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12 Jun 2006: g. [23,24]). The major difficulties then consist in the formulation of accurate internalboundary conditions and in following the evolution of the interfaces through time. ... 104 This study 19.6 16.2 3.53 0.585 2.24[2] 19.51 16.2 3.53 0.586 2.243[3]

22 May 2006: 1.4 Inverse of a matrix. 24. 1.4.1 Uniqueness of inverse. 24. ... . (. 1 4 2). =. . . 6 24 124 16 81 4 2.

4 Sep 2006: 1990. 335.87. 80.22. 1990. 5.6. 4.6. 39.9. 24.9. 5.3. 1991. 335.20. ... 81.54. 1991. 5.4. 4.8. 41.7. 24.5. 5.2. 1992. 338.00. 78.85. 4.

5 May 2006: Received 29 March 2004; received in revised form 24 September 2004; accepted 11 November 2004. ... ykumar and Mao [24] again assuming the interface was sharp. The SPH method, as mentioned earlier, does.

27 Apr 2006: Received 24 November 2004; revised 19 May 2005; accepted 11 August 2005; published 2 February 2006. ... The wider range of melt rates were used toexamine model sensitivity to mi.[24] In an extensive study of four sea ice sites in the.

22 May 2006: gyrus (BA 6) 6 24 69 3.9 19Right precentral gyrus (BA 4) 24 24 72 3.6 11Right precuneus (BA 7) 3 33 54 3.7 13Left precuneus (BA 7) ... cuneus (BA 30) 6 57 15 4.7 48Right cuneus (BA 18) 6 87 24 3.7 6.

13 May 2006: Similarly the ternary cubicx3 2y3 5z3 = 0 has discriminant = 24.39.54 yet is 3-adicallyinsoluble. ... In the case n = 2, we find. c4 (α21 4α0α2 4c)2 (mod 24).We set b2 = α.

24 Apr 2006: Share. Published. 24 Apr 2006. Search news. Sign up to receive our newsletter.

19 Apr 2006: Surprisingly, however, the 24 and 70 µm images of Vegaactually have larger radii than the submillimeter ring or mil-limeter clumps (Su et al., 2005). ... Emission (Additional)Vega A0 200 >90 23,24,25 Eridani K2 <1000 60 26,27η Corvi F2 1000 100 28τ

12 Oct 2006: coli chromosome segregation byorienting the FtsK translocase. EMBO J. 24, 3770–3780 (2005). ... J. Mol. Biol. 343, 547–557 (2004). 24. Ohnishi, T., Hishida, T., Harada, Y., Iwasaki, H. &