[Genetically modified animal models in cardiovascular research] (Q74043611)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11412782%20AND%20SRC:MED&resulttype=core&format=json

8 November 2019

review article

1 reference

title

[Genetically modified animal models in cardiovascular research] (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11412782%20AND%20SRC:MED&resulttype=core&format=json

8 November 2019

author name string

F Dalloz

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11412782%20AND%20SRC:MED&resulttype=core&format=json

8 November 2019

H Osinska

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11412782%20AND%20SRC:MED&resulttype=core&format=json

8 November 2019

J Robbins

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11412782%20AND%20SRC:MED&resulttype=core&format=json

8 November 2019

publication date

1 June 2001

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11412782%20AND%20SRC:MED&resulttype=core&format=json

Revista Española de Cardiología

8 November 2019

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11412782%20AND%20SRC:MED&resulttype=core&format=json

8 November 2019

volume

54

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11412782%20AND%20SRC:MED&resulttype=core&format=json

8 November 2019

issue

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11412782%20AND%20SRC:MED&resulttype=core&format=json

8 November 2019

page(s)

764-789

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11412782%20AND%20SRC:MED&resulttype=core&format=json

Transgenesis in the rat and larger mammals

8 November 2019

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2801%2976391-9

7 January 2021

Genetic manipulation of the rabbit heart via transgenesis

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2801%2976391-9

7 January 2021

A transgenic rabbit model for human hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2801%2976391-9

7 January 2021

Genetic transformation of mouse embryos by microinjection of purified DNA

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2801%2976391-9

7 January 2021

legless insertional mutation: morphological, molecular, and genetic characterization

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2801%2976391-9

7 January 2021

Cardiac transgenic and gene-targeted mice as models of cardiac hypertrophy and failure: a problem of (new) riches

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2801%2976391-9

7 January 2021

Remodeling the cardiac sarcomere using transgenesis

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2801%2976391-9

7 January 2021

Transgenic expression of green fluorescence protein can cause dilatedcardiomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2801%2976391-9

7 January 2021

Gene targeting in embryonic stem cells: the new physiology and metabolism.

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2801%2976391-9

7 January 2021

Gene targeting in the mouse

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2801%2976391-9

7 January 2021

Single-copy transgenic mice with chosen-site integration

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2801%2976391-9

7 January 2021

Regionally restricted developmental defects resulting from targeted disruption of the mouse homeobox gene hox-1.5

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2801%2976391-9

7 January 2021

MLP-deficient mice exhibit a disruption of cardiac cytoarchitectural organization, dilated cardiomyopathy, and heart failure

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2801%2976391-9

7 January 2021

Aortic arch malformations and ventricular septal defect in mice deficient in endothelin-1

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2801%2976391-9

7 January 2021

Cardiac malformation in neonatal mice lacking connexin43.

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2801%2976391-9

7 January 2021

Ablation of the murine alpha myosin heavy chain gene leads to dosage effects and functional deficits in the heart

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2801%2976391-9

7 January 2021

In vivo assessment of embryonic cardiovascular dimensions and function in day-10.5 to -14.5 mouse embryos

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2801%2976391-9

7 January 2021

Dilated cardiomyopathy in homozygous myosin-binding protein-C mutant mice

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2801%2976391-9

7 January 2021

Wall stress and patterns of hypertrophy in the human left ventricle

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2801%2976391-9

7 January 2021

Development and progression of left ventricular hypertrophy in children with hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2801%2976391-9

7 January 2021

Molecular and cellular biology of heart failure.

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2801%2976391-9

7 January 2021

Epidemiology of idiopathic dilated and hypertrophic cardiomyopathy. A population-based study in Olmsted County, Minnesota, 1975-1984

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2801%2976391-9

7 January 2021

Prevalence of hypertrophic cardiomyopathy in a general population of young adults. Echocardiographic analysis of 4111 subjects in the CARDIA Study. Coronary Artery Risk Development in (Young) Adults

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2801%2976391-9

7 January 2021

Congenital heart disease and sudden death in the young

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2801%2976391-9

7 January 2021

Molecular genetics of hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2801%2976391-9

7 January 2021

Mutations in the cardiac myosin binding protein-C gene on chromosome 11 cause familial hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2801%2976391-9

7 January 2021

A molecular basis for familial hypertrophic cardiomyopathy: a beta cardiac myosin heavy chain gene missense mutation

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2801%2976391-9

7 January 2021

Structural interpretation of the mutations in the beta-cardiac myosin that have been implicated in familial hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2801%2976391-9

7 January 2021

Actin Mutations in Dilated Cardiomyopathy, a Heritable Form of Heart Failure

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2801%2976391-9

7 January 2021

Desmin mutation responsible for idiopathic dilated cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2801%2976391-9

7 January 2021

Structural analysis of the titin gene in hypertrophic cardiomyopathy: identification of a novel disease gene

