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DI MAGGIO G 《Bollettino della Società italiana di biologia sperimentale》1950,26(3):335-336
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Sabrina Piombo Gode B. Calleja Bong Yul Yoo Byron F. Johnson 《Cell biochemistry and biophysics》1998,29(3):263-279
Distributions of rupture sites of fission yeast cells ruptured by glass beads have been related to a new morphometric analysis.
As shown previously (Johnson et al.,Cell Biophysics, 1995), ruptures were not randomly distributed nor was their distribution dictated by geometry, rather, ruptures at the extensile
end were related to cell length just as the rate of extension is related to cell length. The extension patterns of early log,
mid-log, late log, and stationary phase cells from suspension cultures were found to approximate the linear growth patterns
of Kubitschek and Clay (1986). The median length of cells was found to decline through the log phase in an unbalanced manner. 相似文献
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Double-stranded RNA unwinding and modifying activity is detected ubiquitously in primary tissues and cell lines. 总被引:19,自引:4,他引:15
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![点击此处可从《Molecular and cellular biology》网站下载免费的PDF全文](/ch/ext_images/free.gif)
R W Wagner C Yoo L Wrabetz J Kamholz J Buchhalter N F Hassan K Khalili S U Kim B Perussia F A McMorris et al. 《Molecular and cellular biology》1990,10(10):5586-5590
A double-stranded RNA unwinding and modifying activity was found to be present in a wide range of tissues and cell types. The level of activity did not vary significantly with respect to the state of cell differentiation, cell cycle, or transformation. Thus, the unwinding and modifying activity, localized in the nucleus in somatic cells and capable of converting many adenosine residues to inosine, appears to be one of the housekeeping genes. 相似文献
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Differentially regulated malate synthase genes participate in carbon and nitrogen metabolism of S. cerevisiae. 总被引:4,自引:0,他引:4
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A Hartig M M Simon T Schuster J R Daugherty H S Yoo T G Cooper 《Nucleic acids research》1992,20(21):5677-5686
We have isolated a second gene (MLS1), which in addition to DAL7, encodes malate synthase from S. cerevisiae. Expression of the two genes is specific for their physiological roles in carbon and nitrogen metabolism. Expression of MLS1, which participates in the utilization of non-fermentable carbon sources, is sensitive to carbon catabolite repression, but nearly insensitive to nitrogen catabolite repression. DAL7, which participates in catabolism of the nitrogenous compound allantoin, is insensitive to carbon catabolite repression, but highly sensitive to nitrogen catabolite repression. Results obtained with null mutations in these genes suggest that S. cerevisiae contains at least one and perhaps two additional malate synthase genes. 相似文献
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Kenneth H. Astrin Cecilia A. Warner Han-Wook Yoo Paul J. Goodfellow Shih-Feng Tsai Robert J. Desnick 《Human genetics》1991,87(1):18-22
Summary Uroporphyrinogen III synthase [UROS; hydroxymethylbilane hydro-lyase (cyclizing), EC 4.2.1.75] is the fourth enzyme in the human heme biosynthetic pathway. The recent isolation of the cDNA encoding human UROS facilitated its chromosomal localization. Human UROS sequences were specifically amplified by the polymerase chain reaction (PCR) from genomic DNA of two independent panels of human-rodent somatic cell hybrids. There was 100% concordance for the presence of the human UROS PCR product and human chromosome 10. For each of the other chromosomes, there was 19%–53% discordance with human UROS. The chromosomal assignment was confirmed by Southern hybridization analysis of DNA from somatic cell hybrids with the full-length UROS cDNA. Using human-rodent hybrids containing different portions of human chromosome 10, we assigned the UROS gene to the region 10q25.2 q26.3. 相似文献
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