B. Costes

发表

IL-4 Is a Potent Modulator of Ion Transport in the Human Bronchial Epithelium In Vitro1

R. Ravazzolo, C. Folli, P. Pagésy, 2002, The Journal of Immunology.

Frequent Occurrence of the CFTR Intron 8 (TG)n 5T Allele in Men with Congenital Bilateral Absence of the Vas Deferens

E. Girodon, M. Goossens, E. Flori, 1995, European journal of human genetics : EJHG.

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

A. Hagège, J. Dubois-Randé, E. Donal, 2016, European heart journal.

Psoralen-modified oligonucleotide primers improve detection of mutations by denaturing gradient gel electrophoresis and provide an alternative to GC-clamping.

E. Girodon, M. Goossens, M. Chassignol, 1993, Human molecular genetics.

Partial C antigen in sickle cell disease patients: clinical relevance and prevention of alloimmunization

P. Bierling, Aurélie Barrault, Jennifer Martret, 2010, Transfusion.

High-dose pegylated interferon-α and ribavirin in nonresponder hepatitis C patients and relationship with IL-28B genotype (SYREN trial).

P. Couzigou, J. Pawlotsky, A. Mallat, 2011, Gastroenterology.

Hepatitis C Patients and Relationship with IL28B Genotype (SYREN Trial)

P. Couzigou, J. Pawlotsky, A. Mallat, 2011 .

Mutational Analysis of the Pro-opiomelanocortin Gene in French Obese Children Led to the Identification of a Novel Deleterious Heterozygous Mutation Located in the α-Melanocyte Stimulating Hormone Domain

K. Clément, C. Vaisse, P. Tounian, 2008, Pediatric Research.

Lack of Evidence of Heterozygosity for Cystic Fibrosis as a Risk Factor for Invasive Aspergillosis in Haematological Patients

E. Girodon, C. Cordonnier, S. Bretagne, 1999, European Journal of Clinical Microbiology and Infectious Diseases.

Factors influencing readthrough therapy for frequent cystic fibrosis premature termination codons

O. Namy, L. Bidou, Matthieu Coupet, 2018, ERJ Open Research.

Alternative Splicing of In‐Frame Exon Associated with Premature Termination Codons: Implications for Readthrough Therapies

L. Galietta, E. Girodon, E. Bieth, 2013, Human mutation.

Detection of cystic fibrosis transmembrane conductance regulator (CFTR) gene rearrangements enriches the mutation spectrum in congenital bilateral absence of the vas deferens and impacts on genetic counselling.

E. Girodon, M. Goossens, M. Legendre, 2007, Human reproduction.

in the Human Bronchial Epithelium In Vitro IL-4 Is a Potent Modulator of Ion Transport

R. Ravazzolo, C. Folli, P. Pagésy, 2001 .

Prenatal detection by real-time quantitative PCR and characterization of a new CFTR deletion, 3600+15kbdel5.3kb (or CFTRdele19).

M. Vidaud, D. Vidaud, E. Girodon, 2000, Clinical chemistry.

Estimation of the difference in HbF expression due to loss of the 5' δ-globin BCL11A binding region

D. Bachir, F. Galactéros, K. Moradkhani, 2013, Haematologica.

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

S. Simon, S. Finet, R. Epaud, 2020, British journal of clinical pharmacology.

Mechanistic study of thermal behaviour and combustion performance of epoxy resins. II. TGDDM/DDS system

G. Camino, L. Costa, M. Luda, 1995 .

Study of binary systems TlVO3-MVO3 : M = Li, Na

M. Touboul, B. Costes, Martine Villatte-Zambetti, 1985 .

Epoxy resins cured with aminophenylmethylphosphine oxide 1: Combustion performance

G. Camino, L. Costa, M. Luda, 1996 .

Thermal oxidative degradation of an epoxy resin

R. Delobel, M. Bras, B. Costes, 1993 .

Comprehensive study of the oxidative degradation of an epoxy resin using the degradation front model

S. Bourbigot, R. Delobel, M. Bras, 1996 .

Epoxy resins cured with aminophenylmethylphosphine oxide—II. Mechanism of thermal decomposition

G. Camino, L. Costa, M. Luda, 1998 .

Synthesis and formulation of novel phosphorylated flame retardant curatives for thermoset resins

B. Costes, M. Buckingham, E. Morel, 1996 .

Mechanistic study of thermal behavior and combustion performance of epoxy resins: I homopolymerized TGDDM

G. Camino, L. Costa, M. Luda, 1995 .

A rapid, efficient, and sensitive assay for simultaneous detection of multiple cystic fibrosis mutations

M. Goossens, N. Ghanem, B. Costes, 1993, Human mutation.

Polyvariant mutant cystic fibrosis transmembrane conductance regulator genes. The polymorphic (Tg)m locus explains the partial penetrance of the T5 polymorphism as a disease mutation.

