B. Hainque

发表

Mechanism of adenovirus improvement of cationic liposome-mediated gene transfer.

M. Perricaudet, C. Meunier-Durmort, R. Picart, 1997, Biochimica et Biophysica Acta.

Efficient transfer of regulated genes in adipocytes and hepatoma cells by the combination of liposomes and replication-deficient adenovirus.

C. Meunier-Durmort, B. Hainque, C. Forest, 1996, European journal of biochemistry.

Hypertrophic Cardiomyopathy: Distribution of Disease Genes, Spectrum of Mutations, and Implications for a Molecular Diagnosis Strategy

M. Komajda, M. Desnos, J. Gueffet, 2003, Circulation.

COOH-terminal truncated cardiac myosin-binding protein C mutants resulting from familial hypertrophic cardiomyopathy mutations exhibit altered expression and/or incorporation in fetal rat cardiomyocytes.

B. Hainque, M. Souchet, K. Schwartz, 1999, Journal of molecular biology.

Systemic low-grade inflammation is related to both circulating and adipose tissue TNFα, leptin and IL-6 levels in obese women

E. Bruckert, J. Capeau, J. Bastard, 2004, International Journal of Obesity.

Plakophilin 2A is the dominant isoform in human heart tissue: consequences for the genetic screening of arrhythmogenic right ventricular cardiomyopathy

M. Komajda, B. Hainque, P. Charron, 2011, Heart.

Desmosomal gene analysis in arrhythmogenic right ventricular dysplasia/cardiomyopathy: spectrum of mutations and clinical impact in practice.

J. Deharo, Y. Lecarpentier, P. Cosnay, 2010, Europace.

Sporadic arrhythmogenic right ventricular cardiomyopathy/dysplasia due to a de novo mutation.

L. Faivre, R. Frank, G. Fontaine, 2009, Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology.

Adipose tissue IL-6 content correlates with resistance to insulin activation of glucose uptake both in vivo and in vitro.

E. Bruckert, J. Capeau, J. Bastard, 2002, The Journal of clinical endocrinology and metabolism.

Lack of association of the potassium channel–associated peptide MiRP2-R83H variant with periodic paralysis

B. Hainque, B. Fontaine, E. Fournier, 2003, Neurology.

Incorporation of non esterified fatty acids into QUICKI is not relevant in obese subjects during diet inducing weight loss.

R. Rabasa-Lhoret, E. Bruckert, M. Laville, 2002, Diabetes & metabolism.

Evidence for a relationship between plasminogen activator inhibitor-1 and gamma glutamyl transferase.

E. Bruckert, J. Bastard, B. Hainque, 1996, Thrombosis research.

Elevated levels of interleukin 6 are reduced in serum and subcutaneous adipose tissue of obese women after weight loss.

E. Bruckert, M. Laville, J. Capeau, 2000, The Journal of clinical endocrinology and metabolism.

C-terminal HERG mutations: the role of hypokalemia and a KCNQ1-associated mutation in cardiac event occurrence.

P. Coumel, E. Schulze-Bahr, B. Hainque, 1999, Circulation.

New KCNQ1 mutations leading to haploinsufficiency in a general population; Defective trafficking of a KvLQT1 mutant.

B. Balkau, S. Demolombe, B. Hainque, 2004, Cardiovascular research.

Intra-laboratory analytical variability of biochemical markers of fibrosis (Fibrotest) and activity (Actitest) and reference ranges in healthy blood donors

D. Thabut, B. Hainque, T. Poynard, 2004, Clinical chemistry and laboratory medicine.

Analytical study of three cystatin C assays and their impact on cystatin C-based GFR-prediction equations.

E. Cavalier, J. Chapelle, B. Hainque, 2008, Clinica chimica acta; international journal of clinical chemistry.

Peroxisome proliferator activated receptor‐γ, leptin and tumor necrosis factor‐α mRNA expression during very low calorie diet in subcutaneous adipose tissue in obese women

E. Bruckert, M. Laville, H. Vidal, 1999 .

Serum apolipoprotein A1 and haptoglobin, in patients with suspected drug-induced liver injury (DILI) as biomarkers of recovery

Y. Ngo, R. Andrade, M. Rudler, 2017, PloS one.

Are free fatty acids related to plasma plasminogen activator inhibitor 1 in android obesity?

