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List of works by Andreas Perrot

"MLP: A Stress Sensor Goes Nuclear" by Sylvia Gunkel, Jörg Heineke, Denise Hilfiker-Kleiner, Ralph Knöll, J Mol Cell Cardiol. 2009;47(4):423-5.

scientific article published on 30 October 2009

A missense variant in desmoglein-2 predisposes to dilated cardiomyopathy

scientific article

A myomesin mutation associated with hypertrophic cardiomyopathy deteriorates dimerisation properties.

scientific article published on 20 January 2011

CCN1 mutation is associated with atrial septal defect.

scientific article published on 19 August 2014

Cardiac alpha-myosin (MYH6) is the predominant sarcomeric disease gene for familial atrial septal defects

scientific article published on 14 December 2011

Cardiac energetics correlates to myocardial hypertrophy in Friedreich's ataxia.

scientific article

Cardiomyopathy mutations reveal variable region of myosin converter as major element of cross-bridge compliance.

scientific article published on August 2009

Composite polymorphisms in the ryanodine receptor 2 gene associated with arrhythmogenic right ventricular cardiomyopathy.

scientific article published on 18 April 2006

Dilated cardiomyopathy: more genes means more phenotypes

scientific article published on 21 March 2005

Doubly heterozygous LMNA and TTN mutations revealed by exome sequencing in a severe form of dilated cardiomyopathy

scientific article published on 06 March 2013

Effects of ACE gene insertion/deletion polymorphism on response to spironolactone in patients with chronic heart failure.

scientific article published in May 2004

Fabry disease: focus on cardiac manifestations and molecular mechanisms.

scientific article published on November 2002

Familial dilated cardiomyopathy

scientific article published in September 2005

Gender-specific differences in major cardiac events and mortality in lamin A/C mutation carriers.

scientific article

Genetic and phenotypic analysis of dilated cardiomyopathy with conduction system disease: demand for strategies in the management of presymptomatic lamin A/C mutant carriers.

scientific article published on 4 January 2006

Hypertrophic cardiomyopathy-related beta-myosin mutations cause highly variable calcium sensitivity with functional imbalances among individual muscle cells

scientific article published on 18 November 2004

Hypertrophic remodelling in cardiac regulatory myosin light chain (MYL2) founder mutation carriers

scientific article published on 24 October 2015

Identification of mutational hot spots in LMNA encoding lamin A/C in patients with familial dilated cardiomyopathy

scientific article published on 15 September 2008

Intrinsic MYH7 expression regulation contributes to tissue level allelic imbalance in hypertrophic cardiomyopathy

scientific article published on 3 November 2017

Is there a common genetic basis for all familial cardiomyopathies?

scientific article published on 07 July 2006

Kardiale Manifestationen bei Muskeldystrophien

scientific article published on 01 May 2005

Letter by Geier et al regarding article, "Hypertrophic cardiomyopathy is predominantly a disease of left ventricular outflow tract obstruction"

scientific article published on 01 June 2007

Molecular genetics of congenital atrial septal defects

scientific article

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

scientific article published on 11 April 2016

Mutations in the cardiac transcription factor GATA4 in patients with lone atrial fibrillation.

scientific article published on 2 April 2010

Novel mutations in the sarcomeric protein myopalladin in patients with dilated cardiomyopathy.

scientific article published on 15 August 2012

Plasma HER2 levels are not associated with cardiac function or hypertrophy in control subjects and heart failure patients

scientific article published on 21 June 2009

Prevalence of cardiac beta-myosin heavy chain gene mutations in patients with hypertrophic cardiomyopathy

scientific article

Recurrent in-stent restenosis is not associated with the angiotensin-converting enzyme D/I, angiotensinogen Thr174Met and Met235Thr, and the angiotensin-II receptor 1 A1166C polymorphism.

scientific article published in June 2007

Returning hypertrophy after surgery in a patient with hypertrophic cardiomyopathy caused by a myosin-binding protein C mutation

scientific article published on 01 April 2005

Risk Factors for Malignant Ventricular Arrhythmias in Lamin A/C Mutation Carriers

scientific article published on 01 January 2012

Sequence analysis of myozenin 2 in 438 European patients with familial hypertrophic cardiomyopathy

scientific article published on 01 July 2008

Sudden cardiac death in familial hypertrophic cardiomyopathy. Identification of high-risk patients

scientific article published in May 2005

Systematic analysis of the regulatory and essential myosin light chain genes: genetic variants and mutations in hypertrophic cardiomyopathy

scientific article (publication date: November 2002)

TIP30 counteracts cardiac hypertrophy and failure by inhibiting translational elongation

scientific article published on 30 August 2019

The G-231A polymorphism in the endothelin-A receptor gene is associated with lower aortic pressure in patients with dilated cardiomyopathy

scientific article published on 01 January 2007

We need a detailed phenome in the phenomenon of genetics and congenital heart disease

article

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