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Lucie Carrier

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Claudia Crocini; Alexandra Eder; Thomas Eschenhagen; Arne Hansen; Akinori Kimura; Silke Reischmann; Takuro Arimura; Ingke Braren; Lucie Carrier
Impact of ANKRD1 mutations associated with hypertrophic cardiomyopathy on contraction parameters of engineered heart tissue.
Felix W Friedrich; Laurent Gouya; Lucie Gueneau; Naima Hammoudi; Richard Isnard; Denise Juhr; Patricia Khattar; Michel Komajda; Pascale Richard; Eric Villard; Jean-Thomas Vilquin; Philippe Charron; Gilles Dilanian; Olivier Dubourg; Thomas Eschenhagen; Véronique Fressart; Gisèle Bonne; Lucie Carrier
A novel genetic variant in the transcription factor Islet-1 exerts gain of function on myocyte enhancer factor 2C promoter activity.
Sonia Donzelli; Jenna F DuMond; Thomas Eschenhagen; Gerry Fischer; Christian Gerloff; Jörg Heeren; Bruce S King; Christin Niemann; Hartwig Wieboldt; Stephan Baldus; Rainer H Böger; Lucie Carrier; Michael G Espey
Pharmacological characterization of 1-nitrosocyclohexyl acetate, a long-acting nitroxyl donor that shows vasorelaxant and antiaggregatory effects.

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2013: Claudia Crocini; Alexandra Eder; Thomas Eschenhagen; Arne Hansen; Akinori Kimura; Silke Reischmann; Takuro Arimura; Ingke Braren; Lucie Carrier
Impact of ANKRD1 mutations associated with hypertrophic cardiomyopathy on contraction parameters of engineered heart tissue.
Basic research in cardiology 2013;108(3):349.
2013: Felix W Friedrich; Laurent Gouya; Lucie Gueneau; Naima Hammoudi; Richard Isnard; Denise Juhr; Patricia Khattar; Michel Komajda; Pascale Richard; Eric Villard; Jean-Thomas Vilquin; Philippe Charron; Gilles Dilanian; Olivier Dubourg; Thomas Eschenhagen; Véronique Fressart; Gisèle Bonne; Lucie Carrier
A novel genetic variant in the transcription factor Islet-1 exerts gain of function on myocyte enhancer factor 2C promoter activity.
European journal of heart failure 2013;15(3):267-76.
2013: Sonia Donzelli; Jenna F DuMond; Thomas Eschenhagen; Gerry Fischer; Christian Gerloff; Jörg Heeren; Bruce S King; Christin Niemann; Hartwig Wieboldt; Stephan Baldus; Rainer H Böger; Lucie Carrier; Michael G Espey
Pharmacological characterization of 1-nitrosocyclohexyl acetate, a long-acting nitroxyl donor that shows vasorelaxant and antiaggregatory effects.
The Journal of pharmacology and experimental therapeutics 2013;344(2):339-47.
2013: Nicolas Vignier; Thomas Voit; Marie Montus; Isabelle Nelson; Jérôme Poupiot; Isabelle Richard; Laurent Servais; Fatima Amor; Michel AROCK; Gisèle Bonne; Lucie Carrier; Sabine Charrier; Angélique Duvallet; Paul Fogel; David Israeli
Distinctive serum miRNA profile in mouse models of striated muscular pathologies.
PloS one 2013;8(2):e55281.
2012: Felix W Friedrich; Lucie Carrier
Genetics of hypertrophic and dilated cardiomyopathy.
Current pharmaceutical biotechnology 2012;13(13):2467-76.
2012: Feriel Azibani; Ludovic Benard; Lucie Carrier; Christos Chatziantoniou; Loubina Fazal; Jean-Marie Launay; Regine Merval; Evelyne Polidano; Jane-Lise Samuel; Saskia Schlossarek; François Tournoux; Claude Delcayre
Aldosterone inhibits antifibrotic factors in mouse hypertensive heart.
Hypertension 2012;59(6):1179-87.
2012: Bodvaël Fraysse; Birgit Geertz; Jonathan C Kentish; Elisabeth Krämer; Jutta Starbatty; Nicolas Vignier; Florian Weinberger; Metin Avkiran; Sonya C Bardswell; Catherine Coirault; Friederike Cuello; Thomas Eschenhagen; Lucie Carrier
Increased myofilament Ca2+ sensitivity and diastolic dysfunction as early consequences of Mybpc3 mutation in heterozygous knock-in mice.
