Citations

Mayo Clinic

Showing 10 of 108376 citations.

Enhancement of DNA Flexibility in Vitro and in Vivo by HMGB Box A Proteins Carrying Box B Residues
Sebastian, Nadia T. , Bystry, Emily M., Becker, Nicole A. , Maher, L. James

Biochemistry | January 26, 2009 | Volume: 48 | Issue: 10 | Pages: 2125-2134

10.1021/bi802269f | PMID 19236006 Get It

Evolutionary Genetics of Coronary Heart Disease
Ding, Keyue , Kullo, Iftikhar J.

Circulation | January 26, 2009 | Volume: 119 | Issue: 3 | Pages: 459-467

10.1161/circulationaha.108.809970 | PMID 19171868 Get It

Vascular risk factors and dementia
Viswanathan, Anand , Rocca, Walter A. , Tzourio, Christophe , Tzourio, Christophe

Neurology | January 26, 2009 | Volume: 72 | Issue: 4 | Pages: 368-374

10.1212/01.wnl.0000341271.90478.8e | PMID 19171835 Get It

Sex Differences in Sympathetic Neural-Hemodynamic Balance
Hart, Emma C. , Charkoudian, Nisha , Wallin, B. Gunnar, Curry, Timothy B. , Eisenach, John H., Joyner, Michael J. , Joyner, Michael J , Hart, Emma C

Hypertension | January 26, 2009 | Volume: 53 | Issue: 3 | Pages: 571-576

10.1161/hypertensionaha.108.126391 | PMID 19171792 Get It

Among young normotensive men, a reciprocal balance between cardiac output and sympathetic nerve activity is important in the regulation of arterial pressure. In young women, the balance among cardiac output, peripheral resistance, and sympathetic nerve activity is unknown. Consequently, the aim of this study was to examine the relationship of cardiac output and total peripheral resistance to muscle sympathetic nerve activity in young women. Multiunit peroneal recordings of muscle sympathetic nerve activity were obtained in 17 women (mean±SEM: age 24±3 years) and 21 men (mean±SEM: age 25±5 years). Mean resting muscle sympathetic nerve activity was lower in women compared with men (19±3 versus 25±1 bursts minute −1 ; P <0.05), as was mean arterial pressure (89±1 versus 94±2 mm Hg; P <0.05). Mean arterial pressure was not related to muscle sympathetic nerve activity in men ( P =0.80) or women ( P =0.62). There was a positive relationship between total peripheral resistance and muscle sympathetic nerve activity ( r =0.62; P <0.05) and an inverse relationship between cardiac output and muscle sympathetic nerve activity ( r =−0.69; P <0.05) in men. Unexpectedly, muscle sympathetic nerve activity had no relationship to either total peripheral resistance ( r =−0.27; P >0.05) or cardiac output ( r =0.23; P >0.05) in women. Our results demonstrate that men and women rely on different integrated physiological mechanisms to maintain a normal arterial pressure despite widely varying sympathetic nerve activity among individuals. These findings may have important implications for understanding how hypertension and other disorders of blood pressure regulation occur in men and women.
Physiological Role of Plasmacytoid Dendritic Cells and Their Potential Use in Cancer Immunity
Schettini, Jorge , Mukherjee, Pinku

Clinical and Developmental Immunology | January 26, 2009 | Volume: 2008 | Issue: No issue available | Pages: 1-10

10.1155/2008/106321 | PMID 19190769 Get It

Dendritic cells (DCs) play a pivotal role in the control of innate and adaptive immune responses. They are a heterogeneous cell population, where plasmacytoid dendritic cells (pDCs) are a unique subset capable of secreting high levels of type I IFNs. It has been demonstrated that pDCs can coordinate events during the course of viral infection, atopy, autoimmune diseases, and cancer. Therefore, pDC, as a main source of type I IFN, is an attractive target for therapeutic manipulations of the immune system to elicit a powerful immune response against tumor antigens in combination with other therapies. The therapeutic vaccination with antigen-pulsed DCs has shown a limited efficacy to generate an effective long-lasting immune response against tumor cells. A rational manipulation and design of vaccines which could include DC subsets outside “Langerhans cell paradigm” might allow us to improve the therapeutic approaches for cancer patients.
Short-Term Rescue of Neonatal Lethality in a Mouse Model of Propionic Acidemia by Gene Therapy
Hofherr, Sean, Senac, Julien S., Chen, Christopher Y. , Palmer, Donna , Ng, Philip , Barry, Michael A. , Barry, Michael A

Human Gene Therapy | January 26, 2009 | Volume: 20 | Issue: 2 | Pages: 169-180

10.1089/hum.2008.158 | PMID 19025475 Get It

Apolipoprotein B and Cardiovascular Disease Risk: Position Statement from the AACC Lipoproteins and Vascular Diseases Division Working Group on Best Practices
Contois, John H. , McConnell, Joseph P., Sethi, Amar A, Csákó, György, Hoefner, Daniel M , Warnick, G. Russell , Devaraj, Sridevi

