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| 1. |
Sumer, Simon: Deciphering the role of SHOX2 in atrial fibrillation and sinus node dysfunction / presented by M.Sc. Simon Alexander Sumer ; referees: Prof. Dr. Gudrun A. Rappold [und ein weiterer G… . -
Heidelberg, 2020. - 1 Online-Ressource (XII, 83 Seiten)
DOI: 10.11588/heidok.00029142
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| 2. |
Hoffmann, Sandra: Functional characterization of rare variants in the SHOX2 gene identified in sinus node dysfunction and atrial fibrillation / Sandra Hoffmann, Christoph Paone, Simon A. Sumer, Sabrina Diebold, Birgit Weiss, Ralph Roeth, Sebast… , 11 July 2019. - 7 S.
In: Frontiers in genetics, ISSN 1664-8021. 10(2019) Artikel-Nummer 648, 7 Seiten
DOI: 10.3389/fgene.2019.00648
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| 3. |
Rädecke, Kristin: Elucidating the role of SHOX2 in atrial fibrillation using a patient-derived human induced pluripotent stem cell model / presented by M.Sc. Kristin Rädecke ; referees: Prof. Dr. Gudrun Rappold, Prof. Dr. Johannes Backs. -
Heidelberg, [2024?]. - XIII, 96 Seiten : Illustrationen, Diagramme
 Buch/keine Angabe |
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| 4. |
Sumer, Simon: Precise correction of heterozygous SHOX2 mutations in hiPSCs derived from patients with atrial fibrillation via genome editing and sib selection / Simon Alexander Sumer, Sandra Hoffmann, Svenja Laue, Birgit Campbell, Kristin Raedecke, Viktoria Fra… , September 24, 2020. - 15 S.
In: Stem cell reports, ISSN 2213-6711. 15(2020), 4, Seite 999-1013
DOI: 10.1016/j.stemcr.2020.08.015
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| 5. |
Schmitteckert, Stefanie: Murine transgenic embryonic stem cell lines for the investigation of sinoatrial node-related molecular pathways / Stefanie Schmitteckert, Anne Griesbeck, Simon Sumer, Anna Jauch, Alexandra Rolletschek, Beate Niesle… . - 5 S.
In: Stem cell research, ISSN 1876-7753. 25(2017), Supplement C, S. 278-282
DOI: 10.1016/j.scr.2017.07.011
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| 6. |
Ho, Kim Hoa: The development and tumorigenesis of choroid plexus / presented by Kim Hoa Ho, M. Sc. ; referee: Prof. Dr. rer. nat. Gudrun Rappold, Dr. Annarita Patrizi. -
Heidelberg, 10 Jul. 2024. - 1 Online-Ressource (160 Seiten) : Illustrationen, Diagramme
DOI: 10.11588/heidok.00035078
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| 7. |
Vergara Dal Pont, Ignacio Andrés: Establishment of an in vitro platform for the characterization of proteins involved in the intestinal epithelial barrier dysfunction of inflammatory bowel disease, with a focus on TNFα/TNR1A/TNR1B / presented by M.Sc. Ignacio Andrés Vergara Dal Pont ; referees: Prof. Dr. Gudrun Rappold [und ein wei… . -
Heidelberg, 23 Nov. 2022. - 1 Online-Ressource (221 Seiten) : Illustrationen, Diagramme
DOI: 10.11588/heidok.00032402
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| 8. |
Rädecke, Kristin: Generation of two homozygous SHOX2 knock-out human induced pluripotent stem cell lines using CRISPR/Cas9 / Kristin Rädecke, Ambuj Gore, Karin Burau, Magdalena Laugsch, Katrin Köhler, Gudrun A Rappold, Sandra… , 5 April 2023. - 7 S.
In: Stem cell research, ISSN 1876-7753. 69(2023) vom: Apr., Artikel-ID 103089, Seite 1-7
DOI: 10.1016/j.scr.2023.103089
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| 9. |
Bohl, Bettina: Deciphering a regulatory function of endolysosomes in asymmetric cell division of human neural stem cells via the Notch signalling pathway / presented by M.Sc. Bettina Bohl ; referees: Prof. Dr. Gudrun Rappold [und ein weiterer Gutachter]. -
Heidelberg, 09 Jul. 2021. - 1 Online-Ressource (135 Seiten) : Illustrationen, Diagramme
DOI: 10.11588/heidok.00030201
Online-Ressource |
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| 10. |
Hoffmann, Sandra: Identification and tissue-specific characterization of novel SHOX-regulated genes in zebrafish highlights SOX family members among other genes / Sandra Hoffmann, Ralph Roeth, Sabrina Diebold, Jasmin Gogel, David Hassel, Steffen Just and Gudrun A… , 27 May 2021. - 11 S.
