9 research outputs found
Relationship between toe grip muscle strength of elementary school student and physical fitness and life style
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PROBABILISTIC MODELING OF SPATIAL VARIATION OF SEISMIC GROUND DEFORMATION
Get PDFThis paper presents a probabilistic method for describing the spatial variability of strong earthquake ground deformation. The intent is to establish a practical procedure to deal with the effect of earthquake on long extended structures. The principal idea of the procedure presented in this paper exists in the interpretation that the seismic ground displacements in a surface plane are resulted from the homogeneous Gaussian space-time process with zero mean. This interpretation makes it possible to derive the extremes of ground displacements, ground strains, and relative displacements between two points on ground surface which are the important factors in seismic design of underground structures, from the spatial correlation functions. Applying the procedure into an analysis of dense instrument array data, the behaviors of these extremes are summarized in a "Spatial Variability Spectra of Seismic Ground Deformation". Also a method of digital simulation of seismic ground deformations varying in a horizontal plane is presented
Expression pattern (in a set of 31 tissues covered by MPSS) of genes belonging to all three types of S-AS pairs (3'3', 5'5'and embedded)
No full text<p><b>Copyright information:</b></p><p>Taken from "Sense-antisense pairs in mammals: functional and evolutionary considerations"</p><p>http://genomebiology.com/2007/8/3/R40</p><p>Genome Biology 2007;8(3):R40-R40.</p><p>Published online 19 Mar 2007</p><p>PMCID:PMC1868933.</p><p></p> Categories are as follows: 'no expression', for S-AS pairs whose expression was not detected (see Materials and methods for details); 'single-gene expression', for S-AS pairs in which expression is observed for only one gene in the pair; 'co-expression', for pairs in which expression is seen for both genes in the pair. Rate of differential expression for the set of co-expressed S-AS pairs. Ratio of sense/antisense genes in the pair is shown on the x-axis
RT-PCR analysis for the internal priming (IP) candidates in fetal liver, colon and lung total RNA
No full text<p><b>Copyright information:</b></p><p>Taken from "Sense-antisense pairs in mammals: functional and evolutionary considerations"</p><p>http://genomebiology.com/2007/8/3/R40</p><p>Genome Biology 2007;8(3):R40-R40.</p><p>Published online 19 Mar 2007</p><p>PMCID:PMC1868933.</p><p></p> RT-PCR was conducted in DNA-free RNA previously treated with (lanes 1 and 2) and in untreated RNA, which was, therefore, contaminated with genomic DNA (gDNA; lanes 3 and 4) for each candidate in the corresponding tissue. As a control, RT-PCR was conducted in the presence (lanes 1 and 3) and absence (lanes 2 and 4) of reverse transcriptase. gDNA was used as a positive control of the PCR reaction (lane 5) and no template as a negative control (lane 6). For fetal liver, in 3 IP candidates (5, 8 and 11) the PCR products (152 bp, 153 bp and 160 bp, respectively) were observed in the treated RNA when RT was added (lane 1) or in untreated RNA independent of the RT (lanes 3 and 4). For colon, in 1 IP candidate (9) the PCR product (158 bp) was observed in the treated RNA when RT was added (lane 1) or in untreated RNA independent of the RT (lanes 3 and 4). For the remaining IP candidates (1, 2, 4, 6, 7, 10 and 12), the PCR products (214 bp, 229 bp, 207 bp, 156 bp, 227 bp, 205 bp and 234 bp, respectively) were observed only in untreated RNA independent of the RT (lanes 3 and 4). The PCR products were analyzed on 8% polyacrylamide gels with silver staining. A 100 bp ladder (M) was used as molecular weight marker. In each gel the lower fragment in lane M correspond to 100 bp
