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Page 1
Reduced social interaction and ultrasonic communication in a mouse model of monogenic heritable autism.
Jamain S, Radyushkin K, Hammerschmidt K, Granon S, Boretius S, Varoqueaux F, Ramanantsoa N, Gallego J, Ronnenberg A, Winter D, Frahm J, Fischer J, Bourgeron T, Ehrenreich H, Brose N. Jamain S, et al. Among authors: ronnenberg a. Proc Natl Acad Sci U S A. 2008 Feb 5;105(5):1710-5. doi: 10.1073/pnas.0711555105. Epub 2008 Jan 28. Proc Natl Acad Sci U S A. 2008. PMID: 18227507 Free PMC article.
Erythropoietin enhances hippocampal long-term potentiation and memory.
Adamcio B, Sargin D, Stradomska A, Medrihan L, Gertler C, Theis F, Zhang M, Müller M, Hassouna I, Hannke K, Sperling S, Radyushkin K, El-Kordi A, Schulze L, Ronnenberg A, Wolf F, Brose N, Rhee JS, Zhang W, Ehrenreich H. Adamcio B, et al. Among authors: ronnenberg a. BMC Biol. 2008 Sep 9;6:37. doi: 10.1186/1741-7007-6-37. BMC Biol. 2008. PMID: 18782446 Free PMC article.
Modification of cognitive performance in schizophrenia by complexin 2 gene polymorphisms.
Begemann M, Grube S, Papiol S, Malzahn D, Krampe H, Ribbe K, Friedrichs H, Radyushkin KA, El-Kordi A, Benseler F, Hannke K, Sperling S, Schwerdtfeger D, Thanhäuser I, Gerchen MF, Ghorbani M, Gutwinski S, Hilmes C, Leppert R, Ronnenberg A, Sowislo J, Stawicki S, Stödtke M, Szuszies C, Reim K, Riggert J, Eckstein F, Falkai P, Bickeböller H, Nave KA, Brose N, Ehrenreich H. Begemann M, et al. Among authors: ronnenberg a. Arch Gen Psychiatry. 2010 Sep;67(9):879-88. doi: 10.1001/archgenpsychiatry.2010.107. Arch Gen Psychiatry. 2010. PMID: 20819981
A myelin gene causative of a catatonia-depression syndrome upon aging.
Hagemeyer N, Goebbels S, Papiol S, Kästner A, Hofer S, Begemann M, Gerwig UC, Boretius S, Wieser GL, Ronnenberg A, Gurvich A, Heckers SH, Frahm J, Nave KA, Ehrenreich H. Hagemeyer N, et al. Among authors: ronnenberg a. EMBO Mol Med. 2012 Jun;4(6):528-39. doi: 10.1002/emmm.201200230. Epub 2012 Apr 4. EMBO Mol Med. 2012. PMID: 22473874 Free PMC article.
Development of an autism severity score for mice using Nlgn4 null mutants as a construct-valid model of heritable monogenic autism.
El-Kordi A, Winkler D, Hammerschmidt K, Kästner A, Krueger D, Ronnenberg A, Ritter C, Jatho J, Radyushkin K, Bourgeron T, Fischer J, Brose N, Ehrenreich H. El-Kordi A, et al. Among authors: ronnenberg a. Behav Brain Res. 2013 Aug 15;251:41-9. doi: 10.1016/j.bbr.2012.11.016. Epub 2012 Nov 23. Behav Brain Res. 2013. PMID: 23183221
Genetic markers of a Munc13 protein family member, BAIAP3, are gender specifically associated with anxiety and benzodiazepine abuse in mice and humans.
Wojcik SM, Tantra M, Stepniak B, Man KN, Müller-Ribbe K, Begemann M, Ju A, Papiol S, Ronnenberg A, Gurvich A, Shin Y, Augustin I, Brose N, Ehrenreich H. Wojcik SM, et al. Among authors: ronnenberg a. Mol Med. 2013 Jul 24;19(1):135-48. doi: 10.2119/molmed.2013.00033. Mol Med. 2013. PMID: 23698091 Free PMC article.
63 results