TAZ-regulated RUNX2 signaling drives pulmonary artery calcification in pulmonary hypertension due to left heart disease
- Alternative title
-
TAZ-reguliertes RUNX2-Signaling fördert die Verkalkung der Lungenarterie bei pulmonaler Hypertonie aufgrund von Linksherzerkrankungen
- Location
-
Deutsche Nationalbibliothek Frankfurt am Main
- Extent
-
Online-Ressource
- Language
-
Englisch
- Notes
-
Berlin, Medizinische Fakultät Charité - Universitätsmedizin Berlin, Dissertation, 2024
- Keyword
-
Lungenkrankheit
Lunge
Tiermodell
- Event
-
Veröffentlichung
- (where)
-
Berlin
- (who)
-
Medizinische Fakultät Charité - Universitätsmedizin Berlin
- (when)
-
2024
- Creator
- DOI
-
10.17169/refubium-43630
- URN
-
urn:nbn:de:kobv:188-refubium-43920-8
- Rights
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
15.08.2025, 7:25 AM CEST
Data provider
This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Liu, Shaofei
- Medizinische Fakultät Charité - Universitätsmedizin Berlin
Time of origin
- 2024
Other Objects (12)
P10.08 Pulmonary Artery Calcification in Racehorses
Poly(ADP-ribose) polymerase 1 accelerates vascular calcification by upregulating Runx2
The mystery of persistent pulmonary hypertension: an idiopathic infantile arterial calcification
Oxygen-regulated transcription factors and their role in pulmonary disease
Pulmonary hypertension complicating pulmonary sarcoidosis
New pathway of icariin-induced MSC osteogenesis: transcriptional activation of TAZ/Runx2 by PI3K/Akt
YAP/TAZ activation mediates PQ-induced lung fibrosis by sustaining senescent pulmonary epithelial cells
SOX9 is a key component of RUNX2-regulated transcriptional circuitry in osteosarcoma
Pulmonary capillary pressure in pulmonary hypertension
Pulmonary hypertension in idiopathic pulmonary fibrosis
Tom70-regulated mitochondrial biogenesis via TFAM improves hypoxia-induced dysfunction of pulmonary vascular endothelial cells and alleviates hypoxic pulmonary hypertension
Right pulmonary to left pulmonary perfusion ratio after percutaneous pulmonary valve implantation
P10.08 Pulmonary Artery Calcification in Racehorses
Poly(ADP-ribose) polymerase 1 accelerates vascular calcification by upregulating Runx2
The mystery of persistent pulmonary hypertension: an idiopathic infantile arterial calcification
Oxygen-regulated transcription factors and their role in pulmonary disease
Pulmonary hypertension complicating pulmonary sarcoidosis
New pathway of icariin-induced MSC osteogenesis: transcriptional activation of TAZ/Runx2 by PI3K/Akt
YAP/TAZ activation mediates PQ-induced lung fibrosis by sustaining senescent pulmonary epithelial cells
SOX9 is a key component of RUNX2-regulated transcriptional circuitry in osteosarcoma
Pulmonary capillary pressure in pulmonary hypertension
Pulmonary hypertension in idiopathic pulmonary fibrosis
Tom70-regulated mitochondrial biogenesis via TFAM improves hypoxia-induced dysfunction of pulmonary vascular endothelial cells and alleviates hypoxic pulmonary hypertension
Right pulmonary to left pulmonary perfusion ratio after percutaneous pulmonary valve implantation
P10.08 Pulmonary Artery Calcification in Racehorses
Poly(ADP-ribose) polymerase 1 accelerates vascular calcification by upregulating Runx2
The mystery of persistent pulmonary hypertension: an idiopathic infantile arterial calcification
Oxygen-regulated transcription factors and their role in pulmonary disease
Pulmonary hypertension complicating pulmonary sarcoidosis
New pathway of icariin-induced MSC osteogenesis: transcriptional activation of TAZ/Runx2 by PI3K/Akt
YAP/TAZ activation mediates PQ-induced lung fibrosis by sustaining senescent pulmonary epithelial cells
SOX9 is a key component of RUNX2-regulated transcriptional circuitry in osteosarcoma
Pulmonary capillary pressure in pulmonary hypertension
Pulmonary hypertension in idiopathic pulmonary fibrosis
Tom70-regulated mitochondrial biogenesis via TFAM improves hypoxia-induced dysfunction of pulmonary vascular endothelial cells and alleviates hypoxic pulmonary hypertension