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Gautier, J. A. C. r. hebd. Séanc. Acad. Sci., Paris 205 (1937) 614; with Renault, J. 225 (1947) 880 ATTRIBUTED TO LOWRY, LAURENCE STEPHEN (1887-1976): In our opinion a work by the artists but less certainty as to authorship is expressed than in the above category.

Besides their adaptation to harsh environments, camels are multipurpose animals used for milk and meat production, racing, transportation and tourism. Pyridine and its Derivatives, ed. Klingsberg, E., Pt. 2, pp. 347, 355, New York (Inter-science) 1961

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With an optimal catalyst in hand, we investigated the scope and limitations for this system. Initially, alkoxycarbonylations of 1a with different alcohols were carried out. To our delight, primary as well as secondary alcohols such as ethanol, tetrahydrofurfuryl alcohol, and iso-propanol worked well and afforded the desired esters 4– 6 in almost quantitative yield (see Supplementary Fig. 10 for details). For a close inspection of the enlarged CDR3-IMGT region, the nucleotide sequences from codon 105 (codon following the 2nd-CYS codon 104 of the V-REGION) to codon 117 (codon preceding the J–PHE 118 or J–TRP 118) that belongs to the F/W–G–X–G motif characteristic of the J–REGION (i.e., coding region of a J gene) (IMGT ®, http://www.imgt.org (accessed on 12 March 2021)), was excised from each clone and reported in Supplementary Figure S7. By comparison with the TRDD genomic sequences, the nucleotides located in each sequence were considered to belong to a TRDD gene if they constituted a stretch of at least five consecutive nucleotides corresponding to one of the six TRDD germline sequences. All TRDD but one (TRDD3) gene, with no preference in the use, were recovered within the cDNA clones. Moreover, in 12 clones the presence of an additional TRDD gene (TRDD* in Supplementary Figure S7) with a nucleotide sequence similar to the TRDD2 and missing in the current genome assembly has been hypothesized. We proved the presence of this additional TRDD gene with an analysis aimed at the TRDD region in C. Bactrianus (CamBac2) and C. ferus (BCGSAC_Cfer_1.0) genome sequences, which revealed the presence of seven TRDD genes, indicating a probably gap between the dromedary TRDD4 and TRDD5 where one more TRDD similar to the TRDD2 gene would lie (see Section 2). Friedman, H. L., Braitberg, L. D., Tolstooukov, A. V. and Tisza, E. T. J. Am. chem. Soc. 69 (1947) 1204

d) Klotz, I. M., Fiess, H. A., Chen Ho, J. Y. and Mellody, M. 76 (1954) 5136; ( e) Brown, H. C., Johnson, S. and Podall, H. ibid. 5556; a) Hassel, O. with Romming, C. Act. chem. scand. 10 (1956) 696; and Tufte, T. 15 (1961) 967; ( b) with Hope, H. ibid. 407 The current development of improved versions of genome assemblies provides invaluable help for the study of complex genomic regions such as TR loci. In this context, the genomic organisation of the dromedary TRG locus has been recently completed by combining previous cloning data [ 6] with the analysis of genomic assemblies [ 10]. The locus is single with respect to ruminants’ TRG1 and TRG2 loci [ 11, 12], and as in cows, sheep and goats it is organised in “cassettes”, each containing the basic V–J–J–C recombination unit. Only three cassettes with six functional TRGV germline genes compose the dromedary TRG locus. In contrast, the ruminant TRG loci, located in two distinct positions of the same chromosome, display a higher number of functional TRGV germline genes (eleven in sheep and goats, 16 in cattle) distributed, as in dromedary, in reiterated V–J–J–C cassettes (six in sheep and seven in cattle and goats). However, the reduced potential diversity of the dromedary TRG repertoire due to the lower number of germline genes is overcome thanks to the somatic hypermutation (SHM) mechanism that allows the expansion of the primary repertoire [ 6, 7]. Cagle, F.W. and Smith, G.F. J.Am.chem.Soc. 69 (1947) 1860; Irving, H. and Hampton, A. J. chem. Soc. (1955) 430 b) Prelog, V., with Szpilfogel, S. Helv. chim. Acta 25 (1942) 1306; 28 (1945) 1684; ( c) with Hinden, W. 27 (1944) 1854;

