- Location
-
Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
-
2045-2322
- Extent
-
Online-Ressource
- Language
-
Englisch
- Notes
-
online resource.
- Bibliographic citation
-
Cross-talk among HMGA1 and FoxO1 in control of nuclear insulin signaling ; volume:8 ; number:1 ; day:4 ; month:6 ; year:2018 ; pages:1-13 ; date:12.2018
Scientific reports ; 8, Heft 1 (4.6.2018), 1-13, 12.2018
- Classification
-
Biowissenschaften, Biologie
- Creator
-
Chiefari, Eusebio
- Contributor
-
Arcidiacono, Biagio
Palmieri, Camillo
Corigliano, Domenica Maria
Morittu, Valeria Maria
Britti, Domenico
Armoni, Michal
Foti, Daniela Patrizia
Brunetti, Antonio
SpringerLink (Online service)
- DOI
-
10.1038/s41598-018-26968-3
- URN
-
urn:nbn:de:101:1-2018080522410078068085
- 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
- Chiefari, Eusebio
- Arcidiacono, Biagio
- Palmieri, Camillo
- Corigliano, Domenica Maria
- Morittu, Valeria Maria
- Britti, Domenico
- Armoni, Michal
- Foti, Daniela Patrizia
- Brunetti, Antonio
- SpringerLink (Online service)
Other Objects (12)
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Transcription factor FoxO1 regulates myoepithelial cell diversity and growth
HMGA1 is a novel transcriptional regulator of the FoxO1 gene
Mesenchymal stem cells promote pancreatic β-cell regeneration through downregulation of FoxO1 pathway
aPKC controls endothelial growth by modulating c-Myc via FoxO1 DNA-binding ability
O-GlcNAcylation of FoxO1 mediates nucleoside diphosphate kinase B deficiency induced endothelial damage
Liver FoxO1 overexpression is positively associated with the degree of liver injury in cirrhotic patients
Mst1-mediated phosphorylation of FoxO1 and C/EBP-β stimulates cell-protective mechanisms in cardiomyocytes
The Regulation of FoxO1 by Glucose-6-Phosphate Dehydrogenase and O-linked N-Acetyl-Glucosamine Modification
Human adipose and synovial-derived MSCs synergistically attenuate osteoarthritis by promoting chondrocyte autophagy through FoxO1 signaling
miR-92a-1-5p enriched prostate cancer extracellular vesicles regulate osteoclast function via MAPK1 and FoxO1
GlcNAcylation of FoxO1 is crucial for the upregulation of Angiopoietin 2 in NDPK B depleted endothelial cells
The role of FoxO1 in neurodegenerative diseases
Transcription factor FoxO1 regulates myoepithelial cell diversity and growth
HMGA1 is a novel transcriptional regulator of the FoxO1 gene
Mesenchymal stem cells promote pancreatic β-cell regeneration through downregulation of FoxO1 pathway
aPKC controls endothelial growth by modulating c-Myc via FoxO1 DNA-binding ability
O-GlcNAcylation of FoxO1 mediates nucleoside diphosphate kinase B deficiency induced endothelial damage
Liver FoxO1 overexpression is positively associated with the degree of liver injury in cirrhotic patients
Mst1-mediated phosphorylation of FoxO1 and C/EBP-β stimulates cell-protective mechanisms in cardiomyocytes
The Regulation of FoxO1 by Glucose-6-Phosphate Dehydrogenase and O-linked N-Acetyl-Glucosamine Modification
Human adipose and synovial-derived MSCs synergistically attenuate osteoarthritis by promoting chondrocyte autophagy through FoxO1 signaling
miR-92a-1-5p enriched prostate cancer extracellular vesicles regulate osteoclast function via MAPK1 and FoxO1
GlcNAcylation of FoxO1 is crucial for the upregulation of Angiopoietin 2 in NDPK B depleted endothelial cells
The role of FoxO1 in neurodegenerative diseases
Transcription factor FoxO1 regulates myoepithelial cell diversity and growth
HMGA1 is a novel transcriptional regulator of the FoxO1 gene
Mesenchymal stem cells promote pancreatic β-cell regeneration through downregulation of FoxO1 pathway
aPKC controls endothelial growth by modulating c-Myc via FoxO1 DNA-binding ability
O-GlcNAcylation of FoxO1 mediates nucleoside diphosphate kinase B deficiency induced endothelial damage
Liver FoxO1 overexpression is positively associated with the degree of liver injury in cirrhotic patients
Mst1-mediated phosphorylation of FoxO1 and C/EBP-β stimulates cell-protective mechanisms in cardiomyocytes
The Regulation of FoxO1 by Glucose-6-Phosphate Dehydrogenase and O-linked N-Acetyl-Glucosamine Modification
Human adipose and synovial-derived MSCs synergistically attenuate osteoarthritis by promoting chondrocyte autophagy through FoxO1 signaling
miR-92a-1-5p enriched prostate cancer extracellular vesicles regulate osteoclast function via MAPK1 and FoxO1