Journal of molecular and cellular cardiology 2012;52(6):1299-307.
2012: Florian Weinberger; Lucie Carrier; Sylvia M Evans; Felix W Friedrich; Xiaoqin Hua; Dennis Mehrkens; Jana Christina Müller; Sonja Schrepfer; Mandy Stubbendorff; Thomas Eschenhagen
Localization of Islet-1-positive cells in the healthy and infarcted adult murine heart.
Circulation research 2012;110(10):1303-10.
2012: Saskia Schlossarek; Friederike Schuermann; Thomas Eschenhagen; Birgit Geertz; Giulia Mearini; Lucie Carrier
Adrenergic stress reveals septal hypertrophy and proteasome impairment in heterozygous Mybpc3-targeted knock-in mice.
Journal of muscle research and cell motility 2012;33(1):5-15.
2012: Daniel Biermann; Rainer H Böger; Lucie Carrier; Michael Didié; Sonia Donzelli; Heimo Ehmke; Süleyman Ergün; Michael Grimm; Andreas Heilmann; Lutz Hein; Hermann Reichenspurner; Maria Römer; Saskia Schlossarek; Anna Steenpass; Karim R Sultan; Azadeh Wahab; Wolfram-Hubertus Zimmermann; Ralf A Benndorf
Impact of AT2 receptor deficiency on postnatal cardiovascular development.
PloS one 2012;7(10):e47916.
2011: Patricia Khattar; Felix W Friedrich; Gisèle Bonne; Lucie Carrier; Thomas Eschenhagen; Sylvia M Evans; Ketty Schwartz; Marc Y Fiszman; Jean-Thomas Vilquin
Distinction between two populations of islet-1-positive cells in hearts of different murine strains.
Stem cells and development 2011;20(6):1043-52.
2011: Catherine Meyer-Schwesinger; Tobias N Meyer; Henning Sievert; Elion Hoxha; Marlies Sachs; Eva-Maria Klupp; Silvia Münster; Stefan Balabanov; Lucie Carrier; Udo Helmchen; Friedrich Thaiss; Rolf A K Stahl
Ubiquitin C-terminal hydrolase-l1 activity induces polyubiquitin accumulation in podocytes and increases proteinuria in rat membranous nephropathy.
The American journal of pathology 2011;178(5):2044-57.
2010: Lucie Carrier
Too much of a good thing is bad: proteasome inhibition induces stressed hearts to fail.
Cardiovascular research 2010;88(3):389-90.
2010: Ali El-Armouche; Azadeh Wahab; Katrin Wittköpper; Thomas Schulze; Felix Böttcher; Lutz Pohlmann; S Bruce King; Jenna F DuMond; Christian Gerloff; Rainer H Böger; Thomas Eschenhagen; Lucie Carrier; Sonia Donzelli
The new HNO donor, 1-nitrosocyclohexyl acetate, increases contractile force in normal and β-adrenergically desensitized ventricular myocytes.
Biochemical and biophysical research communications 2010;402(2):340-4.
2010: Giulia Mearini; Christina Gedicke; Saskia Schlossarek; Christian C Witt; Elisabeth Krämer; Peirang Cao; Marcelo D Gomes; Stewart H Lecker; Siegfried Labeit; Monte Willis; Thomas Eschenhagen; Lucie Carrier
Atrogin-1 and MuRF1 regulate cardiac MyBP-C levels via different mechanisms.
Cardiovascular research 2010;85(2):357-66.
2010: Lucie Carrier; Saskia Schlossarek; Monte Willis; Thomas Eschenhagen
The ubiquitin-proteasome system and nonsense-mediated mRNA decay in hypertrophic cardiomyopathy.
Cardiovascular research 2010;85(2):330-8.
2009: Nicolas Vignier; Saskia Schlossarek; Bodvael Fraysse; Giulia Mearini; Elisabeth Krämer; Hervé Pointu; Nathalie Mougenot; Josiane Guiard; Rudolph Reimer; Heinrich Hohenberg; Ketty Schwartz; Muriel Vernet; Thomas Eschenhagen; Lucie Carrier
Nonsense-mediated mRNA decay and ubiquitin-proteasome system regulate cardiac myosin-binding protein C mutant levels in cardiomyopathic mice.
