A Comparative Analysis of 6T and 10T SRAM Cells for Sub-threshold Operation in 65 nm CMOS Technology

The aggressive approach of the integrated electronics industry towards scaling and the growing trend of low-power applications have led to major research interest in ultra-low power integrated circuits. One of the integrated circuit areas most affected by this revolution is computer memory. In this thesis, a 10-Transistor Static Random Access Memory is compared to a 6-Transistor Static Random Access Memory in the subthreshold region of operation for a 65nm technology node. This comparison focuses primarily on the stability of memory cells in performing read and write operations. The use of 3-dimentional graphs in this thesis is to better compare differences and to give a feedback to memory designers about the design possibilities. A low-power Write Margin improvement method is proposed for the 10-Transistor cell to bring its stability to a standard comparable to that of its 6-transistor counterpart

Comprehensive Gene Expression Analysis of Human Embryonic Stem Cells during Differentiation into Neural Cells

Global gene expression analysis of human embryonic stem cells (hESCs) that differentiate into neural cells would help to further define the molecular mechanisms involved in neurogenesis in humans. We performed a comprehensive transcripteome analysis of hESC differentiation at three different stages: early neural differentiation, neural ectoderm, and differentiated neurons. We identified and validated time-dependent gene expression patterns and showed that the gene expression patterns reflect early ESC differentiation. Sets of genes are induced in primary ectodermal lineages and then in differentiated neurons, constituting consecutive waves of known and novel genes. Pathway analysis revealed dynamic expression patterns of members of several signaling pathways, including NOTCH, mTOR and Toll like receptors (TLR), during neural differentiation. An interaction network analysis revealed that the TGFβ family of genes, including LEFTY1, ID1 and ID2, are possible key players in the proliferation and maintenance of neural ectoderm. Collectively, these results enhance our understanding of the molecular dynamics underlying neural commitment and differentiation

A survey of two submaximal exercise training on a C-reactive protein in the elderly man

The purpose of this research is to survey the effect of eight weeks of sub-maximal training on the C-Reactive Protein (CRP) in elderly males. The subjects of the research consisted of 21 elderly males between 50-80 years old, divided into two groups (one experimental group and one control group), with VO2Peak values of 51.14±2.7, 51.92±3.17, and 43.61±1.85 (based on the 1-mile (1609 meters) Track Jog test). The experimental group carried out Balke-Ware sub-maximal aerobic exercise 5 sessions a week for 8 weeks, while the control group did not participate in the training program. The results of the research showed that the average CRP levels decreased in the experimental group, while they increased in the control group. However, these differences were not statistically significant according to the paired sample T-Test results. On the other hand, a significant difference in Vo2 Peak was observed between the two groups (p<0.039 and p<0.001), with the experimental group showing higher values compared to the control group. Additionally, there was no statistically significant difference in HS-CRP levels between the subjects (experimental group 1, experimental group 2, and control group) before and after the training period. In general, it seems that a longer duration is required to observe better markers of inflammatory and cardiovascular effects of these variables. The pre-study hypothesis of cardiorespiratory fitness on CRP response confirms that assessing control and inflammatory markers of cardiorespiratory fitness in the elderly requires more time

Data in support of comparative physiology and proteomic analysis of two wheat genotypes contrasting in drought tolerance

AbstractHere, we present the data from a comparative physiology and proteomics approach used to analyze the response of two wheat genotypes (SERI M 82 (SE) and SW89.5193/kAu2 (SW)) with contrasting responses to drought stress. Proteomic analysis resulted in identification of 49 unique proteins with significant change in abundance (2-fold) under water shortage in roots and leaves. Gene ontology analysis of drought-responsive proteins (DRPs) suggested an induction of proteins related to cell wall biogenesis, ATP synthesis, photosynthesis, and carbohydrate/energy metabolism in leaves under stress condition. A large fraction of root proteins were identified to be involved in defense and oxidative stress response. In addition, a significant change was detected in proteins related to protein synthesis, ATP synthesis, and germin-like proteins in response to drought stress. A detailed analysis of this data may be obtained from Ref. [1]

Comparative proteomic profiling of Leishmania tropica: investigation of a case infected with simultaneous cutaneous and viscerotropic leishmaniasis by 2-dimentional electrophoresis and mass spectrometry

