... (2007) 36 85 36 94 ª 2007 The Authors Journal compilation ª 2007 FEBS 36 89 T J Winterburn et al N-terminal extension of IA3 Identity Residue number 11 11T 34 45 57 0.1 ± 0.1 *Q S H 30 ± 13 14 MK(H) ... peptides of the indicated length In these forms of IA3, L-norleucine (Z) was substituted for methionine NI = no inhibition at lM 36 86 FEBS Journal 274 (2007) 36 85 36 94 ª 2007 The Authors Journal compilation ... NaCl Fractions containing trimmed IA3 FEBS Journal 274 (2007) 36 85 36 94 ª 2007 The Authors Journal compilation ª 2007 FEBS 36 93 N-terminal extension of IA3 T J Winterburn et al were identified...
... Ca2+ transients Nature 37 5, 784–787 33 Dolmetsch RE, Xu K & Lewis RS (1998) Calcium oscillations increase the efficiency and specificity of gene expression Nature 39 2, 933 – 936 ´ 34 Feijo JA, Sainhas ... transform of the yi in the usual way [45] For Fig 3, we defined a series of 1024-point equally spaced and overlapping windows of the normalized O2 data (points 1–1024, 230 –12 53, 459–1482, ., 35 35 1 36 ... data points for m ⁄ z ¼ 32 (O2) for a 30 -min span starting at 730 h 42 ± (n ¼ 7), the penultimate IBI averaged 36 ± (n ¼ 7), whereas the mean of earlier IBIs reached a plateau of 30 .9 ± 2.4 (when...
... ⁄ 33 .1 32 .0 33 .2 15.6 0.117 ⁄ 0.077 0.04 33 .5 10.4 0. 033 ⁄ 0. 031 0.02 Stereochemical restraints r.m.s (r) ˚ Bond distances (A) 0.011 (0.021) Bond angles (°) 1.609 (1.965) ˚ Chiral centers (A3) ... Gly302-Glu3 03- Ser304-Ser305-Ser306 located at the opposite end of the barrel to the active site has weaker electron density and the temperature factors of the ˚ atoms in this segment are 31 ... Journal compilation ª 2006 FEBS Glu-A 0.15 0.02 0. 13 0.51 )0.46 )0.05 0.15 0.02 0.10 0 .32 )0. 43 )0.06 0. 63 0.44 0.52 0.18 0.56 0 .39 0.46 0.15 21 63 ˇ ˇı J Sevc´k et al Glucoamylase raw starch binding...
... YCplac 33- GAS1 or the YCplac 33- GAS1-C74S plasmid Cells were labelled for with [35 S]methionine and chased for the indicated times before being processed for immunoprecipitation with anti-Gas1p IgG 36 44 ... at 30 °C for 20 min, then pulse-labelled for with 35 0 lCi of [35 S]methionine Pulse labelling was terminated upon the addition of 40 lL of chase solution containing 0 .3% (w/v) methionine and 0 .3 ... residue S 73 For Gas1C103S, the reverse primer Oligo3 (5¢-AGCCTTC ATCGATTCGGAGTGATCTAGAGTG -3 ), partially complementary to nucleotides +288 to +31 8, and Oligo4 (5¢-CTCCGAATCGATGAAGGCTTTGAATGATGC -3 )...
... the whistle, a conditioned reinforcer, is something the animal has learned to want (Some people use the term “primary reinforcer” forfood and “secondary reinforcer” for the signal I avoid those ... trainer too!) before the performance was correct and reliable Also when a trainer uses food without a conditioned reinforcer the animal is apt to look toward the trainer forfood all the time ... not extend to copying for general distribution, for promotion, for creating new works, or for resale Specific permission must be obtained in writing from CRC Press LLC for such copying Direct...
... as an Outbreak Attempt 94 100 106 1 13 1 13 120 127 132 135 139 139 141 147 151 159 167 167 170 175 180 185 191 195 195 200 Notes 205 References 2 23 Index 233 Acknowledgments My engagement with ... ISBN 978-0-7914-7209-5 (hardcover : alk paper) Adorno, Theodor W., 19 03 1969 I Title B3199.A34F67 2007 1 93 dc22 2006 036 599 10 For Hildy This page intentionally left blank Contents Acknowledgments ... object, only in its objectification into the moment of form does it forget how and whereby it is itself constituted” (p 1 63) .37 For Adorno, this “forgetting” is not restricted to idealist philosophies,...
