Citations

Showing 10 of 108036 citations.

Synergy of cancer immunotherapy and radiotherapy
Mansfield, Aaron S. , Park, Sean S. , Dong, Haidong , Mansfield, Aaron S

Mayo Clinic

Aging | March 6, 2016 | Volume: 7 | Issue: 3 | Pages: 144-145

10.18632/aging.100730 | PMID 25868470 Get It

Cardiac BNP gene delivery prolongs survival in aged spontaneously hypertensive rats with overt hypertensive heart disease
Tonne, Jason M., Holditch, Sara J., Oehler, Elise A., Schreiber, Claire A., Ikeda, Yasuhiro , Cataliotti, Alessandro

Mayo Clinic

Aging | March 6, 2016 | Volume: 6 | Issue: 4 | Pages: 311-319

10.18632/aging.100655 | PMID 24799459 Get It

Altered behavioral and metabolic circadian rhythms in mice with disrupted NAD+ oscillation
Sahar, Saurabh, Nin, Verónica , Barbosa, Maria Thereza , Chini, Eduardo N. , Sassone‐Corsi, Paolo

Mayo Clinic

Aging | March 6, 2016 | Volume: 3 | Issue: 8 | Pages: 794-802

10.18632/aging.100368 | PMID 21937766 Get It

Cockayne Syndrome B protein antagonizes OGG1 in modulating CAG repeat length in vivo
Kovtun, Irina V. , Johnson, Kurt O. , McMurray, Cynthia T.

Mayo Clinic

Aging | March 6, 2016 | Volume: 3 | Issue: 5 | Pages: 509-514

10.18632/aging.100324 | PMID 21566259 Get It

Perspectives on cellular senescence and short term dietary restriction in adults
Kirkland, James L.

Mayo Clinic

Aging | March 6, 2016 | Volume: 2 | Issue: 12 | Pages: 894-896

10.18632/aging.100247 | PMID 21164220 Get It

Perspectives on cellular senescence and short term dietary restriction in adults
Kirkland, James L.

Mayo Clinic

Aging | March 6, 2016 | Volume: 2 | Issue: 9 | Pages: 542-544

10.18632/aging.100204 | PMID 20864777 Get It

Epidemiology of Mixed Connective Tissue Disease, 1985–2014: A Population‐Based Study
Ungprasert, Patompong , Crowson, Cynthia S. , Chowdhary, Vaidehi , Ernste, Floranne C. , Moder, Kevin G., Matteson, Eric L. , Chowdhary, Vaidehi R

Mayo Clinic

Arthritis Care & Research | March 6, 2016 | Volume: 68 | Issue: 12 | Pages: 1843-1848

10.1002/acr.22872 | PMID 26946215 Get It

ObjectiveTo characterize the epidemiology of mixed connective tissue disease (MCTD) from 1983 to 2014.MethodsAn inception cohort of patients with incident MCTD in 1985–2014 in Olmsted County, Minnesota was identified based on comprehensive individual medical record review. Diagnosis of MCTD required fulfillment of at least 1 of the 4 widely accepted diagnostic criteria without fulfillment of classification criteria for other connective tissue diseases. Data were collected on demographic characteristics, clinical presentation, laboratory investigations, and mortality.ResultsA total of 50 incident cases of MCTD were identified (mean age 48.1 years and 84% were female). The annual incidence of MCTD was 1.9 per 100,000 population. Raynaud's phenomenon was the most common initial symptoms (50%), followed by arthralgia (30%) and swollen hands (16%). The diagnosis was frequently delayed with the median time from first symptom to fulfillment of criteria of 3.6 years. At fulfillment of criteria, arthralgia was the most prevalent manifestation (86%), followed by Raynaud's phenomenon (80%), swollen hands (64%), leukopenia/lymphopenia (44%), and heartburn (38%). Evolution to other connective tissue occurred infrequently with a 10‐year rate of evolution of 8.5% and 6.3% for systemic lupus erythematosus and systemic sclerosis, respectively. The overall mortality was not different from the general population with a standardized mortality ratio of 1.1 (95% confidence interval 0.4–2.6).ConclusionThis study was the first population‐based study of MCTD to provide a complete picture of epidemiology and clinical characteristics of MCTD. MCTD occurred in about 2 persons per 100,000 per year. Evolution to other connective diseases occurred infrequently and the mortality was not affected.
Removal of growth hormone receptor (GHR) in muscle of male mice replicates some of the health benefits seen in global GHR−/− mice
Berryman, Darlene E. , Ikeno, Yuji , Hubbard, Gene B., Funk, Kevin, Comisford, Ross , Young, Jonathan A., Tchkonia, Tamar , Kirkland, James L. , Miller, Richard A. , Kopchick, John J. , List, Edward Owen , Young, Jonathan A., Stout, Michael B , Masternak, Michal M , Bartke, Andrzej , Tchkonia, T