Circulation research 2009;105(3):239-48.
2009: Felix W Friedrich; Pedro Bausero; Yuli Sun; Andras Treszl; Elisabeth Krämer; Denise Juhr; Pascale Richard; Karl Wegscheider; Ketty Schwartz; Dulce Brito; Eloisa Arbustini; Anders Waldenström; Richard Isnard; Michel Komajda; Thomas Eschenhagen; Lucie Carrier
A new polymorphism in human calmodulin III gene promoter is a potential modifier gene for familial hypertrophic cardiomyopathy.
European heart journal 2009;30(13):1648-55.
2008: Giulia Mearini; Saskia Schlossarek; Monte Willis; Lucie Carrier
The ubiquitin-proteasome system in cardiac dysfunction.
Biochimica et biophysica acta 2008;1782(12):749-63.
2008: L M T Eijssen; B J C van den Bosch; Nicolas Vignier; Patrick J Lindsey; Caroline M M van den Burg; Lucie Carrier; Pieter A Doevendans; Ger J van der Vusse; H J M Smeets
Altered myocardial gene expression reveals possible maladaptive processes in heterozygous and homozygous cardiac myosin-binding protein C knockout mice.
Genomics 2008;91(1):52-60.
2007: Lutz Pohlmann; Irena Kröger; Nicolas Vignier; Saskia Schlossarek; Elisabeth Krämer; Catherine Coirault; Karim R Sultan; Ali El-Armouche; Saul Winegrad; Thomas Eschenhagen; Lucie Carrier
Cardiac myosin-binding protein C is required for complete relaxation in intact myocytes.
Circulation research 2007;101(9):928-38.
2007: Ali El-Armouche; Lutz Pohlmann; Saskia Schlossarek; Jutta Starbatty; Yung-Hsin Yeh; Stanley Nattel; Dobromir Dobrev; Thomas Eschenhagen; Lucie Carrier
Decreased phosphorylation levels of cardiac myosin-binding protein-C in human and experimental heart failure.
Journal of molecular and cellular cardiology 2007;43(2):223-9.
2007: Lucie Carrier
Cardiac myosin-binding protein C in the heart.
Archives des maladies du coeur et des vaisseaux 2007;100(3):238-43.
2006: Ali El-Armouche; Peter Boknik; Thomas Eschenhagen; Lucie Carrier; Michael Knaut; Ursula Ravens; Dobromir Dobrev
Molecular determinants of altered Ca2+ handling in human chronic atrial fibrillation.
Circulation 2006;114(7):670-80.
2006: olivier cazorla; Szabolcs Szilagyi; Nicolas Vignier; Guillermo Salazar; Elisabeth Krämer; Guy Vassort; Lucie Carrier; Alain Lacampagne
Length and protein kinase A modulations of myocytes in cardiac myosin binding protein C-deficient mice.
Cardiovascular research 2006;69(2):370-80.
2005: Jean-François Forissier; Philippe Charron; Sophie Tezenas du Montcel; Albert A Hagège; Richard Isnard; Lucie Carrier; Pascale Richard; Michel Desnos; Jean-Brieuc Bouhour; Ketty Schwartz; Michel Komajda; Olivier Dubourg
Diagnostic accuracy of a 2D left ventricle hypertrophy score for familial hypertrophic cardiomyopathy.
European heart journal 2005;26(18):1882-6.
2005: Andreas H Guse; Xianfeng Gu; Liangren Zhang; Karin Weber; Elisabeth Krämer; Zhenjun Yang; Hongwei Jin; Qin Li; Lucie Carrier; Lihe Zhang
A minimal structural analogue of cyclic ADP-ribose: synthesis and calcium release activity in mammalian cells.
The Journal of biological chemistry 2005;280(16):15952-9.
2005: Antonio Sarikas; Lucie Carrier; Carolus Schenke; Daniela Doll; Jeanne Flavigny; Katrin S Lindenberg; Thomas Eschenhagen; Oliver Zolk
Impairment of the ubiquitin-proteasome system by truncated cardiac myosin binding protein C mutants.
Cardiovascular research 2005;66(1):33-44.
