Microvasculopathy and soft tissue calcification in mice are governed by fetuin-A, magnesium and pyrophosphate
- Standort
-
Deutsche Nationalbibliothek Frankfurt am Main
- Umfang
-
Online-Ressource
- Sprache
-
Englisch
- Erschienen in
-
In: 10.1371/journal.pone.0228938
- Ereignis
-
Veröffentlichung
- (wo)
-
Aachen
- (wer)
-
Universitätsbibliothek der RWTH Aachen
- (wann)
-
2020
- Urheber
-
Babler, Anne
Schmitz, Carlo
Buescher, Andrea
Herrmann, Marietta
Gremse, Felix
Gorgels, Theo
Floege, Juergen
Jahnen-Dechent, Wilhelm
- DOI
-
10.18154/RWTH-CONV-241211
- URN
-
urn:nbn:de:101:1-2021020507314497060276
- Rechteinformation
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
15.08.2025, 07:24 MESZ
Datenpartner
Dieses Objekt wird bereitgestellt von:
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Beteiligte
- Babler, Anne
- Schmitz, Carlo
- Buescher, Andrea
- Herrmann, Marietta
- Gremse, Felix
- Gorgels, Theo
- Floege, Juergen
- Jahnen-Dechent, Wilhelm
- Universitätsbibliothek der RWTH Aachen
Entstanden
- 2020
Ähnliche Objekte (12)
Fetuin-A-based theranostics in ectopic calcification
Oral administration of pyrophosphate inhibits connective tissue calcification
The role of Fetuin-A in ectopic calcification and lipid metabolism
Elevated glucose levels increase vascular calcification risk by disrupting extracellular pyrophosphate metabolism
Fetuin
Tissue chaperoning—the expanded functions of fetuin-A beyond inhibition of systemic calcification
Tissue chaperoning—the expanded functions of fetuin-A beyond inhibition of systemic calcification
Lumenal calcification and microvasculopathy in fetuin-A-deficient mice lead to multiple organ morbidity
Pathology of ectopic calcification in fetuin-a deficient mice : compensatory gene regulation and mineralized matrix metabolism
Pathology of ectopic calcification in fetuin-a deficient mice : compensatory gene regulation and mineralized matrix metabolism
Serum magnesium level and cardiac valve calcification in hemodialysis patients
‘Police-Governed’ Universities
Fetuin-A-based theranostics in ectopic calcification
Oral administration of pyrophosphate inhibits connective tissue calcification
The role of Fetuin-A in ectopic calcification and lipid metabolism
Elevated glucose levels increase vascular calcification risk by disrupting extracellular pyrophosphate metabolism
Fetuin
Tissue chaperoning—the expanded functions of fetuin-A beyond inhibition of systemic calcification
Tissue chaperoning—the expanded functions of fetuin-A beyond inhibition of systemic calcification
Lumenal calcification and microvasculopathy in fetuin-A-deficient mice lead to multiple organ morbidity
Pathology of ectopic calcification in fetuin-a deficient mice : compensatory gene regulation and mineralized matrix metabolism
Pathology of ectopic calcification in fetuin-a deficient mice : compensatory gene regulation and mineralized matrix metabolism
Serum magnesium level and cardiac valve calcification in hemodialysis patients
‘Police-Governed’ Universities
Fetuin-A-based theranostics in ectopic calcification
Oral administration of pyrophosphate inhibits connective tissue calcification
The role of Fetuin-A in ectopic calcification and lipid metabolism
Elevated glucose levels increase vascular calcification risk by disrupting extracellular pyrophosphate metabolism
Fetuin
Tissue chaperoning—the expanded functions of fetuin-A beyond inhibition of systemic calcification
Tissue chaperoning—the expanded functions of fetuin-A beyond inhibition of systemic calcification
Lumenal calcification and microvasculopathy in fetuin-A-deficient mice lead to multiple organ morbidity
Pathology of ectopic calcification in fetuin-a deficient mice : compensatory gene regulation and mineralized matrix metabolism
Pathology of ectopic calcification in fetuin-a deficient mice : compensatory gene regulation and mineralized matrix metabolism
Serum magnesium level and cardiac valve calcification in hemodialysis patients