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Bmpr2 mutation in murine PMVEC
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创建时间：
2011-07-01
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High Altitude Pulmonary Hypertension
The Central Asian Kyrgyz highland population provides a unique opportunity to address genetic diversity and understand the genetic mechanisms underlying hypoxia-induced high altitude pulmonary hyperte
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Characterization of DNA methylation changes associated with lung and right ventricle dysfunction in pulmonary hypertension. Characterization of DNA methylation changes associated with lung and right ventricle dysfunction in pulmonary hypertension
Pulmonary arterial hypertension (PAH) is a lethal vasculopathy associated with pulmonary arteries remodeling and right ventricle (RV) dysfunction. Epigenetic dysregulation, including altered DNA methy
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Comparison of clinical and hemodynamic features of BMPR2 mutation carriers and non-carriers.
Comparison of clinical and hemodynamic features of BMPR2 mutation carriers and non-carriers.
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Remodeling of active endothelial enhancers is associated with aberrant gene-regulatory networks in pulmonary arterial hypertension [ChIP-seq]
Pulmonary Arterial Hypertension (PAH) is a cardiovascular disease characterized by progressively increasing blood pressure as a result of obliteration and loss of pulmonary arteries. We have extracted
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WES of PPHN. WES and TRS of PPHN
Persistent pulmonary hypertension of the newborn (PPHN) is a life-threatening disorder characterized by sustained high levels of pulmonary vascular resistance after birth. Although genetic factors pla
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