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Elaine J. Carlson

Researcher at University of California, San Francisco

Publications -  94
Citations -  14217

Elaine J. Carlson is an academic researcher from University of California, San Francisco. The author has contributed to research in topics: Superoxide dismutase & Transgene. The author has an hindex of 54, co-authored 94 publications receiving 13759 citations. Previous affiliations of Elaine J. Carlson include King's College London.

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Dilated Cardiomyopathy and Neonatal Lethality in Mutant Mice Lacking Manganese Superoxide Dismutase

TL;DR: Cytochemical analysis revealed a severe reduction in succinate dehydrogenase and aconitase activities in the heart and, to a lesser extent, in other organs, which indicates that MnSOD is required for normal biological function of tissues by maintaining the integrity of mitochondrial enzymes susceptible to direct inactivation by superoxide.
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Attenuation of focal cerebral ischemic injury in transgenic mice overexpressing CuZn superoxide dismutase.

TL;DR: Results indicate that increased endogenous SOD activity in brain reduces the level of ischemic damage and support the concept that superoxide radicals play an important role in the pathogenesis of infarction and edema following focal cerebral ischemia.
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Primary afferent tachykinins are required to experience moderate to intense pain

TL;DR: It is concluded that the release of tachykinins from primary afferent pain-sensing receptors (nociceptors) is required to produce moderate to intense pain.
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Human copper-zinc superoxide dismutase transgenic mice are highly resistant to reperfusion injury after focal cerebral ischemia.

TL;DR: It is demonstrated that superoxide radicals play a major role in the pathogenesis of cerebral infarction in reperfusion injury after a focal stroke.
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Severely Impaired Urinary Concentrating Ability in Transgenic Mice Lacking Aquaporin-1 Water Channels

TL;DR: The results suggest that AQP1 knockout mice are unable to create a hypertonic medullary interstitium by countercurrent multiplication, and AQP 1 is thus required for the formation of a concentrated urine by the kidney.