GEXcel Work in Progress Report Volume VI
نویسندگان
چکیده
Institute of Thematic Gender Studies: Department of Gender Studies, Tema Institute, Faculty of Arts and Sciences, Linköping University Division of Gender and Medicine, Faculty of Health Sciences, Linköping University & Centre for Feminist Social Studies (CFS), School of Humanities, Education and Social Sciences (HumES), Örebro University Gender Studies, School of Humanities, Education and Social Sciences (HumES), Örebro University
منابع مشابه
Experimental Study on the Factors Affecting Hexavalent Chromium Bioreduction by Bacillus cereus
Chromium through natural processes and human activities enters the air, soil and water. Chromium-resistant bacteria are capable of reducing toxic Cr(VI) to less toxic Cr(III). In this work, batch studies were conducted to evaluate the effect of environmental factors on the rate of Cr(VI) reduction from synthetic wastewater of metal plating industry by Bacillus cereus under aerobic conditions. T...
متن کاملVolume VI: An Ecological Assessment for Anthropogenic Mercury Emissions in the United States MERCURY STUDY REPORT TO CONGRESS VOLUME VI: AN ECOLOGICAL ASSESSMENT FOR ANTHROPOGENIC MERCURY EMISSIONS IN THE UNITED STATES
متن کامل
Volume VI: An Ecological Assessment for Anthropogenic Mercury Emissions in the United States MERCURY STUDY REPORT TO CONGRESS VOLUME VI: AN ECOLOGICAL ASSESSMENT FOR ANTHROPOGENIC MERCURY EMISSIONS IN THE UNITED STATES
متن کامل
Lipoprotein Lipase (LPL) Gene Mutation: A First Report in Children
Genetic hyperchylomicronemia is a rare autosomal recessive disorder of lipoprotein metabolism estimated to affect approximately one per million individuals. We report a case with a rare mutation identified. It’s a genetic chylomicronemia in a Moroccan newborn baby, with massive hypertriglyceridemia and clinical signs of acute pancreatitis. She was a newborn female, first-degree of consanguineou...
متن کاملEhlers-Danlos syndrome: type VI A – kyphoscoliosis; a case report
Ehlers-Danlos syndrome (EDS) is a clinically heterogeneous groupof inherited disorders with ten different types, all involving agenetic defect in collagen and connective-tissue synthesis andstructure that affecting the skin, joints, and blood vessels. EDStype VIA, a very rare kyphoscoliotic type, is autosomal recessiveand clinically characterized by soft extensible skin, laxity ofjoints and kyp...
متن کامل