- Location
-
Deutsche Nationalbibliothek Frankfurt am Main
- Extent
-
Online-Ressource
- Language
-
Englisch
- Bibliographic citation
-
In: 10.3389/fcell.2023.1302448
- Event
-
Veröffentlichung
- (where)
-
Aachen
- (who)
-
Universitätsbibliothek der RWTH Aachen
- (when)
-
2023
- Creator
-
Puri, Deepika
Maaßen, Catharina
Varona Baranda, Monica
Zeevaert, Kira
Hahnfeld, Lena
Hauser, Annika
Fornero, Giulia
Elsafi Mabrouk, Mohamed H.
Wagner, Wolfgang
- DOI
-
10.18154/RWTH-CONV-252293
- URN
-
urn:nbn:de:101:1-2406160136331.295825865143
- Rights
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
14.08.2025, 10:51 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
- Puri, Deepika
- Maaßen, Catharina
- Varona Baranda, Monica
- Zeevaert, Kira
- Hahnfeld, Lena
- Hauser, Annika
- Fornero, Giulia
- Elsafi Mabrouk, Mohamed H.
- Wagner, Wolfgang
- Universitätsbibliothek der RWTH Aachen
Time of origin
- 2023
Other Objects (12)
Lucky iPSCs
iPSCs are safe!
Modelling urea cycle disorders using iPSCs
Microhomology-assisted scarless genome editing in human iPSCs
Modeling anthracycline-induced cardiotoxicity with patient-specific iPSCs
Generating and characterizing primate iPSCs for evolutionary analyses
Targeted integration of inducible Caspase-9 in human iPSCs allows efficient in vitro clearance of iPSCs and iPSC-macrophages
Genome-wide DNA methylation analysis reveals that mouse chemical iPSCs have closer epigenetic features to mESCs than OSKM-integrated iPSCs
Genomic Instability of iPSCs: Challenges Towards Their Clinical Applications
Modeling xeroderma pigmentosum associated neurological pathologies with patients-derived iPSCs
Advances and challenges in modeling inherited peripheral neuropathies using iPSCs
Improved and Flexible HDR Editing by Targeting Introns in iPSCs
Lucky iPSCs
iPSCs are safe!
Modelling urea cycle disorders using iPSCs
Microhomology-assisted scarless genome editing in human iPSCs
Modeling anthracycline-induced cardiotoxicity with patient-specific iPSCs
Generating and characterizing primate iPSCs for evolutionary analyses
Targeted integration of inducible Caspase-9 in human iPSCs allows efficient in vitro clearance of iPSCs and iPSC-macrophages
Genome-wide DNA methylation analysis reveals that mouse chemical iPSCs have closer epigenetic features to mESCs than OSKM-integrated iPSCs
Genomic Instability of iPSCs: Challenges Towards Their Clinical Applications
Modeling xeroderma pigmentosum associated neurological pathologies with patients-derived iPSCs
Advances and challenges in modeling inherited peripheral neuropathies using iPSCs
Improved and Flexible HDR Editing by Targeting Introns in iPSCs
Lucky iPSCs
iPSCs are safe!
Modelling urea cycle disorders using iPSCs
Microhomology-assisted scarless genome editing in human iPSCs
Modeling anthracycline-induced cardiotoxicity with patient-specific iPSCs
Generating and characterizing primate iPSCs for evolutionary analyses
Targeted integration of inducible Caspase-9 in human iPSCs allows efficient in vitro clearance of iPSCs and iPSC-macrophages
Genome-wide DNA methylation analysis reveals that mouse chemical iPSCs have closer epigenetic features to mESCs than OSKM-integrated iPSCs
Genomic Instability of iPSCs: Challenges Towards Their Clinical Applications
Modeling xeroderma pigmentosum associated neurological pathologies with patients-derived iPSCs
Advances and challenges in modeling inherited peripheral neuropathies using iPSCs