Research of Idiopathic Pulmonary Hypertension has been linked to Hypertensive Disease, Pulmonary Hypertension, Heart Failure, Lung Diseases, Heart Diseases. The study of Idiopathic Pulmonary Hypertension has been mentioned in research publications which can be found using our bioinformatics tool below. Researched pathways related to Idiopathic Pulmonary Hypertension include Pathogenesis, Vasoconstriction, Cell Proliferation, Vasodilation, Muscle Cell Proliferation. These pathways complement our catalog of research reagents for the study of Idiopathic Pulmonary Hypertension including antibodies and ELISA kits against PAH, BMPR2, ENO1, EDN1, ACPP.
Laverne is a handy bioinformatics tool to help facilitate scientific exploration of related genes, diseases and pathways based on co-citations. Explore more on Idiopathic Pulmonary Hypertension below!
For more information on how to use Laverne, please read the How to Guide.
We have 799 products for the study of Idiopathic Pulmonary Hypertension that can be applied to Western Blot, Immunocytochemistry/Immunofluorescence, Flow Cytometry, Immunohistochemistry from our catalog of antibodies and ELISA kits.
Idiopathic Pulmonary Hypertension is also known as Essential Pulmonary Hypertension, Ipah, Primary Pulmonary Hypertension, Pulmonary Arterial Hypertension.
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