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Institution

University of Colorado Denver

EducationDenver, Colorado, United States
About: University of Colorado Denver is a education organization based out in Denver, Colorado, United States. It is known for research contribution in the topics: Population & Poison control. The organization has 27444 authors who have published 57213 publications receiving 2539937 citations. The organization is also known as: CU Denver & UCD.


Papers
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Journal ArticleDOI
TL;DR: There is an increased risk of ACL graft rupture in patients who have undergone allograft reconstruction, and patients in the age group of 10 to 19 years had the highest percentage of graft failures, suggesting allografted ACLRs should be performed with caution in the younger patient population.
Abstract: Background: Tearing an anterior cruciate ligament (ACL) graft is a devastating occurrence after ACL reconstruction (ACLR). Identifying and understanding the independent predictors of ACLR graft failure is important for surgical planning, patient counseling, and efforts to decrease the risk of graft failure.

416 citations

Journal ArticleDOI
14 Apr 1999-JAMA
TL;DR: The Physical Component Summary score from the preoperative SF-36 is an independent risk factor for mortality following CABG surgery, and the baseline Mental component Summary score does not appear to be predictive of mortality.
Abstract: ContextHealth-related quality of life has not been evaluated as a predictor of mortality following coronary artery bypass graft (CABG) surgery. Evaluation of health status as a mortality predictor may be useful for preoperative risk stratification.ObjectiveTo determine whether the Physical and Mental Component Summary scores from the preoperative Short-Form 36 (SF-36) health status survey predict mortality following CABG surgery after adjustment for known clinical risk variables.DesignProspective cohort study conducted between September 1992 and December 1996.SettingFourteen Veterans Affairs hospitals.PatientsOf the 3956 patients undergoing CABG surgery only and who were enrolled in the Processes, Structures, and Outcomes of Care in Cardiac Surgery study, the 2480 who completed a preoperative SF-36.Main Outcome MeasureAll-cause mortality within 180 days after surgery.ResultsA total of 117 deaths (4.7%) occurred within 180 days of CABG surgery. The Physical Component Summary of the preoperative SF-36 was a statistically significant risk factor for 6-month mortality after adjustment for known clinical risk factors for mortality following CABG surgery. In multivariate analysis, a 10-point lower SF-36 Physical Component Summary score had an odds ratio (OR) of 1.39 (95% confidence interval [CI], 1.11-1.77; P=.006) for predicting mortality. The SF-36 Mental Component Summary score was not associated with 6-month mortality in multivariate analyses (OR, 1.09; 95% CI, 0.92-1.29; P=.31).ConclusionsThe Physical Component Summary score from the preoperative SF-36 is an independent risk factor for mortality following CABG surgery. The baseline Mental Component Summary score does not appear to be predictive of mortality. Preoperative patient self-report of the physical component of health status may be helpful for risk stratification and clinical decision making for patients undergoing CABG surgery.

415 citations

Journal ArticleDOI
TL;DR: In this paper, the authors used a simple synchrotron self- Compton model to model the spectral energy distribution (SED) of a set of TeV blazars with good broadband data, to look for a connection of the jet properties to the properties of the central accreting black hole.
Abstract: Following the detection of strong TeV gamma ray flares from the BL Lac object 1 ES 1959+650 with the Whipple 10 m Cerenkov telescope on 2002 May 16 and 17, we performed intensive target of opportunity radio, optical, X-ray, and TeV ?ray observations from 2002 May 18 to August 14. Observations with the X-ray telescope RossiX-Ray Timing Explorer and the Whipple and HEGRA gamma-ray telescopes revealed several strong flares, enabling us to sensitively test the X-ray--gamma-ray flux correlation properties. Although the X-ray and gamma-ray fluxes seemed to be correlated in general, we found an orphan gamma-ray flare that was not accompanied by an X-ray flare. While we detected optical flux variability with the Boltwood and Abastumani observatories, the data did not give evidence for a correlation of the optical flux variability with the observed X-ray and 7-ray flares. Within statistical errors of about 0.03 Jy at 14.5 GHz and 0.05 Jy at 4.8 GHz, the radio fluxes measured with the University of Michigan Radio Astronomy Observatory stayed constant throughout the campaign; the mean values agreed well with the values measured on 2002 May 7 and June 7 at 4.9 and 15 GHz with the Very Large Array and at 4.8 GHz with archival flux measurements. After describing in detail the radio, optical, X-ray and gamma-ray light curves, and spectral energy distributions (SEDs), we present initial modeling of the SED with a simple synchrotron self- Compton model. With the addition of another TeV blazar with good broadband data, we consider the set of all TeV blazars, to begin to look for a connection of the jet properties to the properties of the central accreting black hole thought to drive the jet. Remarkably, the temporal and special X-ray and gamma-ray emission characteristics of TeV blazars are very similar, even though the mass estimates of their central black holes differ by up to 1 order of magnitude.

