Citations

Showing 10 of 108060 citations.

Faculty Opinions recommendation of Developmental transcriptome analysis of human erythropoiesis.
Hu, Wenqian

Mayo Clinic

Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature | July 15, 2016 | Volume: No volume available | Issue: No issue available | Pages: No page available

10.3410/f.718369774.793520916 Get It

Faculty Opinions recommendation of Long noncoding RNAs in cell-fate programming and reprogramming.
Hu, Wenqian

Mayo Clinic

Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature | July 15, 2016 | Volume: No volume available | Issue: No issue available | Pages: No page available

10.3410/f.718437216.793520913 Get It

Faculty Opinions recommendation of Global transcriptome analyses of human and murine terminal erythroid differentiation.
Hu, Wenqian

Mayo Clinic

Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature | July 15, 2016 | Volume: No volume available | Issue: No issue available | Pages: No page available

10.3410/f.718312362.793520915 Get It

Faculty Opinions recommendation of Lineage and species-specific long noncoding RNAs during erythro-megakaryocytic development.
Hu, Wenqian

Mayo Clinic

Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature | July 15, 2016 | Volume: No volume available | Issue: No issue available | Pages: No page available

10.3410/f.718266506.793520914 Get It

FDG-PET and Neuropsychiatric Symptoms among Cognitively Normal Elderly Persons: The Mayo Clinic Study of Aging
Ruider, H, Lowe, Val J. , Stokin, Gorazd B. , Pink, Anna , Roberts, Rosebud O., Mielke, Michelle M. , Christianson, Teresa J., Jack, Clifford R. , Petersen, Ronald C. , Geda, Yonas E. , Krell-Roesch, Janina, Krell‐Roesch, Janina , Knopman, David S. , Machulda, Mary M. , Jack, Clifford R , Mielke, Michelle M , Geda, Yonas E , Stokin, Gorazd

Mayo Clinic

Journal of Alzheimer’s Disease | July 15, 2016 | Volume: 53 | Issue: 4 | Pages: 1609-1616

10.3233/jad-160326 | PMID 27447426 Get It

One of the key research agenda of the field of aging is investigation of presymptomatic Alzheimer’s disease (AD). Furthermore, abnormalities in brain glucose metabolism (as measured by FDG-PET) have been reported among cognitively normal elderly persons. However, little is known about the association of FDG-PET abnormalities with neuropsychiatric symptoms (NPS) in a population-based setting. Thus, we conducted a cross-sectional study derived from the ongoing population-based Mayo Clinic Study of Aging in order to examine the association between brain glucose metabolism and NPS among cognitively normal (CN) persons aged > 70 years. Participants underwent FDG-PET and completed the Neuropsychiatric Inventory Questionnaire (NPI-Q), Beck Depression Inventory (BDI), and Beck Anxiety Inventory (BAI). Cognitive classification was made by an expert consensus panel. We conducted multivariable logistic regression analyses to compute odds ratios (OR) and 95% confidence intervals after adjusting for age, sex, and education. For continuous variables, we used linear regression and Spearman rank-order correlations. Of 668 CN participants (median 78.1 years, 55.4% males), 205 had an abnormal FDG-PET (i.e., standardized uptake value ratio < 1.32 in AD-related regions). Abnormal FDG-PET was associated with depression as measured by NPI-Q (OR = 2.12; 1.23–3.64); the point estimate was further elevated for APOE ɛ 4 carriers (OR = 2.59; 1.00–6.69), though marginally significant. Additionally, we observed a significant association between abnormal FDG-PET and depressive and anxiety symptoms when treated as continuous measures. These findings indicate that NPS, even in community-based samples, can be an important additional tool to the biomarker-based investigation of presymptomatic AD.
Establishing quality indicators for neck dissection: Correlating the number of lymph nodes with oncologic outcomes (NRG Oncology RTOG 9501 and RTOG 0234)
Divi, Vasu , Harari, Paul M. , Cooper, Jay S., McHugh, Jonathan B. , Bell, Diana , Cmelak, Anthony J. , Suntharalingam, Mohan, Raben, David, Kim, Harold , Spencer, Sharon A., Laramore, George E. , Trotti, Andy, Foote, Robert L. , Schultz, Christopher J. , Le, Quynh‐Thu , Harris, Jonathan , Sturgis, Erich M. , Thorstad, Wade , Zhang, Qiang , Holsinger, F. Christopher , Kim, Harold E , Le, Quynh-Thu

