Sticht H - Search Results

1

Assessing clinical utility of preconception expanded carrier screening regarding residual risk for neurodevelopmental disorders.

Boonsawat P, Horn AHC, Steindl K, Baumer A, Joset P, Kraemer D, Bahr A, Ivanovski I, Cabello EM, Papik M, Zweier M, Oneda B, Sirleto P, Burkhardt T, Sticht H, Rauch A. Boonsawat P, et al. Among authors: sticht h. NPJ Genom Med. 2022 Jul 29;7(1):45. doi: 10.1038/s41525-022-00316-x. NPJ Genom Med. 2022. PMID: 35906228 Free PMC article.

2

AMBER force-field parameters for phosphorylated amino acids in different protonation states: phosphoserine, phosphothreonine, phosphotyrosine, and phosphohistidine.

Homeyer N, Horn AH, Lanig H, Sticht H. Homeyer N, et al. Among authors: sticht h. J Mol Model. 2006 Feb;12(3):281-9. doi: 10.1007/s00894-005-0028-4. Epub 2005 Oct 21. J Mol Model. 2006. PMID: 16240095

3

Rare large scale subdomain motions in prion protein can initiate aggregation.

Schwarzinger S, Horn AH, Ziegler J, Sticht H. Schwarzinger S, et al. Among authors: sticht h. J Biomol Struct Dyn. 2006 Jun;23(6):581-90. doi: 10.1080/07391102.2006.10507083. J Biomol Struct Dyn. 2006. PMID: 16615804 Review.

4

Insights into amprenavir resistance in E35D HIV-1 protease mutation from molecular dynamics and binding free-energy calculations.

Meiselbach H, Horn AH, Harrer T, Sticht H. Meiselbach H, et al. Among authors: sticht h. J Mol Model. 2007 Feb;13(2):297-304. doi: 10.1007/s00894-006-0121-3. Epub 2006 Jun 23. J Mol Model. 2007. PMID: 16794810

5

Human TBX1 missense mutations cause gain of function resulting in the same phenotype as 22q11.2 deletions.

Zweier C, Sticht H, Aydin-Yaylagül I, Campbell CE, Rauch A. Zweier C, et al. Among authors: sticht h. Am J Hum Genet. 2007 Mar;80(3):510-7. doi: 10.1086/511993. Epub 2007 Jan 18. Am J Hum Genet. 2007. PMID: 17273972 Free PMC article.

6

Two novel mutations in the insulin binding subunit of the insulin receptor gene without insulin binding impairment in a patient with Rabson-Mendenhall syndrome.

Thiel CT, Knebel B, Knerr I, Sticht H, Müller-Wieland D, Zenker M, Reis A, Dörr HG, Rauch A. Thiel CT, et al. Among authors: sticht h. Mol Genet Metab. 2008 Jul;94(3):356-62. doi: 10.1016/j.ymgme.2008.02.013. Epub 2008 Apr 14. Mol Genet Metab. 2008. PMID: 18411068

7

Insight into the phosphoryl transfer of the Escherichia coli glucose phosphotransferase system from QM/MM simulations.

Jardin C, Horn AH, Schürer G, Sticht H. Jardin C, et al. Among authors: sticht h. J Phys Chem B. 2008 Oct 23;112(42):13391-400. doi: 10.1021/jp801319k. Epub 2008 Sep 25. J Phys Chem B. 2008. PMID: 18816086

8

Independent NF1 and PTPN11 mutations in a family with neurofibromatosis-Noonan syndrome.

Thiel C, Wilken M, Zenker M, Sticht H, Fahsold R, Gusek-Schneider GC, Rauch A. Thiel C, et al. Among authors: sticht h. Am J Med Genet A. 2009 Jun;149A(6):1263-7. doi: 10.1002/ajmg.a.32837. Am J Med Genet A. 2009. PMID: 19449407

9

Effect of pathogenic mutations on the structure and dynamics of Alzheimer's A beta 42-amyloid oligomers.

Kassler K, Horn AH, Sticht H. Kassler K, et al. Among authors: sticht h. J Mol Model. 2010 May;16(5):1011-20. doi: 10.1007/s00894-009-0611-1. Epub 2009 Nov 12. J Mol Model. 2010. PMID: 19908073

10

Amyloid-beta42 oligomer structures from fibrils: a systematic molecular dynamics study.

Horn AH, Sticht H. Horn AH, et al. Among authors: sticht h. J Phys Chem B. 2010 Feb 18;114(6):2219-26. doi: 10.1021/jp100023q. J Phys Chem B. 2010. PMID: 20104925

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