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2005 1
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Page 1
SPRED2 loss-of-function causes a recessive Noonan syndrome-like phenotype.
Motta M, Fasano G, Gredy S, Brinkmann J, Bonnard AA, Simsek-Kiper PO, Gulec EY, Essaddam L, Utine GE, Guarnetti Prandi I, Venditti M, Pantaleoni F, Radio FC, Ciolfi A, Petrini S, Consoli F, Vignal C, Hepbasli D, Ullrich M, de Boer E, Vissers LELM, Gritli S, Rossi C, De Luca A, Ben Becher S, Gelb BD, Dallapiccola B, Lauri A, Chillemi G, Schuh K, Cavé H, Zenker M, Tartaglia M. Motta M, et al. Among authors: ullrich m. Am J Hum Genet. 2021 Nov 4;108(11):2112-2129. doi: 10.1016/j.ajhg.2021.09.007. Epub 2021 Oct 8. Am J Hum Genet. 2021. PMID: 34626534 Free PMC article.
[Practical use of electronic patient records: findings from two care projects in centers for rare diseases].
Rashid A, Choukair D, Bauer C, Ullrich M, Maisch T. Rashid A, et al. Among authors: ullrich m. Bundesgesundheitsblatt Gesundheitsforschung Gesundheitsschutz. 2022 Nov;65(11):1143-1150. doi: 10.1007/s00103-022-03599-8. Epub 2022 Oct 24. Bundesgesundheitsblatt Gesundheitsforschung Gesundheitsschutz. 2022. PMID: 36278976 Free PMC article. Review. German.
SPRED2 deficiency elicits cardiac arrhythmias and premature death via impaired autophagy.
Ullrich M, Aßmus B, Augustin AM, Häbich H, Abeßer M, Martin Machado J, Werner F, Erkens R, Arias-Loza AP, Umbenhauer S, Wagner H, Benz PM, Unger A, Linke WA, Frantz S, Baba HA, Kuhn M, Schuh K. Ullrich M, et al. J Mol Cell Cardiol. 2019 Apr;129:13-26. doi: 10.1016/j.yjmcc.2019.01.023. Epub 2019 Feb 13. J Mol Cell Cardiol. 2019. PMID: 30771306
Gene disruption of Spred-2 causes dwarfism.
Bundschu K, Knobeloch KP, Ullrich M, Schinke T, Amling M, Engelhardt CM, Renné T, Walter U, Schuh K. Bundschu K, et al. Among authors: ullrich m. J Biol Chem. 2005 Aug 5;280(31):28572-80. doi: 10.1074/jbc.M503640200. Epub 2005 Jun 9. J Biol Chem. 2005. PMID: 15946934 Free article.
Gene trap: knockout on the fast lane.
Ullrich M, Schuh K. Ullrich M, et al. Methods Mol Biol. 2009;561:145-59. doi: 10.1007/978-1-60327-019-9_10. Methods Mol Biol. 2009. PMID: 19504070
Mena/VASP and αII-Spectrin complexes regulate cytoplasmic actin networks in cardiomyocytes and protect from conduction abnormalities and dilated cardiomyopathy.
Benz PM, Merkel CJ, Offner K, Abeßer M, Ullrich M, Fischer T, Bayer B, Wagner H, Gambaryan S, Ursitti JA, Adham IM, Linke WA, Feller SM, Fleming I, Renné T, Frantz S, Unger A, Schuh K. Benz PM, et al. Among authors: ullrich m. Cell Commun Signal. 2013 Aug 12;11:56. doi: 10.1186/1478-811X-11-56. Cell Commun Signal. 2013. PMID: 23937664 Free PMC article.
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