E. Bruckert, J. Bastard, B. Hainque, 1995, International journal of obesity and related metabolic disorders : journal of the International Association for the Study of Obesity.

0021-972X/04/$15.00/0 The Journal of Clinical Endocrinology & Metabolism 89(6):2684–2689 Printed in U.S.A. Copyright © 2004 by The Endocrine Society doi: 10.1210/jc.2003-031978 Adiponutrin: A New Gene Regulated by Energy Balance

K. Clément, E. Bruckert, N. Viguerie, 2022 .

Evidence for a link between adipose tissue interleukin-6 content and serum C-reactive protein concentrations in obese subjects.

E. Bruckert, J. Bastard, B. Hainque, 1999, Circulation.

Increased adiponectin receptor-1 expression in adipose tissue of impaired glucose-tolerant obese subjects during weight loss.

K. Clément, E. Bruckert, J. Capeau, 2006, European journal of endocrinology.

Subcutaneous adipose tissue expression of plasminogen activator inhibitor-1 gene during very low calorie diet in obese subjects

E. Bruckert, H. Vidal, J. Bastard, 2000, International Journal of Obesity.

Percutaneous adipose tissue biopsy by mini-liposuction for metabolic studies.

J. Bastard, B. Hainque, C. Jardel, 1994, JPEN. Journal of parenteral and enteral nutrition.

Long term regulation of glucose transporters by insulin in mature 3T3-F442A adipose cells. Differential effects on two glucose transporter subtypes.

B. Hainque, M. Guerre-Millo, L. J. Wardzala, 1990, The Journal of biological chemistry.

Analysis of gene expression during adipogenesis in 3T3‐F442A preadipocytes: Insulin and dexamethasone control

B. Hainque, F. Lasnier, J. Pairault, 1990, Journal of cellular biochemistry.

A new mutation in PRKAG2 gene causing hypertrophic cardiomyopathy with conduction system disease and muscular glycogenosis

N. Romero, J. Hogrel, P. Laforêt, 2006, Neuromuscular Disorders.

A simple index of insulin resistance.

E. Bruckert, J. Bastard, B. Hainque, 1997, Diabetes & metabolism.

Hepatic stellate cell hypertrophy is associated with metabolic liver fibrosis

K. Clément, A. Danckaert, C. Hoffmann, 2020, Scientific Reports.

New mutations of SCN4A cause a potassium-sensitive normokalemic periodic paralysis

P. Laforêt, B. Eymard, T. Kuntzer, 2004, Neurology.

Codon 102 of the cardiac troponin T gene is a putative hot spot for mutations in familial hypertrophic cardiomyopathy.

M. Yacoub, M. Komajda, A. Hagège, 1996, Circulation.

Low incidence of cardiac events with beta-blocking therapy in children with long QT syndrome.

B. Hainque, P. Guicheney, I. Denjoy, 2004, European heart journal.

First description of germline mosaicism in familial hypertrophic cardiomyopathy

M. Komajda, C. Moraine, B. Hainque, 2000, Journal of medical genetics.

Severe neonatal non‐dystrophic myotonia secondary to a novel mutation of the voltage‐gated sodium channel (SCN4A) gene

L. Faivre, C. Thauvin-Robinet, B. Hainque, 2008, American journal of medical genetics. Part A.

Defective trafficking of a KvLQT1 mutant

B. Balkau, S. Demolombe, B. Hainque, 2004 .

Novel mutations in KvLQT 1 that affect I activation through interactionsks with Isk

J. Barhanin, B. Hainque, P. Guicheney, 2000 .

[T wave abnormalities on Holter monitoring of congenital long QT syndrome: phenotypic marker of a mutation of LQT2 (HERG)].

P. Coumel, B. Hainque, P. Guicheney, 2001, Archives des maladies du coeur et des vaisseaux.

Comparison of bathophenanthroline sulfonate and ferene as chromogens in colorimetric measurement of low hepatic iron concentration.

B. Hainque, T. Poynard, F. Charlotte, 2001, Clinical chemistry.

Hypokalaemic periodic paralysis type 2 caused by mutations at codon 672 in the muscle sodium channel gene SCN4A.

