Berger S - Search Results

1

Lipid profiling of the Arabidopsis hypersensitive response reveals specific lipid peroxidation and fragmentation processes: biogenesis of pimelic and azelaic acid.

Zoeller M, Stingl N, Krischke M, Fekete A, Waller F, Berger S, Mueller MJ. Zoeller M, et al. Among authors: berger s. Plant Physiol. 2012 Sep;160(1):365-78. doi: 10.1104/pp.112.202846. Epub 2012 Jul 22. Plant Physiol. 2012. PMID: 22822212 Free PMC article.

2

Light conditions influence specific defence responses in incompatible plant-pathogen interactions: uncoupling systemic resistance from salicylic acid and PR-1 accumulation.

Zeier J, Pink B, Mueller MJ, Berger S. Zeier J, et al. Among authors: berger s. Planta. 2004 Aug;219(4):673-83. doi: 10.1007/s00425-004-1272-z. Epub 2004 Apr 20. Planta. 2004. PMID: 15098125

3

B1-phytoprostanes trigger plant defense and detoxification responses.

Loeffler C, Berger S, Guy A, Durand T, Bringmann G, Dreyer M, von Rad U, Durner J, Mueller MJ. Loeffler C, et al. Among authors: berger s. Plant Physiol. 2005 Jan;137(1):328-40. doi: 10.1104/pp.104.051714. Epub 2004 Dec 23. Plant Physiol. 2005. PMID: 15618427 Free PMC article.

4

Yeast increases resistance in Arabidopsis against Pseudomonas syringae and Botrytis cinerea by salicylic acid-dependent as well as -independent mechanisms.

Raacke IC, von Rad U, Mueller MJ, Berger S. Raacke IC, et al. Among authors: berger s. Mol Plant Microbe Interact. 2006 Oct;19(10):1138-46. doi: 10.1094/MPMI-19-1138. Mol Plant Microbe Interact. 2006. PMID: 17022178 Free article.

5

Visualization of dynamics of plant-pathogen interaction by novel combination of chlorophyll fluorescence imaging and statistical analysis: differential effects of virulent and avirulent strains of P. syringae and of oxylipins on A. thaliana.

Berger S, Benediktyová Z, Matous K, Bonfig K, Mueller MJ, Nedbal L, Roitsch T. Berger S, et al. J Exp Bot. 2007;58(4):797-806. doi: 10.1093/jxb/erl208. Epub 2006 Nov 30. J Exp Bot. 2007. PMID: 17138624

6

General detoxification and stress responses are mediated by oxidized lipids through TGA transcription factors in Arabidopsis.

Mueller S, Hilbert B, Dueckershoff K, Roitsch T, Krischke M, Mueller MJ, Berger S. Mueller S, et al. Among authors: berger s. Plant Cell. 2008 Mar;20(3):768-85. doi: 10.1105/tpc.107.054809. Epub 2008 Mar 11. Plant Cell. 2008. PMID: 18334669 Free PMC article.

7

Reactive electrophilic oxylipins: pattern recognition and signalling.

Mueller MJ, Berger S. Mueller MJ, et al. Among authors: berger s. Phytochemistry. 2009 Sep;70(13-14):1511-21. doi: 10.1016/j.phytochem.2009.05.018. Epub 2009 Jun 24. Phytochemistry. 2009. PMID: 19555983 Review.

8

New bioactive oxylipins formed by non-enzymatic free-radical-catalyzed pathways: the phytoprostanes.

Durand T, Bultel-Poncé V, Guy A, Berger S, Mueller MJ, Galano JM. Durand T, et al. Among authors: berger s. Lipids. 2009 Oct;44(10):875-88. doi: 10.1007/s11745-009-3351-1. Epub 2009 Sep 30. Lipids. 2009. PMID: 19789901 Review.

9

Differential impact of lipoxygenase 2 and jasmonates on natural and stress-induced senescence in Arabidopsis.

Seltmann MA, Stingl NE, Lautenschlaeger JK, Krischke M, Mueller MJ, Berger S. Seltmann MA, et al. Among authors: berger s. Plant Physiol. 2010 Apr;152(4):1940-50. doi: 10.1104/pp.110.153114. Epub 2010 Feb 26. Plant Physiol. 2010. PMID: 20190093 Free PMC article.

10

DONGLE and DEFECTIVE IN ANTHER DEHISCENCE1 lipases are not essential for wound- and pathogen-induced jasmonate biosynthesis: redundant lipases contribute to jasmonate formation.

Ellinger D, Stingl N, Kubigsteltig II, Bals T, Juenger M, Pollmann S, Berger S, Schuenemann D, Mueller MJ. Ellinger D, et al. Among authors: berger s. Plant Physiol. 2010 May;153(1):114-27. doi: 10.1104/pp.110.155093. Epub 2010 Mar 26. Plant Physiol. 2010. PMID: 20348210 Free PMC article.

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