Lista de obras -

A Cypher/ZASP mutation associated with dilated cardiomyopathy alters the binding affinity to protein kinase C.

artículo científico publicado en 2003

A novel disease gene for Brugada syndrome: sarcolemmal membrane-associated protein gene mutations impair intracellular trafficking of hNav1.5.

artículo científico publicado en 2012

A novel link of HLA locus to the regulation of immunity and infection: NFKBIL1 regulates alternative splicing of human immune-related genes and influenza virus M gene ⬇️

artículo científico publicado el 14 de agosto de 2013

A novel protein found in the I bands of myofibrils is produced by alternative splicing of the DLST gene

artículo científico publicado en 2009

ANKRD1, the gene encoding cardiac ankyrin repeat protein, is a novel dilated cardiomyopathy gene

artículo científico publicado en 2009

Alpha B-crystallin mutation in dilated cardiomyopathy

article by Natsuko Inagaki et al published 7 April 2006 in Biochemical and Biophysical Research Communications

Autophagic degradation of nuclear components in mammalian cells

artículo científico publicado en 2009

Cardiac ankyrin repeat protein gene (ANKRD1) mutations in hypertrophic cardiomyopathy

artículo científico publicado en 2009

DelK32-lamin A/C has abnormal location and induces incomplete tissue maturation and severe metabolic defects leading to premature death

artículo científico publicado en 2011

Dilated cardiomyopathy-associated BAG3 mutations impair Z-disc assembly and enhance sensitivity to apoptosis in cardiomyocytes

artículo científico publicado el 29 de septiembre de 2011

Endothelin-1 induces myofibrillar disarray and contractile vector variability in hypertrophic cardiomyopathy-induced pluripotent stem cell-derived cardiomyocytes

artículo científico publicado en 2014

Functional characterization of a trafficking-defective HCN4 mutation, D553N, associated with cardiac arrhythmia

artículo científico publicado en 2004

Genetic defects in a His-Purkinje system transcription factor, IRX3, cause lethal cardiac arrhythmias.

artículo científico publicado en 2015

Genetics of Laminopathies

article

Genetics of laminopathies.

artículo científico publicado en 2005

Heart-specific small subunit of myosin light chain phosphatase activates rho-associated kinase and regulates phosphorylation of myosin phosphatase target subunit 1.

artículo científico publicado en 2010

Hypertrophic Cardiomyopathy Accompanied by Spinocerebellar Atrophy With a Novel Mutation in Troponin I Gene

artículo científico publicado en 2016

Identification and functional analysis of a caveolin-3 mutation associated with familial hypertrophic cardiomyopathy

artículo científico publicado en 2004

Impact of ANKRD1 mutations associated with hypertrophic cardiomyopathy on contraction parameters of engineered heart tissue.

artículo científico publicado en 2013

Impaired binding of ZASP/Cypher with phosphoglucomutase 1 is associated with dilated cardiomyopathy

scientific journal article

Improvement of Left Ventricular Dysfunction and of Survival Prognosis of Dilated Cardiomyopathy by Administration of Calcium Sensitizer SCH00013 in a Mouse Model

artículo científico publicado en 2010

Interaction of BMP10 with Tcap may modulate the course of hypertensive cardiac hypertrophy

artículo científico publicado en 2007

Megakaryoblastic leukemia factor-1 gene in the susceptibility to coronary artery disease

artículo científico publicado en 2009

Molecular basis for clinical heterogeneity in inherited cardiomyopathies due to myopalladin mutations

artículo científico publicado en 2012

Mouse model carrying H222P- Lmna mutation develops muscular dystrophy and dilated cardiomyopathy similar to human striated muscle laminopathies

artículo científico publicado en 2004

Mutational analysis of fukutin gene in dilated cardiomyopathy and hypertrophic cardiomyopathy

artículo científico publicado en 2009

Nebulette Mutations Are Associated With Dilated Cardiomyopathy and Endocardial Fibroelastosis ⬇️

artículo científico publicado el 26 de octubre de 2010

Novel SCN3B mutation associated with brugada syndrome affects intracellular trafficking and function of Nav1.5.

artículo científico publicado en 2012

Novel mechanisms of trafficking defect caused by KCNQ1 mutations found in long QT syndrome.

artículo científico publicado en 2009

Novel mutation in the α-myosin heavy chain gene is associated with sick sinus syndrome

artículo científico publicado en 2015

Nuclear accumulation of androgen receptor in gender difference of dilated cardiomyopathy due to lamin A/C mutations.

