scholarly journals DNA Microarray Analysis of Temporal and Spatial Variation of Bacterial Communities in Japanese Rivers

2008 ◽  
Vol 44 (2) ◽  
pp. 109-120
Author(s):  
RAHUL R. UPADHYE ◽  
DAISUKE INOUE ◽  
MASAKI INABA ◽  
KAZUNARI SEI ◽  
MICHIHIKO IKE
Keyword(s):  
Spatial Variation ◽  
Microarray Analysis ◽  
Dna Microarray ◽  
Bacterial Communities ◽  
Temporal And Spatial Variation ◽  
Dna Microarray Analysis ◽  
Japanese Rivers ◽  
Temporal And Spatial

Impact of sewage sludge on the soil bacterial communities by DNA microarray analysis

2011 ◽  
Vol 27 (9) ◽  
pp. 1997-2003 ◽  
Author(s):  
Silvana P. Val-Moraes ◽  
Jackson Marcondes ◽  
Lúcia M. Carareto Alves ◽  
Eliana G. M. Lemos
Keyword(s):  
Sewage Sludge ◽  
Microarray Analysis ◽  
Dna Microarray ◽  
Bacterial Communities ◽  
Dna Microarray Analysis ◽  
Soil Bacterial Communities ◽  
Soil Bacterial

scholarly journals Phylogenetic paleoecology: macroecology within an evolutionary framework

Paleobiology ◽  
2021 ◽  
Vol 47 (2) ◽  
pp. 171-177
Author(s):  
James C. Lamsdell ◽  
Curtis R. Congreve
Keyword(s):  
Species Diversity ◽  
Spatial Variation ◽  
Geographic Distribution ◽  
Evolutionary Biology ◽  
Phylogenetic Signal ◽  
Evolutionary Rates ◽  
The Other ◽  
Ecological Data ◽  
Temporal And Spatial Variation ◽  
Temporal And Spatial

The burgeoning field of phylogenetic paleoecology (Lamsdell et al. 2017) represents a synthesis of the related but differently focused fields of macroecology (Brown 1995) and macroevolution (Stanley 1975). Through a combination of the data and methods of both disciplines, phylogenetic paleoecology leverages phylogenetic theory and quantitative paleoecology to explain the temporal and spatial variation in species diversity, distribution, and disparity. Phylogenetic paleoecology is ideally situated to elucidate many fundamental issues in evolutionary biology, including the generation of new phenotypes and occupation of previously unexploited environments; the nature of relationships among character change, ecology, and evolutionary rates; determinants of the geographic distribution of species and clades; and the underlying phylogenetic signal of ecological selectivity in extinctions and radiations. This is because phylogenetic paleoecology explicitly recognizes and incorporates the quasi-independent nature of evolutionary and ecological data as expressed in the dual biological hierarchies (Eldredge and Salthe 1984; Congreve et al. 2018; Fig. 1), incorporating both as covarying factors rather than focusing on one and treating the other as error within the dataset.

scholarly journals The Potential of 2-aza-8-Oxohypoxanthine as a Cosmetic Ingredient

Cosmetics ◽  
2021 ◽  
Vol 8 (3) ◽  
pp. 60
Author(s):  
Hisae Aoshima ◽  
Masayuki Ito ◽  
Rinta Ibuki ◽  
Hirokazu Kawagishi
Keyword(s):  
Gene Expression ◽  
Cell Proliferation ◽  
Microarray Analysis ◽  
Dna Microarray ◽  
Cell Activation ◽  
Skin Barrier ◽  
Efficacy Evaluation ◽  
Activation Effect ◽  
Expression Levels ◽  
Dna Microarray Analysis

In this study, we verified the effects of 2-aza-8-oxohypoxanthine (AOH) on human epidermal cell proliferation by performing DNA microarray analysis. Cell proliferation was assessed using the 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide assay, which measures mitochondrial respiration in normal human epidermal keratinocyte (NHEK) cells. Gene expression levels were determined by DNA microarray analysis of 177 genes involved in skin aging and disease. AOH showed a significant increase in cell viability at concentrations between 7.8 and 31.3 μg/mL and a significant decrease at concentrations above 250 μg/mL. DNA microarray analysis showed that AOH significantly increased the gene expression of CLDN1, DSC1, DSG1, and CDH1 (E-cadherin), which are involved in intercellular adhesion and skin barrier functioning. AOH also up-regulated the expression of KLK5, KLK7, and SPIMK5, which are proteases involved in stratum corneum detachment. Furthermore, AOH significantly stimulated the expression of KRT1, KRT10, TGM1, and IVL, which are considered general differentiation indicators, and that of SPRR1B, a cornified envelope component protein. AOH exerted a cell activation effect on human epidermal cells. Since AOH did not cause cytotoxicity, it was considered that the compound had no adverse effects on the skin. In addition, it was found that AOH stimulated the expression levels of genes involved in skin barrier functioning by DNA microarray analysis. Therefore, AOH has the potential for practical use as a cosmetic ingredient. This is the first report of efficacy evaluation tests performed for AOH.

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