F. Lehmann-Horn, K. Jurkat-Rott, T. Maisonobe, 2001, Brain : a journal of neurology.

Dexamethasone regulation of terminal differentiation in 3T3-F442A preadipocyte cell line

B. Hainque, N. Moustaïd, A. Quignard‐Boulangé, 1988, Cytotechnology.

Glucocorticoid binding during the differentiation of 3T3-F442A fibroblasts into adipocytes. A possible regulatory effect of insulin.

B. Hainque, M. Lavau, B. Ardouin, 1987, Biochimica et biophysica acta.

Effects of dexamethasone on the growth of cultured rabbit articular chondrocytes:relation with the nuclear glucocorticoid-receptor complex.

X. Ronot, B. Hainque, M. Adolphe, 1987, Annals of the rheumatic diseases.

Familial hypertrophic cardiomyopathy: from mutations to functional defects.

B. Hainque, K. Schwartz, P. Richard, 1998, Circulation research.

PCR based mutation screening of the laminin alpha2 chain gene (LAMA2): application to prenatal diagnosis and search for founder effects in congenital muscular dystrophy.

V. Frey, J. Harpey, C. Cruaud, 1998, Journal of medical genetics.

Decreased expression of ABCD4 and BG1 genes early in the pathogenesis of X-linked adrenoleukodystrophy.

A. Moser, I. Bièche, M. Vidaud, 2005, Human molecular genetics.

[The microRNAs as biomarkers: What prospects?]

B. Hainque, C. Tse, S. Favard, 2017, Comptes rendus biologies.

Eicosapentaenoic acid induces mRNA expression of peroxisome proliferator-activated receptor gamma.

M. Laville, H. Vidal, J. Riou, 2002, Obesity research.

Cardiac myosin binding protein–C gene splice acceptor site mutation is associated with familial hypertrophic cardiomyopathy

J. Beckmann, J. Weissenbach, M. Komajda, 1995, Nature Genetics.

Organization and sequence of human cardiac myosin binding protein C gene (MYBPC3) and identification of mutations predicted to produce truncated proteins in familial hypertrophic cardiomyopathy.

M. Komajda, A. Hagège, M. Desnos, 1997, Circulation research.

In vitro aging of articular chondrocytes identified by analysis of DNA and tubulin content and relationship to cell size and protein content.

X. Ronot, B. Hainque, M. Adolphe, 1988, Cytometry.

G2 arrest, binucleation, and single-parameter DNA flow cytometric analysis.

C. Hecquet, X. Ronot, B. Hainque, 1986, Cytometry.

Female predominance and transmission distortion in the long-QT syndrome.

S. Priori, M. Imboden, C. Napolitano, 2006, The New England journal of medicine.

MOG1: A New Susceptibility Gene for Brugada Syndrome

A. Leenhardt, V. Probst, J. Schott, 2011, Circulation. Cardiovascular genetics.

Identification of the genotypes causing hypertrophic cardiomyopathy in northern Sweden.

U. Hellman, B. Hainque, K. Schwartz, 2003, Journal of molecular and cellular cardiology.

Long QT syndrome in neonates: conduction disorders associated with HERG mutations and sinus bradycardia with KCNQ1 mutations.

A. Bozio, B. Hainque, P. Guicheney, 2004, Journal of the American College of Cardiology.

Genomic organization of the KCNQ1 K+ channel gene and identification of C-terminal mutations in the long-QT syndrome.

P. Coumel, B. Hainque, P. Guicheney, 1999, Circulation research.

Identification of two novel mutations in the ventricular regulatory myosin light chain gene (MYL2) associated with familial and classical forms of hypertrophic cardiomyopathy

Pascale Richard, Philippe Charron, Gisèle Bonne, 1998, Journal of Molecular Medicine.

