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Gopherus agassizii agassizs desert tortoise scute dysecdysis / scute sloughing


, : Gopherus agassizii agassizs desert tortoise scute dysecdysis / scute sloughing. Herpetological Review 43(3): 473-474


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Other references

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Adriaenssens, N.; Belsack, D.; Buyl, R.; Ruggiero, L.; Breucq, C.; D.M.y, J.; Lievens, P.; Lamote, J., 2013: Ultrasound elastography as an objective diagnostic measurement tool for lymphoedema of the treated breast in breast cancer patients following breast conserving surgery and radiotherapy. BACKGROUND.: Lymphoedema of the operated and irradiated breast is a common complication following early breast cancer treatment. There is no consensus on objective diagnostic criteria and standard measurement tools. This study investigates the use...

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Kuyper, L.F.; Baccanari, D.P.; Jones, M.L.; Hunter, R.N.; Tansik, R.L.; Joyner, S.S.; Boytos, C.M.; Rudolph, S.K.; Knick, V.; Wilson, H.R.; Caddell, J.M.; Friedman, H.S.; Comley, J.C.; Stables, J.N., 1996: High-affinity inhibitors of dihydrofolate reductase: antimicrobial and anticancer activities of 7,8-dialkyl-1,3-diaminopyrrolo[3,2-f]quinazolines with small molecular size. A series of 7,8-dialkylpyrrolo[3,2-f]quinazolines were prepared as inhibitors of dihydrofolate reductase (DHFR). On the basis of an apparent inverse relationship between compound size and antifungal activity, the compounds were designed to be rela...

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Dahlbäck, H.; Holmberg, I., 1990: Oxidation of 5 beta-cholestane-3 alpha,7 alpha, 12 alpha-triol into 3 alpha,7 alpha,12 alpha-trihydroxy-5 beta-cholestanoic acid by cytochrome P-450(26) from rabbit liver mitochondria. The mitochondrial cytochrome P-450(26), previously shown to catalyze 26-hydroxylation of 5 beta-cholestane-3 alpha, 7 alpha, 12 alpha-triol, was found to convert this substrate also into 3 alpha,7 alpha,12 alpha-trihydroxy-5 beta-cholestanoic acid...

Katz, E.; M.J.ngYuan; Kyle, D.; Ziffer, H., 1999: Structure and antimalarial activity of adducts of 11-azaartemisinin with conjugated terminal acetylenes. Several N-substituted 11-azaartemisinins were prepared from 11-azaartemisinin in high yield by the DMAP catalysed addition of terminal acetylenes conjugated with electron-withdrawing groups. Their antimalarial activities against 2 drug-resistant s...