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Karrer, P., with Schwarzenbach, G., Benz, F. and Solmssen, U. Helv. chim. Acta 19 (1936) 811; with Ringier, B. H., Büchi, J., Fritzsche, H. and Solmssen, U. 20 (1937) 55; with Kahnt, F. W., Epstein, R., Jaffé, W. and Ishii, T. 21 (1938) 223; with Blumer, F. 30 (1947) 1157; Kuhnis, H., Traber, W. and Karrer, P. 40 (1957) 751 Katritzky, A. R., Monro, A. M., Beard, J. A. T., Dearnaley, D. P. and Earl, N.J. J.chem. Soc. (1958) 2182 Hamer, J., Link, W. J., Jurjevich, A. and Vigo, T. L. Recl Trav. chim. Pays-Bas Belg. 81 (1962) 1058

Group B and D are representative of genes belonging to artiodactyls as they include dromedary and sheep TRDV5 and TRDV4 genes, respectively.

Reference

a) Biddiscombe, D. P., Herington, E. F. G., Lawrenson, I. J. and Martin, J. F. J. chem. Soc. (1963) 444; ( b) Katritzky, A. R. and Lagowski, J. M. (1961) 43 Goates, H., Cook, A. H., Heilbron, I. M., Hey, D. H., Lambert, A. and Lewis, F. B. J. chem. Soc. (1943) 401; Abramovitch, R. A. (1954) 3839 Eastham, G. R. et al. Synthesis and spectroscopic characterisation of the intermediates in the Pd-catalysed methoxycarbonylation of ethene. Chem. Commun. 7, 609–610 (2000). d) Krollpfeiffer, F. and Müller, A. Ber. dtsch. chem. Ges. 68 (1935) 1169; ( e) Kröhnke, F. ibid. 1177 Absentee (Auto bid) and live bids can be submitted bid.richardwinterton.co.uk, please note that there is an additional 3% (plus VAT) premium for this service.

a) Tschitschibabin, A. E. with Zeide, O. A. Zh. russk. fiz.-khim. Obshch. ( b) 50 (1918) 522; ( c) ibid. 512; Ostromislensky, I. U.S. Pat. 1,680,109; 1,680,111 (1928); 1,724,305 (1929); 1,809,352; 1,820,483 (1931); Tisza, E. T. and Joos, B. U.S. Pat. 1,856,602 (1932); 2,029,315 (1936); Renshaw, R. R. and Tisza, E. T., 2,135,293 (1938); Penfold, B. R. Acta crystallogr. 6 (1953) ( a) 591 ( b) 707; ( c) Wright, W. B. and King, G. D. S. ibid. 305 a) Cunliffe-Jones, D. B. Spectrochim. Acta 21 (1965) 747; ( b) Medhi, K. G. and Mukher-jee, D. K. ibid. 895 a) Abramovitch, R. A., Helmer, F. and Saha, J. G. Chemy Ind. (1964) 659; ( b) Ban, Y. and Wakamatsu, T. ibid. 710; ( c) Childs, R. F. and Johnson, A. W. ibid. 542; ( d) Levitt, L. S. and B. W. (1963) 1621; ( e) Barrett, G. G. and Schofield, K. ibid. 1980 Mauzerall, D. and Westheimer, F. H. J. Am. chem. Soc. 77 (1955) 2261; Loewus, F. A., Vennesland, B. and Harris, D. L. ibid. 3391

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Haszeldine, R. N. J. chem. Soc. (1950) 1638, 1966; (1951) 102; Simmons, T. C., Hoffmann, F. W. et al., J. Am. chem. Soc. 79 (1957) 3429 a) Quagliano, J. V., Fujita, J., Franz, G., Phillips, D. J., Walmsley, J. A. and Tyree, S. Y. J. Am. chem. Soc. 86 (1964) 586; Heller, A., Marcus, Y. and Eliezer, I. J. chem. Soc. (1963) 1579; The issue is that, the colors to mix , suggested by the software, are only available in urethane paint in the shop. Not only is utherene paint 4 times more expensive than acrlylic paint, it also needs extra step of clear coating. My Painter offers me higher price for 2 stage paint job . Since it is white color (forgiving color againts UV related fading and swirl marks), i do not think i need extra protection by clear coat. The car is an old/cheap car too. This gene is a sterile transcript. It has been found with a leader L region and a germline V region. L-V-sequence is in germline configuration. a) Foster, R. W., Ph.D. Thesis, London University, 1954; ( b) Jones, J. and J. Tetrahedron Lett. (1964) 2117; ( c) Beattie, I. R. and Webster, M. J. chem. Soc. (1961) 1730