90 research outputs found

    Utilization of Information Sources by the Biologists in Madurai Kamaraj University, Madurai: An Analytical Study

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    This study revealed importance of information sources among the biological faculty members and research scholars of Madurai Kamaraj University. In this studies the relative importance of information sources among the biologist on the basis of statistical tests concludes that the personal attributes of biologists such as designation, gender, age, qualification, subject, experience, nature of work and nature of research in a university level have bearing on the use of information resources. The results show that position and education are good predictors of information use while professional experience has little power in explaining variations in information source use. The findings of the study support the notion that information source use is a result of complex set of interactions among variables. The examination of the interaction of some of the variables such as education, position, and experience provides insight in understanding the factors that influence the use of information sources. The study reveals that the Reprints/Prints, Abstracting and Indexing Journal, primary periodicals, Newspaper, Dictionaries, Subject Bibliographies and Monographs / Text books were the sources of information which were most frequently used by the largest majority of the biologists

    Profiling extra cellular matrix associated proteome of human fetal nucleus pulposus in search for regenerative targets

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    Degeneration of the intervertebral disc is associated with a decrease in extra-cellular matrix (ECM) content due to an imbalance in anabolic and catabolic signaling. Our previous study profiled the core matrisome of fetal NP's and identified various proteins with anabolic potential for regenerative therapies. This study aims to complement those results by exploring ECM regulators, associated proteins and secreted factors of the fetal nucleus pulposus (NP). Proteomic data of 9 fetal, 7 healthy adults (age 22-79), and 11 degenerated NP's was analyzed. Based on the selection criteria, a total of 45 proteins were identified, of which 14 were uniquely expressed or upregulated in fetus compared to adult NP's. Pathway analysis with these proteins revealed a significant upregulation of one pathway and two biological processes, in which 12 proteins were involved. Prolyl 4 hydroxylase (P4HA) 1 and 2, Procollagen-lysine, 2-oxoglutarate 5-dioxygenase (PLOD) 1, and Heat shock protein 47 (SERPINH1) were involved in 'collagen biosynthesis' pathway. In addition, PLOD 1, SERPINH1, Annexin A1 and A4, CD109 and Galectin 3 (LGALS3) were all involved in biological process of 'tissue development'. Furthermore Annexin A1, A4 and A5, LGALS-3 and SERPINF1 were featured in 'negative regulation of cell death'. In conclusion, additionally to core ECM proteome, this study reveals ECM regulators and ECM affiliated proteins of interest to study for regenerative therapies, and their potential should be validated in future mechanistic experiments.Scientific Assessment and Innovation in Neurosurgical Treatment Strategie

    Genetic Variants of APOL1 Are Major Determinants of Kidney Failure in People of African Ancestry With HIV

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    INTRODUCTION: Variants of the APOL1 gene are associated with chronic kidney disease (CKD) in people of African ancestry, although evidence for their impact in people with HIV are sparse. METHODS: We conducted a cross-sectional study investigating the association between APOL1 renal risk alleles and kidney disease in people of African ancestry with HIV in the UK. The primary outcome was end-stage kidney disease (ESKD; estimated glomerular filtration rate [eGFR] of 30 mg/mmol), and biopsy-proven HIV-associated nephropathy (HIVAN). Multivariable logistic regression was used to estimate the associations between APOL1 high-risk genotypes (G1/G1, G1/G2, G2/G2) and kidney disease outcomes. RESULTS: A total of 2864 participants (mean age 48.1 [SD 10.3], 57.3% female) were genotyped, of whom, 354 (12.4%) had APOL1 high-risk genotypes, and 99 (3.5%) had ESKD. After adjusting for demographic, HIV, and renal risk factors, individuals with APOL1 high-risk genotypes were at increased odds of ESKD (odds ratio [OR] 10.58, 95% CI 6.22–17.99), renal impairment (OR 5.50, 95% CI 3.81–7.95), albuminuria (OR 3.34, 95% CI 2.00–5.56), and HIVAN (OR 30.16, 95% CI 12.48–72.88). An estimated 49% of ESKD was attributable to APOL1 high-risk genotypes. CONCLUSION: APOL1 high-risk genotypes were strongly associated with kidney disease in people of African ancestry with HIV and accounted for approximately half of ESKD cases in this cohort

    Vegetal fibers in polymeric composites: a review

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