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Titlebook: Literary and Cultural Production, World-Ecology, and the Global Food System; Chris Campbell,Michael Niblett,Kerstin Oloff Book 2021 The Ed

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Made in Cod’s Image: Food, Fuel, and World-Ecological Decline in Michael Crummey’s cultural recognition of the post-peak North Atlantic fishery, and narrates the erasure of Newfoundland’s outport communities following the 1992 northwest Atlantic cod moratorium. Focusing on . local manifestations of world-ecological breakdown, this chapter argues that the narrative moves from a sen
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White Flight from Planet Earth: Reading Race, Cheap Food, and Capitalism’s Crisis State in l crisis is understood and symbolically managed. In ., Blight has affected the world’s food supply, rendering Earth an uninhabitable Dust Bowl where human survivability is quickly coming to an end. The chapter shows how the movie offers a compelling and seemingly progressive visual representation of
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cy (maternal levels 68–96 μmol/l, target level 30–60 μmol/l). Tyrosine levels during pregnancy were between 500 and 693 μmol/l (normal values 20–120 μmol/l) and phenylalanine levels between 8 and 39 μmol/l (normal values 30–100 μmol/l). Nitisinone was measurable in neonatal blood immediately after b
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Chris Campbellestigated this by studying rat P19 cells, an established model for neuronal and glial differentiation. Our results show that (1) the .-serine synthesizing enzyme serine racemase was expressed upon differentiation, (2) extracellular .-serine concentrations increased upon differentiation, which was in
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Treasa De Loughrys implementation. It has so far focused on the detection of congenital hypothyroidism (CH) and phenylketonuria (PKU) to prevent or reduce mental and physical developmental retardation in children. Throughout this period, a total of 35,795,550 dried blood samples (DBS) of newborns (NB) have been anal
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Lucy Potter,Stephanie Lambertared to that of patients in the rest of the world. Observational data reported to the Fabry Registry were obtained from untreated patients or prior to treatment with enzyme replacement therapy. As of October 1, 2010, 3,752 patients were enrolled in the Fabry Registry worldwide, including 333 patient
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of the mitochondrial fatty-acid oxidation disorders. MADD is caused by a defect in the electron transfer flavoprotein (ETF) or ETF dehydrogenase (ETFDH) molecule, but as yet, inherited MADD has not been reported in animals. Here we present the first report of MADD in a cat. The affected animal prese
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