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2801%2976391-9

7 January 2021

The mammalian myosin heavy chain gene family

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2801%2976391-9

7 January 2021

Myosin heavy chain isoform expression in the failing and nonfailing human heart

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2801%2976391-9

7 January 2021

Myosin heavy chain gene expression in human heart failure

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2801%2976391-9

7 January 2021

Characteristics and prognostic implications of myosin missense mutations in familial hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2801%2976391-9

7 January 2021

Differences in clinical expression of hypertrophic cardiomyopathy associated with two distinct mutations in the beta-myosin heavy chain gene. A 908Leu----Val mutation and a 403Arg----Gln mutation

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2801%2976391-9

7 January 2021

Sudden cardiac death in hypertrophic cardiomyopathy. Variability in phenotypic expression of beta-myosin heavy chain mutations

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2801%2976391-9

7 January 2021

Malignant familial hypertrophic cardiomyopathy in a family with a 453Arg-->Cys mutation in the beta-myosin heavy chain gene: coexistence of sudden death and end-stage heart failure

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2801%2976391-9

7 January 2021

Prognostic implications of novel beta cardiac myosin heavy chain gene mutations that cause familial hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2801%2976391-9

7 January 2021

Early expression of a malignant phenotype of familial hypertrophic cardiomyopathy associated with a Gly716Arg myosin heavy chain mutation in a Korean family

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2801%2976391-9

7 January 2021

Sudden cardiac death in familial hypertrophic cardiomyopathy: are “benign” mutations really benign?

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2801%2976391-9

7 January 2021

A missense mutation in the beta-myosin heavy chain gene in a Japanese patient with hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2801%2976391-9

7 January 2021

Genotype-phenotype correlations in hypertrophic cardiomyopathy. Insights provided by comparisons of kindreds with distinct and identical beta-myosin heavy chain gene mutations

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2801%2976391-9

7 January 2021

Multiple disease genes cause hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2801%2976391-9

7 January 2021

A mouse model of familial hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2801%2976391-9

7 January 2021

Neonatal cardiomyopathy in mice homozygous for the Arg403Gln mutation in the alpha cardiac myosin heavy chain gene

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2801%2976391-9

7 January 2021

The pathogenesis of familial hypertrophic cardiomyopathy: early and evolving effects from an alpha-cardiac myosin heavy chain missense mutation

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2801%2976391-9

7 January 2021

Diastolic dysfunction and altered energetics in the alphaMHC403/+ mouse model of familial hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2801%2976391-9

7 January 2021

Altered cardiac excitation-contraction coupling in mutant mice with familial hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2801%2976391-9

7 January 2021

Familial hypertrophic cardiomyopathy mice display gender differences in electrophysiological abnormalities

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2801%2976391-9

7 January 2021

QT dispersion in alpha-myosin heavy-chain familial hypertrophic cardiomyopathy mice

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2801%2976391-9

7 January 2021

Single-molecule mechanics of R403Q cardiac myosin isolated from the mouse model of familial hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2801%2976391-9

7 January 2021

Altered crossbridge kinetics in the alphaMHC403/+ mouse model of familial hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2801%2976391-9

7 January 2021

Functional analysis of myosin mutations that cause familial hypertrophic cardiomyopathy.

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2801%2976391-9

7 January 2021

Animal models of cardiac arrhythmias

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2801%2976391-9

7 January 2021

Light chain-dependent myosin structural dynamics in solution investigated by transient electrical birefringence

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2801%2976391-9

7 January 2021

Mutations in either the essential or regulatory light chains of myosin are associated with a rare myopathy in human heart and skeletal muscle

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2801%2976391-9

7 January 2021

The molecular biology and pathophysiology of hypertrophic cardiomyopathy due to mutations in the beta myosin heavy chains and the essential and regulatory light chains.

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2801%2976391-9

7 January 2021

Identification of two novel mutations in the ventricular regulatory myosin light chain gene (MYL2) associated with familial and classical forms of hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2801%2976391-9

7 January 2021

The stretch-activation response may be critical to the proper functioning of the mammalian heart

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2801%2976391-9

7 January 2021

Abnormal cardiac structure and function in mice expressing nonphosphorylatable cardiac regulatory myosin light chain 2

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2801%2976391-9

7 January 2021

In vivo analysis of an essential myosin light chain mutation linked to familial hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2801%2976391-9

7 January 2021

A new protein of the thick filaments of vertebrate skeletal myofibrils. Extractions, purification and characterization

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2801%2976391-9

7 January 2021

Isolation and characterization of a cDNA clone encoding avian skeletal muscle C-protein: an intracellular member of the immunoglobulin superfamily

