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Author Correction: The AP-1 transcription factor Fosl-2 drives cardiac fibrosis and arrhythmias under immunofibrotic conditions.
Stellato M, Dewenter M, Rudnik M, Hukara A, Özsoy Ç, Renoux F, Pachera E, Gantenbein F, Seebeck P, Uhtjaerv S, Osto E, Razansky D, Klingel K, Henes J, Distler O, Błyszczuk P, Kania G. Stellato M, et al. Among authors: dewenter m. Commun Biol. 2023 Feb 23;6(1):213. doi: 10.1038/s42003-023-04600-z. Commun Biol. 2023. PMID: 36823451 Free PMC article. No abstract available.
The AP-1 transcription factor Fosl-2 drives cardiac fibrosis and arrhythmias under immunofibrotic conditions.
Stellato M, Dewenter M, Rudnik M, Hukara A, Özsoy Ç, Renoux F, Pachera E, Gantenbein F, Seebeck P, Uhtjaerv S, Osto E, Razansky D, Klingel K, Henes J, Distler O, Błyszczuk P, Kania G. Stellato M, et al. Among authors: dewenter m. Commun Biol. 2023 Feb 9;6(1):161. doi: 10.1038/s42003-023-04534-6. Commun Biol. 2023. PMID: 36759717 Free PMC article.
CNP Promotes Antiarrhythmic Effects via Phosphodiesterase 2.
Cachorro E, Günscht M, Schubert M, Sadek MS, Siegert J, Dutt F, Bauermeister C, Quickert S, Berning H, Nowakowski F, Lämmle S, Firneburg R, Luo X, Künzel SR, Klapproth E, Mirtschink P, Mayr M, Dewenter M, Vettel C, Heijman J, Lorenz K, Guan K, El-Armouche A, Wagner M, Kämmerer S. Cachorro E, et al. Among authors: dewenter m. Circ Res. 2023 Feb 17;132(4):400-414. doi: 10.1161/CIRCRESAHA.122.322031. Epub 2023 Jan 30. Circ Res. 2023. PMID: 36715019 Free PMC article.
Endothelial deletion of the cytochrome P450 reductase leads to cardiac remodelling.
Lopez M, Malacarne PF, Ramanujam DP, Warwick T, Müller N, Hu J, Dewenter M, Weigert A, Günther S, Gilsbach R, Engelhardt S, Brandes RP, Rezende F. Lopez M, et al. Among authors: dewenter m. Front Physiol. 2022 Dec 2;13:1056369. doi: 10.3389/fphys.2022.1056369. eCollection 2022. Front Physiol. 2022. PMID: 36531184 Free PMC article.
Deep phenotyping of two preclinical mouse models and a cohort of RBM20 mutation carriers reveals no sex-dependent disease severity in RBM20 cardiomyopathy.
Lennermann DC, Pepin ME, Grosch M, Konrad L, Kemmling E, Hartmann J, Nolte JL, Clauder-Münster S, Kayvanpour E, Sedaghat-Hamedani F, Haas J, Meder B, van den Boogaard M, Amin AS, Dewenter M, Krüger M, Steinmetz LM, Backs J, van den Hoogenhof MMG. Lennermann DC, et al. Among authors: dewenter m. Am J Physiol Heart Circ Physiol. 2022 Dec 1;323(6):H1296-H1310. doi: 10.1152/ajpheart.00328.2022. Epub 2022 Nov 11. Am J Physiol Heart Circ Physiol. 2022. PMID: 36367695 Free article.
Acral lamellar ichthyosis with amino acid substitution in the C-terminus of keratin 2.
Frommherz L, Komlosi K, Hewel C, Kopp J, Dewenter M, Zimmer A, Bartsch O, Linke M, Technau-Hafsi K, Gerber S, Fischer J, Has C. Frommherz L, et al. Among authors: dewenter m. J Eur Acad Dermatol Venereol. 2023 Apr;37(4):817-822. doi: 10.1111/jdv.18719. Epub 2022 Nov 17. J Eur Acad Dermatol Venereol. 2023. PMID: 36331357
Assessment of the Genetic Spectrum of Uncombable Hair Syndrome in a Cohort of 107 Individuals.
Basmanav FB, Cesarato N, Kumar S, Borisov O, Kokordelis P, Ralser DJ, Wehner M, Axt D, Xiong X, Thiele H, Dolgin V, Gossmann Y, Fricker N, Dewenter MK, Weller K, Suri M, Reichenbach H, Oji V, Addor MC, Ramirez K, Stewart H, Garcia Bartels N, Weibel L, Wagner N, George S, Kilic A, Tantcheva-Poor I, Stewart A, Dikow N, Blaumeiser B, Medvecz M, Blume-Peytavi U, Farrant P, Grimalt R, Bertok S, Bradley L, Eskin-Schwartz M, Birk OS, Bygum A, Simon M, Krawitz P, Fischer C, Hamm H, Fritz G, Betz RC. Basmanav FB, et al. Among authors: dewenter mk. JAMA Dermatol. 2022 Nov 1;158(11):1245-1253. doi: 10.1001/jamadermatol.2022.2319. JAMA Dermatol. 2022. PMID: 36044230 Free PMC article.
Further characterization of Borjeson-Forssman-Lehmann syndrome in females due to de novo variants in PHF6.
Gerber CB, Fliedner A, Bartsch O, Berland S, Dewenter M, Haug M, Hayes I, Marin-Reina P, Mark PR, Martinez-Castellano F, Maystadt I, Karadurmus D, Steindl K, Wiesener A, Zweier M, Sticht H, Zweier C. Gerber CB, et al. Among authors: dewenter m. Clin Genet. 2022 Sep;102(3):182-190. doi: 10.1111/cge.14173. Epub 2022 Jun 14. Clin Genet. 2022. PMID: 35662002 Free PMC article.
40 results