Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Johannes Hutzler"'
Autor:
Eva Hollenbach, Johannes Hutzler, Thomas Mietzner, Stefan Tresch, Helmut Kraus, Janneke Hendriks, Hans Wolfgang Höffken, Matthias Witschel, Ruth Campe, Lara Kämmerer, Jens Lerchl
Publikováno v:
Pesticide Biochemistry and Physiology. 148:116-125
The prevalent occurrence of herbicide resistant weeds increases the necessity for new site of action herbicides for effective control as well as to relax selection pressure on the known sites of action. As a consequence, interest increased in the une
Autor:
Johannes Hutzler, Markus Aebi, Martin Loibl, Lina Wunderle, Benjamin L. Schulz, Sabine Strahl
Publikováno v:
Journal of Biological Chemistry. 289:8599-8611
O-Mannosylation and N-glycosylation are essential protein modifications that are initiated in the endoplasmic reticulum (ER). Protein translocation across the ER membrane and N-glycosylation are highly coordinated processes that take place at the tra
Autor:
Xinghua Ma, Anthony C. Willis, Trevor William Newton, Tobias Seiser, Amanda Benton, Prue Guest, Ehab S. Taher, Johannes Hutzler, Martin G. Banwell
Publikováno v:
The Journal of organic chemistry. 82(1)
A series of 28 analogues of the phytotoxic geranylcyclohexentriol (−)-phomentrioloxin A (1) has been synthesized through cross-couplings of various enantiomerically pure haloconduritols or certain deoxygenated derivatives with either terminal alkyn
Autor:
Thomas Ehrhardt, Johannes Hutzler, Ralf Looser, Klaus Grossmann, Stefan Tresch, Nicole Christiansen
Publikováno v:
Pest Management Science. 68:482-492
BACKGROUND: The mode of action of the grass herbicides cinmethylin and 5-benzyloxymethyl-1,2-isoxazolines substituted with methylthiophene (methiozolin) or pyridine (ISO1, ISO2) was investigated. RESULTS: Physiological profiling using a series of bio
Publikováno v:
Weed Science. 59:290-298
Saflufenacil (Kixor™) is a new protoporphyrinogen IX oxidase (PPO) inhibiting herbicide for preplant burndown and selective PRE dicot weed control in multiple crops, including corn. The biokinetic properties and the mechanism of selectivity of safl
Autor:
Pedro Botías, Johannes Hutzler, Andrea Schott, Jesús García-Cantalejo, Enrico Ragni, Heidi Piberger, Sabine Strahl, Ana Belen Sanz, Javier Arroyo, Clara Bermejo
Publikováno v:
Molecular Microbiology. 79:1529-1546
Summary O-mannosylation is a crucial protein modification in eukaryotes that is initiated by the essential family of protein O-mannosyltransferases (PMTs). Here we demonstrate that in the model yeast Saccharomyces cerevisiae rhodanine-3-acetic acid d
Publikováno v:
Proceedings of the National Academy of Sciences. 104:7827-7832
Protein O-mannosylation represents an evolutionarily conserved, essential posttranslational modification with immense impact on a variety of cellular processes. In humans, O-mannosylation defects result in Walker–Warburg syndrome, a severe recessiv
Autor:
Klaus Grossmann, Stefan Tresch, Ralf Looser, Johannes Hutzler, Thomas Ehrhardt, Nicole Christiansen, Stephan Pollmann
Publikováno v:
Pest management science. 68(4)
BACKGROUND: For novel herbicides identified in greenhouse screens, efficient research is important to discover and chemically optimise new leads with new modes of action (MoAs). RESULTS: The metabolic and physiological response pattern to a herbicide
Autor:
Javier, Arroyo, Johannes, Hutzler, Clara, Bermejo, Enrico, Ragni, Jesús, García-Cantalejo, Pedro, Botías, Heidi, Piberger, Andrea, Schott, Ana Belén, Sanz, Sabine, Strahl
Publikováno v:
Molecular microbiology. 79(6)
O-mannosylation is a crucial protein modification in eukaryotes that is initiated by the essential family of protein O-mannosyltransferases (PMTs). Here we demonstrate that in the model yeast Saccharomyces cerevisiae rhodanine-3-acetic acid derivativ
Autor:
Maurizio Vurro, Antonio Evidente, Michele Fiore, Ralf Looser, Stephen O. Duke, Nicole Christiansen, Johannes Hutzler, Agnes M. Rimando, Klaus Grossmann, Franck E. Dayan
Publikováno v:
Pesticide biochemistry and physiology 100 (2011): 41–50. doi:10.1016/j.pestbp.2011.02.002
info:cnr-pdr/source/autori:Duke S.O., Evidente A., Fiore M., Rimando A.M., Dayan F.E., Vurro M., Christiansen N., Looser R., Hutzler J., Grossmann K./titolo:Effects of the aglycone of ascaulitoxin on amino acid metabolism in Lemna paucicostata./doi:10.1016%2Fj.pestbp.2011.02.002/rivista:Pesticide biochemistry and physiology/anno:2011/pagina_da:41/pagina_a:50/intervallo_pagine:41–50/volume:100
info:cnr-pdr/source/autori:Duke S.O., Evidente A., Fiore M., Rimando A.M., Dayan F.E., Vurro M., Christiansen N., Looser R., Hutzler J., Grossmann K./titolo:Effects of the aglycone of ascaulitoxin on amino acid metabolism in Lemna paucicostata./doi:10.1016%2Fj.pestbp.2011.02.002/rivista:Pesticide biochemistry and physiology/anno:2011/pagina_da:41/pagina_a:50/intervallo_pagine:41–50/volume:100
Ascaulitoxin and its aglycone (2,4,7-triamino-5-hydroxyoctanoic acid, CAS 212268-55-8) are potent phytotoxins produced by Ascochyta caulina , a plant pathogen being developed for biocontrol of weeds. The mode of action of this non-protein amino acid
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1d32ff7da322d1c2211905f1922083d2