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2801%2976391-9

7 January 2021

Cardiac myosin binding protein C

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2801%2976391-9

7 January 2021

Modulation of myosin filament organization by C-protein family members

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2801%2976391-9

7 January 2021

Mutations in the gene for cardiac myosin-binding protein C and late-onset familial hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2801%2976391-9

7 January 2021

Cardiac myosin binding protein-C gene splice acceptor site mutation is associated with familial hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2801%2976391-9

7 January 2021

Novel splice donor site mutation in the cardiac myosin-binding protein-C gene in familial hypertrophic cardiomyopathy. Characterization Of cardiac transcript and protein

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2801%2976391-9

7 January 2021

Clinical Features and Prognostic Implications of Familial Hypertrophic Cardiomyopathy Related to the Cardiac Myosin-Binding Protein C Gene

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2801%2976391-9

7 January 2021

A mouse model of myosin binding protein C human familial hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2801%2976391-9

7 January 2021

In vivo modeling of myosin binding protein C familial hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2801%2976391-9

7 January 2021

Abnormal blood pressure response during exercise in hypertrophic cardiomyopathy.

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2801%2976391-9

7 January 2021

Clinical implications of hypertrophic cardiomyopathy associated with mutations in the alpha-tropomyosin gene

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2801%2976391-9

7 January 2021

Novel missense mutation in alpha-tropomyosin gene found in Japanese patients with hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2801%2976391-9

7 January 2021

Alpha-tropomyosin and cardiac troponin T mutations cause familial hypertrophic cardiomyopathy: a disease of the sarcomere

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2801%2976391-9

7 January 2021

A Mutant Tropomyosin That Causes Hypertrophic Cardiomyopathy Is Expressed In Vivo and Associated With an Increased Calcium Sensitivity

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2801%2976391-9

7 January 2021

Mouse model of a familial hypertrophic cardiomyopathy mutation in alpha-tropomyosin manifests cardiac dysfunction

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2801%2976391-9

7 January 2021

Targeted Ablation of the Murine α-Tropomyosin Gene

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2801%2976391-9

7 January 2021

Molecular and Physiological Effects of α-Tropomyosin Ablation in the Mouse

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2801%2976391-9

7 January 2021

Troponin T isoform expression in humans. A comparison among normal and failing adult heart, fetal heart, and adult and fetal skeletal muscle

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2801%2976391-9

7 January 2021

Molecular basis of human cardiac troponin T isoforms expressed in the developing, adult, and failing heart.

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2801%2976391-9

7 January 2021

Structural aspects of troponin-tropomyosin regulation of skeletal muscle contraction

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2801%2976391-9

7 January 2021

Troponin T: genetics, properties and function

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2801%2976391-9

7 January 2021

Mutations in the genes for cardiac troponin T and alpha-tropomyosin in hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2801%2976391-9

7 January 2021

Codon 102 of the cardiac troponin T gene is a putative hot spot for mutations in familial hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2801%2976391-9

7 January 2021

Novel missense mutation in cardiac troponin T gene found in Japanese patient with hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2801%2976391-9

7 January 2021

Clinical manifestations of hypertrophic cardiomyopathy with mutations in the cardiac beta-myosin heavy chain gene or cardiac troponin T gene

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2801%2976391-9

7 January 2021

A truncated cardiac troponin T molecule in transgenic mice suggests multiple cellular mechanisms for familial hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2801%2976391-9

7 January 2021

Dominant-negative effect of a mutant cardiac troponin T on cardiac structure and function in transgenic mice

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2801%2976391-9

7 January 2021

Decreased left ventricular ejection fraction in transgenic mice expressing mutant cardiac troponin T-Q(92), responsible for human hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2801%2976391-9

7 January 2021

Cardiac troponin T mutations result in allele-specific phenotypes in a mouse model for hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2801%2976391-9

7 January 2021

In vivo short-term expression of a hypertrophic cardiomyopathy mutation in adult rabbit myocardium: myofibrillar incorporation without early disarray

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2801%2976391-9

7 January 2021

Altered interactions among thin filament proteins modulate cardiac function

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2801%2976391-9

7 January 2021

The C Terminus of Cardiac Troponin I Is Essential for Full Inhibitory Activity and Ca2+ Sensitivity of Rat Myofibrils

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2801%2976391-9

7 January 2021

Mutations in the cardiac troponin I gene associated with hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2801%2976391-9

7 January 2021

Altered regulatory properties of human cardiac troponin I mutants that cause hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2801%2976391-9

7 January 2021

Transgenic modeling of a cardiac troponin I mutation linked to familial hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2801%2976391-9

7 January 2021

A gene defect that causes conduction system disease and dilated cardiomyopathy maps to chromosome 1p1-1q1

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2801%2976391-9

7 January 2021

Localization of a gene responsible for familial dilated cardiomyopathy to chromosome 1q32.

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2801%2976391-9

7 January 2021

Familial dilated cardiomyopathy locus maps to chromosome 2q31.