2005: Thien Phong Vu Manh; Mustapha Mokrane; Emmanuelle Georgenthum; Jeanne Flavigny; Lucie Carrier; Michel Sémériva; Michel Piovant; Laurence Röder
Expression of cardiac myosin-binding protein-C (cMyBP-C) in Drosophila as a model for the study of human cardiomyopathies.
Human molecular genetics 2005;14(1):7-17.
2004: George B McClellan; Irina Kulikovskaya; Jeanne Flavigny; Lucie Carrier; Saul Winegrad
Effect of cardiac myosin-binding protein C on stability of the thick filament.
Journal of molecular and cellular cardiology 2004;37(4):823-35.
2004: Lucie Carrier; Ralph Knöll; Nicolas Vignier; Dagmar I Keller; Pedro Bausero; Bernard Prudhon; Richard Isnard; Marie-Lory Ambroisine; Marc Fiszman; John Ross; Ketty Schwartz; Kenneth R Chien
Asymmetric septal hypertrophy in heterozygous cMyBP-C null mice.
Cardiovascular research 2004;63(2):293-304.
2004: Dagmar I Keller; Catherine Coirault; Thomas Rau; Theary Cheav; Michael Weyand; Kerstin Amann; Yves Lecarpentier; Pascale Richard; Thomas Eschenhagen; Lucie Carrier
Human homozygous R403W mutant cardiac myosin presents disproportionate enhancement of mechanical and enzymatic properties.
Journal of molecular and cellular cardiology 2004;36(3):355-62.
2003: Irina Kulikovskaya; George B McClellan; Jeanne Flavigny; Lucie Carrier; Saul Winegrad
Effect of MyBP-C binding to actin on contractility in heart muscle.
The Journal of general physiology 2003;122(6):761-74.
2003: Jeanne Flavigny; Philippe Robert; Jean-Claude Camelin; Ketty Schwartz; Lucie Carrier; Isabelle Berrebi-Bertrand
Biomolecular interactions between human recombinant beta-MyHC and cMyBP-Cs implicated in familial hypertrophic cardiomyopathy.
Cardiovascular research 2003;60(2):388-96.
2003: Pascale Richard; Philippe Charron; Lucie Carrier; Céline Ledeuil; Theary Cheav; Claire Pichereau; Abdelaziz Benaiche; Richard Isnard; Olivier Dubourg; Marc Burban; Jean-Pierre Gueffet; Alain Millaire; Michel Desnos; Ketty Schwartz; Bernard Hainque; Michel Komajda
Hypertrophic cardiomyopathy: distribution of disease genes, spectrum of mutations, and implications for a molecular diagnosis strategy.
Circulation 2003;107(17):2227-32.
2002: Philippe Charron; Delphine Héron; Marcela Gargiulo; Pascale Richard; Olivier Dubourg; Michel Desnos; Jean-Brieuc Bouhour; Josué Feingold; Lucie Carrier; Bernard Hainque; Ketty Schwartz; Michel Komajda
Genetic testing and genetic counselling in hypertrophic cardiomyopathy: the French experience.
Journal of medical genetics 2002;39(10):741-6.
2002: Xavier Jouven; Albert A Hagege; Philippe Charron; Lucie Carrier; Olivier Dubourg; JM Langlard; S Aliaga; Jean-Brieuc Bouhour; Ketty Schwartz; Michel Desnos; Michel Komajda
Relation between QT duration and maximal wall thickness in familial hypertrophic cardiomyopathy.
Heart (British Cardiac Society) 2002;88(2):153-7.
2002: Dagmar I Keller; Lucie Carrier; Ketty Schwartz
Genetics of familial cardiomyopathies and arrhythmias.
Swiss medical weekly 2002;132(29-30):401-7.
2001: Pascale Sébillon; Gisèle Bonne; Jeanne Flavigny; S Venin; Andrée Rouche; Marc Fiszman; Karen Lynn Vikstrom; L Leinwand; Lucie Carrier; Ketty Schwartz
COOH-terminal truncated human cardiac MyBP-C alters myosin filament organization.
Comptes rendus de l'Académie des sciences. Série III, Sciences de la vie 2001;324(3):251-60.
2000: Pascale Richard; Philippe Charron; C Leclercq; Céline Ledeuil; Lucie Carrier; Olivier Dubourg; Michel Desnos; Jean-Brieuc Bouhour; Ketty Schwartz; J C Daubert; Michel Komajda; Bernard Hainque
Homozygotes for a R869G mutation in the beta -myosin heavy chain gene have a severe form of familial hypertrophic cardiomyopathy.
