(Q28203734)

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900242-2

7 January 2021

South Africa: setting the wrong example

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900242-2

7 January 2021

Mutations in the gene encoding lamin A/C cause autosomal dominant Emery-Dreifuss muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900242-2

7 January 2021

Mapping of a novel gene for familial hypertrophic cardiomyopathy to chromosome 11

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900242-2

7 January 2021

Complexity in simplicity: monogenic disorders and complex cardiomyopathies

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900242-2

7 January 2021

Report of the National Heart, Lung, and Blood Institute Special Emphasis Panel on Heart Failure Research

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900242-2

7 January 2021

The in vitro motility activity of beta-cardiac myosin depends on the nature of the beta-myosin heavy chain gene mutation in hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900242-2

7 January 2021

Crystal structure of a vertebrate smooth muscle myosin motor domain and its complex with the essential light chain: visualization of the pre-power stroke state

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900242-2

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%2FS0092-8674%2801%2900242-2

7 January 2021

Missense mutations in the rod domain of the lamin A/C gene as causes of dilated cardiomyopathy and conduction-system disease

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900242-2

7 January 2021

An abnormal Ca(2+) response in mutant sarcomere protein-mediated familial hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900242-2

7 January 2021

A mouse model of familial hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900242-2

7 January 2021

The nuclear envelope lamina is reversibly depolymerized during mitosis.

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900242-2

7 January 2021

Missense mutations in desmin associated with familial cardiac and skeletal myopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900242-2

7 January 2021

Frequency and phenotypes of familial dilated cardiomyopathy.

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900242-2

7 January 2021

Homozygous mutation in cardiac troponin T: implications for hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900242-2

7 January 2021

Endothelin and angiotensin II stimulation of Na+-H+ exchange is impaired in cardiac hypertrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900242-2

7 January 2021

The cardiac beta-myosin heavy chain gene is not the predominant gene for hypertrophic cardiomyopathy in the Finnish population.

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900242-2

7 January 2021

Mapping a gene for familial hypertrophic cardiomyopathy to chromosome 14q1

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900242-2

7 January 2021

Mutations in sarcomere protein genes as a cause of dilated cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900242-2

7 January 2021

Mutations in the cardiac troponin I gene associated with hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900242-2

7 January 2021

Desmin mutation responsible for idiopathic dilated cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900242-2

7 January 2021

Protein-protein interactions in intracellular Ca2+-release channel function.

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900242-2

7 January 2021

A transgenic rabbit model for human hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900242-2

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%2FS0092-8674%2801%2900242-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900242-2

7 January 2021

Familial dilated cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900242-2

7 January 2021

Disruption of muscle architecture and myocardial degeneration in mice lacking desmin

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900242-2

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%2FS0092-8674%2801%2900242-2

7 January 2021

A calcineurin-dependent transcriptional pathway for cardiac hypertrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900242-2

7 January 2021

Alpha-cardiac actin is a novel disease gene in familial hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900242-2

7 January 2021

Identification of mutations in the gene encoding lamins A/C in autosomal dominant limb girdle muscular dystrophy with atrioventricular conduction disturbances (LGMD1B)

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900242-2

7 January 2021

Identification of the Syrian hamster cardiomyopathy gene.

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900242-2

7 January 2021

Possible gene dose effect of a mutant cardiac beta-myosin heavy chain gene on the clinical expression of familial hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900242-2

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%2FS0092-8674%2801%2900242-2

7 January 2021

Evidence for a dystrophin missense mutation as a cause of X-linked dilated cardiomyopathy.

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900242-2

7 January 2021

Actin mutations in dilated cardiomyopathy, a heritable form of heart failure

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900242-2

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%2FS0092-8674%2801%2900242-2

7 January 2021

Structure of the actin-myosin complex and its implications for muscle contraction

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900242-2

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%2FS0092-8674%2801%2900242-2

7 January 2021

Identification of a contractile deficit in adult cardiac myocytes expressing hypertrophic cardiomyopathy-associated mutant troponin T proteins

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900242-2

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%2FS0092-8674%2801%2900242-2

7 January 2021

Molecular diversity of myofibrillar proteins: gene regulation and functional significance

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900242-2

7 January 2021

Dilated cardiomyopathy and sensorineural hearing loss: a heritable syndrome that maps to 6q23-24.

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900242-2

7 January 2021

LMNA, encoding lamin A/C, is mutated in partial lipodystrophy.

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900242-2

7 January 2021

Three-dimensional atomic model of F-actin decorated with Dictyostelium myosin S1

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900242-2

7 January 2021

The management of hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900242-2

7 January 2021

Muscular dystrophies and the dystrophin-glycoprotein complex

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900242-2

7 January 2021

Nuclear lamins: their structure, assembly, and interactions

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900242-2

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%2FS0092-8674%2801%2900242-2

7 January 2021

A familial hypertrophic cardiomyopathy locus maps to chromosome 15q2.

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900242-2

7 January 2021

Etiologies of cardiomyopathy and heart failure

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900242-2

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%2FS0092-8674%2801%2900242-2

7 January 2021

Sporadic hypertrophic cardiomyopathy due to de novo myosin mutations

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900242-2

7 January 2021

A disease locus for familial hypertrophic cardiomyopathy maps to chromosome 1q3.

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900242-2

7 January 2021

Expression and functional assessment of a truncated cardiac troponin T that causes hypertrophic cardiomyopathy. Evidence for a dominant negative action

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900242-2

7 January 2021

A 35-A movement of smooth muscle myosin on ADP release.

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900242-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900242-2

7 January 2021

Alteration of intracellular Ca2(+)-handling and receptor regulation in hypertensive cardiac hypertrophy: insights from Ren2-transgenic rats

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900242-2

7 January 2021