Clinical Chemistry | January 23, 2009 | Volume: 55 | Issue: 3 | Pages: 407-419

10.1373/clinchem.2008.118356 | PMID 19168552 Get It

Abstract Background: Low-density lipoprotein cholesterol (LDL-C) has been the cornerstone measurement for assessing cardiovascular risk for nearly 20 years. Content: Recent data demonstrate that apolipoprotein B (apo B) is a better measure of circulating LDL particle number (LDL-P) concentration and is a more reliable indicator of risk than LDL-C, and there is growing support for the idea that addition of apo B measurement to the routine lipid panel for assessing and monitoring patients at risk for cardiovascular disease (CVD) would enhance patient management. In this report, we review the studies of apo B and LDL-P reported to date, discuss potential advantages of their measurement over that of LDL-C, and present information related to standardization. Conclusions: In line with recently adopted Canadian guidelines, the addition of apo B represents a logical next step to National Cholesterol Education Program Adult Treatment Panel III (NCEP ATPIII) and other guidelines in the US. Considering that it has taken years to educate physicians and patients regarding the use of LDL-C, changing perceptions and practices will not be easy. Thus, it appears prudent to consider using apo B along with LDL-C to assess LDL-related risk for an interim period until the superiority of apo B is generally recognized.
Analytic and Clinical Utility of a Next-Generation, Highly Sensitive Cardiac Troponin I Assay for Early Detection of Myocardial Injury
Kavsak, Peter A. , MacRae, Andrew R., Yerna, Marie-Jeanne, Jaffe, Allan S. , Jaffe, Allan S.

Clinical Chemistry | January 23, 2009 | Volume: 55 | Issue: 3 | Pages: 573-577

10.1373/clinchem.2008.116020 | PMID 19168557 Get It

Abstract Background: Improvements in cardiac troponin (cTn) assays have increased the rapidity with which clinicians can identify patients with changing cTn concentrations (rise or fall) indicative of acute myocardial injury. The aim of the present study was to characterize a new, high-sensitivity cTnI (hs-cTnI) assay and examine whether increased sensitivity can result in still earlier detection of evolving injury. Methods: We determined the limit of detection, precision profiles, and preliminary estimates of the 99th percentile for the Beckman Coulter hs-cTnI assay in 125 healthy individuals (age &lt;55 years, 54% male). We compared AccuTnI® and hs-cTnI to assess whether change criteria for early concentration changes (i.e., ≥3SD for low concentrations and 20% difference for concentrations &gt;0.10 μg/L) were exceeded in the first 2 specimens (median time between specimens, 1 h; 25th–75th percentile, 1–3 h) from subjects with symptoms suggestive of cardiac ischemia (n = 290). Results: The limit of detection for the hs-cTnI assay was 2.06 ng/L, and the 20% CV and 10% CV concentrations were 2.95 and 8.66 ng/L, respectively. The preliminary 99th percentile estimates in lithium heparin, serum, and EDTA plasma were 9.20, 8.00, and 8.60 ng/L, respectively. In 108 patients with myocardial injury based on the peak AccuTnI concentration, applying the change criteria on the 2 earliest specimens identified 81% (95% CI 73%–88%) of patients using the hs-cTnI assay compared to 62% (53%–71%) using the AccuTnI assay (P &lt; 0.001). Conclusions: Although more extensive validation studies are required, this Beckman Coulter hs-cTnI assay appears to detect patients with evolving myocardial injury earlier.
A Metric to Evaluate the Comparative Performance of an Institution's Graduate Medical Education Program
Murray, Peter M. , Valdivia, Jennifer H., Berquist, Mary R.

Academic Medicine | January 23, 2009 | Volume: 84 | Issue: 2 | Pages: 212-219

10.1097/acm.0b013e3181939705 | PMID 19174668 Get It

Abstract The economics of medicine have drastically changed during the past quarter century. Institutions may be faced with difficult decisions concerning graduate medical education (GME), particularly as it relates to the growth of existing programs and the creation of new programs. The authors describe a tool that they developed that can consistently measure the value of individual training programs while aligning with an institution's strategic priorities. This tool, the assessment metric scorecard, permits the annual prioritization of GME programs by the leadership of Mayo Clinic, Jacksonville, Florida. The scorecard also provides valuable data regarding the strengths and weaknesses of individual programs. The metric seeks to evaluate GME programs on the basis of four broad areas: Research, Teaching, Patient Service, and a General category. The assessment metric scorecard has been used since 2004; this article reports on its use for the academic years 2004–2005 and 2005–2006. The scorecard has proved to be a helpful tool for the yearly evaluation and prioritization of GME programs at the authors' institution. The overall mean score of the GME programs increased, which suggests a positive trend. This scorecard is flexible; modifications of the relative weights of the metrics can be made to align it with the strategic priorities of other institutions. The resources necessary to implement the scorecard are minimal.
Androgen Modulation of Coregulator Expression in Prostate Cancer Cells
Heemers, Hannelore V. , Regan, Kevin M., Schmidt, Lucy J., Anderson, S. Keith , Ballman, Karla V. , Tindall, Donald J., Ballman, Karla

Molecular Endocrinology | January 23, 2009 | Volume: 23 | Issue: 4 | Pages: 572-583

10.1210/me.2008-0363 | PMID 19164447 Get It