Journal of molecular and cellular cardiology 2000;32(8):1575-83.
2000: Jean-François Forissier; Pascale Richard; Sylvain Briault; Céline Ledeuil; Olivier Dubourg; Bernard Charbonnier; Lucie Carrier; Claude Moraine; Gisèle Bonne; Michel Komajda; Ketty Schwartz; Bernard Hainque
First description of germline mosaicism in familial hypertrophic cardiomyopathy.
Journal of medical genetics 2000;37(2):132-4.
1999: Jeanne Flavigny; Michel Souchet; Pascale Sébillon; Isabelle Berrebi-Bertrand; Bernard Hainque; A Mallet; Antoine Bril; Ketty Schwartz; Lucie Carrier
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.
Journal of molecular biology 1999;294(2):443-56.
1999: Pascale Richard; Richard Isnard; Lucie Carrier; Olivier Dubourg; Y Donatien; B Mathieu; Gisèle Bonne; F Gary; Philippe Charron; M Hagege; Michel Komajda; Ketty Schwartz; Bernard Hainque
Double heterozygosity for mutations in the beta-myosin heavy chain and in the cardiac myosin binding protein C genes in a family with hypertrophic cardiomyopathy.
Journal of medical genetics 1999;36(7):542-5.
1998: Gisèle Bonne; Lucie Carrier; Pascale Richard; Bernard Hainque; Ketty Schwartz
Familial hypertrophic cardiomyopathy: from mutations to functional defects.
Circulation research 1998;83(6):580-93.
1998: Philippe Charron; Olivier Dubourg; Michel Desnos; Jean-Brieuc Bouhour; Richard Isnard; Albert A Hagege; Lucie Carrier; Gisèle Bonne; Frédérique Tesson; Pascale Richard; Bernard Hainque; Ketty Schwartz; Michel Komajda
Diagnostic value of electrocardiography and echocardiography for familial hypertrophic cardiomyopathy in genotyped children.
European heart journal 1998;19(9):1377-82.
1998: Philippe Charron; Olivier Dubourg; Michel Desnos; Mohamed Bennaceur; Lucie Carrier; A C Camproux; Richard Isnard; Albert A Hagege; JM Langlard; Gisèle Bonne; Pascale Richard; Bernard Hainque; Jean-Brieuc Bouhour; Ketty Schwartz; Michel Komajda
Clinical features and prognostic implications of familial hypertrophic cardiomyopathy related to the cardiac myosin-binding protein C gene.
Circulation 1998;97(22):2230-6.
1998: H Farza; PJ Townsend; Lucie Carrier; Paul J R Barton; L Mesnard; E Bährend; Jean-François Forissier; Marc Fiszman; Magdi H Yacoub; Ketty Schwartz
Genomic organisation, alternative splicing and polymorphisms of the human cardiac troponin T gene.
Journal of molecular and cellular cardiology 1998;30(6):1247-53.
1998: Lucie Carrier; Gisèle Bonne; Ketty Schwartz
Cardiac Myosin-binding protein C and hypertrophic cardiomyopathy.
Trends in cardiovascular medicine 1998;8(4):151-7.
1998: Albert A Hagège; O Dubourg; Michel Desnos; R Mirochnik; G Isnard; Gisèle Bonne; Lucie Carrier; P Guicheney; Jean-Brieuc Bouhour; K Schwartz; M Komajda
Familial hypertrophic cardiomyopathy. Cardiac ultrasonic abnormalities in genetically affected subjects without echocardiographic evidence of left ventricular hypertrophy.
European heart journal 1998;19(3):490-9.
1998: Bing Yu; J A French; Lucie Carrier; Richmond W Jeremy; D R McTaggart; M R Nicholson; Brett D Hambly; Christopher Semsarian; David R Richmond; K Schwartz; Ronald J Trent
Molecular pathology of familial hypertrophic cardiomyopathy caused by mutations in the cardiac myosin binding protein C gene.
Journal of medical genetics 1998;35(3):205-10.
