Search Results for: tennstedt
A novel missense mutation in TNNI3K causes recessively inherited cardiac conduction disease in a consanguineous Pakistani family
Ramzan S, Tennstedt S, Tariq M, Khan S, Ul Ayan HN, Ali A, Munz M, Thiele H, Korejo AA, Mughal AR, Jamal SZ, Nürnberg P, Baig SM, Erdmann J, Ahmad I.
Genes 2021, 12(8), 1282
Genome-wide association meta-analysis of coronary artery disease and periodontitis reveals a novel shared risk locus.
Munz M, Richter GM, Loos BG, Jepsen S, Divaris K, Offenbacher S, Teumer A, Holtfreter B, Kocher T, Bruckmann C, Jockel-Schneider Y, Graetz C, Munoz L, Bhandari A, Tennstedt S, Staufenbiel I, van der Velde N, Uitterlinden AG, de Groot LCPGM, Wellmann J, Berger K, Krone B, Hoffmann P, Laudes M, Lieb W, Franke A, Dommisch H, Erdmann J, Schaefer AS.
Sci Rep. 2018 Sep 12;8(1):13678. doi: 10.1038/s41598-018-31980-8.
Stimulators of the soluble guanylyl cyclase: promising functional insights from rare coding atherosclerosis-related GUCY1A3 variants
Wobst J, von Ameln S, Wolf B, Wierer M, Dang TA, Sager HB, Tennstedt S, Hengstenberg C, Koesling D, Friebe A, Braun SL, Erdmann J, Schunkert H, Kessler T.
Basic Res Cardiol. 2016 Jul;111(4):51. doi: 10.1007/s00395-016-0570-5. Epub 2016 Jun 24. PMID: 27342234 [PubMed – in process]
Classification of ADAMTS binding sites: The first step toward selective ADAMTS7 inhibitors
Müller M, Kessler T, Schunkert H, Erdmann J, Tennstedt S.
Biochem Biophys Res Commun. 2016 Mar 11;471(3):380-5. doi: 10.1016/j.bbrc.2016.02.025. Epub 2016 Feb 10. PubMed PMID: 26872430.
Screening of synthetic and natural product databases: Identification of novel androgens and antiandrogens.
Bobach C, Tennstedt S, Palberg K, Denkert A, Brandt W, de Meijere A, Seliger B, Wessjohann LA.
Eur J Med Chem. 2015 Jan 27;90:267-79. doi: 10.1016/j.ejmech.2014.11.026. Epub 2014 Nov 13.
A novel missense mutation in CACNA1A evaluated by in silico protein modeling is associated with non-episodic spinocerebellar ataxia with slow progression.
Bürk K, Kaiser FJ, Tennstedt S, Schöls L, Kreuz FR, Wieland T, Strom TM, Büttner T, Hollstein R, Braunholz D, Plaschke J, Gillessen-Kaesbach G, Zühlke C.
Eur J Med Genet. 2014 Apr;57(5):207-11. doi: 10.1016/j.ejmg.2014.01.005. Epub 2014 Jan 29.
Dysfunctional nitric oxide signalling increases risk of myocardial infarction
Erdmann, J., Stark, K., Esslinger, U. B., Rumpf, P. M., Koesling, D., de Wit, C., Kaiser, F. J., Braunholz, D., Medack, A., Fischer, M., Zimmermann, M. E., Tennstedt, S., Graf, E., Eck, S., Aherrahrou, Z., Nahrstaedt, J., Willenborg, C., Bruse, P., Braenne, I., Nothen, M. M., Hofmann, P., Braund, P. S., Mergia, E., Reinhard, W., Burgdorf, C., Schreiber, S., Balmforth, A. J., Hall, A. S., Bertram, L., Steinhagen-Thiessen, E., Li, S. C., Marz, W., Reilly, M., Kathiresan, S., McPherson, R., Walter, U., CardioGram, Ott, J., Samani, N. J., Strom, T. M., Meitinger, T., Hengstenberg, C., Schunkert, H.
Nature. 2013 Dec 19;504(7480):432-6. doi: 10.1038/nature12722. Epub 2013 Nov 10.
RAD21 mutations cause a human cohesinopathy.
Deardorff MA, Wilde JJ, Albrecht M, Dickinson E, Tennstedt S, Braunholz D, Mönnich M, Yan Y, Xu W, Gil-Rodríguez MC, Clark D, Hakonarson H, Halbach S, Michelis LD, Rampuria A, Rossier E, Spranger S, Van Maldergem L, Lynch SA, Gillessen-Kaesbach G, Lüdecke HJ, Ramsay RG, McKay MJ, Krantz ID, Xu H, Horsfield JA, Kaiser FJ.
Am J Hum Genet. 2012 Jun 8;90(6):1014-27. doi: 10.1016/j.ajhg.2012.04.019. Epub 2012 May 24.