Epigenetic dysregulation in the developing Down syndrome cortex von El Hajj, Nady, Dittrich, Marcus, Böck, Julia, Kraus, Theo F. J., Nanda, Indrajit, Müller, Tobias, Seidmann, Larissa, Tralau, Tim, Galetzka, Danuta, Schneider, Eberhard, Haaf, Thomas

Volltext

CpG sites with continuously increasing or decreasing methylation from early to late human fetal brain development von Schneider, Eberhard, Dittrich, Marcus, Böck, Julia, Nanda, Indrajit, Müller, Tobias, Seidmann, Larissa, Tralau, Tim, Galetzka, Danuta, El Hajj, Nady, Haaf, Thomas

Volltext

Human laminin β2 deficiency causes congenital nephrosis with mesangial sclerosis and distinct eye abnormalities von Zenker, Martin, Aigner, Thomas, Wendler, Olaf, Tralau, Tim, Müntefering, Horst, Fenski, Regina, Pitz, Susanne, Schumacher, Valérie, Royer-Pokora, Brigitte, Wühl, Elke, Cochat, Pierre, Bouvier, Raymonde, Kraus, Cornelia, Mark, Karlheinz, Madlon, Henry, Dötsch, Jörg, Rascher, Wolfgang, Maruniak-Chudek, Iwona, Lennert, Thomas, Neumann, Luitgard M., Reis, André

Volltext

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 von Galetzka, Danuta, Weis, Eva, Tralau, Tim, Seidmann, Larissa, Haaf, Thomas

Volltext

Congenital nephrosis, mesangial sclerosis, and distinct eye abnormalities with microcoria: An autosomal recessive syndrome von Zenker, Martin, Tralau, Tim, Lennert, Thomas, Pitz, Susanne, Mark, Karlheinz, Madlon, Henry, Dötsch, Jörg, Reis, André, Müntefering, Horst, Neumann, Luitgard M.

Volltext

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 inact... von Galetzka, Danuta, Tralau, Tim, Stein, Raimund, Haaf, Thomas

Volltext

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

Volltext

Human laminin ²2 deficiency causes congenital nephrosis with mesangial sclerosis and distinct eye abnormalities von Zenker, Martin, Aigner, Thomas, Wendler, Olaf, Tralau, Tim, Müntefering, Horst, Fenski, Regina, Pitz, Susanne, Schumacher, Valérie, Royer-Pokora, Brigitte, Wühl, Elke, Cochat, Pierre, Bouvier, Raymonde, Kraus, Cornelia, Karlheinz, Mark, Madlon, Henry, Dötsch, Jörg

Volltext

Human laminin beta2 deficiency causes congenital nephrosis with mesangial sclerosis and distinct eye abnormalities von Zenker, Martin, Aigner, Thomas, Wendler, Olaf, Tralau, Tim, Müntefering, Horst, Fenski, Regina, Pitz, Susanne, Schumacher, Valérie, Royer-Pokora, Brigitte, Wühl, Elke, Cochat, Pierre, Bouvier, Raymonde, Kraus, Cornelia, Mark, Karlheinz, Madlon, Henry, Dötsch, Jörg, Rascher, Wolfgang, Maruniak-Chudek, Iwona, Lennert, Thomas, Neumann, Luitgard M, Reis, André

Volltext