941 resultados para Parallel and Series Connection


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Each vol. has also distinctive title.

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The "Register" (containing index to v.6-10 only) form a separate volume, with special t.-p. and series t.-p. added.

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"Geschichte Deutschlands von 1806-1830 von Prof. Friedrich Bülau. Zugleich als Fortsetzung von Pfisters Geschichte der Teutschen," published as a part of this series, Hamburg, F. Perthes, 1842, is commonly regarded as the 6th volume of Pfister's history.

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Reprinted in part from various periodicals.

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Title and series title within illustrated border.

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Title and series title within illustrated border.

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Reprinted, in part, from various periodicals.

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Department name and series title at head of title.

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Vol. 2, edited by S. C. Freden, E. P. Mercanti, and D. E. Witten, published by Goddard Space Flight Center, Greenbelt, Md.; v. 3, edited by S. C. Freden and E. P. Mercanti, also published by Goddard.

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Each issue also has a distinctive title.

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Editor: 19 A. Baumstark.

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Dicks was active from 313 The Strand between 1863 and 1878--cf. Brown.

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Braided m-Lie algebras induced by multiplication are introduced, which generalize Lie algebras, Lie color algebras and quantum Lie algebras. The necessary and sufficient conditions for the braided m-Lie algebras to be strict Jacobi braided Lie algebras are given. Two classes of braided m-Lie algebras are given, which are generalized matrix braided m-Lie algebras and braided m-Lie subalgebras of End(F)M, where M is a Yetter-Drinfeld module over B with dimB < infinity. In particular, generalized classical braided m-Lie algebras sl(q,f)(GM(G)(A),F) and osp(q,l)(GM(G)(A),M,F) of generalized matrix algebra GMG(A) are constructed and their connection with special generalized matrix Lie superalgebra sl(s,f)(GM(Z2)(A(s)),F) and orthosymplectic generalized matrix Lie super algebra osp(s,l) (GM(Z2)(A(s)),M-s,F) are established. The relationship between representations of braided m-Lie algebras and their associated algebras are established.

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Pharmacodynamics (PD) is the study of the biochemical and physiological effects of drugs. The construction of optimal designs for dose-ranging trials with multiple periods is considered in this paper, where the outcome of the trial (the effect of the drug) is considered to be a binary response: the success or failure of a drug to bring about a particular change in the subject after a given amount of time. The carryover effect of each dose from one period to the next is assumed to be proportional to the direct effect. It is shown for a logistic regression model that the efficiency of optimal parallel (single-period) or crossover (two-period) design is substantially greater than a balanced design. The optimal designs are also shown to be robust to misspecification of the value of the parameters. Finally, the parallel and crossover designs are combined to provide the experimenter with greater flexibility.