Institution
University of North Texas
Education•Denton, Texas, United States•
About: University of North Texas is a education organization based out in Denton, Texas, United States. It is known for research contribution in the topics: Population & Poison control. The organization has 11866 authors who have published 26984 publications receiving 705376 citations. The organization is also known as: Fight, North Texas & UNT.
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TL;DR: In this article, the authors examined the effects of human capital, organizational demography, and interpersonal processes on partner evaluations of venture performance, defined as the presence of profit and growth, and proposed that this perspective be included in future venture viability assessment, and used for intervention to enhance venture success.
170 citations
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TL;DR: Previous and most recent evidence is emphasized suggesting that early programming of the thymus, sexual dimorphism, and the efficiency of specific T-cell progenitors and theThymic microenvironment are all crucial determinants of immune activity from early life through advanced ages.
Abstract: Age-related thymic involution is characterized by a progressive regression in thymus size and a diminishment of thymic structure. A decrease in thymic compartments leads to the reduction of thymopoiesis. Thymic involution is closely associated with immunosenescence, a degeneration of the immune system primarily due to the alterations in T-cell composition. Strategies to improve the consequences of the aging thymus are currently under investigation. A wide array of knowledge has revealed a series of factors that are essential in the overall determination of thymic function and immune response. Evidence indicates that early programming of the thymus, sexual dimorphism, and the efficiency of specific T-cell progenitors and the thymic microenvironment are all crucial determinants of immune activity from early life through advanced ages. To fully understand the processes involved in age-related thymic involution, such determinants must be considered. The central purpose of this review is to emphasize previous and most recent evidence suggesting that these factors contribute to the influence of long-term immunity and ultimately shape the progression of thymic involution in advanced age.
170 citations
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TL;DR: In this study, the density functional theory (DFT) method was applied to study the electronic structure and catalytic properties of graphene clusters containing various point and line defects and found that the graphene cluster with the point defect having pentagon rings at the zigzag edge shows the electrocatalytic capability for ORR.
Abstract: Defects are common but important in graphene, which could significantly tailor the electronic structures and physical and chemical properties. In this study, the density functional theory (DFT) method was applied to study the electronic structure and catalytic properties of graphene clusters containing various point and line defects. The electron transfer processes in oxygen reduction reaction (ORR) on perfect and defective graphene clusters in fuel cells was simulated, and the free energy and reaction energy barrier of the elementary reactions were calculated to determine the reaction pathways. It was found that the graphene cluster with the point defect having pentagon rings at the zigzag edge, or line defects (grain boundaries) consisting of pentagon-pentagon-octagon or pentagon-heptagon chains also at the edges, shows the electrocatalytic capability for ORR. Four-electron and two-electron transfer processes could occur simultaneously on graphene clusters with certain types of defects. The energy barriers of the reactions are comparable to that of platinum(111). The catalytic active sites were determined on the defective graphene.
170 citations
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TL;DR: It is proposed that plasma membrane PKD2 is under negative regulation by PIP2, and EGF may reduce the threshold ofPKD2 activation by mechanical and other stimuli by releasing it from PIP1-mediated inhibition.
Abstract: PKD2, or polycystin 2, the product of the gene mutated in type 2 autosomal dominant polycystic kidney disease, belongs to the transient receptor potential channel superfamily and has been shown to function as a nonselective cation channel in the plasma membrane. However, the mechanism of PKD2 activation remains elusive. We show that PKD2 overexpression increases epidermal growth factor (EGF)-induced inward currents in LLC-PK1 kidney epithelial cells, while the knockdown of endogenous PKD2 by RNA interference or the expression of a pathogenic missense variant, PKD2-D511V, blunts the EGF-induced response. Pharmacological experiments indicate that the EGF-induced activation of PKD2 occurs independently of store depletion but requires the activity of phospholipase C (PLC) and phosphoinositide 3-kinase (PI3K). Pipette infusion of purified phosphatidylinositol-4,5-bisphosphate (PIP2) suppresses the PKD2-mediated effect on EGF-induced conductance, while pipette infusion of phosphatidylinositol-3,4,5-trisphosphate (PIP3) does not have any effect on this conductance. Overexpression of type Iα phosphatidylinositol-4-phosphate 5-kinase [PIP(5)Kα], which catalyzes the formation of PIP2, suppresses EGF-induced currents. Biochemical experiments show that PKD2 physically interacts with PLC-γ2 and EGF receptor (EGFR) in transfected HEK293T cells and colocalizes with EGFR and PIP2 in the primary cilium of LLC-PK1 cells. We propose that plasma membrane PKD2 is under negative regulation by PIP2. EGF may reduce the threshold of PKD2 activation by mechanical and other stimuli by releasing it from PIP2-mediated inhibition.
170 citations
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TL;DR: Results of this experiment begin to show that exposure to chronic low levels of ibuprofen alter the pattern of reproduction and may produce sex-specific responses in teleosts.
170 citations
Authors
Showing all 12053 results
Name | H-index | Papers | Citations |
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Steven N. Blair | 165 | 879 | 132929 |
Scott D. Solomon | 137 | 1145 | 103041 |
Richard A. Dixon | 126 | 603 | 71424 |
Thomas E. Mallouk | 122 | 549 | 52593 |
Hong-Cai Zhou | 114 | 489 | 66320 |
Qian Wang | 108 | 2148 | 65557 |
Boris I. Yakobson | 107 | 443 | 45174 |
J. N. Reddy | 106 | 926 | 66940 |
David Spiegel | 106 | 733 | 46276 |
Charles A. Nelson | 103 | 557 | 40352 |
Robert J. Vallerand | 98 | 301 | 41840 |
Gerald R. Ferris | 93 | 332 | 29478 |
Michael H. Abraham | 89 | 726 | 37868 |
Jere H. Mitchell | 88 | 337 | 24386 |
Alan Needleman | 86 | 373 | 39180 |