Institution
University of North Texas Health Science Center
Education•Fort Worth, Texas, United States•
About: University of North Texas Health Science Center is a education organization based out in Fort Worth, Texas, United States. It is known for research contribution in the topics: Population & Receptor. The organization has 2972 authors who have published 5401 publications receiving 153180 citations. The organization is also known as: UNT Health Science Center & UNTHSC.
Topics: Population, Receptor, Health care, Neuroprotection, Cancer
Papers published on a yearly basis
Papers
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TL;DR: A systematic study of the quenching efficiency of Förster-type energy-transfer (FRET) for multiple fluorophores immobilized on a single antibody as a function of the number of identical emitters bound to a single IgG antibody.
Abstract: Advancements in single molecule detection (SMD) continue to unfold powerful ways to study the behavior of individual and complex molecular systems in real time. SMD enables the characterization of complex molecular interactions and reveals basic physical phenomena underlying chemical and biological processes. We present here a systematic study of the quenching efficiency of Forster-type energy-transfer (FRET) for multiple fluorophores immobilized on a single antibody. We simultaneously monitor the fluorescence intensity, fluorescence lifetime, and the number of available photons before photobleaching as a function of the number of identical emitters bound to a single IgG antibody. The detailed studies of FRET between individual fluorophores reveal complex through-space interactions. In general, even for two or three fluorophores immobilized on a single protein, homo-FRET interactions lead to an overall non-linear intensity increase and shortening of fluorescence lifetime. Over-labeling of protein in solution (ensemble) results in the loss of fluorescence signal due to the self-quenching of fluorophores making it useless for assays applications. However, in the single molecule regime, over-labeling may bring significant benefits in regards to the number of available photons and the overall survival time. Our investigation reveals possibilities to significantly increase the observation time for a single macromolecule allowing studies of macromolecular interactions that are not obscured by ensemble averaging. Extending the observation time will be crucial for developing immunoassays based on single-antibody.
61 citations
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TL;DR: Altered expression of splice variants of CS1 and 2B4 that mediate differential signalling in PBMC from patients with SLE are demonstrated.
Abstract: CS1 (CRACC, CD319) and 2B4 (CD244), members of the signalling lymphocyte activation molecule (SLAM) family receptors, regulate various immune functions. Genes encoding SLAM family receptors are located at 1q23, implicated in systemic lupus erythematosus (SLE). In this study, we have investigated the expression and alternative splicing of CS1 and 2B4 in immune cells from SLE patients. The surface expression of CS1 and 2B4 on total peripheral blood mononuclear cells (PBMCs), T, B, natural killer (NK) cells and monocytes in 45 patients with SLE and 30 healthy individuals was analysed by flow cytometry. CS1-positive B cell population was increased significantly in SLE patients. Because CS1 is a self-ligand and homophilic interaction of CS1 induces B cell proliferation and autocrine cytokine secretion, this could account for autoreactive B cell proliferation in SLE. The proportion of NK cells and monocytes expressing 2B4 on their surface was significantly lower in patients with SLE compared to healthy controls. Our study demonstrated altered expression of splice variants of CS1 and 2B4 that mediate differential signalling in PBMC from patients with SLE.
61 citations
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TL;DR: The results suggest that ischemia/reperfusion cerebral damage induces signalings at the G1/S cell‐cycle transition, and may constitute a critical step in the neuronal apoptotic pathway in ischemIA/rePerfusion induced neuronal damage.
61 citations
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TL;DR: Anabolic steroids may potentiate concentric left ventricular hypertrophy with decreasing ventricular compliance without affecting cardiac function and is coupled with a significantly disproportionate septal and posterior wall thickness in DUs when indexed to body mass compared to DFs.
Abstract: ObjectiveTo investigate the relationship between resistance training, anabolic steroid use, and left ventricular function.DesignSixteen competitive bodybuilders were recruited for an echocardiography study.SettingUniversity of North Texas Health Science Center (Fort Worth, TX, U.S.A.); the cardiolog
60 citations
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TL;DR: In this paper, the authors examined cardiac protection effects of normobaric intermittent hypoxia training for 20 consecutive days in a normalobaric chamber with N2 to reduce fraction of inspired oxygen (FiO2) to 9.5%-10%.
Abstract: This investigation examined cardiac protective effects of normobaric intermittent hypoxia training. Six dogs underwent intermittent hypoxic training for 20 consecutive days in a normobaric chamber ventilated intermittently with N2 to reduce fraction of inspired oxygen (FiO2) to 9.5%-10%. Hypoxic periods, initially 5 mins and increasing to 10 mins, were followed by 4-min normoxic periods. This hypoxia-normoxia protocol was repeated, initially 5 times and increasing to 8 times. The dogs showed no discomfort during intermittent hypoxic training. After 20 days of hypoxic training, the resistance of ventricular myocardium to infarction was assessed in an acute experiment. The left anterior descending (LAD) coronary artery was occluded for 60 mins and then reperfused for 5 hrs. At 30 mins of LAD occlusion, radioactive microspheres were injected through a left atrial catheter to assess coronary collateral blood flow into the ischemic region. After 5 hrs reperfusion, the heart was dyed to delineate the area at risk (AAR) of infarction and stained with triphenyl tetrazolium chloride to identify infarcted myocardium. During LAD occlusion and reperfusion, systemic hemodynamics and global left ventricular function were stable. Infarction was not detected in 4 hearts and was 1.6% of AAR in the other 2 hearts. In contrast, 6 dogs sham-trained in a chamber ventilated with compressed air and 5 untrained dogs subjected to the same LAD occlusion/reperfusion protocol had infarcts of 36.8% +/- 5.8% and 35.2% +/- 9.5% of the AAR, respectively. The reduction in infarct size of four of the six hypoxia-trained dogs could not be explained by enhanced collateral blood flow to the AAR. Hypoxia-trained dogs had no ventricular tachycardia or ventricular fibrillation. Three sham-trained dogs had ventricular tachycardia and two had ventricular fibrillation. Three untrained dogs had ventricular fibrillation. In conclusion, intermittent hypoxic training protects canine myocardium from infarction and life-threatening arrhythmias during coronary artery occlusion and reperfusion. The mechanism responsible for this potent cardioprotection merits further study.
60 citations
Authors
Showing all 3001 results
Name | H-index | Papers | Citations |
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John T. Potts | 90 | 359 | 29359 |
Evan A. Stein | 80 | 340 | 36392 |
James W. Simpkins | 79 | 431 | 20574 |
Robert J. Gatchel | 79 | 494 | 25583 |
Douglas B. Cines | 79 | 397 | 27792 |
Ranajit Chakraborty | 77 | 407 | 25474 |
Kunlin Jin | 75 | 258 | 23282 |
Bruce Budowle | 70 | 613 | 20227 |
Lisa L. Barnes | 69 | 280 | 20190 |
Abbot F. Clark | 65 | 297 | 13938 |
Yong Fang Kuo | 65 | 447 | 14938 |
Alexander C. Wagenaar | 63 | 241 | 13661 |
David P. Siderovski | 62 | 180 | 19698 |
Yogesh C. Awasthi | 61 | 254 | 12304 |
Ignacy Gryczynski | 61 | 545 | 16705 |