Mayo Clinic

Aging | March 5, 2016 | Volume: 7 | Issue: 7 | Pages: 500-512

10.18632/aging.100766 | PMID 26233957 Get It

Aspirin use and the risk of cholangiocarcinoma‡
Ghoz, Hassan , Peeraphatdit, Thoetchai , Baichoo, Esha, Addissie, Benyam D., Harmsen, William S. , Therneau, Terry M. , Chaiteerakij, Roongruedee , Roberts, Lewis R. , Choi, Jonggi, Ghoz, Hassan M, Choi, Jonggi , Olson, Janet E. , Chaiteerakij, Roongruedee , Roberts, Lewis R

Mayo Clinic

Hepatology | March 5, 2016 | Volume: 64 | Issue: 3 | Pages: 785-796

10.1002/hep.28529 | PMID 26940227 Get It

Whether aspirin use is protective against cholangiocarcinoma (CCA) remains unclear. We determined the association between aspirin use and other risk factors for each CCA subtype individually. In a hospital‐based case‐control study, 2395 CCA cases (1169 intrahepatic, 995 perihilar, and 231 distal) seen at the Mayo Clinic, Rochester, MN, from 2000 through 2014 were enrolled. Controls selected from the Mayo Clinic Biobank were matched two to one with cases by age, sex, race, and residence (n = 4769). Associations between aspirin use, other risk factors, and CCA risk were determined. Aspirin was used by 591 (24.7%) CCA cases and 2129 (44.6%) controls. There was a significant inverse association of aspirin use with all CCA subtypes, with adjusted odds ratios (AORs) of 0.35 (95% confidence interval [CI], 0.29‐0.42), 0.34 (95% CI 0.27‐0.42), and 0.29 (95% CI 0.19‐0.44) for intrahepatic, perihilar, and distal CCA, respectively (P < 0.001 for all). Primary sclerosing cholangitis was more strongly associated with perihilar (AOR = 453, 95% CI 104‐999) than intrahepatic (AOR = 93.4, 95% CI 27.1‐322) or distal (AOR = 34.0, 95% CI 3.6‐323) CCA, whereas diabetes was more associated with distal (AOR = 4.2, 95% CI 2.5‐7.0) than perihilar (AOR = 2.9, 95% CI 2.2‐3.8) or intrahepatic (AOR = 2.5, 95% CI 2.0‐3.2) CCA. Cirrhosis not related to primary sclerosing cholangitis was associated with both intrahepatic and perihilar CCA, with similar AORs of 14. Isolated inflammatory bowel disease without primary sclerosing cholangitis was not associated with any CCA subtype. Conclusions: Aspirin use was significantly associated with a 2.7‐fold to 3.6‐fold decreased risk for the three CCA subtypes; our study demonstrates that individual risk factors confer risk of different CCA subtypes to different extents. (Hepatology 2016;64:785‐796)