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Vandana Dixit Ashok V. Kurup A K Gupta O M Kataria G B K S Prasad 《Indian journal of clinical biochemistry : IJCB》1997,12(1):39-43
Lymphatic filariasis caused byWuchereria bancrofti is a major health problem next only to malaria. A study had been conducted to estimate the prevalence of microfilaraemia in a rural endemic community near Raipur. The incidence of microfilaramia in the community was found to be about 14% when studied by night finger prick method. The incidence appears to be more in males as compared to females. The infection rate in vector population i.e.,Culex quinquefasciatus was recorded at a rate of 10%. No relationship could be drawn between the rates of vector and human filarial infections or between the density of vector population and the rate of vector/human infection(s). Prior health education is essential before taking up control and preventive measures in given endemic zone. 相似文献
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The cellular manufacturing （CM） has been proved as a well-known manufacturing strategy that helps to improve manufacturing efficiency and productivity by utilizing the philosophy of group technology. Large num- ber of papers has been published in the area of design issues of CM system. Unfortunately, the issues related to acceptability of CM in Indian industries are typically not examined rigorously as technical issues. This paper pre- sents the results of a survey carded out to find the status, enabler and barrier of implementing CM system in Indian industries. 相似文献
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Pratibha Dixit Shally Awasthi Nutan Maurya Sarita Agarwal M. Srinivasan 《Indian journal of clinical biochemistry : IJCB》2015,30(1):35-42
Cystic Fibrosis Trans membrane conductance regulator (CFTR) gene is an asthma susceptibility gene. In the present study we investigated the possible association of CFTR gene mutations in Indian asthmatic children as compared to controls. The study included 250 asthmatics and 250 age and sex matched controls. Case to control ratio for sample size was 1:1. Genotyping was performed for 24 CFTR gene mutations by ARMS-PCR and PCR–RFLP method. Among 24 CFTR gene mutations, heterozygous allele of R553X mutation was found in 4 (1.6 %) asthmatic cases and 2 (0.8 %) controls. Value of FVC and FEV1/FVC ratio were significantly lower in heterozygous individuals (p value <0.05). No significant difference was observed in the genotype and allele frequency of R553X mutation (OR = 1.339, 95 % CI = 0.755–2.374, p value = 0.685). Furthermore, all wild type homozygous alleles were observed in remaining 23 CFTR gene mutations. Our data concludes that R553X mutation was not significantly associated in Indian asthmatic children. 相似文献
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N. Pattanaik Ajita V Singh R. S. Pandey B. S. Singh Mohan Kumar S. K. Dixit Yamini B. Tripathi 《Indian journal of clinical biochemistry : IJCB》2003,18(2):181-189
Free radicals are implicated in various chronic diseases. There has always been a search for new antioxidants. In this paper
we have investigated Tamra bhasma, a metallic ayurvedic preparation. It is a time-tested medicine in Ayurveda and is in clinical
use for various ailments specifically the free radical mediated diseases. Our results show that Tamra bhasma inhibits lipid
peroxidation (LPO), prevents the rate of aerial oxidation of reduced glutathione (GSH) content and induces the activity of
superoxide dismutase (SOD) in rat liver homogenate in the bi-phasic manner. The drug was orally given for 7, 15 and 30 days
in different doses. Best protective response was found at the dose of 0.5mg/100g body weight in albino rats, although it showed
some histopathological changes at the dose of 20mg/100g body weight. The results suggest that this Ayurvedic preparation is
not merely a source of copper metal, but it is a strong anti-oxidant with no detectable adverse effect in lower doses of therapeutic
range. 相似文献
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R.P. Dixit 《International Information and Library Review》2013,45(3):165-182
AbstractThe paper describes succinctly the historical development of Indian health science libraries. With this background it illustrates the outcome of a study conducted for the purpose of assessing the strengths and weaknesses of prevalent health literature information services such as bibliographical, current awareness, selective dissemination of information, MEDLARS/MEDLINE, indexing and abstracting, translation and reprographic of 240 medical libraries belonging to modern medicine (allopathy system) and recommends the suitable steps to be undertaken to optimize the utilization of available resources and services. 相似文献
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Manjusha Dixit Anvesha Srivastava Gourdas Choudhuri Balraj Mittal 《Indian journal of clinical biochemistry : IJCB》2008,23(2):123-129
Background: Imbalance in cholesterol homeostasis may lead to gallstone disease. Apolipoprotein B is sole component of low-density
lipoprotein and plays an important role in cholesterol metabolism. The present study was carried out to explore the association
of APOB 3′ VNTR, exon 26 XbaI and signal peptide insertion/ deletion polymorphisms with gallstone disease. 214 ultrasonographically proven gallstone patients
and 322 healthy, age and sex matched controls were taken for the study. Genotyping was done using PCR followed by polyacrylamide
gel electrophoresis for VNTR and insertion/ deletion analysis. For APOB XbaI polymorphism PCR product was digested with XbaI restriction enzyme, followed by agarose gel electrophoresis. All statistical analyses were done using SPSS v11.5. Higher
repeat alleles of APOB 3′ VNTR polymorphism were more frequent in gallstone patients than in controls. Alleles with more than 57 repeats were present
only in patient group. Long (L) alleles with repeat higher than 49, were significantly higher (P=0.000; OR=3.705, 95% CI 2.577–5.326) and medium (M) alleles were lower (P=0.000; OR=0.406, 95% CI 0.304–0.542) in patients than in controls. To nullify the effect of gender, data was further stratified
into male and female population. APOB 3′ VNTR, L alleles were imposing risk and M alleles were protective in both male and female population. APOB
XbaI and insertion/deletion polymorphisms were not found to be associated with the gallstone disease. Longer alleles of APOB 3′ VNTR occur more frequently in gallstone patients, and may be an important risk factor for the development of gallstone
disease. APOB XbaI and signal peptide insertion/deletion polymorphisms may not be contributing to the risk for gallstone disease. 相似文献
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The path of charged particles is affected when they enter a magnetic field. This change of path largely depends on the angle between the applied magnetic field and the direction of motion of the charged particle (and its velocity) entering the magnetic field. This is demonstrated by means of a simple, low-cost experiment. A high voltage is used to ionize the air between a spark gap. The flow of charged particles between the spark gap is altered by applying a magnetic field from a rare earth permanent magnet having surface magnetic field induction of 0.12 T. 相似文献
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