Schneider A - Search Results

1

Rsk2 Knockdown in PC12 Cells Results in Sp1 Dependent Increased Expression of the Gria2 Gene, Encoding the AMPA Receptor Subunit GluR2.

Mehmood T, Schneider A, Pannetier S, Hanauer A. Mehmood T, et al. Among authors: schneider a. Int J Mol Sci. 2013 Feb 6;14(2):3358-75. doi: 10.3390/ijms14023358. Int J Mol Sci. 2013. PMID: 23389038 Free PMC article.

2

Coffin-Lowry syndrome.

Pereira PM, Schneider A, Pannetier S, Heron D, Hanauer A. Pereira PM, et al. Among authors: schneider a. Eur J Hum Genet. 2010 Jun;18(6):627-33. doi: 10.1038/ejhg.2009.189. Epub 2009 Nov 4. Eur J Hum Genet. 2010. PMID: 19888300 Free PMC article. Review.

3

Transcriptome profile reveals AMPA receptor dysfunction in the hippocampus of the Rsk2-knockout mice, an animal model of Coffin-Lowry syndrome.

Mehmood T, Schneider A, Sibille J, Marques Pereira P, Pannetier S, Ammar MR, Dembele D, Thibault-Carpentier C, Rouach N, Hanauer A. Mehmood T, et al. Among authors: schneider a. Hum Genet. 2011 Mar;129(3):255-69. doi: 10.1007/s00439-010-0918-0. Epub 2010 Nov 30. Hum Genet. 2011. PMID: 21116650

4

Altered ERK/MAPK signaling in the hippocampus of the mrsk2_KO mouse model of Coffin-Lowry syndrome.

Schneider A, Mehmood T, Pannetier S, Hanauer A. Schneider A, et al. J Neurochem. 2011 Nov;119(3):447-59. doi: 10.1111/j.1471-4159.2011.07423.x. Epub 2011 Sep 28. J Neurochem. 2011. PMID: 21838783 Free article.

5

Identification of the first deep intronic mutation in the RPS6KA3 gene in a patient with a severe form of Coffin-Lowry syndrome.

Schneider A, Maas SM, Hennekam RC, Hanauer A. Schneider A, et al. Eur J Med Genet. 2013 Mar;56(3):150-2. doi: 10.1016/j.ejmg.2012.11.007. Epub 2012 Dec 20. Eur J Med Genet. 2013. PMID: 23261961

6

Sam68 sequestration and partial loss of function are associated with splicing alterations in FXTAS patients.

Sellier C, Rau F, Liu Y, Tassone F, Hukema RK, Gattoni R, Schneider A, Richard S, Willemsen R, Elliott DJ, Hagerman PJ, Charlet-Berguerand N. Sellier C, et al. Among authors: schneider a. EMBO J. 2010 Apr 7;29(7):1248-61. doi: 10.1038/emboj.2010.21. Epub 2010 Feb 25. EMBO J. 2010. PMID: 20186122 Free PMC article.

7

Cell-Type-Specific Gene Expression Profiling in Adult Mouse Brain Reveals Normal and Disease-State Signatures.

Merienne N, Meunier C, Schneider A, Seguin J, Nair SS, Rocher AB, Le Gras S, Keime C, Faull R, Pellerin L, Chatton JY, Neri C, Merienne K, Déglon N. Merienne N, et al. Among authors: schneider a. Cell Rep. 2019 Feb 26;26(9):2477-2493.e9. doi: 10.1016/j.celrep.2019.02.003. Cell Rep. 2019. PMID: 30811995 Free article.

8

Symptomatic Clusters Related to Amyloid Positivity in Cognitively Unimpaired Individuals.

Sannemann L, Bartels C, Brosseron F, Buerger K, Fliessbach K, Freiesleben SD, Frommann I, Glanz W, Heneka MT, Janowitz D, Kilimann I, Kleineidam L, Lammerding D, Laske C, Munk MHJ, Perneczky R, Peters O, Priller J, Rauchmann BS, Rostamzadeh A, Roy-Kluth N, Schild AK, Schneider A, Schneider LS, Spottke A, Spruth EJ, Teipel S, Wagner M, Wiltfang J, Wolfsgruber S, Duezel E, Jessen F; DELCODE Study Group. Sannemann L, et al. Among authors: schneider a. J Alzheimers Dis. 2024 Jun 5. doi: 10.3233/JAD-231335. Online ahead of print. J Alzheimers Dis. 2024. PMID: 38848176

9

Averaged versus Persistent Reduction in Urine Output to Define Oliguria in Critically Ill Patients, an Observational Study.

Monard C, Bianchi N, Kelevina T, Altarelli M, Chaouch A, Schneider A. Monard C, et al. Among authors: schneider a. Clin J Am Soc Nephrol. 2024 Jun 7. doi: 10.2215/CJN.0000000000000493. Online ahead of print. Clin J Am Soc Nephrol. 2024. PMID: 38848126

10

Diagnosis and treatment of Parkinson´s disease (guideline of the German Society for Neurology).

Höglinger G; German Parkinson’s Guidelines Committee; Trenkwalder C. Höglinger G, et al. Neurol Res Pract. 2024 Jun 6;6(1):30. doi: 10.1186/s42466-024-00325-4. Neurol Res Pract. 2024. PMID: 38845028

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