415 citations

Journal ArticleDOI
25 May 2012-PLOS ONE
TL;DR: It is observed that the preclinical phase of RA is characterized by an accumulation of multiple autoantibody specificities reflecting the process of epitope spread, and a biomarker profile including autoantsibodies and cytokines which predicts the imminent onset of clinical arthritis is identified.
Abstract: Rheumatoid arthritis (RA) is a prototypical autoimmune arthritis affecting nearly 1% of the world population and is a significant cause of worldwide disability. Though prior studies have demonstrated the appearance of RA-related autoantibodies years before the onset of clinical RA, the pattern of immunologic events preceding the development of RA remains unclear. To characterize the evolution of the autoantibody response in the preclinical phase of RA, we used a novel multiplex autoantigen array to evaluate development of the anti-citrullinated protein antibodies (ACPA) and to determine if epitope spread correlates with rise in serum cytokines and imminent onset of clinical RA. To do so, we utilized a cohort of 81 patients with clinical RA for whom stored serum was available from 1–12 years prior to disease onset. We evaluated the accumulation of ACPA subtypes over time and correlated this accumulation with elevations in serum cytokines. We then used logistic regression to identify a profile of biomarkers which predicts the imminent onset of clinical RA (defined as within 2 years of testing). We observed a time-dependent expansion of ACPA specificity with the number of ACPA subtypes. At the earliest timepoints, we found autoantibodies targeting several innate immune ligands including citrullinated histones, fibrinogen, and biglycan, thus providing insights into the earliest autoantigen targets and potential mechanisms underlying the onset and development of autoimmunity in RA. Additionally, expansion of the ACPA response strongly predicted elevations in many inflammatory cytokines including TNF-α, IL-6, IL-12p70, and IFN-γ. Thus, we observe that the preclinical phase of RA is characterized by an accumulation of multiple autoantibody specificities reflecting the process of epitope spread. Epitope expansion is closely correlated with the appearance of preclinical inflammation, and we identify a biomarker profile including autoantibodies and cytokines which predicts the imminent onset of clinical arthritis.

415 citations

Journal ArticleDOI
TL;DR: It is shown that regulatory components of the venom secretory system may have evolved from a pancreatic origin and that venom toxin genes were co-opted by distinct genomic mechanisms, which provides insight into mechanisms of protein evolution under strong selection.
Abstract: Snakes are limbless predators, and many species use venom to help overpower relatively large, agile prey. Snake venoms are complex protein mixtures encoded by several multilocus gene families that function synergistically to cause incapacitation. To examine venom evolution, we sequenced and interrogated the genome of a venomous snake, the king cobra (Ophiophagus hannah), and compared it, together with our unique transcriptome, microRNA, and proteome datasets from this species, with data from other vertebrates. In contrast to the platypus, the only other venomous vertebrate with a sequenced genome, we find that snake toxin genes evolve through several distinct co-option mechanisms and exhibit surprisingly variable levels of gene duplication and directional selection that correlate with their functional importance in prey capture. The enigmatic accessory venom gland shows a very different pattern of toxin gene expression from the main venom gland and seems to have recruited toxin-like lectin genes repeatedly for new nontoxic functions. In addition, tissue-specific microRNA analyses suggested the co-option of core genetic regulatory components of the venom secretory system from a pancreatic origin. Although the king cobra is limbless, we recovered coding sequences for all Hox genes involved in amniote limb development, with the exception of Hoxd12. Our results provide a unique view of the origin and evolution of snake venom and reveal multiple genome-level adaptive responses to natural selection in this complex biological weapon system. More generally, they provide insight into mechanisms of protein evolution under strong selection.

415 citations


Authors

Showing all 27683 results

NameH-indexPapersCitations
Matthew Meyerson194553243726
Charles A. Dinarello1901058139668
Gad Getz189520247560
Gordon B. Mills1871273186451
Jasvinder A. Singh1762382223370
David Haussler172488224960
Donald G. Truhlar1651518157965
Charles M. Perou156573202951
David Cella1561258106402
Bruce D. Walker15577986020
Marco A. Marra153620184684
Thomas E. Starzl150162591704
Marc Humbert1491184100577
Rajesh Kumar1494439140830
Martin J. Blaser147820104104
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Performance
Metrics
No. of papers from the Institution in previous years
YearPapers
20241
202383
2022358
20213,830
20203,913
20193,632