Mayo Clinic

Cancer | July 15, 2016 | Volume: 122 | Issue: 22 | Pages: 3464-3471

10.1002/cncr.30204 | PMID 27419843 Get It

BACKGROUNDProspective quality metrics for neck dissection have not been established for patients with head and neck squamous cell carcinoma. The purpose of this study was to investigate the association between lymph node counts from neck dissection, local‐regional recurrence, and overall survival.METHODSThe number of lymph nodes counted from neck dissection in patients treated in 2 NRG Oncology trials (Radiation Therapy Oncology Group [RTOG] 9501 and RTOG 0234) was evaluated for its prognostic impact on overall survival with a multivariate Cox model adjusted for demographic, tumor, and lymph node data and stratified by the postoperative treatment group.RESULTSFive hundred seventy‐two patients were analyzed at a median follow‐up of 8 years. Ninety‐eight percent of the patients were pathologically N+. The median numbers of lymph nodes recorded on the left and right sides were 24 and 25, respectively. The identification of fewer than 18 nodes was associated with worse overall survival in comparison with 18 or more nodes (hazard ratio [HR], 1.38; 95% confidence interval [CI], 1.09‐1.74; P = .007). The difference appeared to be driven by local‐regional failure (HR, 1.46; 95% CI, 1.02‐2.08; P = .04) but not by distant metastases (HR, 1.08; 95% CI, 0.77‐1.53; P = .65). When the analysis was limited to NRG Oncology RTOG 0234 patients, adding the p16 status to the model did not affect the HR for dissected nodes, and the effect of nodes did not differ with the p16 status.CONCLUSIONSThe removal and identification of 18 or more lymph nodes was associated with improved overall survival and lower rates of local‐regional failure, and this should be further evaluated as a measure of quality in neck dissections for mucosal squamous cell carcinoma. Cancer 2016;122:3464–71. © 2016 American Cancer Society.
Historical Underpinnings of Bipolar Disorder Diagnostic Criteria
Mason, Brittany L. , Brown, E. Sherwood , Croarkin, Paul E. , Croarkin, Paul E

Mayo Clinic

Behavioral Sciences | July 15, 2016 | Volume: 6 | Issue: 3 | Pages: 14

10.3390/bs6030014 | PMID 27429010 Get It

Mood is the changing expression of emotion and can be described as a spectrum. The outermost ends of this spectrum highlight two states, the lowest low, melancholia, and the highest high, mania. These mood extremes have been documented repeatedly in human history, being first systematically described by Hippocrates. Nineteenth century contemporaries Falret and Baillarger described two forms of an extreme mood disorder, with the validity and accuracy of both debated. Regardless, the concept of a cycling mood disease was accepted before the end of the 19th century. Kraepelin then described “manic depressive insanity” and presented his description of a full spectrum of mood dysfunction which could be exhibited through single episodes of mania or depression or a complement of many episodes of each. It was this concept which was incorporated into the first DSM and carried out until DSM-III, in which the description of episodic mood dysfunction was used to build a diagnosis of bipolar disorder. Criticism of this approach is explored through discussion of the bipolar spectrum concept and some recent examinations of the clinical validity of these DSM diagnoses are presented. The concept of bipolar disorder in children is also explored.
A systematic review of faculty development initiatives designed to enhance teaching effectiveness: A 10-year update: BEME Guide No. 40
Mann, Karen, Barnett, Bonnie Maureen, Centeno, Angel , Naismith, Laura , Spencer, John, Tullo, Ellen, Viggiano, Thomas R., Ward, H. Marshall , Viggiano, Thomas, Steinert, Yvonne , Anderson, M. Brownell , Prideaux, David J. , Dolmans, Diana H. J. M.

Mayo Clinic

Medical Teacher | July 15, 2016 | Volume: 38 | Issue: 8 | Pages: 769-786

10.1080/0142159x.2016.1181851 | PMID 27420193 Get It

The Chicago Collaborative-Working Together to Address the Grand Challenges of Scholarly Communication
Yokote, Gail, Homan, J. , Shipman, Jean P.

Mayo Clinic

Against the Grain | July 15, 2016 | Volume: 24 | Issue: 3 | Pages: No page available

10.7771/2380-176x.6267 Get It

Animal models of gastrointestinal and liver diseases. Animal models of acute and chronic pancreatitis
Zhan, Xianbao , Bi, Yan , Ji, Baoan , Zhan, Xianbao , Wang, Fan

Mayo Clinic

American Journal of Physiology-Gastrointestinal and Liver Physiology | July 15, 2016 | Volume: 311 | Issue: 3 | Pages: G343-G355

10.1152/ajpgi.00372.2015 | PMID 27418683 Get It

Animal models of pancreatitis are useful for elucidating the pathogenesis of pancreatitis and developing and testing novel interventions. In this review, we aim to summarize the most commonly used animal models, overview their pathophysiology, and discuss their strengths and limitations. We will also briefly describe common animal study procedures and refer readers to more detailed protocols in the literature. Although animal models include pigs, dogs, opossums, and other animals, we will mainly focus on rodent models because of their popularity. Autoimmune pancreatitis and genetically engineered animal models will be reviewed elsewhere.