about
Transcription Factor Runx2 Promotes Aortic Fibrosis and Stiffness in Type 2 Diabetes Mellitus.Loss of somatostatin receptor subtype 2 in prostate cancer is linked to an aggressive cancer phenotype, high tumor cell proliferation and predicts early metastatic and biochemical relapseN-terminal pro-brain natriuretic peptide is a useful prognostic marker in patients with pre-capillary pulmonary hypertension and renal insufficiency.BMPR2 preserves mitochondrial function and DNA during reoxygenation to promote endothelial cell survival and reverse pulmonary hypertensionElafin Reverses Pulmonary Hypertension via Caveolin-1-Dependent Bone Morphogenetic Protein Signaling.RNA Sequencing Analysis Detection of a Novel Pathway of Endothelial Dysfunction in Pulmonary Arterial Hypertension.Acute effects of exercise on the inflammatory state in patients with idiopathic pulmonary arterial hypertension.In Pulmonary Arterial Hypertension, Reduced BMPR2 Promotes Endothelial-to-Mesenchymal Transition via HMGA1 and Its Target SlugAmphetamines promote mitochondrial dysfunction and DNA damage in pulmonary hypertensionFibrinogen plasma concentration is an independent marker of haemodynamic impairment in chronic thromboembolic pulmonary hypertension.The endothelial ADMA/NO pathway in hypoxia-related chronic respiratory diseases.Sweet taste receptor interacting protein CIB1 is a general inhibitor of InsP3-dependent Ca2+ release in vivo.Increased Pyruvate Dehydrogenase Kinase 4 Expression in Lung Pericytes Is Associated with Reduced Endothelial-Pericyte Interactions and Small Vessel Loss in Pulmonary Arterial Hypertension.Intrinsic BMP Antagonist Gremlin-1 as a Novel Circulating Marker in Pulmonary Arterial Hypertension.Role of Toll-like receptors and interferon regulatory factors in different experimental heart failure models of diverse etiology: IRF7 as novel cardiovascular stress-inducible factor.[Pathobiology, pathology and genetics of pulmonary hypertension: Recommendations of the Cologne Consensus Conference 2016].Enhanced caspase activity contributes to aortic wall remodeling and early aneurysm development in a murine model of Marfan syndrome.Myeloperoxidase aggravates pulmonary arterial hypertension by activation of vascular Rho-kinase.Pathobiology, pathology and genetics of pulmonary hypertension: Update from the Cologne Consensus Conference 2018Complete resolution of idiopathic pulmonary arterial hypertension following chemotherapyPPARγ Interaction with UBR5/ATMIN Promotes DNA Repair to Maintain Endothelial HomeostasisDoes circulating IL-17 identify a subset of patients with idiopathic pulmonary arterial hypertension?Subcellular Compartmentalization of Survivin is Associated with Biological Aggressiveness and Prognosis in Prostate CancerSmooth Muscle Contact Drives Endothelial Regeneration by BMPR2-Notch1-Mediated Metabolic and Epigenetic ChangesThe Actin Binding Protein Plastin-3 Is Involved in the Pathogenesis of Acute Myeloid LeukemiaThe P2-receptor-mediated Ca2+ signalosome of the human pulmonary endothelium - implications for pulmonary arterial hypertension
P50
Q27339475-0526B921-B88A-43E2-ADBE-68FB3E972C82Q28540624-9BDF1959-5590-4D03-8688-D6CDCF41AAFDQ35153971-9BA2712D-8D18-462E-AFE3-F37BD4367C14Q35376926-8B7B8B5E-315A-4291-AC0C-78ECDA35313AQ35766693-0A71BC8E-AD48-4DDE-BD59-E5900D4D5184Q36096312-2ED6C1E3-E9F0-4A09-9E1D-6897B7BED6FFQ36190169-133583FA-D71A-40E8-8FE6-0F31466FBEC4Q36869381-A8F44181-AC85-467C-89DA-8FB847B2AD86Q37599544-5B0C8847-C01A-4E45-ADD7-02FBC7314679Q37738172-1FD2EDC8-C63F-4CF7-9BE1-5B3BCEDE1D45Q38203518-9950C382-0D0C-4361-9712-3EA7AF0D0CE9Q39961290-F6E4E727-226C-4768-9C20-02A5A60CEBF4Q41022731-4FF76531-4E75-4894-A438-BE10B509F957Q48201616-D51F1879-9AFF-456A-9C03-785120C6CF64Q52655959-18CD4F6D-6068-4DBC-924A-C86E65239AEAQ52874616-F4A2ECD7-EC75-4DDA-93F5-C0A0AF772573Q53042878-4740FF3A-C499-4B6E-A89F-909E96FDA439Q54976862-7BFF503D-028B-4401-A905-DF94E2D442D3Q57492750-A27E3127-5214-4352-8472-F4FF561F2196Q61766950-B5ADF749-44E4-448F-9DDD-A6EB4CBDD778Q64282162-EF342F08-31DD-4C0F-8102-497B4E19FBB4Q86385610-AB7B2345-DE85-4DBA-BA76-C0A6F8C12DF3Q89865924-4CBB258D-BB21-435E-8AB7-CC7115394878Q90735599-37CB6C7D-7B95-4DF3-BC73-583F1D954620Q91254108-442D8B8D-EA8C-42AB-869B-9608F47242D0Q92515097-2598A3CE-9B28-477B-8A42-9D73363F34C8
P50
description
investigador
@es
researcher
@en
wetenschapper
@nl
name
Jan K Hennigs
@en
Jan K Hennigs
@nl
type
label
Jan K Hennigs
@en
Jan K Hennigs
@nl
prefLabel
Jan K Hennigs
@en
Jan K Hennigs
@nl
P31
P496
0000-0002-7784-8267