Gender-specific differences in major cardiac events and mortality in lamin A/C mutation carriers.
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Skeletal Muscle Laminopathies: A Review of Clinical and Molecular FeaturesInherited bradyarrhythmia: A diverse genetic backgroundGenetics and genotype-phenotype correlations in Finnish patients with dilated cardiomyopathyGenetic Variation in Cardiomyopathy and Cardiovascular Disorders.CAP2 in cardiac conduction, sudden cardiac death and eye development.Where genotype is not predictive of phenotype: towards an understanding of the molecular basis of reduced penetrance in human inherited disease.Clinical disease presentation and ECG characteristics of LMNA mutation carriersIs gender becoming relevant in uro-oncological research? A bibliographical analysis.Pregnancy, cardiomyopathies, and genetics.Sex differences in cardiomyopathies.Role of nuclear Lamin A/C in cardiomyocyte functions.Proposal for a revised definition of dilated cardiomyopathy, hypokinetic non-dilated cardiomyopathy, and its implications for clinical practice: a position statement of the ESC working group on myocardial and pericardial diseases.Sexual dimorphisms of mRNA and miRNA in human/murine heart disease.Current applications of biomarkers in cardiomyopathies.Lamin A/C Cardiomyopathies: Current Understanding and Novel Treatment Strategies.Truncating titin mutations are associated with a mild and treatable form of dilated cardiomyopathy.Lamin A/C cardiomyopathy: young onset, high penetrance, and frequent need for heart transplantation.Lipodystrophic laminopathies: Diagnostic clues.Elevated dual specificity protein phosphatase 4 in cardiomyopathy caused by lamin A/C gene mutation is primarily ERK1/2-dependent and its depletion improves cardiac function and survival.Whole exome sequencing identified 1 base pair novel deletion in BCL2-associated athanogene 3 (BAG3) gene associated with severe dilated cardiomyopathy (DCM) requiring heart transplant in multiple family members.Clinical aspects of Emery-Dreifuss muscular dystrophy.Exploring the Crosstalk Between and Splicing Machinery Gene Mutations in Dilated CardiomyopathyLamin mutation location predicts cardiac phenotype severity: combined analysis of the published literature
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P2860
Gender-specific differences in major cardiac events and mortality in lamin A/C mutation carriers.
description
2012 nî lūn-bûn
@nan
2012年の論文
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2012年学术文章
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2012年学术文章
@zh-cn
2012年学术文章
@zh-hans
2012年学术文章
@zh-my
2012年学术文章
@zh-sg
2012年學術文章
@yue
2012年學術文章
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2012年學術文章
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name
Gender-specific differences in ...... n lamin A/C mutation carriers.
@en
Gender-specific differences in ...... n lamin A/C mutation carriers.
@nl
type
label
Gender-specific differences in ...... n lamin A/C mutation carriers.
@en
Gender-specific differences in ...... n lamin A/C mutation carriers.
@nl
prefLabel
Gender-specific differences in ...... n lamin A/C mutation carriers.
@en
Gender-specific differences in ...... n lamin A/C mutation carriers.
@nl
P2093
P2860
P50
P356
P1476
Gender-specific differences in ...... in lamin A/C mutation carriers
@en
P2093
Aeilko H Zwinderman
Anneke J van der Kooi
Camilla Rowland
Eline A Nannenberg
Imke Christiaans
Ingrid A W van Rijsingen
J Peter van Tintelen
Johanna F Hermans-van Ast
Maarten P van den Berg
Maurizia Grasso
P2860
P304
P356
10.1093/EURJHF/HFS191
P50
P577
2012-11-25T00:00:00Z