4,877 research outputs found
Funiculi - Funicula : Yamoh - Yamoh
https://digitalcommons.library.umaine.edu/mmb-ps/1188/thumbnail.jp
High dose multiple micronutrient supplementation improves villous morphology in environmental enteropathy without HIV enteropathy: results from a double-blind randomised placebo controlled trial in Zambian adults
PMCID: PMC3897937This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated
Woodland Echoes
https://digitalcommons.library.umaine.edu/mmb-ps/1723/thumbnail.jp
Inbuilt Mechanisms for Overcoming Functional Problems Inherent in Hepatic Microlobular Structure
This paper is funded by an MRC/EPSRC Discipline Bridging Initiative Grant (G0502256-77947) to W. Wan
Empirical Game-Theoretic Analysis: A Survey
In the empirical approach to game-theoretic analysis (EGTA), the model of the
game comes not from declarative representation, but is derived by interrogation
of a procedural description of the game environment. The motivation for
developing this approach was to enable game-theoretic reasoning about strategic
situations too complex for analytic specification and solution. Since its
introduction over twenty years ago, EGTA has been applied to a wide range of
multiagent domains, from auctions and markets to recreational games to
cyber-security. We survey the extensive methodology developed for EGTA over the
years, organized by the elemental subproblems comprising the EGTA process. We
describe key EGTA concepts and techniques, and the questions at the frontier of
EGTA research. Recent advances in machine learning have accelerated progress in
EGTA, and promise to significantly expand our capacities for reasoning about
complex game situations.Comment: 72 pages, 17 figure
In-Vitro steroidogenesis of newly formed corpora lutea and the non-luteal ovary in the rat, rabbit, hamster and guinea-pig
The steroidogenic abilities of the newly formed corpus luteum (8-10 h after ovulation) and the non-luteal ovary were compared in the guinea-pig, hamster, rabbit and rat using an invitro incubation technique. Histologically, newly formed rat corpora lutea (CL) were highly luteinized whereas the CL of the rabbit and guinea-pig were only partially luteinized. The CL of the hamster showed the least amount of luteinization. Serum progesterone was highest in the rat (18 ± 3 (s.e.m.) ng/ml). In the hamster, it was about 8 ng/ml, whereas in the rabbit and guinea-pig it was about 1 ng/ml. Serum androstenedione ranged between 0.5 and 1 ng/ml. Serum testosterone was lowest in the hamster (60 pg/ml) and highest in the rabbit (470 pg/ml), whereas in the rat and guinea-pig, testosterone levels were similar (about 240 pg/ml). Serum oestrogens were at baseline levels in all species. The CL of the rat exhibited considerably greater steroidogenic ability than the CL of the other species, producing 70 ± 6 ng progesterone/mg per h, 215 ± 14 pg androstenedione/mg per h, 49 ± 3 pg testosterone/mg per h, 3 pg oestrone/mg per h and 1 pg oestradiol/mg per h. Rabbit CL produced only progesterone (7 ± 2 ng/mg per h). Newly formed hamster CL produced none of the above steroids. In general, the ability of the CL to produce progesterone in vitro correlated with the degree of luteinization found by histological observation. Guinea-pig CL were embedded deeply in the ovary and could not be obtained without damage. Consequently, a portion of the ovary containing a corpus luteum was incubated. There was no difference in the steroid production by this portion of the ovary compared with the non-luteal ovary. The non-luteal ovary of the rat produced the highest amount of progesterone (10 ± 2 ng/mg per h). The guinea-pig non-luteal ovary produced about 5 ± 2 ng progesterone/mg per h, whereas the non-luteal ovary of the rabbit did not produce any. On the other hand, the hamster non-luteal ovary lost progesterone. Non-luteal ovaries from all species produced androgens. The non-luteal ovary of the guinea-pig contained especially large numbers of atretic antral follicles. The guinea-pig non-luteal ovary produced extremely large amounts of androstenedione (1110 ± 210 pg/mg per h) and testosterone (606 ± 154 pg/mg per h) compared with the amounts produced by the non-luteal ovary of the rat, hamster and rabbit. In the non-luteal ovary, interstitium and atretic antral follicles are the probable source of androgens. Oestrogen production by the non-luteal ovary was at baseline levels in the four species studied correlating with the absence of healthy antral follicles. The results indicate the extreme species differences that exist in ovarian function in the early postovulatory period
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