Background: Viscerotropic leishmaniasis caused by Leishmania tropica poses a significant prob­lem in the diagnosis and treatment management. Since differential gene expression is more im­portant in outcome of the infection, we employed proteomic approach to identify potential pro­teins involved in visceralization of L. tropica. Methods: The proteomes profiling of L. tropica isolated from cutaneous and visceral tissues of one host were compared by 2-DE/MS proteomics study. Moreover, the transcript level of some identified proteins was confirmed using real-time RT-PCR. Results: Of the 700 protein spots that were detected reproducibly on each gel, 135 were found to be differentially expressed (P≤ 0.05). Most of responsive proteins in visceral isolate changed in less abundant compared to cutaneous isolate. Among differentially expressed proteins, 56 proteins were confidently identified and classified according to the biological process. The larg­est groups consist of proteins involved in carbohydrate metabolism and protein synthesis. Most of the identified proteins, which implicated in energy metabolism, cell signaling and virulence were down-regulated, whereas some proteins that have a role in protein folding, antioxidant defense and proteolysis were up-regulated in visceral form. Moreover, the transcript level of some identified proteins such as co-chaperon was confirmed using real-time RT-PCR. Conclusion: L. tropica probably uses different mechanisms for survival and multiplication in viscera to establish viscerotropic leishmaniasis. The current study provides some clues into the mechanisms underlying the dissemination of L. tropica

Comparative proteomic profiling of Leishmania tropica: investigation of a case infected with simultaneous cutaneous and viscerotropic leishmaniasis by 2-dimentional electrophoresis and mass spectrometry

Background: Viscerotropic leishmaniasis caused by Leishmania tropica poses a significant prob­lem in the diagnosis and treatment management. Since differential gene expression is more im­portant in outcome of the infection, we employed proteomic approach to identify potential pro­teins involved in visceralization of L. tropica. Methods: The proteomes profiling of L. tropica isolated from cutaneous and visceral tissues of one host were compared by 2-DE/MS proteomics study. Moreover, the transcript level of some identified proteins was confirmed using real-time RT-PCR. Results: Of the 700 protein spots that were detected reproducibly on each gel, 135 were found to be differentially expressed (P≤ 0.05). Most of responsive proteins in visceral isolate changed in less abundant compared to cutaneous isolate. Among differentially expressed proteins, 56 proteins were confidently identified and classified according to the biological process. The larg­est groups consist of proteins involved in carbohydrate metabolism and protein synthesis. Most of the identified proteins, which implicated in energy metabolism, cell signaling and virulence were down-regulated, whereas some proteins that have a role in protein folding, antioxidant defense and proteolysis were up-regulated in visceral form. Moreover, the transcript level of some identified proteins such as co-chaperon was confirmed using real-time RT-PCR. Conclusion: L. tropica probably uses different mechanisms for survival and multiplication in viscera to establish viscerotropic leishmaniasis. The current study provides some clues into the mechanisms underlying the dissemination of L. tropica

Identification of candidate Glutathione S-transferase (GST) genes in Sunn pest, Eurygaster integriceps Put. (Hem.: Scutelleridae), using RNA-seq analysis

Glutathione S-transferase (GST) genes control vital traits for metabolism of the variety of toxins that expose insects to the environment (insecticide) or plant defense systems. Sunn pest is the most important pest of wheat and barley in the Middle East where it threats food security throughout the region. Sequencing the sunn pest's RNA provides an opportunity to identify the structure and function of the different gene families. To our knowledge, this is the first study to identify 43 GST candidate genes in sunn pest using bioinformatics tools. The identified candidate genes clustered in 5 cytosolic GST (Delta, Theta, Zeta, Omega, and Sigma) and Microsomal GST using phylogenetic analysis. The Sigma subclass was identified as the biggest subclass with 22 candidate genes, while microsomal GST  found to be the smallest group with one candidate gene. Given the role of GST in the interactions among the insect, toxins, and environment, our results facilitate future investigations on insecticide resistance and their utilization in pest management programs against sunn pest

Comparison of Dynamics of Udder Skin Microbiota From Grazing Yak and Cattle During the Perinatal Period on the Qinghai-Tibetan Plateau

he perinatal period has an important impact on the health of ruminants, and the imbalance of udder skin microbiota might be an important inducement of bovine mastitis. However, it is not clear how the perinatal period affects the microbial structure and stability of the udder skin of yak and cattle. Here, we used 16S rRNA gene high-throughput sequencing to analyze the udder skin microbiota of yak and cattle during the perinatal period. We found that the diversity and richness of microbiota of bovine udder skin during 1–2 weeks postpartum were significantly lower than those in the 1–2 weeks prenatal and 1-month postpartum period (Wilcoxon, p &lt; 0.05). Besides, we found sharing of 2,533 OTUs in the udder skin microbiota of yak and cattle during the perinatal period, among which the core microbiota at the genera level was mainly composed of Staphylococcus, Moraxella, and Acinetobacter. However, the genus Acinetobacter was significantly abundant in the udder skin of cattle during 1–2 weeks postpartum. The NMDS and LEfSe results showed that the perinatal period had more effects on the composition and stability of microbial community in the udder skin of cattle compared to yak, particularly during 1–2 weeks postpartum. In addition, the average content of total whey proteins and immunoglobulin G of whey protein were significantly higher in the yak colostrum when compared to those found in the cattle (p &lt; 0.05). In conclusion, the structure of udder skin microbiota of yak during the perinatal period is more stable than that of cattle in the same habitat, and 1–2 weeks postpartum may be a potential window period to prevent cattle mastitis