Applications of genome editing technology in the targeted therapy of human diseases: mechanisms, advances and prospects
H Li, Y Yang, W Hong, M Huang, M Wu… - Signal transduction and …, 2020 - nature.com
Based on engineered or bacterial nucleases, the development of genome editing
technologies has opened up the possibility of directly targeting and modifying genomic …
technologies has opened up the possibility of directly targeting and modifying genomic …
Cardiomyocyte maturation: new phase in development
Y Guo, WT Pu - Circulation research, 2020 - Am Heart Assoc
Maturation is the last phase of heart development that prepares the organ for strong,
efficient, and persistent pum** throughout the mammal's lifespan. This process is …
efficient, and persistent pum** throughout the mammal's lifespan. This process is …
Epidemiology of the inherited cardiomyopathies
WJ McKenna, DP Judge - Nature Reviews Cardiology, 2021 - nature.com
In the absence of contemporary, population-based epidemiological studies, estimates of the
incidence and prevalence of the inherited cardiomyopathies have been derived from …
incidence and prevalence of the inherited cardiomyopathies have been derived from …
CRISPR modeling and correction of cardiovascular disease
Cardiovascular disease remains the leading cause of morbidity and mortality in the
developed world. In recent decades, extraordinary effort has been devoted to defining the …
developed world. In recent decades, extraordinary effort has been devoted to defining the …
Genetics of congenital heart disease
Congenital heart disease (CHD) is one of the most common birth defects. Studies in animal
models and humans have indicated a genetic etiology for CHD. About 400 genes have been …
models and humans have indicated a genetic etiology for CHD. About 400 genes have been …
Genetic modifiers and rare Mendelian disease
Despite advances in high-throughput sequencing that have revolutionized the discovery of
gene defects in rare Mendelian diseases, there are still gaps in translating individual …
gene defects in rare Mendelian diseases, there are still gaps in translating individual …
[HTML][HTML] Transcription factor protein interactomes reveal genetic determinants in heart disease
Congenital heart disease (CHD) is present in 1% of live births, yet identification of causal
mutations remains challenging. We hypothesized that genetic determinants for CHDs may …
mutations remains challenging. We hypothesized that genetic determinants for CHDs may …
Molecular genetics and complex inheritance of congenital heart disease
Congenital heart disease (CHD) is the most common congenital malformation and the
leading cause of mortality therein. Genetic etiologies contribute to an estimated 90% of CHD …
leading cause of mortality therein. Genetic etiologies contribute to an estimated 90% of CHD …
Precision medicine and therapies of the future
SM Sisodiya - Epilepsia, 2021 - Wiley Online Library
Precision medicine in the epilepsies has gathered much attention, especially with gene
discovery pushing forward new understanding of disease biology. Several targeted …
discovery pushing forward new understanding of disease biology. Several targeted …
[HTML][HTML] Genetics of congenital heart disease: a narrative review of recent advances and clinical implications
Congenital heart disease (CHD) is the most common human birth defect and remains a
leading cause of mortality in childhood. Although advances in clinical management have …
leading cause of mortality in childhood. Although advances in clinical management have …