artículo científico publicado en 2013

Overexpression of heart-specific small subunit of myosin light chain phosphatase results in heart failure and conduction disturbance

artículo científico publicado en 2018

Replication of the association between a chromosome 9p21 polymorphism and coronary artery disease in Japanese and Korean populations

scientific article published on 09 February 2008

Structural analysis of four and half LIM protein-2 in dilated cardiomyopathy.

artículo científico publicado en 2007

Structural analysis of obscurin gene in hypertrophic cardiomyopathy

artículo científico publicado en 2007

Subchronic toxicity study of dietary N-acetylglucosamine in F344 rats

artículo científico publicado en 2004

Tcap gene mutations in hypertrophic cardiomyopathy and dilated cardiomyopathy

artículo científico publicado en 2004

Titin mutations as the molecular basis for dilated cardiomyopathy

artículo científico publicado en 2002

Lista de obras de

A Cypher/ZASP mutation associated with dilated cardiomyopathy alters the binding affinity to protein kinase C.

A novel disease gene for Brugada syndrome: sarcolemmal membrane-associated protein gene mutations impair intracellular trafficking of hNav1.5.

A novel link of HLA locus to the regulation of immunity and infection: NFKBIL1 regulates alternative splicing of human immune-related genes and influenza virus M gene ⬇️

A novel protein found in the I bands of myofibrils is produced by alternative splicing of the DLST gene

ANKRD1, the gene encoding cardiac ankyrin repeat protein, is a novel dilated cardiomyopathy gene

Alpha B-crystallin mutation in dilated cardiomyopathy

Autophagic degradation of nuclear components in mammalian cells

Cardiac ankyrin repeat protein gene (ANKRD1) mutations in hypertrophic cardiomyopathy

DelK32-lamin A/C has abnormal location and induces incomplete tissue maturation and severe metabolic defects leading to premature death

Dilated cardiomyopathy-associated BAG3 mutations impair Z-disc assembly and enhance sensitivity to apoptosis in cardiomyocytes

Endothelin-1 induces myofibrillar disarray and contractile vector variability in hypertrophic cardiomyopathy-induced pluripotent stem cell-derived cardiomyocytes

Functional characterization of a trafficking-defective HCN4 mutation, D553N, associated with cardiac arrhythmia

Genetic defects in a His-Purkinje system transcription factor, IRX3, cause lethal cardiac arrhythmias.

Genetics of Laminopathies

Genetics of laminopathies.

Heart-specific small subunit of myosin light chain phosphatase activates rho-associated kinase and regulates phosphorylation of myosin phosphatase target subunit 1.

Hypertrophic Cardiomyopathy Accompanied by Spinocerebellar Atrophy With a Novel Mutation in Troponin I Gene

Identification and functional analysis of a caveolin-3 mutation associated with familial hypertrophic cardiomyopathy

Impact of ANKRD1 mutations associated with hypertrophic cardiomyopathy on contraction parameters of engineered heart tissue.

Impaired binding of ZASP/Cypher with phosphoglucomutase 1 is associated with dilated cardiomyopathy

Improvement of Left Ventricular Dysfunction and of Survival Prognosis of Dilated Cardiomyopathy by Administration of Calcium Sensitizer SCH00013 in a Mouse Model

Interaction of BMP10 with Tcap may modulate the course of hypertensive cardiac hypertrophy

Megakaryoblastic leukemia factor-1 gene in the susceptibility to coronary artery disease

Molecular basis for clinical heterogeneity in inherited cardiomyopathies due to myopalladin mutations

Mouse model carrying H222P- Lmna mutation develops muscular dystrophy and dilated cardiomyopathy similar to human striated muscle laminopathies

Mutational analysis of fukutin gene in dilated cardiomyopathy and hypertrophic cardiomyopathy

Nebulette Mutations Are Associated With Dilated Cardiomyopathy and Endocardial Fibroelastosis ⬇️

Novel SCN3B mutation associated with brugada syndrome affects intracellular trafficking and function of Nav1.5.

Novel mechanisms of trafficking defect caused by KCNQ1 mutations found in long QT syndrome.

Novel mutation in the α-myosin heavy chain gene is associated with sick sinus syndrome

Nuclear accumulation of androgen receptor in gender difference of dilated cardiomyopathy due to lamin A/C mutations.

Overexpression of heart-specific small subunit of myosin light chain phosphatase results in heart failure and conduction disturbance

Replication of the association between a chromosome 9p21 polymorphism and coronary artery disease in Japanese and Korean populations

Structural analysis of four and half LIM protein-2 in dilated cardiomyopathy.

Structural analysis of obscurin gene in hypertrophic cardiomyopathy

Subchronic toxicity study of dietary N-acetylglucosamine in F344 rats

Tcap gene mutations in hypertrophic cardiomyopathy and dilated cardiomyopathy

Titin mutations as the molecular basis for dilated cardiomyopathy