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2801%2976391-9

7 January 2021

Mapping a cardiomyopathy locus to chromosome 3p22-p25.

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2801%2976391-9

7 January 2021

Gene mapping of familial autosomal dominant dilated cardiomyopathy to chromosome 10q21-23.

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2801%2976391-9

7 January 2021

Trans-cellular desmin-lamin B intermediate filament network in cardiac myocytes

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2801%2976391-9

7 January 2021

Missense mutations in desmin associated with familial cardiac and skeletal myopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2801%2976391-9

7 January 2021

A missense mutation in the desmin rod domain is associated with autosomal dominant distal myopathy, and exerts a dominant negative effect on filament formation

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2801%2976391-9

7 January 2021

A dysfunctional desmin mutation in a patient with severe generalized myopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2801%2976391-9

7 January 2021

Desmin myopathy, a skeletal myopathy with cardiomyopathy caused by mutations in the desmin gene

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2801%2976391-9

7 January 2021

Myopathy associated with desmin type intermediate filaments. An immunoelectron microscopic study

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2801%2976391-9

7 January 2021

The pattern of desmin filaments in myocardial disarray

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2801%2976391-9

7 January 2021

Desmin myopathy involving cardiac, skeletal, and vascular smooth muscle: report of a case with immunoelectron microscopy

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2801%2976391-9

7 January 2021

Desmin myopathy: a multisystem disorder involving skeletal, cardiac, and smooth muscle

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2801%2976391-9

7 January 2021

Disruption of muscle architecture and myocardial degeneration in mice lacking desmin

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2801%2976391-9

7 January 2021

Desmin in muscle formation and maintenance: knockouts and consequences

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2801%2976391-9

7 January 2021

Null mutation in the desmin gene gives rise to a cardiomyopathy.

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2801%2976391-9

7 January 2021

The absence of desmin leads to cardiomyocyte hypertrophy and cardiac dilation with compromised systolic function

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2801%2976391-9

7 January 2021

X linked fatal infantile cardiomyopathy maps to Xq28 and is possibly allelic to Barth syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2801%2976391-9

7 January 2021

X-linked dilated cardiomyopathy. Molecular genetic evidence of linkage to the Duchenne muscular dystrophy (dystrophin) gene at the Xp21 locus

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2801%2976391-9

7 January 2021

A mouse model for mitochondrial myopathy and cardiomyopathy resulting from a deficiency in the heart/muscle isoform of the adenine nucleotide translocator

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2801%2976391-9

7 January 2021

Disruption of the sarcoglycan-sarcospan complex in vascular smooth muscle: a novel mechanism for cardiomyopathy and muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2801%2976391-9

7 January 2021

Primary systemic carnitine deficiency is caused by mutations in a gene encoding sodium ion-dependent carnitine transporter

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2801%2976391-9

7 January 2021

Complexity in simplicity: monogenic disorders and complex cardiomyopathies

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2801%2976391-9

7 January 2021

Stress pathways and heart failure

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2801%2976391-9

7 January 2021

Chronic phospholamban-sarcoplasmic reticulum calcium ATPase interaction is the critical calcium cycling defect in dilated cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2801%2976391-9

7 January 2021

Signaling pathways for cardiac hypertrophy and failure

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2801%2976391-9

7 January 2021

Meeting Koch's postulates for calcium signaling in cardiac hypertrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2801%2976391-9

7 January 2021

Incidence of congenital heart disease: I. Postnatal incidence.

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2801%2976391-9

7 January 2021

Advances in understanding the molecular regulation of cardiac development

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2801%2976391-9

7 January 2021

Molecular genetics of congenital heart disease

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2801%2976391-9

7 January 2021

Toward molecular strategies for heart disease--past, present, future

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2801%2976391-9

7 January 2021

Doxycycline-mediated quantitative and tissue-specific control of gene expression in transgenic mice

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2801%2976391-9

7 January 2021

Controlling genes with tetracyclines

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2801%2976391-9

7 January 2021

Tetracycline-regulated cardiac gene expression in vivo.

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2801%2976391-9

7 January 2021

Conditional expression of a Gi-coupled receptor causes ventricular conduction delay and a lethal cardiomyopathy.

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2801%2976391-9

7 January 2021

Conditional lineage ablation to model human diseases

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2801%2976391-9

7 January 2021

Gene recombination in postmitotic cells. Targeted expression of Cre recombinase provokes cardiac-restricted, site-specific rearrangement in adult ventricular muscle in vivo.

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2801%2976391-9

7 January 2021

Inducible Gene Targeting in Mice Using the Cre/loxSystem

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2801%2976391-9

7 January 2021

10.1016/S0300-8932(01)76391-9

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11412782%20AND%20SRC:MED&resulttype=core&format=json

8 November 2019

1 reference