In: Frontiers in genetics, ISSN 1664-8021. 12(2021) vom: 27. Mai, Artikel-ID 688806, Seite 1-11
DOI: 10.3389/fgene.2021.688808
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| 11. |
Wang, Jing: Mitochondrial dysfunction and oxidative stress contribute to cognitive and motor impairment in FOXP1 syndrome / Jing Wang, Henning Fröhlich, Felipe Bodaleo Torres, Rangel Leal Silva, Gernot Poschet, Amit Agarwal,… , February 14, 2022. - 11 S.
In: Proceedings of the National Academy of Sciences of the United States of America, ISSN 1091-6490. 119(2022), 8, Artikel-ID e2112852119, Seite 1-11
DOI: 10.1073/pnas.2112852119
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| 12. |
Weiß, Birgit: Identification of novel genes including NAV2 associated with isolated tall stature / Birgit Weiss, Tim Ott, Philipp Vick, Julian C. Lui, Ralph Roeth, Sebastian Vogel, Stephan Waldmüller… , 12 December 2023. - 11 S.
In: Frontiers in endocrinology, ISSN 1664-2392. 14(2023) vom: Dez., Artikel-ID 1258313, Seite 1-11
DOI: 10.3389/fendo.2023.1258313
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| 13. |
Niesler, Beate: Emerging evidence for gene mutations driving both brain and gut dysfunction in autism spectrum disorder / Beate Niesler, Gudrun A. Rappold, 2021. - 3 S.
In: Molecular psychiatry, ISSN 1476-5578. 26(2021), 5, Seite 1442-1444
DOI: 10.1038/s41380-020-0778-5
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| 14. |
Bohl, Bettina: Deciphering a regulatory function of endolysosomes in asymmetric cell division of human neural stem cells via the Notch signalling pathway / presented by M.Sc. Bettina Gudrun Bohl ; referees: Prof. Dr. Gudrun Rappold [und ein weiterer Gutac… . -
Heidelberg, [2021?]. - IX, 92, XL Blätter : Illustrationen, Diagramme
Buch/keine Angabe |
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| 15. |
Vergara Dal Pont, Ignacio Andrés: Establishment of an in vitro platform for the characterization of proteins involved in the intestinal epithelial barrier dysfunction of inflammatory bowel disease, with a focus on TNFα/TNR1A/TNR1B / presented by M.Sc. Ignacio Andrés Vergara Dal Pont ; referees: Prof. Dr. Gudrun Rappold, Prof. Dr. C… . -
Heidelberg, [2022?]. - XXXVII, 182 Seiten : Illustrationen, Diagramme
Buch/keine Angabe |
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| 16. |
Rheinert, David: Vom Gen zum Phänotyp: die SHOX-Gene und ihr Netzwerk / vorgelegt von David Rheinert ; Doktormutter: Frau Prof. Dr. rer. nat. Gudrun Rappold. -
Heidelberg, 2021. - IV, 72 Blätter : Illustrationen, Diagramme
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| 17. |
Wang, Jing: Disrupted mitochondrial network drives deficits of learning and memory in a mouse model of FOXP1 haploinsufficiency / Jing Wang, Gudrun A. Rappold and Henning Fröhlich, 11 January 2022. - 12 S.
In: Genes, ISSN 2073-4425. 13(2022), 1, Artikel-ID 127, Seite 1-12
DOI: 10.3390/genes13010127
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| 18. |
Montalbano, Antonino: Identification and functional characterization of genetic modifiers for SHOX deficiency / presented by Diplom-M.Sc. Antonino Montalbano ; referees: Prof. Dr. Gudrun Rappold, Prof. Dr. Thomas… . -
Heidelberg, 2016. - 1 Online-Ressource (121 Seiten)
DOI: 10.11588/heidok.00021940
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| 19. |
Rappold, Gudrun: Wenn die Intelligenz beeinträchtigt ist / Gudrun A. Rappold, 2021-08-21. - 14 S.
In: Heidelberger Jahrbücher online, ISSN 2509-2464. 6(2021), Seite 165-178
DOI: 10.17885/heiup.hdjbo.2021.1.24384
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| 20. |
Berens, Sabrina: Serotonin type 3 receptor subunit gene polymorphisms associated with psychosomatic symptoms in irritable bowel syndrome : a multicenter retrospective study / Sabrina Berens, Yuanjun Dong, Nikola Fritz, Jutta Walstab, Mauro D'Amato, Tenghao Zheng, Verena Wahl… , June 7, 2022. - 16 S.
In: World journal of gastroenterology, ISSN 2219-2840. 28(2022), 21, Seite 2334-2349
DOI: 10.3748/wjg.v28.i21.2334
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