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Eine Ebene höherGruppiert nach: Dokumententyp |
Veröffentlichungsdatum
Anzahl der Publikationen: 4
2022
Kogan, Palgit-S.; Wirth, Felix; Tomar, Archana; Darr, Jonatan; Teperino, Raffaele; Lahm, Harald; Dressen, Martina; Puluca, Nazan; Zhang, Zhong; Neb, Irina; Beck, Nicole; Luzius, Tatjana; Osa de la Rosa, Luis de la; Gärtner, Kathrin; Hüls, Corinna; Zeidler, Reinhard; Ramanujam, Deepak; Engelhardt, Stefan; Wenk, Catharina; Holdt, Lesca M.; Mononen, Mimmi; Sahara, Makoto; Cleuziou, Julie; Hörer, Jürgen; Lange, Rüdiger; Krane, Markus und Doppler, Stefanie A.
(2022):
Uncovering the molecular identity of cardiosphere-derived cells (CDCs) by single-cell RNA sequencing.
In: Basic Research in Cardiology, Bd. 117, Nr. 1, 11
Lahm, Harald; Heinrich, Paul; Zierler, Elisabeth; Dzilic, Elda; Neb, Irina; Luzius, Tatjana; Doppler, Stefanie A.; Schneider, Stephanie; Lange, Rüdiger; Krane, Markus und Dressen, Martina
(2022):
Generation of a CRISPR/Cas edited human induced pluripotent stem cell line DHMi005-A-1 carrying a patient-specific disease-causing point mutation in the TBX5 gene.
In: Stem Cell Research, Bd. 60, 102691
2021
Krane, Markus; Dressen, Martina; Santamaria, Gianluca; My, Ilaria; Schneider, Christine M.; Dorn, Tatjana; Laue, Svenja; Mastantuono, Elisa; Berutti, Riccardo; Rawat, Hilansi; Gilsbach, Ralf; Schneider, Pedro; Lahm, Harald; Schwarz, Sascha; Doppler, Stefanie A.; Paige, Sharon; Puluca, Nazan; Doll, Sophia; Neb, Irina; Brade, Thomas; Zhang, Zhong; Abou-Ajram, Claudia; Northoff, Bernd; Holdt, Lesca M.; Sudhop, Stefanie; Sahara, Makoto; Goedel, Alexander; Dendorfer, Andreas; Tjong, Fleur V. Y.; Rijlaarsdam, Maria E.; Cleuziou, Julie; Lang, Nora; Kupatt, Christian; Bezzina, Connie; Lange, Rudiger; Bowles, Neil E.; Mann, Matthias; Gelb, Bruce D.; Crotti, Lia; Hein, Lutz; Meitinger, Thomas; Wu, Sean; Sinnecker, Daniel; Gruber, Peter J.; Laugwitz, Karl-Ludwig und Moretti, Alessandra
(2021):
Sequential Defects in Cardiac Lineage Commitment and Maturation Cause Hypoplastic Left Heart Syndrome.
In: Circulation, Bd. 144, Nr. 17: S. 1409-1428
Lahm, Harald; Jia, Meiwen; Dressen, Martina; Wirth, Felix; Puluca, Nazan; Gilsbach, Ralf; Keavney, Bernard D.; Cleuziou, Julie; Beck, Nicole; Bondareva, Olga; Dzilic, Elda; Burri, Melchior; König, Karl C.; Ziegelmüller, Johannes A.; Abou-Ajram, Claudia; Neb, Irina; Zhang, Zhong; Doppler, Stefanie A.; Mastantuono, Elisa; Lichtner, Peter; Eckstein, Gertrud; Hörer, Jürgen; Ewert, Peter; Priest, James R.; Hein, Lutz; Lange, Rüdiger; Meitinger, Thomas; Cordell, Heather J.; Mueller-Myhsok, Bertram und Krane, Markus
(2021):
Congenital heart disease risk loci identified by genome-wide association study in European patients.
In: Journal of Clinical Investigation, Bd. 131, Nr. 2, e141837
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