Wiesmüller L - Search Results

1

MCM3AP and POMP Mutations Cause a DNA-Repair and DNA-Damage-Signaling Defect in an Immunodeficient Child.

Gatz SA, Salles D, Jacobsen EM, Dörk T, Rausch T, Aydin S, Surowy H, Volcic M, Vogel W, Debatin KM, Stütz AM, Schwarz K, Pannicke U, Hess T, Korbel JO, Schulz AS, Schumacher J, Wiesmüller L. Gatz SA, et al. Among authors: wiesmuller l. Hum Mutat. 2016 Mar;37(3):257-68. doi: 10.1002/humu.22939. Epub 2015 Dec 30. Hum Mutat. 2016. PMID: 26615982

2

p53 in recombination and repair.

Gatz SA, Wiesmüller L. Gatz SA, et al. Among authors: wiesmuller l. Cell Death Differ. 2006 Jun;13(6):1003-16. doi: 10.1038/sj.cdd.4401903. Cell Death Differ. 2006. PMID: 16543940 Review.

3

Resveratrol modulates DNA double-strand break repair pathways in an ATM/ATR-p53- and -Nbs1-dependent manner.

Gatz SA, Keimling M, Baumann C, Dörk T, Debatin KM, Fulda S, Wiesmüller L. Gatz SA, et al. Among authors: wiesmuller l. Carcinogenesis. 2008 Mar;29(3):519-27. doi: 10.1093/carcin/bgm283. Epub 2008 Jan 3. Carcinogenesis. 2008. PMID: 18174244

4

Take a break--resveratrol in action on DNA.

Gatz SA, Wiesmüller L. Gatz SA, et al. Among authors: wiesmuller l. Carcinogenesis. 2008 Feb;29(2):321-32. doi: 10.1093/carcin/bgm276. Epub 2008 Jan 3. Carcinogenesis. 2008. PMID: 18174251

5

Identification of a novel pro-apopotic function of NF-kappaB in the DNA damage response.

Karl S, Pritschow Y, Volcic M, Häcker S, Baumann B, Wiesmüller L, Debatin KM, Fulda S. Karl S, et al. Among authors: wiesmuller l. J Cell Mol Med. 2009 Oct;13(10):4239-56. doi: 10.1111/j.1582-4934.2009.00888.x. Epub 2009 Sep 1. J Cell Mol Med. 2009. PMID: 19725919 Free PMC article.

6

Role of SIRT1 in homologous recombination.

Uhl M, Csernok A, Aydin S, Kreienberg R, Wiesmüller L, Gatz SA. Uhl M, et al. Among authors: wiesmuller l. DNA Repair (Amst). 2010 Apr 4;9(4):383-93. doi: 10.1016/j.dnarep.2009.12.020. Epub 2010 Jan 25. DNA Repair (Amst). 2010. PMID: 20097625

7

BCR-ABL stimulates mutagenic homologous DNA double-strand break repair via the DNA-end-processing factor CtIP.

Salles D, Mencalha AL, Ireno IC, Wiesmüller L, Abdelhay E. Salles D, et al. Among authors: wiesmuller l. Carcinogenesis. 2011 Jan;32(1):27-34. doi: 10.1093/carcin/bgq216. Epub 2010 Oct 25. Carcinogenesis. 2011. PMID: 20974687

8

Functional characterization connects individual patient mutations in ataxia telangiectasia mutated (ATM) with dysfunction of specific DNA double-strand break-repair signaling pathways.

Keimling M, Volcic M, Csernok A, Wieland B, Dörk T, Wiesmüller L. Keimling M, et al. Among authors: wiesmuller l. FASEB J. 2011 Nov;25(11):3849-60. doi: 10.1096/fj.11-185546. Epub 2011 Jul 21. FASEB J. 2011. PMID: 21778326

9

NF-κB regulates DNA double-strand break repair in conjunction with BRCA1-CtIP complexes.

Volcic M, Karl S, Baumann B, Salles D, Daniel P, Fulda S, Wiesmüller L. Volcic M, et al. Among authors: wiesmuller l. Nucleic Acids Res. 2012 Jan;40(1):181-95. doi: 10.1093/nar/gkr687. Epub 2011 Sep 9. Nucleic Acids Res. 2012. PMID: 21908405 Free PMC article.

10

BRCA1-mediated repression of mutagenic end-joining of DNA double-strand breaks requires complex formation with BACH1.

Dohrn L, Salles D, Siehler SY, Kaufmann J, Wiesmüller L. Dohrn L, et al. Among authors: wiesmuller l. Biochem J. 2012 Feb 1;441(3):919-26. doi: 10.1042/BJ20110314. Biochem J. 2012. PMID: 22032289

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