Brendel C - Search Results

1

Prediction of Clinical Outcomes with Explainable Artificial Intelligence in Patients with Chronic Lymphocytic Leukemia.

Hoffmann J, Eminovic S, Wilhelm C, Krause SW, Neubauer A, Thrun MC, Ultsch A, Brendel C. Hoffmann J, et al. Among authors: brendel c. Curr Oncol. 2023 Feb 4;30(2):1903-1915. doi: 10.3390/curroncol30020148. Curr Oncol. 2023. PMID: 36826109 Free PMC article.

2

Very mild cases of Rett syndrome with skewed X inactivation.

Huppke P, Maier EM, Warnke A, Brendel C, Laccone F, Gärtner J. Huppke P, et al. Among authors: brendel c. J Med Genet. 2006 Oct;43(10):814-6. doi: 10.1136/jmg.2006.042077. Epub 2006 May 11. J Med Genet. 2006. PMID: 16690727 Free PMC article.

3

Multiple factors prevent transcriptional interference at the yeast ARO4-HIS7 locus.

Valerius O, Brendel C, Düvel K, Braus GH. Valerius O, et al. Among authors: brendel c. J Biol Chem. 2002 Jun 14;277(24):21440-5. doi: 10.1074/jbc.M201841200. Epub 2002 Apr 5. J Biol Chem. 2002. PMID: 11937506 Free article.

4

Mutation analysis of the HDAC 1, 2, 8 and CDKL5 genes in Rett syndrome patients without mutations in MECP2.

Huppke P, Ohlenbusch A, Brendel C, Laccone F, Gärtner J. Huppke P, et al. Among authors: brendel c. Am J Med Genet A. 2005 Aug 30;137(2):136-8. doi: 10.1002/ajmg.a.30764. Am J Med Genet A. 2005. PMID: 16086395

5

ABCG2 is expressed in late spermatogenesis and is associated with the acrosome.

Scharenberg C, Mannowetz N, Robey RW, Brendel C, Repges P, Sahrhage T, Jähn T, Wennemuth G. Scharenberg C, et al. Among authors: brendel c. Biochem Biophys Res Commun. 2009 Jan 9;378(2):302-7. doi: 10.1016/j.bbrc.2008.11.058. Epub 2008 Nov 24. Biochem Biophys Res Commun. 2009. PMID: 19032939

6

Monitoring of donor chimerism in sorted CD34+ peripheral blood cells allows the sensitive detection of imminent relapse after allogeneic stem cell transplantation.

Bornhäuser M, Oelschlaegel U, Platzbecker U, Bug G, Lutterbeck K, Kiehl MG, Schetelig J, Kiani A, Illmer T, Schaich M, Theuser C, Mohr B, Brendel C, Fauser AA, Klein S, Martin H, Ehninger G, Thiede C. Bornhäuser M, et al. Among authors: brendel c. Haematologica. 2009 Nov;94(11):1613-7. doi: 10.3324/haematol.2009.007765. Haematologica. 2009. PMID: 19880783 Free PMC article.

7

Readthrough of nonsense mutations in Rett syndrome: evaluation of novel aminoglycosides and generation of a new mouse model.

Brendel C, Belakhov V, Werner H, Wegener E, Gärtner J, Nudelman I, Baasov T, Huppke P. Brendel C, et al. J Mol Med (Berl). 2011 Apr;89(4):389-98. doi: 10.1007/s00109-010-0704-4. Epub 2010 Dec 1. J Mol Med (Berl). 2011. PMID: 21120444 Free PMC article.

8

Molecular and biochemical characterization of a unique mutation in CCS, the human copper chaperone to superoxide dismutase.

Huppke P, Brendel C, Korenke GC, Marquardt I, Donsante A, Yi L, Hicks JD, Steinbach PJ, Wilson C, Elpeleg O, Møller LB, Christodoulou J, Kaler SG, Gärtner J. Huppke P, et al. Among authors: brendel c. Hum Mutat. 2012 Aug;33(8):1207-15. doi: 10.1002/humu.22099. Epub 2012 May 16. Hum Mutat. 2012. PMID: 22508683 Free PMC article.

9

Characterization of Staufen 1 ribonucleoprotein complexes.

Brendel C, Rehbein M, Kreienkamp HJ, Buck F, Richter D, Kindler S. Brendel C, et al. Biochem J. 2004 Dec 1;384(Pt 2):239-46. doi: 10.1042/BJ20040812. Biochem J. 2004. PMID: 15303970 Free PMC article.

10

Characterization of the MeCP2R168X knockin mouse model for Rett syndrome.

Wegener E, Brendel C, Fischer A, Hülsmann S, Gärtner J, Huppke P. Wegener E, et al. Among authors: brendel c. PLoS One. 2014 Dec 26;9(12):e115444. doi: 10.1371/journal.pone.0115444. eCollection 2014. PLoS One. 2014. PMID: 25541993 Free PMC article.

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