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AN ASSOCIATION BETWEEN INTRONIC VARIANT OF ZINC TRANSPORTER 7 OF SLC30A7 GENE AND SALT-SENSITIVE HYPERTENSION IN CAUCASIAN POPULATION

Canadian journal of cardiology, 2023-10, Vol.39 (10), p.S19-S20

2023

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AN ASSOCIATION BETWEEN INTRONIC VARIANT OF ZINC TRANSPORTER 7 OF SLC30A7 GENE AND SALT-SENSITIVE HYPERTENSION IN CAUCASIAN POPULATION

Canadian journal of diabetes, 2023-11, Vol.47 (7), p.S1-S2

2023

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Guidelines for the study of familial dilated cardiomyopathies

European heart journal, 1999-01, Vol.20 (2), p.93-102

1999

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Differential Motif and Transcription Factor Binding Predictions Link to ULK4 Gene Polymorphisms and Associated with Essential Hypertension in Caucasian Females

Canadian journal of cardiology, 2023-05, Vol.39 (5), p.S7-S7

2023

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In vivo and in vitro examination of the functional significances of novel lamin gene mutations in heart failure patients

Journal of medical genetics, 2005-08, Vol.42 (8), p.639-647

2005

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A QUANTITATIVE ASSOCIATION BETWEEN A ULK4 GENE POLYMORPHISM AND ESSENTIAL HYPERTENSION IN CAUCASIAN FEMALES

Canadian journal of cardiology, 2021-10, Vol.37 (10), p.S4-S4

2021

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Somatic Mutations in the Connexin 40 Gene (GJA5) in Atrial Fibrillation

The New England journal of medicine, 2006-06, Vol.354 (25), p.2677-2688

2006

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Association between the NEDD4L rs4149601 single nucleotide polymorphism and early onset essential hypertension in Caucasian females: a case-control study

Canadian journal of cardiology, 2021-02, Vol.37 (2), p.e5-e5

2021

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When the département number becomes a vested symbol: an unexpected and involuntary ally in the resiliance of regional institutions

Annales de géographie, 2011-11, Vol.120 (682), p.673-682

Tesson, F

2011

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Influence of Pro12Ala peroxisome proliferator-activated receptor γ2 polymorphism on glucose response to exercise training in type 2 diabetes

Diabetologia, 2005-08, Vol.48 (8), p.1503-1509

2005

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Se reconnaître et se revendiquer comme ville moyenne : postures d'acteurs locaux en France, en Espagne et au Portugal dans le cadre du programme INTERREG ATI: Villes petites et moyennes

Norois, 2012 (223), p.31-42

TESSON, F

2012

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A New Locus for Autosomal Dominant Dilated Cardiomyopathy Identified on Chromosome 6q12-q16

American journal of human genetics, 2001, Vol.68 (1), p.241-246

2001

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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, 1997-02, Vol.29 (2), p.831-838

1997

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Identification of a genetic risk factor for idiopathic dilated cardiomyopathy. Involvement of a polymorphism in the endothelin receptor type A gene

European heart journal, 1999-11, Vol.20 (21), p.1587-1591

1999

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Decreased Mitochondrial Proton Leak and Reduced Expression of Uncoupling Protein 3 in Skeletal Muscle of Obese Diet-Resistant Women

Diabetes (New York, N.Y.), 2002-08, Vol.51 (8), p.2459-2466

2002

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Subcellular distribution of imidazoline-guanidinium-receptive sites in human and rabbit liver. Major localization to the mitochondrial outer membrane

The Journal of biological chemistry, 1991-01, Vol.266 (1), p.155-160

1991

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

European heart journal, 1998-09, Vol.19 (9), p.1377-1382

1998

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Mutations in the laminin α2-chain gene ( LAMA2 ) cause merosin-deficient congenital muscular dystrophy

Nature genetics, 1995-10, Vol.11 (2), p.216-218

1995

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Specific contribution of lamin A and lamin C in the development of laminopathies

Experimental cell research, 2008-08, Vol.314 (13), p.2362-2375

2008

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Mutations in the laminin alpha 2-chain gene (LAMA2) cause merosin-deficient congenital muscular dystrophy