Genetic testing and genetic counselling in hypertrophic cardiomyopathy: the French experience

M. Komajda, M. Desnos, B. Hainque, 2002, Journal of medical genetics.

Overview of the diagnostic value of biochemical markers of liver fibrosis (FibroTest, HCV FibroSure) and necrosis (ActiTest) in patients with chronic hepatitis C

D. Thabut, B. Hainque, T. Poynard, 2004, Comparative hepatology.

Relationship between plasma plasminogen activator inhibitor 1 and insulin resistance

J. Bastard, B. Hainque, L. Piéroni, 2000, Diabetes/metabolism research and reviews.

Interpretation of circulating C-reactive protein levels in adults: body mass index and gender are a must.

J. Bastard, B. Hainque, C. Jardel, 2003, Diabetes & metabolism.

Effects of Glucocorticoid Immunosuppression on Se- Rum Cystatin C Concentrations in Renal Transplant

B. Hainque, T. Poynard, F. Charlotte, 2022 .

Deletion in the cardiac troponin I gene in a family from northern Sweden with hypertrophic cardiomyopathy.

B. Hainque, K. Schwartz, P. Richard, 2000, Journal of molecular and cellular cardiology.

Clinical features and prognostic implications of familial hypertrophic cardiomyopathy related to the cardiac myosin-binding protein C gene.

M. Komajda, A. Camproux, A. Hagège, 1998, Circulation.

Novel mutations in KvLQT1 that affect Iks activation through interactions with Isk.

J. Barhanin, B. Hainque, P. Guicheney, 2000, Cardiovascular research.

Hypokalemic Periodic Paralysis

P. Lory, S. Bendahhou, B. Hainque, 2014 .

Double heterozygosity for mutations in the β-myosin heavy chain and in the cardiac myosin binding protein C genes in a family with hypertrophic cardiomyopathy

M. Komajda, A. Hagège, B. Hainque, 1999, Journal of medical genetics.

Intra-individual fasting versus postprandial variation of biochemical markers of liver fibrosis (FibroTest) and activity (ActiTest)

D. Thabut, B. Hainque, T. Poynard, 2004, Comparative hepatology.

Hepatic stellate cell hypertrophy is associated with metabolic liver fibrosis

K. Clément, A. Danckaert, C. Hoffmann, 2020, Scientific Reports.

Variations in plasma soluble tumour necrosis factor receptors after diet‐induced weight loss in obesity

E. Bruckert, H. Vidal, J. Bastard, 2000, Diabetes, obesity & metabolism.

Regulation of glucose transporters in cultured rat adipocytes: synergistic effect of insulin and dexamethasone on GLUT4 gene expression through promoter activation.

É. Hajduch, B. Hainque, C. Jardel, 1995, Endocrinology.

Diagnostic value of electrocardiography and echocardiography for familial hypertrophic cardiomyopathy in genotyped children.

M. Komajda, A. Hagège, M. Desnos, 1998, European heart journal.

Possible founder effect of rapsyn N88K mutation and identification of novel rapsyn mutations in congenital myasthenic syndromes

A. Barois, B. Eymard, B. Hainque, 2003, Journal of medical genetics.

Homozygotes for a R869G mutation in the beta -myosin heavy chain gene have a severe form of familial hypertrophic cardiomyopathy.

J. Daubert, C. Leclercq, M. Komajda, 2000, Journal of molecular and cellular cardiology.

Effects ofdexamethasone on thegrowth ofcultured rabbit articular chondrocytes:relation

X. Ronot, B. Hainque, M. Adolphe, 1987 .

Electrochemical DNA-biosensors based on long-range electron transfer: optimization of the amperometric detection in the femtomolar range using two-electrode setup and ultramicroelectrode

E. Markova, P. Bigey, B. Hainque, 2016 .

Genotype‐phenotype analysis in four families with mutations in β‐myosin heavy chain gene responsible for familial hypertrophic cardiomyopathy

M. Komajda, M. Desnos, C. Cruaud, 1998, Human mutation.

RABBIT ARTICULAR CHONDROCYTES: AN IN VITRO MODEL FOR STUDYING THE EFFECT OF SODIUM AURO‐THIOPROPANOL SULFONATE ON PROLIFERATION KINETICS, TYPE II COLLAGEN PHENOTYPE AND MITOCHONDRIAL ACTIVITY

D. Hartmann, X. Ronot, B. Hainque, 1988, Fundamental & clinical pharmacology.

[Results transferability on RXL, ARX, X-Pand, BN2 (Dade Behring) and modular DP (Roche Diagnostics) analysers: application to component assays of fibrotest and Actitest].

