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The contribution of astrocyte glycogen to brain energy homeostasisForsyth, Robert J. January 1994 (has links)
No description available.
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Control of glucokinase and mRNA levels in hepatocytesBeresford, Guy William January 1994 (has links)
No description available.
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Structural basis of substrate binding to human facilitative sugar transportersKane, Susan January 1997 (has links)
No description available.
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Preservation of blood glucose.January 1992 (has links)
Leung Kwok-ming, Victor. / Thesis (M.Sc.)--Chinese University of Hong Kong, 1992. / Includes bibliographical references (leaves 74-78). / Chapter 1. --- SUMMARY --- p.1 / Chapter 2. --- INTRODUCTION / Chapter 2.1 --- Glycolysis : magnitude of the problem --- p.2 / Chapter 2.2 --- Glycolysis : individual variations --- p.2 / Chapter 2.2.1 --- Erythrocyte --- p.2 / Chapter 2.2.2 --- Leucocyte --- p.3 / Chapter 2.2.3 --- Age of individual --- p.3 / Chapter 2.3 --- Methods of blood glucose preservation --- p.3 / Chapter 2.3.1 --- Sodium fluoride --- p.4 / Chapter 2.3.1.1 --- Delayed effectiveness of NaF ; clinical implications --- p.6 / Chapter 2.3.2 --- D-mannose --- p.7 / Chapter 2.3.3 --- Citric acid --- p.9 / Chapter 2.3.4 --- Cooling --- p.10 / Chapter 2.3.5 --- Haemolysis --- p.11 / Chapter 2.4 --- Aims of the project --- p.12 / Chapter 3. --- MATERIALS & METHODS / Chapter 3.1 --- Evaluation of the YSI 23 AM glucose analyser for the measurement of glucose in haemolysate --- p.15 / Chapter 3.1.1 --- Principle of measurement --- p.15 / Chapter 3.1.2 --- Preparation of haemolysate --- p.16 / Chapter 3.1.3 --- Procedure --- p.16 / Chapter 3.2 --- Development of a glucose assay in haemolysate in Cobas Bio and Cobas Mira --- p.17 / Chapter 3.2.1 --- Glucose measurement --- p.17 / Chapter 3.2.2 --- Preparation of haemolysate --- p.17 / Chapter 3.2.3 --- Cobas Bio --- p.17 / Chapter 3.2.3.1 --- Optimisation of sample size --- p.17 / Chapter 3.2.3.2 --- Discussion --- p.21 / Chapter 3.2.4 --- Cobas Mira --- p.22 / Chapter 3.2.4.1 --- Optimisation of sample/reagent volume ratio --- p.22 / Chapter 3.2.4.2 --- Discussion --- p.22 / Chapter 3.2.4.3 --- Optimisation of the assay protocol --- p.26 / Chapter 3.2.4.4 --- Evaluation of the RS-SR1 protocol --- p.34 / Chapter 3.2.4.5 --- Discussion --- p.36 / Chapter 3.2.5 --- To study the effect of variations in haematological parameters on the re- covery of glucose inhaemolysate --- p.36 / Chapter 3.2.5.1 --- Procedure / :Experiment (i) --- p.36 / :Experiment (ii) --- p.43 / Chapter 3.2.5.2 --- Discussion --- p.48 / Chapter 3.2.6 --- Interference study of saponin --- p.50 / Chapter 3.2.6.1 --- Procedure --- p.50 / Chapter 3.2.6.2 --- Discussion --- p.50 / Chapter 3.2.7 --- Interference study of SDS --- p.53 / Chapter 3.2.7.1 --- Procedure --- p.53 / Chapter 3.2.7.2 --- Discussion --- p.53 / Chapter 3.3 --- Stability of glucose in haemolysate --- p.55 / Chapter 3.3.1 --- Preparation of haemolysate --- p.55 / Chapter 3.3.2 --- Glucose measurement --- p.55 / Chapter 3.3.3 --- Procedure --- p.55 / Chapter 3.3.3.1 --- Experiment (i) --- p.55 / Chapter 3.3.3.2 --- Experiment (ii) --- p.55 / Chapter 3.3.4 --- Statistical analysis --- p.56 / Chapter 4. --- RESULTS / Chapter 4.1 --- Evaluation of the YSI 23 AM glucose analyser for the measurement of glucose in haemolysate --- p.57 / Chapter 4.2 --- Stability of glucose in haemolysate --- p.60 / Chapter 5. --- DISCUSSION --- p.66 / Chapter 6. --- ACKNOWLEDGMENT --- p.73 / Chapter 7. --- REFERENCES --- p.74
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Reactions of glucose in H-Y zeolite catalystsLourvanij, Khavinet 26 June 1991 (has links)
Y-Zeolite catalysts have the potential to promote the
shape-selective conversion of glucose to oxygenated
hydrocarbons at fairly low temperature (100 to 130°C).
Reaction of glucose solution with H-Y Zeolite catalyst
powder was carried out in a well-mixed batch reactor. This
reaction was studied as a function of reaction time (0 to 24
hours), temperature (100 to 130°C), catalyst loading (10:1
to 1:1 glucose:Y-Zeolite), and initial glucose concentration
(12% to 58% g glucose/g solution). Unreacted glucose and
reaction products were analyzed by HPLC.
The dehydration of glucose solution by H-Y Zeolite
catalyst powder resulted in 90% conversion at 2:1 glucose:
H-Y Zeolite and 130°C. At these conditions, maximum
levulinic acid and formic acid yields were 15% and 30%
respectively.
A pseudo first-order process was used to estimate the
apparent rate constant for glucose conversion at various
temperatures. From the Arrhenius equation, the apparent
activation energy was estimated as 22.06 kCal/mole for
glucose solution initially at 12% weight.
Based on the product distribution data, a reaction
model for glucose dehydration to HMF, levulinic acid, and
formic acid in Y-Zeolite catalysts was proposed. / Graduation date: 1992
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Scanning Electrochemical Microscopy in Couple with Flow Injection Analysis for Determination of Biochemical CompoundsLai, Jyun-jie 30 August 2006 (has links)
µL
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Fermentation of D-xylose and mixtures of D-xylose and glucose by Candida shehataeKastner, James Robert 12 1900 (has links)
No description available.
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Regulation of glucose transport and insulin-stimulated glut4 translocation in skeletal muscle /Rincón Viatela, Jorge E., January 1900 (has links)
Diss. (sammanfattning) Stockholm : Karol. inst. / Härtill 6 uppsatser.
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Effect of hyperglycemia on glucose transport and intracellular signal transduction in skeletal muscle /Kawano, Yuichi, January 1900 (has links)
Diss. (sammanfattning) Stockholm : Karol. inst. / Härtill 5 uppsatser.
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Gluconeogenesis in the developing lamb /Warnes, Deidre Margaret. January 1976 (has links) (PDF)
Thesis (Ph.D.) -- University of Adelaide, Dept. of Obstetrics and Gynaecology, 1977.
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