Nature genetics, 1995-10, Vol.11 (2), p.216-218

1995

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Diagnostic value of electrocardiography and echocardiography for familial hypertrophic cardiomyopathy in a genotyped adult population

Circulation (New York, N.Y.), 1997-07, Vol.96 (1), p.214-219

1997

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Modalités et enjeux de l’insertion territoriale d’une université en ville moyenne. Approche à partir de la recherche scientifique à l’université de Pau et des Pays de l’Adour

Cybergeo, 2011 (570), p.1-20

2011

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Les ressources du département et du canton dans la petite fabrique des territoires

Annales de géographie, 2006, Vol.115 (648), p.197-216

TESSON, F

2006

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Penetrance of familial hypertrophic cardiomyopathy

Genetic counseling, 1997, Vol.8 (2), p.107

1997

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Localization of I2-imidazoline binding sites on monoamine oxidases

The Journal of biological chemistry, 1995-04, Vol.270 (17), p.9856-9861

1995

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AN ASSOCIATION BETWEEN INTRONIC VARIANT OF ZINC TRANSPORTER 7 OF SLC30A7 GENE AND SALT-SENSITIVE HYPERTENSION IN CAUCASIAN POPULATION

AN ASSOCIATION BETWEEN INTRONIC VARIANT OF ZINC TRANSPORTER 7 OF SLC30A7 GENE AND SALT-SENSITIVE HYPERTENSION IN CAUCASIAN POPULATION

Guidelines for the study of familial dilated cardiomyopathies

Differential Motif and Transcription Factor Binding Predictions Link to ULK4 Gene Polymorphisms and Associated with Essential Hypertension in Caucasian Females

In vivo and in vitro examination of the functional significances of novel lamin gene mutations in heart failure patients

A QUANTITATIVE ASSOCIATION BETWEEN A ULK4 GENE POLYMORPHISM AND ESSENTIAL HYPERTENSION IN CAUCASIAN FEMALES

Somatic Mutations in the Connexin 40 Gene (GJA5) in Atrial Fibrillation

Association between the NEDD4L rs4149601 single nucleotide polymorphism and early onset essential hypertension in Caucasian females: a case-control study

When the département number becomes a vested symbol: an unexpected and involuntary ally in the resiliance of regional institutions

Influence of Pro12Ala peroxisome proliferator-activated receptor γ2 polymorphism on glucose response to exercise training in type 2 diabetes

Se reconnaître et se revendiquer comme ville moyenne : postures d'acteurs locaux en France, en Espagne et au Portugal dans le cadre du programme INTERREG ATI: Villes petites et moyennes

A New Locus for Autosomal Dominant Dilated Cardiomyopathy Identified on Chromosome 6q12-q16

The Influence of the Angiotensin I Converting Enzyme Genotype in Familial Hypertrophic Cardiomyopathy Varies with the Disease Gene Mutation

Identification of a genetic risk factor for idiopathic dilated cardiomyopathy. Involvement of a polymorphism in the endothelin receptor type A gene

Decreased Mitochondrial Proton Leak and Reduced Expression of Uncoupling Protein 3 in Skeletal Muscle of Obese Diet-Resistant Women

Subcellular distribution of imidazoline-guanidinium-receptive sites in human and rabbit liver. Major localization to the mitochondrial outer membrane

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

Mutations in the laminin α2-chain gene ( LAMA2 ) cause merosin-deficient congenital muscular dystrophy

Specific contribution of lamin A and lamin C in the development of laminopathies

Mutations in the laminin alpha 2-chain gene (LAMA2) cause merosin-deficient congenital muscular dystrophy

Diagnostic value of electrocardiography and echocardiography for familial hypertrophic cardiomyopathy in a genotyped adult population

Modalités et enjeux de l’insertion territoriale d’une université en ville moyenne. Approche à partir de la recherche scientifique à l’université de Pau et des Pays de l’Adour

Les ressources du département et du canton dans la petite fabrique des territoires

Penetrance of familial hypertrophic cardiomyopathy

Localization of I2-imidazoline binding sites on monoamine oxidases

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