Research Article
Development of an improved technique for the perfusion of the isolated caudal lobe of sheep liver
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- 02 November 2000, pp. 469-478
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Possible contribution of central gamma-aminobutyric acid receptors to resting vascular tone in freely moving rats
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- 02 November 2000, pp. 479-485
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Regional distribution of potassium currents in the rabbit pulmonary arterial circulation
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- 02 November 2000, pp. 487-496
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Hypotonic swelling increases L-type calcium current in smooth muscle cells of the human stomach
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- 02 November 2000, pp. 497-504
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Differences in the calcium-handling response of isolated rat and guinea-pig cardiomyocytes to metabolic inhibition: implications for cell damage
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- 02 November 2000, pp. 505-510
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Nerve-evoked secretion of immunoglobulin A in relation to other proteins by parotid glands in anaesthetized rat
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- 02 November 2000, pp. 511-518
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Ageing modulates some aspects of the non-specific immune response of murine macrophages and lymphocytes
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- 02 November 2000, pp. 519-525
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The preoptic area in the hypothalamus is the source of the additional respiratory drive at raised body temperature in anaesthetised rats
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- Published online by Cambridge University Press:
- 03 November 2000, pp. 527-537
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Equine uteroplacental metabolism at mid- and late gestation
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- 02 November 2000, pp. 539-545
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Left ventricular diastolic filling and cardiovascular functional capacity in older men
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- 02 November 2000, pp. 547-555
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Cardiovascular effects of 8 h of isocapnic hypoxia with and without beta-blockade in humans
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- 02 November 2000, pp. 557-565
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Selective long-term electrical stimulation of fast glycolytic fibres increases capillary supply but not oxidative enzyme activity in rat skeletal muscles
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- 02 November 2000, pp. 567-573
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Angiotensin-converting enzyme genotype affects the response of human skeletal muscle to functional overload
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- 02 November 2000, pp. 575-579
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Carbohydrate ingestion prior to exercise augments the exercise-induced activation of the pyruvate dehydrogenase complex in human skeletal muscle
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- 02 November 2000, pp. 581-586
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