Anzahl der Publikationen: 9
Zeitschriftenartikel
Maity-Kumar, Gandhari; Staender, Lisa; DeAngelis, Meri; Lee, Sooyeon; Molenaar, Anna; Becker, Lore; Garrett, Lillian; Amerie, Oana; Hoelter, Sabine M.; Wurst, Wolfgang; Fuchs, Helmut; Feuchtinger, Annette; Gailus-Durner, Valerie; Gárcia-Cáceres, Cristina; Othman, Ahmed E.; Brockmann, Caroline; Schoeffling, Vanessa I.; Beiser, Katja; Krude, Heiko; Mroz, Piotr A.; Hofmann, Susanna; Tuckermann, Jan; DiMarchi, Richard D.; de Angelis, Martin Hrabe; Tschoep, Matthias H.; Pfluger, Paul T. und Mueller, Timo D.
(2022):
Validation of Mct8/Oatp1c1 dKO mice as a model organism for the Allan-Herndon-Dudley Syndrome.
In: Molecular Metabolism, Bd. 66, 101616
[PDF, 3MB]
Choukair, Daniela; Hauck, Fabian; Bettendorf, Markus; Krude, Heiko; Klein, Christoph; Baeumer, Tobias; Berner, Reinhard; Lee-Kirsch, Min Ae; Grasemann, Corinna; Burgard, Peter und Hoffmann, Georg F.
(2021):
An Integrated clinical pathway for diagnosis, treatment and care of rare diseases: model, operating procedures, and results of the project TRANSLATE-NAMSE funded by the German Federal Joint Committee.
In: Orphanet Journal of Rare Diseases, Bd. 16, Nr. 1, 474
Khajavi, Noushafarin; Finan, Brian; Kluth, Oliver; Müller, Timo D.; Mergler, Stefan; Schulz, Angela; Kleinau, Gunnar; Scheerer, Patrick; Schürmann, Annette; Gudermann, Thomas; Tschoep, Matthias H.; Krude, Heiko; DiMarchi, Richard D. und Biebermann, Heike
(2018):
An incretin-based tri-agonist promotes superior insulin secretion from murine pancreatic islets via PLC activation.
In: Cellular Signalling, Bd. 51: S. 13-22
Griese, Matthias; Lorenz, Elke; Hengst, Meike; Schams, Andrea; Wesselak, Traudl; Rauch, Daniela; Wittmann, Thomas; Kirchberger, Valerie; Escribano, Amparo; Schaible, Thomas; Baden, Winfried; Schulze, Johannes; Krude, Heiko; Aslanidis, Charalampos; Schwerk, Nicolaus; Kappler, Matthias; Hartl, Dominik; Lohse, Peter und Zarbock, Ralf
(2016):
Surfactant proteins in pediatric interstitial lung disease.
In: Pediatric Research, Bd. 79, Nr. 1: S. 34-41
Thorwarth, Anne; Schnittert-Hübener, Sarah; Ullmann, Reinhard; Krude, Heiko; Schrumpf, Pamela; Müller, Ines; Jyrch, Sabine; Dame, Christof; Biebermann, Heike; Kleinau, Gunnar; Katchanov, Juri; Schülke, Markus; Ebert, Grit; Steininger, Anne; Bönnemann, Carsten; Brockmann, Knut; Christen, Hans-Jürgen; Crock, Patricia; Zegher, Francis de; Griese, Matthias; Hewitt, Jacqueline; Ivarsson, Sten; Hübner, Christoph; Kapelari, Klaus; Plecko, Barbara; Rating, Dietz; Stoeva, Iva; Ropers, Hans-Hilger und Grüters, Annette
(2014):
Comprehensive genotyping and clinical characterisation reveal 27 novel NKX2-1 mutations and expand the phenotypic spectrum.
In: Journal of Medical Genetics, Bd. 51, Nr. 6: S. 375-387
[PDF, 2MB]
Kleinlein, Barbara; Griese, Matthias; Liebisch, Gerhard; Krude, Heiko; Lohse, Peter; Aslanidis, Charalampos; Schmitz, Gerd; Peters, Jochen und Holzinger, Andreas
(November 2011):
Fatal neonatal respiratory failure in an infant with congenital hypothyroidism due to haploinsufficiency of the NKX2-1 gene: alteration of pulmonary surfactant homeostasis.
