clinical pharmacology
Published: June 30, 2020

Exon identity influences splicing induced by exonic variants and in silico prediction efficacy.

Exon identity influences splicing induced by exonic variants and in silico prediction efficacy.

Journal: Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society
Published: March 27, 2020

Argon attenuates multiorgan failure following experimental aortic cross-clamping.

Argon attenuates multiorgan failure following experimental aortic cross-clamping.

Journal: British journal of clinical pharmacology
Published: August 21, 2017

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

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

Journal: Human mutation
Published: August 10, 2017

Factors influencing readthrough therapy for frequent cystic fibrosis premature termination codons.

Factors influencing readthrough therapy for frequent cystic fibrosis premature termination codons.

Journal: ERJ open research
Published: July 03, 2017

Deciphering the mechanism of Q145H SFTPC mutation unmasks a splicing defect and explains the severity of the phenotype.

Deciphering the mechanism of Q145H SFTPC mutation unmasks a splicing defect and explains the severity of the phenotype.

Journal: European journal of human genetics : EJHG
Published: October 08, 2016

A Brief Period of Hypothermia Induced by Total Liquid Ventilation Decreases End-Organ Damage and Multiorgan Failure Induced by Aortic Cross-Clamping.

A Brief Period of Hypothermia Induced by Total Liquid Ventilation Decreases End-Organ Damage and Multiorgan Failure Induced by Aortic Cross-Clamping.

Journal: Anesthesia and analgesia
Published: August 03, 2016

The importance of functional tests to assess the effect of a new CFTR variant when genotype-phenotype correlation is not possible.

The importance of functional tests to assess the effect of a new CFTR variant when genotype-phenotype correlation is not possible.

Journal: Clinical case reports
Published: March 07, 2016

Prevalence and clinical phenotype of hereditary transthyretin amyloid cardiomyopathy in patients with increased left ventricular wall thickness.

Prevalence and clinical phenotype of hereditary transthyretin amyloid cardiomyopathy in patients with increased left ventricular wall thickness.

Journal: European heart journal
Published: July 31, 2015
Showing 1-12 of 17

Last Updated: 09/26/2026