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  • 1
    ISSN: 1437-7772
    Keywords: Key words FGF ; Renal cell carcinoma ; Tumor progression
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Background. Recently, several investigators have demonstrated that fibroblast growth factor-2 (FGF-2) plays a crucial role in the malignant progression of human renal cell carcinoma (RCC). However, the significance of other FGFs in RCC remains largely unknown. Methods. We investigated the expression of FGFs (FGF-1 to FGF-9) in 50 RCCs and surrounding ten normal kidney tissues using the reverse transcription-polymerase chain reaction (RT-PCR). We also analyzed the correlation between the incidence of FGF expression and the clinicopathological findings. Results. FGF-1, FGF-2, and FGF-9 were expressed in all the normal and malignant kidney specimens, whereas FGF-3, FGF-4, FGF-6, and FGF-7 were not detected in any specimens. FGF-5 and FGF-8 were expressed in all normal kidney tissues; however, FGF-5 was detected in only 27 of the 50 (54%) RCC specimens and FGF-8 was also detected in only 27 of the 50 (54%) RCC specimens. The incidence of FGF-5 expression in high-stage RCC was significantly greater than that in low-stage RCC (P 〈 0.01), whereas no significant difference was observed in the incidence of FGF-8 expression by tumor stage. In addition, the frequency of FGF-5 expression was significantly higher in the clear-cell subtype of RCC than in the granular-cell subtype (P 〈 0.05). Conclusion. We demonstrated a close relationship between the expression of FGF-5 and the development of RCC. Our result suggests that FGF-5 expression in RCC tissues may be a useful prognostic marker for this cancer.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Molecular genetics and genomics 250 (1996), S. 241-251 
    ISSN: 1617-4623
    Keywords: mukF ; mukE ; Chromosome partitioning ; Leucine zipper ; Escherichia coli
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract We have previously reported that the MukB protein is essential for chromosome partitioning inEscherichia coli and thatmukB mutants produce anucleate cells and are temperature-sensitive for colony formation. ThemukB gene maps at 21 min on theE. coli chromosome andsmtA-mukF-mukE-mukB genes might comprise an operon, which is transcribed in a clockwise direction. Here, we report thatmukF andmukE null mutants are both temperature-sensitive for colony formation and produce anucleate cells even at the permissive temperature. These phenotypes are the same as those observed in themukB null mutant. The primary sequence of MukF includes a leucine zipper structure and an acidic domain. Mutational analysis revealed that both are required for MukF function. When the MukF protein was overproduced in the wild-type strain, anucleate cells were produced. In contrast, overproduction of either MukE or MukB did not cause the defect. In null mutants for themukF, mukE, andmukB genes, the synchronous initiation of chromosome replication was not affected. The mini-F plasmid was as stably maintained in these mutants as in the wild-type strain. These results indicate that the MukF, MukE, and MukB proteins are involved in the chromosome partitioning steps, but are not required for mini-F plasmid partitioning.
    Type of Medium: Electronic Resource
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