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30 Nov 1998: 05 46 10.7 47 00 38 97 105 0.17 6.1 67P13 05 46 13.3 44 05 16 1469 1523 0.20 53.4 67P14 05 46 ... 67P484 06 32 19.9 47 33 30 592 665 0.10 17.3 67P485 06 32 20.1 44 46 36 215 0.15 8.8.

30 Nov 1998: 17.1 48 49 15 343 374 0.18 11.2 51P4 09 49 13.3 47 20 23 279 416 0.33 11.3 51P5 09 49 15.7 44 ... 13.5 51P165 10 33 35.7 48 50 02 883 1057 0.11 20.3.

30 Nov 1998: 69P94 06 06 18.10 46 20 44.2 33.5 53.3 0.27 45.8 69P95 06 06 20.20 44 34 46.1 2.9 3.4 ... 22 33.9 23.2 24.6 0.20 20.5 69P246 06 13 39.89 44 00 55.4 12.1 15.3 0.09 6.2 69P247 06 13

30 Nov 1998: 2 34.2 33.7 0.41 41.3 54P7 10 40 29.46 46 36 53.0 17.7 17.9 0.43 20.3 54P8 10 40 30.43 ... 25.1 29.5 0.20 17.6 54P120 10 53 20.02 46 35 02.3 41.6 41.8 0.22 26.8.

30 Nov 1998: 4 7.2 7.7 0.16 6.7 70P7 06 40 46.74 44 45 34.5 11.1 10.7 0.20 9.0 70P8 06 40 47.96 ... 6 24.6 0.29 24.6 70P16 06 41 20.56 45 22 05.7 25.1 24.7 0.31 29.4 70P17 06 41 22.51 44 16

14 Oct 1998: DR. AFT. 20 What is Percolation? [1.5]. 1.5 The Main Questions. ... χ(p) = Pp(|C| =). n=1n Pp(|C| = n)(1.20). =θ(p). n=1n Pp(|C|= n),.

15 Jan 1998: 1995)(hum-b2)K463R K440 20 (PIP2) Salt-bridge to 5-phosphoryl of PIP2 SimoÄ es et al. ... Thealignment of T. brucei GPI-PLC with bPI-PLC(Figure 5) shows a sequence identity of 20% for theN-terminal half of the protein and 13% for the C-terminal half.

30 Nov 1998: 53P1 10 01 04.41 46 40 51.9 34.0 32.6 0.20 24.5 53P2 10 01 51.97 46 19 57.6 20.6 21.2 ... 46 38 35.3 23.6 30.7 0.42 29.7 53P9 10 03 11.65 47 37 57.5 32.4 32.9 0.20 23.1 53P10 10

28 Feb 1998: in the experiment shown above were approxi- promiscuous event than would be the case otherwise.mately 80%, 50%, 20%, and 20% for RM, rRM, cRM, and cRM 1TRAM, respectively.

30 Nov 1998: 52P1 10 17 48.9 48 45 06 2116 4010 0.07 19.8 52P2 10 20 06.2 48 06 50 1188 1259 0.12 26.6 52P3 10 20 ... 24.6 48 39 43 824 877 0.11 17.2 52P4 10 24 02.8 45 01 10 566 612 0.18 20.8 52P5 10 24 12.8 46