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Characterizing C6+P2-graphic Sequences
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作者 HU Li-li 《Chinese Quarterly Journal of Mathematics》 CSCD 2014年第2期238-243,共6页
For a given graph H, a graphic sequence π =(d1, d2, ···, dn) is said to be potentially H-graphic if π has a realization containing H as a subgraph. In this paper, we characterize the potentially C6+ P... For a given graph H, a graphic sequence π =(d1, d2, ···, dn) is said to be potentially H-graphic if π has a realization containing H as a subgraph. In this paper, we characterize the potentially C6+ P2-graphic sequences where C6+ P2 denotes the graph obtained from C6 by adding two adjacent edges to the three pairwise nonadjacent vertices of C6. Moreover, we use the characterization to determine the value of σ(C6+ P2, n). 展开更多
关键词 GRAPH degree sequence potentially c6 P2-graphic sequences
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INFINITELY MANY SOLUTIONS FOR ELLIPTIC SYSTEMS WITH STRONGLY INDEFINITE VARIATIONAL STRUCTURE 被引量:1
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作者 刘朝霞 《Acta Mathematica Scientia》 SCIE CSCD 2010年第1期55-64,共10页
Based on the multiplicity results of Benci and Fortunato [4], we consider some elliptic systems with strongly indefinite quadratic part, and establish the existence of infinitely many nontrivial solutions in a suitabl... Based on the multiplicity results of Benci and Fortunato [4], we consider some elliptic systems with strongly indefinite quadratic part, and establish the existence of infinitely many nontrivial solutions in a suitable family of products of fractional Sobolev spaces. 展开更多
关键词 semilinear elliptic systems variational functional (P.S.)c sequence criticalpoint
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Characteristics of mRNA dynamic expression related to spinal cord ischemia/reperfusion injury:a transcriptomics study 被引量:6
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作者 Zhi-ping Qi Peng Xia +3 位作者 Ting-ting Hou Ding-yang Li Chang-jun Zheng Xiao-yu Yang 《Neural Regeneration Research》 SCIE CAS CSCD 2016年第3期480-486,共7页
Following spinal cord ischemia/reperfusion injury,an endogenous damage system is immediately activated and participates in a cascade reaction.It is difficult to interpret dynamic changes in these pathways,but the exam... Following spinal cord ischemia/reperfusion injury,an endogenous damage system is immediately activated and participates in a cascade reaction.It is difficult to interpret dynamic changes in these pathways,but the examination of the transcriptome may provide some information.The transcriptome reflects highly dynamic genomic and genetic information and can be seen as a precursor for the proteome.We used DNA microarrays to measure the expression levels of dynamic evolution-related m RNA after spinal cord ischemia/reperfusion injury in rats.The abdominal aorta was blocked with a vascular clamp for 90 minutes and underwent reperfusion for 24 and 48 hours.The simple ischemia group and sham group served as controls.After rats had regained consciousness,hindlimbs showed varying degrees of functional impairment,and gradually improved with prolonged reperfusion in spinal cord ischemia/reperfusion injury groups.Hematoxylin-eosin staining demonstrated that neuronal injury and tissue edema were most severe in the 24-hour reperfusion group,and mitigated in the 48-hour reperfusion group.There were 8,242 differentially expressed m RNAs obtained by Multi-Class Dif in the simple ischemia group,24-hour and 48-hour reperfusion groups.Sixteen m RNA dynamic expression patterns were obtained by Serial Test Cluster.Of them,five patterns were significant.In the No.28 pattern,all differential genes were detected in the 24-hour reperfusion group,and their expressions showed a trend in up-regulation.No.11 pattern showed a decreasing trend in m RNA whereas No.40 pattern showed an increasing trend in m RNA from ischemia to 48 hours of reperfusion,and peaked at 48 hours.In the No.25 and No.27 patterns,differential expression appeared only in the 24-hour and 48-hour reperfusion groups.Among the five m RNA dynamic expression patterns,No.11 and No.40 patterns could distinguish normal spinal cord from pathological tissue.No.25 and No.27 patterns could distinguish simple ischemia from ischemia/reperfusion.No.28 pattern could analyze the need for inducing reperfusion injury.The study of specific pathways and functions for different dynamic patterns can provide a theoretical basis for clinical differential diagnosis and treatment of spinal cord ischemia/reperfusion injury. 展开更多
关键词 nerve regeneration spinal cord injury ischemia/reperfusion injury messenger RNA transcription oligonucleotide sequence microarray transcriptome c DNA sequence NADPH oxidase neural regeneration
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