1992
DOI: 10.1016/0048-3575(92)90008-n
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The herbicide sindone B disrupts spindle microtubule organizing centers

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Cited by 20 publications
(10 citation statements)
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“…This is strengthened by references available in literature (Romagni et al, 2000). Several reasons have been put forward to determine the factors that disrupt mitosis including disruption of microtubule organization or alternation of cell wall biosynthesis (Lehnen and Vaughn, 1992).…”
Section: Resultsmentioning
confidence: 99%
“…This is strengthened by references available in literature (Romagni et al, 2000). Several reasons have been put forward to determine the factors that disrupt mitosis including disruption of microtubule organization or alternation of cell wall biosynthesis (Lehnen and Vaughn, 1992).…”
Section: Resultsmentioning
confidence: 99%
“…The interruption in fatty acid assembly results in inhibition of cell division [7]. The herbicides might inhibit cell divi sion in several ways [8][9][10][11]. The uses of herbicides in cereal crops were become very popular and common for the reason that tremendous crop pro tection, satisfactory residual action, wide range weed control, flexibility in application timing and the most important cost effective.…”
mentioning
confidence: 99%
“…In large studies where rapid determination is of importance, paraffin sectioning might prove to be Microscopic analysis is another method for studying the effects of herbicides on cell division. Many authors including Lehnen and Vaughn (1992), , Armbruster et al (1991), and have used microscopy in elucidating the effects of herbicides on mitosis. Microtechnique is as varied as the researcher doing the work.…”
Section: Methods Of Studying Herbicides Which Affect Cell Divisionmentioning
confidence: 99%
“…In addition to using general light microscopy in studying herbicidal effects on roots (specifically microtubules), immunofluorescence microscopy has substantially enhanced analysis of mitotic disrupter herbicides (Sherman and Vaughn, 1991). These authors, along with Lehnen and Vaughn (1992) described methods by which monoclonal anti-atubulin primary and goat anti-mouse IgG fluorescein-conjugated secondary antibodies are used to stain tubulin. When viewed with a microscope using a short-wavelength (blue or ultraviolet energy) light source, the fluorescent tracer, bound to the tubulin, illuminates allowing the microtubule arrays to be seen, and aberrations detected.…”
Section: Methods Of Studying Herbicides Which Affect Cell Divisionmentioning
confidence: 99%
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