Sperling SR - Search Results

1

Comparative DNA methylation and gene expression analysis identifies novel genes for structural congenital heart diseases.

Grunert M, Dorn C, Cui H, Dunkel I, Schulz K, Schoenhals S, Sun W, Berger F, Chen W, Sperling SR. Grunert M, et al. Among authors: sperling sr. Cardiovasc Res. 2016 Oct;112(1):464-77. doi: 10.1093/cvr/cvw195. Epub 2016 Aug 5. Cardiovasc Res. 2016. PMID: 27496870

2

Genome-wide array analysis of normal and malformed human hearts.

Kaynak B, von Heydebreck A, Mebus S, Seelow D, Hennig S, Vogel J, Sperling HP, Pregla R, Alexi-Meskishvili V, Hetzer R, Lange PE, Vingron M, Lehrach H, Sperling S. Kaynak B, et al. Circulation. 2003 May 20;107(19):2467-74. doi: 10.1161/01.CIR.0000066694.21510.E2. Epub 2003 May 12. Circulation. 2003. PMID: 12742993

3

Identification and functional analysis of CITED2 mutations in patients with congenital heart defects.

Sperling S, Grimm CH, Dunkel I, Mebus S, Sperling HP, Ebner A, Galli R, Lehrach H, Fusch C, Berger F, Hammer S. Sperling S, et al. Hum Mutat. 2005 Dec;26(6):575-82. doi: 10.1002/humu.20262. Hum Mutat. 2005. PMID: 16287139

4

Array analysis applied to malformed hearts: Molecular dissection of tetralogy of Fallot.

Sperling S. Sperling S. Methods Mol Med. 2006;126:233-46. doi: 10.1385/1-59745-088-X:233. Methods Mol Med. 2006. PMID: 16930016

5

Characterization of TBX20 in human hearts and its regulation by TFAP2.

Hammer S, Toenjes M, Lange M, Fischer JJ, Dunkel I, Mebus S, Grimm CH, Hetzer R, Berger F, Sperling S. Hammer S, et al. J Cell Biochem. 2008 Jun 1;104(3):1022-33. doi: 10.1002/jcb.21686. J Cell Biochem. 2008. PMID: 18275040

6

Prediction of cardiac transcription networks based on molecular data and complex clinical phenotypes.

Toenjes M, Schueler M, Hammer S, Pape UJ, Fischer JJ, Berger F, Vingron M, Sperling S. Toenjes M, et al. Mol Biosyst. 2008 Jun;4(6):589-98. doi: 10.1039/b800207j. Epub 2008 Apr 2. Mol Biosyst. 2008. PMID: 18493657

7

Regulation of muscle development by DPF3, a novel histone acetylation and methylation reader of the BAF chromatin remodeling complex.

Lange M, Kaynak B, Forster UB, Tönjes M, Fischer JJ, Grimm C, Schlesinger J, Just S, Dunkel I, Krueger T, Mebus S, Lehrach H, Lurz R, Gobom J, Rottbauer W, Abdelilah-Seyfried S, Sperling S. Lange M, et al. Genes Dev. 2008 Sep 1;22(17):2370-84. doi: 10.1101/gad.471408. Genes Dev. 2008. PMID: 18765789 Free PMC article.

8

MicroRazerS: rapid alignment of small RNA reads.

Emde AK, Grunert M, Weese D, Reinert K, Sperling SR. Emde AK, et al. Among authors: sperling sr. Bioinformatics. 2010 Jan 1;26(1):123-4. doi: 10.1093/bioinformatics/btp601. Epub 2009 Oct 29. Bioinformatics. 2010. PMID: 19880369

9

Evaluation of the LightCycler 1536 Instrument for high-throughput quantitative real-time PCR.

Schlesinger J, Tönjes M, Schueler M, Zhang Q, Dunkel I, Sperling SR. Schlesinger J, et al. Among authors: sperling sr. Methods. 2010 Apr;50(4):S19-22. doi: 10.1016/j.ymeth.2010.01.007. Methods. 2010. PMID: 20215016 Review.

10

Mutations in the sarcomere gene MYH7 in Ebstein anomaly.

Postma AV, van Engelen K, van de Meerakker J, Rahman T, Probst S, Baars MJ, Bauer U, Pickardt T, Sperling SR, Berger F, Moorman AF, Mulder BJ, Thierfelder L, Keavney B, Goodship J, Klaassen S. Postma AV, et al. Among authors: sperling sr. Circ Cardiovasc Genet. 2011 Feb;4(1):43-50. doi: 10.1161/CIRCGENETICS.110.957985. Epub 2010 Dec 2. Circ Cardiovasc Genet. 2011. PMID: 21127202

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