Lista de obras - Eric Villard - Dominio Público Uruguay

A genetic study of angiotensin I-converting enzyme levels in human semen

artículo científico publicado en 1995

A genome-wide association study identifies 6p21 as novel risk locus for dilated cardiomyopathy

artículo científico publicado en 2013

A genome-wide association study identifies two loci associated with heart failure due to dilated cardiomyopathy

artículo científico publicado en 2011

A novel genetic variant in the transcription factor Islet-1 exerts gain of function on myocyte enhancer factor 2C promoter activity

artículo científico publicado en 2012

Angiotensin I-converting enzyme genotype influences arterial response to injury in normotensive rats.

artículo científico publicado en 1998

Atlas of the clinical genetics of human dilated cardiomyopathy

artículo científico publicado en 2015

Charcot-Marie-Tooth features and maculopathy in a patient with Danon disease

artículo científico publicado en 2004

Co-expression of PC2 and proenkephalin in human tumoral adrenal medullary tissues

artículo científico publicado en 1994

Contribution of exome sequencing for genetic diagnostic in arrhythmogenic right ventricular cardiomyopathy/dysplasia

artículo científico publicado en 2017

Cytochrome P450 2C19 loss-of-function polymorphism is a major determinant of clopidogrel responsiveness in healthy subjects

artículo científico publicado en 2006

Cytochrome P450 2C19 polymorphism in young patients treated with clopidogrel after myocardial infarction: a cohort study

artículo científico publicado en 2008

Danon's disease as a cause of hypertrophic cardiomyopathy: a systematic survey.

artículo científico publicado en 2004

Desmosomal cadherins are decreased in explanted arrhythmogenic right ventricular dysplasia/cardiomyopathy patient hearts

artículo científico publicado en 2013

Differential Sarcomere and Electrophysiological Maturation of Human iPSC-Derived Cardiac Myocytes in Monolayer vs. Aggregation-Based Differentiation Protocols

artículo científico publicado en 2017

Exome sequencing in arrhythmogenic right ventricular cardiomyopathy: a new diagnostic tool?

artículo científico publicado en 2017

Exome-wide association study reveals novel susceptibility genes to sporadic dilated cardiomyopathy

artículo científico publicado en 2017

Expanding the phenotype of LMNA mutations in dilated cardiomyopathy and functional consequences of these mutations.

artículo científico publicado en 2003

Expression of PC2 and PC1/PC3 in human pheochromocytomas

scientific article published on 01 March 1994

Genetic association study identifies HSPB7 as a risk gene for idiopathic dilated cardiomyopathy

artículo científico publicado en 2010

Identification of new polymorphisms of the angiotensin I-converting enzyme (ACE) gene, and study of their relationship to plasma ACE levels by two-QTL segregation-linkage analysis.

artículo científico publicado en 1996

Impact of ABCC2 polymorphisms on high-dose methotrexate pharmacokinetics in patients with lymphoid malignancy

artículo científico publicado en 2012

Induction of angiotensin I-converting enzyme transcription by a protein kinase C-dependent mechanism in human endothelial cells

artículo científico publicado en 1998

Involvement of BAG3 and HSPB7 loci in various etiologies of systolic heart failure: Results of a European collaboration assembling more than 2000 patients

artículo científico publicado en 2015

Molecular biology and genetics of the angiotensin-I-converting enzyme: potential implications in cardiovascular diseases.

artículo científico publicado en 1996

Mutation screening in dilated cardiomyopathy: prominent role of the beta myosin heavy chain gene

article

Mutational analysis of the beta- and delta-sarcoglycan genes in a large number of patients with familial and sporadic dilated cardiomyopathy

artículo científico publicado en 2003

Mutations in NEBL encoding the cardiac Z-disk protein nebulette are associated with various cardiomyopathies.

artículo científico publicado en 2016

Mutations in the ANKRD1 gene encoding CARP are responsible for human dilated cardiomyopathy

artículo científico publicado en 2009

Mutations in the Z-band protein myopalladin gene and idiopathic dilated cardiomyopathy

artículo científico publicado en 2007

Natural genetic variation of the cardiac transcriptome in non-diseased donors and patients with dilated cardiomyopathy.

