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- W2912084914 endingPage "157" @default.
- W2912084914 startingPage "150" @default.
- W2912084914 abstract "Congenital malformations, or structural birth defects, are now the leading cause of infant mortality in the United States and Europe (Dolk et al., 2010; Heron et al., 2009). Of the congenital malformations, congenital heart disease (CHD) is the most common (Dolk et al., 2010; Heron et al., 2009). Thus, a molecular understanding of heart development is an essential goal for improving clinical approaches to CHD. However, CHDs are commonly a result of genetic defects that manifest themselves in a spatial and temporal manner during the early stages of embryogenesis, leaving them mostly intractable to mass spectrometry-based analysis. Here, we describe the technologies and advancements in the field of mass spectrometry over the past few years that have begun to provide insights into the molecular and cellular basis of CHD and prospects for these types of approaches in the future." @default.
- W2912084914 created "2019-02-21" @default.
- W2912084914 creator A5001468756 @default.
- W2912084914 creator A5037078937 @default.
- W2912084914 date "2019-02-01" @default.
- W2912084914 modified "2023-09-25" @default.
- W2912084914 title "Proteomic-based approaches to cardiac development and disease" @default.
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