Publications by authors named "Tim Tralau"

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CpG sites with continuously increasing or decreasing methylation from early to late human fetal brain development.
Eberhard Schneider, Marcus Dittrich, Julia Böck, Indrajit Nanda, Tobias Müller, Tim Tralau

Gene· October 2016

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Epigenetic dysregulation in the developing Down syndrome cortex.
Nady El Hajj, Marcus Dittrich, Julia Böck, Theo F J Kraus, Indrajit Nanda, Tim Tralau

Epigenetics· August 2016

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Sex-specific windows for high mRNA expression of DNA methyltransferases 1 and 3A and methyl-CpG-binding domain proteins 2 and 4 in human fetal gonads.
Danuta Galetzka, Eva Weis, Tim Tralau, Larissa Seidmann, Thomas Haaf

Mol Reprod Dev· February 2007

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Expression of DNMT3A transcripts and nucleolar localization of DNMT3A protein in human testicular and fibroblast cells suggest a role for de novo DNA methylation in nucleolar inactivation.
Danuta Galetzka, Tim Tralau, Raimund Stein, Thomas Haaf

J Cell Biochem· July 2006

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Human laminin beta2 deficiency causes congenital nephrosis with mesangial sclerosis and distinct eye abnormalities.
Martin Zenker, Thomas Aigner, Olaf Wendler, Tim Tralau, Horst Müntefering

Hum Mol Genet· November 2004

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Congenital nephrosis, mesangial sclerosis, and distinct eye abnormalities with microcoria: an autosomal recessive syndrome.
Martin Zenker, Tim Tralau, Thomas Lennert, Susanne Pitz, Karlheinz Mark

Am J Med Genet A· October 2004

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Human leukocyte elastase and cathepsin G are specific inhibitors of C5a-dependent neutrophil enzyme release and chemotaxis.
Tim Tralau, Ulf Meyer-Hoffert, Jens-M Schröder, Oliver Wiedow

Exp Dermatol· May 2004

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