artículo científico publicado en 2017

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

artículo científico publicado en 2011

Plakophilin-2 c.419C>T and risk of heart failure and arrhythmias in the general population

artículo científico publicado en 2015

Screening of genes encoding junctional candidates in arrhythmogenic right ventricular cardiomyopathy/dysplasia

artículo científico publicado en 2013

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

scientific article published on 16 January 2009

[Genetics and dilated cardiomyopathy]

artículo científico publicado en 2003

[Review: genetics of familial dilated cardiomyopathy]

artículo científico publicado en 2005

Lista de obras de Eric Villard

A genetic study of angiotensin I-converting enzyme levels in human semen

A genome-wide association study identifies 6p21 as novel risk locus for dilated cardiomyopathy

A genome-wide association study identifies two loci associated with heart failure due to dilated cardiomyopathy

A novel genetic variant in the transcription factor Islet-1 exerts gain of function on myocyte enhancer factor 2C promoter activity

Angiotensin I-converting enzyme genotype influences arterial response to injury in normotensive rats.

Atlas of the clinical genetics of human dilated cardiomyopathy

Charcot-Marie-Tooth features and maculopathy in a patient with Danon disease

Co-expression of PC2 and proenkephalin in human tumoral adrenal medullary tissues

Contribution of exome sequencing for genetic diagnostic in arrhythmogenic right ventricular cardiomyopathy/dysplasia

Cytochrome P450 2C19 loss-of-function polymorphism is a major determinant of clopidogrel responsiveness in healthy subjects

Cytochrome P450 2C19 polymorphism in young patients treated with clopidogrel after myocardial infarction: a cohort study

Danon's disease as a cause of hypertrophic cardiomyopathy: a systematic survey.

Desmosomal cadherins are decreased in explanted arrhythmogenic right ventricular dysplasia/cardiomyopathy patient hearts

Differential Sarcomere and Electrophysiological Maturation of Human iPSC-Derived Cardiac Myocytes in Monolayer vs. Aggregation-Based Differentiation Protocols

Exome sequencing in arrhythmogenic right ventricular cardiomyopathy: a new diagnostic tool?

Exome-wide association study reveals novel susceptibility genes to sporadic dilated cardiomyopathy

Expanding the phenotype of LMNA mutations in dilated cardiomyopathy and functional consequences of these mutations.

Expression of PC2 and PC1/PC3 in human pheochromocytomas

Genetic association study identifies HSPB7 as a risk gene for idiopathic dilated cardiomyopathy

Identification of new polymorphisms of the angiotensin I-converting enzyme (ACE) gene, and study of their relationship to plasma ACE levels by two-QTL segregation-linkage analysis.

Impact of ABCC2 polymorphisms on high-dose methotrexate pharmacokinetics in patients with lymphoid malignancy

Induction of angiotensin I-converting enzyme transcription by a protein kinase C-dependent mechanism in human endothelial cells

Involvement of BAG3 and HSPB7 loci in various etiologies of systolic heart failure: Results of a European collaboration assembling more than 2000 patients

Molecular biology and genetics of the angiotensin-I-converting enzyme: potential implications in cardiovascular diseases.

Mutation screening in dilated cardiomyopathy: prominent role of the beta myosin heavy chain gene

Mutational analysis of the beta- and delta-sarcoglycan genes in a large number of patients with familial and sporadic dilated cardiomyopathy

Mutations in NEBL encoding the cardiac Z-disk protein nebulette are associated with various cardiomyopathies.

Mutations in the ANKRD1 gene encoding CARP are responsible for human dilated cardiomyopathy

Mutations in the Z-band protein myopalladin gene and idiopathic dilated cardiomyopathy

Natural genetic variation of the cardiac transcriptome in non-diseased donors and patients with dilated cardiomyopathy.

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

Plakophilin-2 c.419C>T and risk of heart failure and arrhythmias in the general population

Screening of genes encoding junctional candidates in arrhythmogenic right ventricular cardiomyopathy/dysplasia

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

[Genetics and dilated cardiomyopathy]

[Review: genetics of familial dilated cardiomyopathy]