M. Goossens, B. Nilius, G. Droogmans, 1998, The Journal of clinical investigation.

Haplotype analysis of 94 cystic fibrosis mutations with seven polymorphic CFTR DNA markers

X. Estivill, L. Tsui, J. Zieleński, 1996, Human mutation.

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

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

Spectroscopic characterization of 1,5-diphenyl-3,7-dihydroxy-1,5-diazacyclooctane — (8C ring compound) formed in N,N-diglycidylanaline/aniline curing systems

L. Matějka, K. Dušek, B. Costes, 1988 .

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

H. Wajcman, F. Galactéros, N. Arous, 1998 .

Combined Computational–Experimental Analyses of CFTR Exon Strength Uncover Predictability of Exon‐Skipping Level

E. Girodon, C. Vasseur, M. Goossens, 2013, Human mutation.

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

I. Sermet-Gaudelus, E. Girodon, J. Varilh, 2020, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

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

S. Simon, R. Epaud, X. Decrouy, 2017, European Journal of Human Genetics.

A recurrent deep-intronic splicing CF mutation emphasizes the importance of mRNA studies in clinical practice.

M. Claustres, R. Epaud, E. Girodon, 2011, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Molecular characterization of cystic fibrosis: 16 novel mutations identified by analysis of the whole cystic fibrosis conductance transmembrane regulator (CFTR) coding regions and splice site junctions.

M. Vidaud, M. Goossens, N. Ghanem, 1992, Genomics.

part of transcripts UTR ' expression via influence of MAPK cascades on 3 Cell-specific posttranscriptional regulation of CFTR gene

A. Edelman, A. Hinzpeter, B. Costes, 2016 .

Cell-specific posttranscriptional regulation of CFTR gene expression via influence of MAPK cascades on 3'UTR part of transcripts.

A. Edelman, A. Hinzpeter, F. Brouillard, 2005, American journal of physiology. Cell physiology.

Alternative Splicing at a NAGNAG Acceptor Site as a Novel Phenotype Modifier

Bruno Costes, E. Girodon, M. Goossens, 2010, PLoS genetics.

Identification of eight mutations and three sequence variations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene.

E. Girodon, M. Goossens, N. Ghanem, 1994, Genomics.

Rapid detection of CFTR gene rearrangements impacts on genetic counselling in cystic fibrosis

E. Girodon, M. Goossens, F. Niel, 2004, Journal of Medical Genetics.

Genetic characterization of Plasmodium falciparum allelic variants infecting mothers at delivery and their children during their first plasmodial infections.

André Garcia, F. Migot-Nabias, E. Renard, 2013, Infection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases.

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

P. Fergelot, D. Lacombe, I. Callebaut, 2017, Clinical case reports.

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

P. Fergelot, D. Lacombe, E. Girodon, 2016 .

Screening for cystic fibrosis in dried blood spots of newborns.

C. Férec, M. Audrézet, B. Mercier, 1993, Molecular and cellular probes.

CFTR Gene Mutations in Adults with Disseminated Bronchiectasis

B. Housset, C. Cazeneuve, F. Lebargy, 1997, European journal of human genetics : EJHG.

Twenty-Four Novel Hemophilia B Mutations Revealed by Rapid Scanning of the Whole Factor IX Gene in a French Population Sample

M. Vidaud, C. Rothschild, M. Goossens, 1993, European journal of human genetics : EJHG.

pic& Efficient9 and Sensitive Fibrosis tations

J. Mandel, M. Goossens, N. Ghanem, 2005 .

Erratum: Haplotype analysis of 94 cystic fibrosis mutations with seven polymorphic CFTR DNA markers (Human Mutation (1996) 8 (149-159))

X. Estivill, L. Tsui, J. Zieleński, 1996 .

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

S. Simon, R. Epaud, X. Decrouy, 2017, European Journal of Human Genetics.