... Convention Oxford University Press, pp 30 9 31 8 Savitzky, A and Golay, M J E (1964) Smoothing and differentiation of data by simplified least squares procedures Anal Chem 36 , 1627–1 633 Schofield, ... root and vector methods used in multivariate analysis Biometrika 53, 32 5 33 8 Griffiths, P R and de Haseth, J A (1986) Fourier Transform Infrared Spectrometry John Wiley, New York Hough, J S (1957) ... Timmins and Goodacre (1997) Conditions used for each experiment involved heating the sample to 100 C for s followed by Curie-point pyrolysis at 530 C for s with a temperature rise time of 0·5 s...
... 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 Gesellschaft für Psychologie: 23 27 September; Kiel Edited by: Frey D Göttingen: Hogrefe; 1990:1 23- 124 Potthoff RD, Schmielau F: Specific ... den 37 Kongress der Deutschen Page 15 of 16 (page number not for citation purposes) Journal of NeuroEngineering and Rehabilitation 2007, 4 :31 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 ... for example he performed 130 correct responses when tested after treatment, his detection rate would be 130 :35 0 = 37 .1% The improvement due to treatment in that case would be 37 .1% - 28.6% = 8.5%...
... 5'-ATGACCAGGACGAGGAGATG -3' (maps to residues 8 831 -8812 of vRNA), ABV2r, 5'-CCTGTGAATGTCTCGTTTCTG -3' (maps to residues 5754-5 733 of vRNA), and ABV3r 5-TTCTTTCAGCAACCACTGACG -3' (maps to residues 25 63- 25 43 of vRNA) ... polymerase and dATP for 10 minutes at 72°C For each product, independent transformants were prepared for standard dideoxy sequencing on an ABI3 730 sequencer (ElimBio, Hayward CA) Forward and reverse ... sequenced with M13F and M13R primers For the 3' RACE products, independent transformants from independently generated PCR products were subcloned and sequenced with M13F and M13R primers Terminal...
... 0. 03 Figure C (3, 2 ,3) : Probability of detection compared with Pe For the C (3, 2 ,3) encoder, the probability of detecting the true encoder is depicted compared with the channel error probability for ... http://jwcn.eurasipjournals.com/content/2011/1/168 • C (3, 2, 3) convolutional encoder: Figure shows the probability of detecting the true encoder (Pdet) compared with Pe for 1, 10, and 50 iterations It shows that, for the C (3, 2, 3) convolutional ... Indeed, the algorithm performances are excellent: P det is close to when P e corresponds to either BERr < × 10-4 for C (3, 2 ,3) convolutional encoder or BERr < 0.67 × 10-4 for the C (3, 1,4) encoder Conclusion...
... B-frame one GOP size (kbit) 1080 36 0 180 36 00 GOP = {IBBPBBPBBPBB}, 25 frames/s, 7.5 Mbit/s video bitrate # MPEG-2 TS packets # IP packets 714 102 238 34 119 17 238 0 34 0 Table 2: Value of Eb /N0 ... IEEE Transactions on Multimedia, vol 8, no 2, pp 34 1– 35 5, 2006 [21] M Watson, “Proposal for evaluation process for forward error correction codes for DVB-IPI,” DVB IPI document TMIPI2084 edition, ... packet groups (N = 5, Ncoh = 3, Ngroup = 3) where Ppack is the probability that a packet is erased and irrespective of the channel condition Ppack = +∞ Ppack (x)p(x)dx ( 23) For large Eb /N0 , Ppack...
... side of (35 ), we obtain M gk1 According to (41), gR, = gI, (42) Then (41) can be reduced to M = 1, 2 gR,k1 + 2gR, − = (36 ) k=1 ( 43) k=1,k= M gk1 Thus = (37 ) M gR, = 3 Therefore, (36 ) and (37 ) dictate ... that is, g12 = Hence, g2 will take the form g2 = | g T T , (32 ) which results in H g1 g2 = (33 ) Therefore, (26) is reduced to J g2 = E zR,2 (n) − R g2 , (34 ) A Ikhlef and D Le Guennec T where ... Imaginary −2 −4 −4 3 −2 −1 Real −6 −6 −4 −2 (a) −4 3 −2 −1 Imaginary Imaginary −2 −4 Real −6 −6 −4 −2 (d) 4 Equalizer output −4 3 −2 −1 Real (c) Mixture −1 −2 3 −4 Real −1 −2 3 −4 (b) Source...