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41.
Lal R Ellenbogen A Chen D Zomorodi K Atluri H Luo W Tovera J Hurt J Bonzo D Lassauzet ML Vu A Cundy KC 《Clinical neuropharmacology》2012,35(4):165-173
42.
Chandrashekhar T Sreeramareddy Pathiyil R Shankar VS Binu Chiranjoy Mukhopadhyay Biswabina Ray Ritesh G Menezes 《BMC medical education》2007,7(1):26
Background
In recent years there has been a growing appreciation of the issues of quality of life and stresses involved medical training as this may affect their learning and academic performance. However, such studies are lacking in medical schools of Nepal. Therefore, we carried out this study to assess the prevalence of psychological morbidity, sources and severity of stress and coping strategies among medical students in our integrated problem-stimulated undergraduate medical curriculum. 相似文献43.
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47.
Bellay J Atluri G Sing TL Toufighi K Costanzo M Ribeiro PS Pandey G Baller J VanderSluis B Michaut M Han S Kim P Brown GW Andrews BJ Boone C Kumar V Myers CL 《Genome research》2011,21(8):1375-1387
Genetic interactions provide a powerful perspective into gene function, but our knowledge of the specific mechanisms that give rise to these interactions is still relatively limited. The availability of a global genetic interaction map in Saccharomyces cerevisiae, covering ~30% of all possible double mutant combinations, provides an unprecedented opportunity for an unbiased assessment of the native structure within genetic interaction networks and how it relates to gene function and modular organization. Toward this end, we developed a data mining approach to exhaustively discover all block structures within this network, which allowed for its complete modular decomposition. The resulting modular structures revealed the importance of the context of individual genetic interactions in their interpretation and revealed distinct trends among genetic interaction hubs as well as insights into the evolution of duplicate genes. Block membership also revealed a surprising degree of multifunctionality across the yeast genome and enabled a novel association of VIP1 and IPK1 with DNA replication and repair, which is supported by experimental evidence. Our modular decomposition also provided a basis for testing the between-pathway model of negative genetic interactions and within-pathway model of positive genetic interactions. While we find that most modular structures involving negative genetic interactions fit the between-pathway model, we found that current models for positive genetic interactions fail to explain 80% of the modular structures detected. We also find differences between the modular structures of essential and nonessential genes. 相似文献
48.
Uretsky S Rozanski A Singh P Supariwala A Atluri P Bangalore S Pappas TW Fisher EA Peters MR 《The international journal of cardiovascular imaging》2011,27(6):805-812
Patients with coronary artery calcium (CAC) scores of zero are generally considered not to have atherosclerosis. Recent studies
involving computed tomography coronary angiography (CTCA) challenge this assumption. This goal of the present study is to
assess the frequency, morphology, location, and the prognosis of patients with plaque detected on CTCA and zero CAC. 1,119
patients (51 ± 12 years, 52% male) with a zero CAC score during CTCA study were retrospectively identified. The CTCA studies
were assessed for the presence, morphology, location and severity of all coronary plaques. All-cause mortality was assessed.
The prevalence of coronary plaque was 13% (147 patients). Among the 212 plaques identified 154 (73%) were non-calcified, 28
(13%) were calcified, and 30 (14%) were of mixed morphology. Notably, ≥70% stenosis was noted among only 0.4% of all patients.
ROC analysis revealed that coronary artery disease risk factors did not add to the prediction of plaque among our patients.
Over a mean follow-up of 2.5 ± 0.6 years there were 4 deaths (0.4%), all in patients without coronary plaque on CTCA. The
presence of coronary plaque is not uncommon among patients with zero CAC scores. These plaques were rarely associated with
hemodynamically significant stenoses and were associated with an excellent prognosis. Clinical factors do not appear to be
useful in predicting which patients with zero CAC scores have undetected coronary plaque. 相似文献
49.
VS Gurunadh A Banarji S Patyal TS Ahluwalia AK Upadhyay M Bhadauria 《Medical Journal Armed Forces India》2010,66(2):147-150
Background
Proliferative vitreo-retinopathy (PVR) is the most common cause of failed repair of a primary rhegmatogenous retinal detachment (RRD). The success rates for the surgery of complicated RRD has doubled with improved vitreous techniques from 35–40% to approximately 65–75% at six months. However, despite these advances, recurrent vitreo-retinal traction leads to re-detachment in more than one-fourths of the initially successful cases. The use of adjunctive treatments to prevent cellular proliferation holds promise for the prevention of PVR or recurrences after surgery. One focus has been on the use of intra-vitreal antimetabolites to prevent the occurrence of PVR.Methods
Thirty patients of complicated retinal detachment associated with PVR, C1 or more were managed by vitreo-retinal (VR) surgery with the addition of 250 μg / ml of 5-fluorouracil (5FU) and 1 IU / ml of low molecular weight heparin (LMWH) to the vitreous infusion. The patients were examined for any evidence of PVR till 180 days as also for any systemic or other ophthalmic complication.Result
Out of the 30 cases in the study group, 25 (83.34%) cases had retinal settlement at the end of six weeks, which is similar to the outcomes of conventional VR surgery. There was no case of any serious complication.Conclusion
The addition of LMWH and 5FU did not enhance the outcome of VR surgery.Key Words: Proliferative vitreo-retinopathy, Rhegmatogenons retinal detachment, 5-fluorouracil, Low molecular weight heparin 相似文献50.
Suash Sharma Asis K Karak Rajvir Singh VS Mehta Chitra Sarkar Horst P Schmitt 《Pathology oncology research : POR》1999,5(2):134-141
An in vivo bromodeoxyuridine (BrdU) labeling index (LI) was estimated in 43 cases of astrocytic tumors and mixed gliomas by one hour intra-operative intravenous infusion at a dose of 200 mg/m2 and correlated with (a) histological grading using a computer aided malignancy classifier TESTAST-268; and (b) histological typing using WHO classification. The lowest BrdU LI was seen in pilocytic and gemistocytic astrocytomas followed by astrocytomas, anaplastic astrocytomas and glioblastoma multiforme in that order. Mixed oligoastrocytomas followed the pattern of their astrocytic counterparts. Tumors of similar histological type showed different BrdU LI values especially amongst astrocytomas and glioblastomas. A statistically significant difference in the BrdU LI was also noted between the higher TESTAST grades of astrocytomas (T III and IV) versus the lower TESTAST grades (T II). Unlike earlier reports in literature, in the present study the category of BrdU LI of <1 contained no case of anaplastic astrocytoma or glioblastoma multiforme (TESTAST grades III and IV). Likewise, the category of BrdU LI >5 contained only anaplastic astrocytoma and glioblastoma multiforme (TESTAST grades III and IV). Maximum spread of cases was seen in the BrdU LI category of 1-5, not only in terms of histological types but also TESTAST grades. Thus there appeared to be a positive trend of increasing BrdU LI values both with histological types and increasing TESTAST grades. Further, an interesting observation was that by using a combination of TESTAST grades and BrdU LI, the histologically homogenous glioblastoma group could be further subdivided into 4 categories which showed a trend towards prognostic correlation. Thus, this study though preliminary with number of cases being small in some groups, highlights the possible usefulness of combined histological typing, TESTAST grading and in vivo BrdU LI for prognostication of gliomas especially glioblastoma multiforme. 相似文献