In: Archives of disease in childhood. Fetal and neonatal edition, Bd. 96, Nr. 6:
F453-F456
[PDF, 196kB]
Scherag, Andre; Dina, Christian; Hinney, Anke; Vatin, Vincent; Scherag, Susann; Vogel, Carla I. G.; Mueller, Timo D.; Grallert, Harald; Wichmann, Heinz-Erich; Balkau, Beverley; Heude, Barbara; Jarvelin, Marjo-Riitta; Hartikainen, Anna-Liisa; Levy-Marchal, Claire; Weill, Jacques; Delplanque, Jerome; Koerner, Antje; Kiess, Wieland; Kovacs, Peter; Rayner, Nigel W.; Prokopenko, Inga; McCarthy, Mark I.; Schaefer, Helmut; Jarick, Ivonne; Boeing, Heiner; Fisher, Eva; Reinehr, Thomas; Heinrich, Joachim ORCID: https://orcid.org/0000-0002-9620-1629; Rzehak, Peter; Berdel, Dietrich; Borte, Michael; Biebermann, Heike; Krude, Heiko; Rosskopf, Dieter; Rimmbach, Christian; Rief, Winfried; Fromme, Tobias; Klingenspor, Martin; Schuermann, Annette; Schulz, Nadja; Noethen, Markus M.; Muehleisen, Thomas W.; Erbel, Raimund; Joeckel, Karl-Heinz; Moebus, Susanne; Boes, Tanja; Illig, Thomas; Froguel, Philippe; Hebebrand, Johannes und Meyre, David
(April 2010):
Two New Loci for Body-Weight Regulation Identified in a Joint Analysis of Genome-Wide Association Studies for Early-Onset Extreme Obesity in French and German Study Groups.
In: PLOS Genetics
6(4), e1000916
[PDF, 251kB]
Heid, Iris M.; Huth, Cornelia; Loos, Ruth J. F.; Kronenberg, Florian; Adamkova, Vera; Anand, Sonia S.; Ardlie, Kristin; Biebermann, Heike; Bjerregaard, Peter; Boeing, Heiner; Bouchard, Claude; Ciullo, Marina; Cooper, Jackie A.; Corella, Dolores; Dina, Christian; Engert, James C.; Fisher, Eva; Frances, Francesc; Froguel, Philippe; Hebebrand, Johannes; Hegele, Robert A.; Hinney, Anke; Hoehe, Margret R.; Hu, Frank B.; Hubacek, Jaroslav A.; Humphries, Steve E.; Hunt, Steven C.; Illig, Thomas; Jarvelin, Marjo-Riita; Kaakinen, Marika; Kollerits, Barbara; Krude, Heiko; Kumar, Jitender; Lange, Leslie A.; Langer, Birgit; Li, Shengxu; Luchner, Andreas; Lyon, Helen N.; Meyre, David; Mohlke, Karen L.; Mooser, Vincent; Nebel, Almut; Nguyen, Thuy Trang; Paulweber, Bernhard; Perusse, Louis; Qi, Lu; Rankinen, Tuomo; Rosskopf, Dieter; Schreiber, Stefan; Sengupta, Shantanu; Sorice, Rossella; Suk, Anita; Thorleifsson, Gudmar; Thorsteinsdottir, Unnur; Voelzke, Henry; Vimaleswaran, Karani S.; Wareham, Nicholas J.; Waterworth, Dawn; Yusuf, Salim; Lindgren, Cecilia; McCarthy, Mark I.; Lange, Christoph; Hirschhorn, Joel N.; Laird, Nan und Wichmann, Heinz-Erich
(Oktober 2009):
Meta-Analysis of the INSIG2 Association with Obesity Including 74,345 Individuals. Does Heterogeneity of Estimates Relate to Study Design?
In: PLOS Genetics
5(10), e1000694
[PDF, 297kB]
Konferenzbeitrag
Kühnen, Peter; Vetter, Celine; Jessen, Elena; Roenneberg, Till ORCID: https://orcid.org/0000-0003-2939-0332; Liesenkoetter, Klaus-Peter; Neumann, Uta; Lankes, Erwin; Werner, Helene; Jenni, Oskar G.; Schnurbein, Julia von; Wiegand, Susanna und Krude, Heiko
(2017):
Analysis of Sleep-Wake Behavior in Patients with Precocious and Delayed Puberty.
10th International Meeting of Pediatric Endocrinology, Washington DC, September 14-17, 2017.
Hormone Research in Paediatrics.
Bd. 88, Nr. Suppl. 1
Karger. S. 537
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