Schanze D - Search Results

1

Profiling of the Bacterial Microbiota along the Murine Alimentary Tract.

Vilchez-Vargas R, Salm F, Znalesniak EB, Haupenthal K, Schanze D, Zenker M, Link A, Hoffmann W. Vilchez-Vargas R, et al. Among authors: schanze d. Int J Mol Sci. 2022 Feb 4;23(3):1783. doi: 10.3390/ijms23031783. Int J Mol Sci. 2022. PMID: 35163705 Free PMC article.

2

MOTA Syndrome: Molecular Genetic Confirmation of the Diagnosis in a Newborn with Previously Unreported Clinical Features.

Mitter D, Schanze D, Sterker I, Müller D, Till H, Zenker M. Mitter D, et al. Among authors: schanze d. Mol Syndromol. 2012 Sep;3(3):136-139. doi: 10.1159/000341501. Epub 2012 Jul 25. Mol Syndromol. 2012. PMID: 23112756 Free PMC article.

3

Haploinsufficiency of SOX5, a member of the SOX (SRY-related HMG-box) family of transcription factors is a cause of intellectual disability.

Schanze I, Schanze D, Bacino CA, Douzgou S, Kerr B, Zenker M. Schanze I, et al. Among authors: schanze d. Eur J Med Genet. 2013 Feb;56(2):108-13. doi: 10.1016/j.ejmg.2012.11.001. Epub 2012 Dec 5. Eur J Med Genet. 2013. PMID: 23220431

4

Ablepharon macrostomia syndrome: A distinct genetic entity clinically related to the group of FRAS-FREM complex disorders.

Schanze D, Harakalova M, Stevens CA, Brancati F, Dallapiccola B, Farndon P, Ferraz VE, McDonald-McGinn DM, Zackai EH, Wright M, van Lieshout S, Vogel MJ, van Haelst MM, Zenker M. Schanze D, et al. Am J Med Genet A. 2013 Dec;161A(12):3012-7. doi: 10.1002/ajmg.a.36119. Epub 2013 Sep 24. Am J Med Genet A. 2013. PMID: 24115501

5

Fraser syndrome due to mutations in GRIP1--clinical phenotype in two families and expansion of the mutation spectrum.

Schanze D, Kayserili H, Satkın BN, Altunoglu U, Zenker M. Schanze D, et al. Am J Med Genet A. 2014 Mar;164A(3):837-40. doi: 10.1002/ajmg.a.36343. Epub 2013 Dec 19. Am J Med Genet A. 2014. PMID: 24357607 No abstract available.

6

Deletions in the 3' part of the NFIX gene including a recurrent Alu-mediated deletion of exon 6 and 7 account for previously unexplained cases of Marshall-Smith syndrome.

Schanze D, Neubauer D, Cormier-Daire V, Delrue MA, Dieux-Coeslier A, Hasegawa T, Holmberg EE, Koenig R, Krueger G, Schanze I, Seemanova E, Shaw AC, Vogt J, Volleth M, Reis A, Meinecke P, Hennekam RC, Zenker M. Schanze D, et al. Among authors: schanze i. Hum Mutat. 2014 Sep;35(9):1092-100. doi: 10.1002/humu.22603. Epub 2014 Jul 8. Hum Mutat. 2014. PMID: 24924640

7

Valenced action/inhibition learning in humans is modulated by a genetic variant linked to dopamine D2 receptor expression.

Richter A, Guitart-Masip M, Barman A, Libeau C, Behnisch G, Czerney S, Schanze D, Assmann A, Klein M, Düzel E, Zenker M, Seidenbecher CI, Schott BH. Richter A, et al. Among authors: schanze d. Front Syst Neurosci. 2014 Aug 6;8:140. doi: 10.3389/fnsys.2014.00140. eCollection 2014. Front Syst Neurosci. 2014. PMID: 25147510 Free PMC article.

8

A cryptic unbalanced translocation der(4)t(4;17)(p16.1;q25.3) identifies Wittwer syndrome as a variant of Wolf-Hirschhorn syndrome.

Wieland I, Schanze D, Schanze I, Volleth M, Muschke P, Zenker M. Wieland I, et al. Among authors: schanze d, schanze i. Am J Med Genet A. 2014 Dec;164A(12):3213-4. doi: 10.1002/ajmg.a.36765. Epub 2014 Sep 23. Am J Med Genet A. 2014. PMID: 25251057 No abstract available.

9

Pilot study of association of catechol-O-methyl transferase rs4680 genotypes with acute kidney injury and tubular stress after open heart surgery.

Albert C, Kube J, Haase-Fielitz A, Dittrich A, Schanze D, Zenker M, Kuppe H, Hetzer R, Bellomo R, Mertens PR, Haase M. Albert C, et al. Among authors: schanze d. Biomark Med. 2014;8(10):1227-38. doi: 10.2217/bmm.14.85. Biomark Med. 2014. PMID: 25525983

10

Synaptic activity controls localization and function of CtBP1 via binding to Bassoon and Piccolo.

Ivanova D, Dirks A, Montenegro-Venegas C, Schöne C, Altrock WD, Marini C, Frischknecht R, Schanze D, Zenker M, Gundelfinger ED, Fejtova A. Ivanova D, et al. Among authors: schanze d. EMBO J. 2015 Apr 15;34(8):1056-77. doi: 10.15252/embj.201488796. Epub 2015 Feb 4. EMBO J. 2015. PMID: 25652077 Free PMC article.

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