B. Hainque, T. Poynard, F. Imbert‐Bismut, 2005, Annales de biologie clinique.

Peroxisome proliferator activated receptor-gamma, leptin and tumor necrosis factor-alpha mRNA expression during very low calorie diet in subcutaneous adipose tissue in obese women.

E. Bruckert, M. Laville, H. Vidal, 1999, Diabetes/metabolism research and reviews.

Notched T Waves on Holter Recordings Enhance Detection of Patients With LQT2 (HERG) Mutations

L. Demay, D. Klug, I. Denjoy, 2001, Circulation.

Abstract 2713: MOG1 Mutations Associated With Brugada Syndrome Electrocardiogram Pattern

B. Hainque, P. Guicheney, S. Maugenre, 2009 .

Analysis of the glucocorticoid receptor during differentiation of 3T3-F442A preadipocyte cell line in culture.

M. Agarwal, B. Hainque, N. Moustaid, 1990, Biochemical medicine and metabolic biology.

Response to the Letter by Kattygnarath et al

A. Leenhardt, V. Probst, J. Schott, 2011 .

The occurrence of Brugada syndrome and isolated cardiac conductive disease in the same family could be due to a single SCN5A mutation or to the accidental association of both diseases.

B. Hainque, P. Guicheney, I. Denjoy, 2007, Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology.

[Cellular energetic metabolism of cerebral tissue: metabolic characteristics of glial tumours].

F. Lamari, B. Hainque, J. Beaudeux, 2008, Annales de biologie clinique.

Is quantitative insulin sensitivity check index, a fair insulin sensitivity index in humans?

E. Bruckert, J. Bastard, B. Hainque, 2001, Diabetes & metabolism.

Penetrance of familial hypertrophic cardiomyopathy.

M. Komajda, M. Desnos, B. Hainque, 1997, Genetic counseling.

Familial hypertrophic cardiomyopathy: from mutations to functional defects.

B. Hainque, K. Schwartz, P. Richard, 1998, Circulation research.

224 INTEREST OF FIBROTEST-ACTITEST (FT-AT) IN THE FOLLOW-UP OF LIVER TRANSPLANTED (LT) PATIENTS: A PILOT STUDY

B. Hainque, T. Poynard, M. Munteanu, 2008 .

Differential analysis in Transcriptomic: The strength of randomly picking 'reference' genes

Y. Rozenholc, C. Hoffmann, B. Hainque, 2021, 2103.09872.

Clinical features and prognostic implications of familial hypertrophic cardiomyopathy related to the cardiac myosin-binding protein C gene.

M. Komajda, A. Camproux, A. Hagège, 1998, Circulation.

Desmosomal gene analysis in arrhythmogenic right ventricular dysplasia/cardiomyopathy: spectrum of mutations and clinical impact in practice.

J. Deharo, Y. Lecarpentier, P. Cosnay, 2010, Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology.

[The microRNAs as biomarkers: What prospects?]

B. Hainque, C. Tse, S. Favard, 2017, Comptes rendus biologies.

[Course of the concentration of serum free amino acids as a function of time and the method of preservation].

B. Hainque, S. Troupel, D. Gerbet, 1985, Annales de biologie clinique.

Subcutaneous adipose tissue expression of tumour necrosis factor‐α is not associated with whole body insulin resistance in obese nondiabetic or in type‐2 diabetic subjects

Laville, H. Koistinen, M. Laville, 2000, European journal of clinical investigation.

Elevated levels of interleukin 6 are reduced in serum and subcutaneous adipose tissue of obese women after weight loss.

E. Bruckert, M. Laville, J. Capeau, 2000, The Journal of clinical endocrinology and metabolism.

[Biochemical exploration of energetic metabolism and oxidative stress in low grade gliomas: central and peripheral tumor tissue analysis].

F. Lamari, B. Hainque, J. Beaudeux, 2008, Annales de biologie clinique.

Soluble transferrin receptor in hemochromatosis patients during phlebotomy therapy.

B. Hainque, C. Jardel, J. Thiolières, 2005, Clinica chimica acta; international journal of clinical chemistry.