1998: Jeanne Flavigny; Pascale Richard; Richard Isnard; Lucie Carrier; Philippe Charron; Gisèle Bonne; Jean-François Forissier; Michel Desnos; Olivier Dubourg; Michel Komajda; Ketty Schwartz; Bernard Hainque
Identification of two novel mutations in the ventricular regulatory myosin light chain gene (MYL2) associated with familial and classical forms of hypertrophic cardiomyopathy.
Journal of molecular medicine (Berlin, Germany) 1998;76(3-4):208-14.
1998: Frédérique Tesson; Pascale Richard; Philippe Charron; B Mathieu; C Cruaud; Lucie Carrier; Olivier Dubourg; N Lautié; Michel Desnos; Alain Millaire; Richard Isnard; Albert A Hagege; Jean-Brieuc Bouhour; Mohamed Bennaceur; Bernard Hainque; Pascale Guicheney; Ketty Schwartz; Michel Komajda
Genotype-phenotype analysis in four families with mutations in beta-myosin heavy chain gene responsible for familial hypertrophic cardiomyopathy.
Human mutation 1998;12(6):385-92.
1998: Philippe Charron; Olivier Dubourg; Michel Desnos; Richard Isnard; Albert A Hagege; Gisèle Bonne; Lucie Carrier; Frédérique Tesson; Jean-Brieuc Bouhour; J C Buzzi; Josué Feingold; Ketty Schwartz; Michel Komajda
Genotype-phenotype correlations in familial hypertrophic cardiomyopathy. A comparison between mutations in the cardiac protein-C and the beta-myosin heavy chain genes.
European heart journal 1998;19(1):139-45.
1997: Philippe Charron; Olivier Dubourg; Michel Desnos; Richard Isnard; Albert A Hagege; Alain Millaire; Lucie Carrier; Gisèle Bonne; Frédérique Tesson; Pascale Richard; Jean-Brieuc Bouhour; Ketty Schwartz; Michel Komajda
Diagnostic value of electrocardiography and echocardiography for familial hypertrophic cardiomyopathy in a genotyped adult population.
Circulation 1997;96(1):214-9.
1997: Lucie Carrier; Gisèle Bonne; E Bährend; B Yu; Pascale Richard; F Niel; Bernard Hainque; C Cruaud; F Gary; Siegfried Labeit; Jean-Brieuc Bouhour; Olivier Dubourg; Michel Desnos; Albert A Hagège; R J Trent; Michel Komajda; Marc Fiszman; Ketty Schwartz
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.
Circulation research 1997;80(3):427-34.
1997: Frédérique Tesson; C Dufour; J C Moolman; Lucie Carrier; S al-Mahdawi; L Chojnowska; Olivier Dubourg; E Soubrier; P Brink; Michel Komajda; Pascale Guicheney; Ketty Schwartz; Josué Feingold
The influence of the angiotensin I converting enzyme genotype in familial hypertrophic cardiomyopathy varies with the disease gene mutation.
Journal of molecular and cellular cardiology 1997;29(2):831-8.
1997: Philippe Charron; Lucie Carrier; Olivier Dubourg; Frédérique Tesson; Michel Desnos; Pascale Richard; Gisèle Bonne; Pascale Guicheney; Bernard Hainque; Jean-Brieuc Bouhour; A Mallet; Josué Feingold; Ketty Schwartz; Michel Komajda
Penetrance of familial hypertrophic cardiomyopathy.
Genetic counseling (Geneva, Switzerland) 1997;8(2):107-14.
1996: Jean-François Forissier; Lucie Carrier; H Farza; Gisèle Bonne; J Bercovici; Pascale Richard; Bernard Hainque; PJ Townsend; M H Yacoub; S Fauré; Olivier Dubourg; Alain Millaire; Albert A Hagège; Michel Desnos; Michel Komajda; Ketty Schwartz
Codon 102 of the cardiac troponin T gene is a putative hot spot for mutations in familial hypertrophic cardiomyopathy.
Circulation 1996;94(12):3069-73.
1995: Gisèle Bonne; Lucie Carrier; J Bercovici; C Cruaud; Pascale Richard; Bernard Hainque; Mathias Gautel; Siegfried Labeit; M James; Jacques Beckmann; Jean Weissenbach; H P Vosberg; Marc Fiszman; Michel Komajda; Ketty Schwartz
Cardiac myosin binding protein-C gene splice acceptor site mutation is associated with familial hypertrophic cardiomyopathy.
Nature genetics 1995;11(4):438-40.
