Tralau T - Search Results

1

CpG sites with continuously increasing or decreasing methylation from early to late human fetal brain development.

Schneider E, Dittrich M, Böck J, Nanda I, Müller T, Seidmann L, Tralau T, Galetzka D, El Hajj N, Haaf T. Schneider E, et al. Among authors: tralau t. Gene. 2016 Oct 30;592(1):110-118. doi: 10.1016/j.gene.2016.07.058. Epub 2016 Jul 25. Gene. 2016. PMID: 27468947 Free article.

2

Epigenetic dysregulation in the developing Down syndrome cortex.

El Hajj N, Dittrich M, Böck J, Kraus TF, Nanda I, Müller T, Seidmann L, Tralau T, Galetzka D, Schneider E, Haaf T. El Hajj N, et al. Among authors: tralau t. Epigenetics. 2016 Aug 2;11(8):563-78. doi: 10.1080/15592294.2016.1192736. Epub 2016 May 31. Epigenetics. 2016. PMID: 27245352 Free PMC article.

3

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.

Galetzka D, Tralau T, Stein R, Haaf T. Galetzka D, et al. Among authors: tralau t. J Cell Biochem. 2006 Jul 1;98(4):885-94. doi: 10.1002/jcb.20798. J Cell Biochem. 2006. PMID: 16453278

4

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.

Galetzka D, Weis E, Tralau T, Seidmann L, Haaf T. Galetzka D, et al. Among authors: tralau t. Mol Reprod Dev. 2007 Feb;74(2):233-41. doi: 10.1002/mrd.20615. Mol Reprod Dev. 2007. PMID: 16998846

5

Human laminin beta2 deficiency causes congenital nephrosis with mesangial sclerosis and distinct eye abnormalities.

Zenker M, Aigner T, Wendler O, Tralau T, Müntefering H, Fenski R, Pitz S, Schumacher V, Royer-Pokora B, Wühl E, Cochat P, Bouvier R, Kraus C, Mark K, Madlon H, Dötsch J, Rascher W, Maruniak-Chudek I, Lennert T, Neumann LM, Reis A. Zenker M, et al. Among authors: tralau t. Hum Mol Genet. 2004 Nov 1;13(21):2625-32. doi: 10.1093/hmg/ddh284. Epub 2004 Sep 14. Hum Mol Genet. 2004. PMID: 15367484

6

Congenital nephrosis, mesangial sclerosis, and distinct eye abnormalities with microcoria: an autosomal recessive syndrome.

Zenker M, Tralau T, Lennert T, Pitz S, Mark K, Madlon H, Dötsch J, Reis A, Müntefering H, Neumann LM. Zenker M, et al. Among authors: tralau t. Am J Med Genet A. 2004 Oct 1;130A(2):138-45. doi: 10.1002/ajmg.a.30310. Am J Med Genet A. 2004. PMID: 15372515 Review.

7

Comparative case study on NAMs: towards enhancing specific target organ toxicity analysis.

Jochum K, Miccoli A, Sommersdorf C, Poetz O, Braeuning A, Tralau T, Marx-Stoelting P. Jochum K, et al. Among authors: tralau t. Arch Toxicol. 2024 Nov;98(11):3641-3658. doi: 10.1007/s00204-024-03839-7. Epub 2024 Aug 29. Arch Toxicol. 2024. PMID: 39207506 Free PMC article.

8

Thresholds of adversity for endocrine disrupting substances: a conceptual case study.

Choi J, Rotter S, Ritz V, Kneuer C, Marx-Stoelting P, de Lourdes Marzo Solano M, Oertel A, Rudzok S, Ziková-Kloas A, Tralau T, Hensel A. Choi J, et al. Among authors: tralau t. Arch Toxicol. 2024 Jul;98(7):2019-2045. doi: 10.1007/s00204-024-03748-9. Epub 2024 May 5. Arch Toxicol. 2024. PMID: 38704806 Free PMC article.

9

In vitro and in vivo investigation of a thyroid hormone system-specific interaction with triazoles.

Kadic A, Oles P, Fischer BC, Reetz AE, Sylla BS, Feiertag K, Ritz V, Heise T, Marx-Stoelting P, Tralau T, Renko K, Solano MLM. Kadic A, et al. Among authors: tralau t. Sci Rep. 2024 Mar 18;14(1):6503. doi: 10.1038/s41598-024-55019-3. Sci Rep. 2024. PMID: 38499550 Free PMC article.

10

Adverse outcome pathway-based analysis of liver steatosis in vitro using human liver cell lines.

Karaca M, Fritsche K, Lichtenstein D, Vural Ö, Kreuzer K, Alarcan J, Braeuning A, Marx-Stoelting P, Tralau T. Karaca M, et al. Among authors: tralau t. STAR Protoc. 2023 Sep 15;4(3):102500. doi: 10.1016/j.xpro.2023.102500. Epub 2023 Aug 23. STAR Protoc. 2023. PMID: 37616165 Free PMC article.

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