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Elucidation of the genetic causes of bicuspid aortic valve disease.
Gehlen J, Stundl A, Debiec R, Fontana F, Krane M, Sharipova D, Nelson CP, Al-Kassou B, Giel AS, Sinning JM, Bruenger CMH, Zelck CF, Koebbe LL, Braund PS, Webb TR, Hetherington S, Ensminger S, Fujita B, Mohamed SA, Shrestha M, Krueger H, Siepe M, Kari FA, Nordbeck P, Buravezky L, Kelm M, Veulemans V, Adam M, Baldus S, Laugwitz KL, Haas Y, Karck M, Mehlhorn U, Conzelmann LO, Breitenbach I, Lebherz C, Urbanski P, Kim WK, Kandels J, Ellinghaus D, Nowak-Goettl U, Hoffmann P, Wirth F, Doppler S, Lahm H, Dreßen M, von Scheidt M, Knoll K, Kessler T, Hengstenberg C, Schunkert H, Nickenig G, Nöthen MM, Bolger AP, Abdelilah-Seyfried S, Samani NJ, Erdmann J, Trenkwalder T, Schumacher J. Gehlen J, et al. Among authors: lahm h. Cardiovasc Res. 2023 May 2;119(3):857-866. doi: 10.1093/cvr/cvac099. Cardiovasc Res. 2023. PMID: 35727948 Free PMC article.
A novel de novo TBX5 mutation in a patient with Holt-Oram syndrome leading to a dramatically reduced biological function.
Dreßen M, Lahm H, Lahm A, Wolf K, Doppler S, Deutsch MA, Cleuziou J, Pabst von Ohain J, Schön P, Ewert P, Malcic I, Lange R, Krane M. Dreßen M, et al. Among authors: lahm h, lahm a. Mol Genet Genomic Med. 2016 Jul 14;4(5):557-67. doi: 10.1002/mgg3.234. eCollection 2016 Sep. Mol Genet Genomic Med. 2016. PMID: 27652283 Free PMC article.
Cardiac fibroblasts: more than mechanical support.
Doppler SA, Carvalho C, Lahm H, Deutsch MA, Dreßen M, Puluca N, Lange R, Krane M. Doppler SA, et al. Among authors: lahm h. J Thorac Dis. 2017 Mar;9(Suppl 1):S36-S51. doi: 10.21037/jtd.2017.03.122. J Thorac Dis. 2017. PMID: 28446967 Free PMC article. Review.
161 results