1995: Gisèle Bonne; Lucie Carrier; Ketty Schwartz; Michel Komajda
The COX8 gene is not the disease gene of the CMH4 locus in familial hypertrophic cardiomyopathy.
Journal of medical genetics 1995;32(8):670-1.
1995: Ketty Schwartz; Lucie Carrier; Pascale Guicheney; Michel Komajda
Molecular basis of familial cardiomyopathies.
Circulation 1995;91(2):532-40.
1994: C Hengstenberg; Lucie Carrier; K Schwartz; Bernhard Maisch
Clinical and genetical heterogeneity of familial hypertrophic cardiomyopathy.
Herz 1994;19(2):84-90.
1993: E Dausse; Michel Komajda; L Fetler; Olivier Dubourg; C Dufour; Lucie Carrier; C Wisnewsky; J Bercovici; C Hengstenberg; S al-Mahdawi
Familial hypertrophic cardiomyopathy. Microsatellite haplotyping and identification of a hot spot for mutations in the beta-myosin heavy chain gene.
The Journal of clinical investigation 1993;92(6):2807-13.
1993: Lucie Carrier; C Hengstenberg; Jacques Beckmann; Pascale Guicheney; C Dufour; J Bercovici; E Dausse; I Berebbi-Bertrand; C Wisnewsky; D Pulvenis
Mapping of a novel gene for familial hypertrophic cardiomyopathy to chromosome 11.
Nature genetics 1993;4(3):311-3.
1993: C Dufour; Lucie Carrier; C Hengstenberg; J Bercovici; E Dausse; J Weissenbach; Olivier Dubourg; Michel Komajda; Ketty Schwartz; Jacques Beckmann
Exclusion of genes coding for proteins of the cytoskeleton and the extracellular matrix in familial hypertrophic cardiomyopathy using a candidate gene approach.
Comptes rendus de l'Académie des sciences. Série III, Sciences de la vie 1993;316(5):474-81.
1993: Ketty Schwartz; C Chassagne; Lucie Carrier; Kenneth R Boheler
[Left ventricular hypertrophy: molecular aspects].
Archives des maladies du coeur et des vaisseaux 1993;86 Spec No 1():73-5.
1992: Lucie Carrier; C Chassagne; Kenneth R Boheler; Ketty Schwartz
[Molecular bases of cardiac aging].
Presse médicale (Paris, France : 1983) 1992;21(26):1196-8.
1992: Ketty Schwartz; Jacques Beckmann; C Dufour; L Faure; Françoise Fougerousse; Lucie Carrier; C Hengstenberg; D Cohen; H P Vosberg; A Sacrez
Exclusion of cardiac myosin heavy chain and actin gene involvement in hypertrophic cardiomyopathy of several French families.
Circulation research 1992;71(1):3-8.
1992: Lucie Carrier; Kenneth R Boheler; C Chassagne; D de la Bastie; C Wisnewsky; E G Lakatta; Ketty Schwartz
Expression of the sarcomeric actin isogenes in the rat heart with development and senescence.
Circulation research 1992;70(5):999-1005.
1992: Ketty Schwartz; Lucie Carrier; Anne-Marie Lompré; Jean-Jacques Mercadier; Kenneth R Boheler
Contractile proteins and sarcoplasmic reticulum calcium-ATPase gene expression in the hypertrophied and failing heart.
Basic research in cardiology 1992;87 Suppl 1():285-90.
1992: Ketty Schwartz; Lucie Carrier; C Chassagne; C Wisnewsky; Kenneth R Boheler
Regulation of myosin heavy chain and actin isogenes during cardiac growth and hypertrophy.
Symposia of the Society for Experimental Biology 1992;46():265-72.
1991: Kenneth R Boheler; Lucie Carrier; D de la Bastie; P D Allen; Michel Komajda; Jean-Jacques Mercadier; Ketty Schwartz
Skeletal actin mRNA increases in the human heart during ontogenic development and is the major isoform of control and failing adult hearts.
The Journal of clinical investigation 1991;88(1):323-30.
1991: Kenneth R Boheler; Lucie Carrier; C Chassagne; D de la Bastie; Jean-Jacques Mercadier; Ketty Schwartz
Regulation of myosin heavy chain and actin isogenes expression during cardiac growth.
Molecular and cellular biochemistry 1991;104(1-2):101-7.