Search

18 Mar 2008: Now, (A-3) can be expressed as:( ). _f anþ1 _f an þ Dt va _riĵaij þ _Ei bDai þ ka Xb. ... Lett. 78. (24), 3878–3880.Li, Y.L., Hu, S.Y., Liu, Z.K., Chen, L.Q., 2002.

8 Feb 2008: topology that led to the hypothesisthat topology, not sequence, is the major contribut-ing factor in how a protein folds.23,24 If proteinfolding rates and mechanisms are determinedlargely by the ... Activation energies were estimated using

27 Nov 2008: based measure dN (Yang 1997) and thenucleotide-based measure KA (Comeron 1995); seeBierne & Eyre-Walker (2003) and Haddrill et al. ... Evol. 24,2222–2234. (doi:10.1093/molbev/msm150). Charlesworth, B. & Charlesworth, D. 2000 The degener-ation of Y

18 Mar 2008: eA00fA D 0; (24)eA10fA D 0: (25). Anti-self-dual conformal structures in neutral signature 123. ... 4Other terminology includes neutral hyper-Kähler [28] and hyper-para-Kähler [24]. Anti-self-dual conformal structures in neutral signature 127.

19 Aug 2008: 24]. So we are keen to define the notion of Kleisli bicategoryin a way that includes such variants. ... for each pair (A, B) a natural transformation. C(A, B)K - D(KA, KB).

5 Feb 2008: 75) >3 (75) >1 (25) >2 (50) 0.25-16.6 (6-400) 0.1-72 (2.5-1800) <12 (300) <12 (300) 0.25-24 (6-600) 0.25-24 ... 6-600) >0.5 (12) >0.5 (12) 3 (75) 1.5-16 (40-400) <16 (400) >1.5 (40) 0.25-6 (6-150) <72 (1800) <24 (600) <8 (200)

4 Aug 2008: The 32 nm spacing between RS1 and RS2 and the 24 nm spacing between RS2 and RS3 are indicated bydouble-headed arrows. ... Curr Biol 2005, 1155::R514-R526. 40. Michie KA, Löwe J: DDyynnaammiicc ffiillaammeennttss ooff tthhee bbaacctteerriiaall

21 Oct 2008:

18 Feb 2008: adaptively. Although we chose to select genes on the. basis of nonsynonymous divergence (Ka), using the ratio. ... nonsynonymous : synonymous substitutions (Ka/Ks). would have made little difference to the list of genes.

31 Jul 2008: 9.3.9]:. u0(t) = 1, u1(t) =3t 5t3. 24, u2(t) =. 81t2 462t4 385t61152. , ... 9.6.24]. Kν (νz) =1. 2. eνφ(v) dv, φ(v) = z cosh v v.