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Koenigs, W. and Bernhart, K. Ber. dtsch. chem. Ges. 38 (1905) 3042; Tschitschibabin, A. E. ibid. 3834; Koenigs, W. 40 (1907) 3199 b) Koenigs, E., Gerdes, H. C. and Sirot, A. Ber. dtsch. chem. Ges. 61 (1928) 1022; ( c) Maier-Bode, H. 69 (1936) 1534; Although the general structure is shared between the three species, interesting differences in the gene content can be observed. In dromedary, the total number of TRAV genes (83 TRAV genes) is higher than in humans (56 TRAV genes) (IMGT ® Repertoire, http://www.imgt.org (accessed on 12 March 2021)), but is much lower than in the sheep (277 TRAV genes) [ 17]; whereas the number of the dromedary TRAV subgroups (33 subgroups) is lower with respect to both humans (42 subgroups) and sheep (39 subgroups). Therefore, the dromedary germline TRAV repertoire is mainly due to the complexity of the duplication events that have caused the expansion of genes within some subgroups rather than the birth and/or the maintenance of other subgroups. As a matter of a fact, the clustering of the genes in the phylogenetic tree shows that gene duplication, involving ancestral TRAV gene subgroups followed by diversification, is the major mode of evolution of the dromedary TRAV genes. However, the dromedary TRAV42, TRAV43 and TRAV45 subgroups, shared with sheep but not with humans, are distinctive of the artiodactyl lineage, only. a) Wiley, R. H. and Slaymaker, S. C. J. Am. chem. Soc. 79 (1957) 2233; ( b) Katritzky, A. R. with Gardner, J. N. J. chem. Soc. (1958) 2192; ( c) with Hands, A. R. (1958) 2195; ( d) with Beard, J. A. T. and Coats, N. A. (1959) 3680

Sandborn, L. T. and Marvel, C. S. J. Am. chem. Soc. 50 (1928) 563; Renshaw, R. R., Ziff, M., Brodie, B. B. and Kornblum, N. 61 (1939) 638 Gautier, J. A. C. r. hebd. Séanc. Acad. Sci., Paris 205 (1937) 614; with Renault, J. 225 (1947) 880 Musante, C. and Fabbrini, L. Gazz. chim. ital. 84 (1954) 584; Germ. Pat. 936,071 (1955); Katritzky, A. R. and Jones, R. A. J. chem. Soc. (1960) 2947; Elkaschef, M. A.-F., Nosseir, M. H. and Abdel-Kader, A. (1963) 4647 Surrey, A. R. and Lindwall, H. G. J. Am. chem. Soc. 62 (1940) 1697; Boarland, M. P. V. and McOmie, J. F. W. J. chem. Soc. (1951) 1218; The phylogenetic relationship of the TRDJ genes were investigated by aligning the nucleotide sequences of all dromedary TRDJ genes (coding region plus RS) with those of sheep and humans.a) Katritzky, A. R. and Jones, R. A. Y. Proc. chem. Soc. (1960) 313; ( b) Katritzky, A. R. and Reavill, R. E. J. chem. Soc. (1963) 753; ( c) van der Haak, P. J. and de Boer, Th. J. Recl Trav. chim. Pays-Bas Belg. 83 (1964) 186

By comparison, in sheep, the mean length of δ CDR3 is 17.15 AA (range 8–26 AA) with only one clone out of 56 containing four TRDD genes [ 34]. Similarly, pig δ chains can involve up to four TRDD genes [ 39], and the cattle δ CDR3 shows combinations from one up to five TRDD genes [ 38]. Locations of the TRA and TRD genes are provided in Supplementary Table S1. The locations of the olfactory receptor ( OR) genes intermingled with the TRV genes at the 5′ of the locus are also provided ( Supplementary Table S1). Moreover, the phylogenetic tree also attests that the gene duplications that affected the birth of the expanded TRDV1 subgroup occurred independently in sheep and dromedary genome, although the model of duplication can be the same as indicated by the dot-plot matrix information.

a&&a.mc

Heil, B. & Markó, L. Hydroformylierung von Olefinen mit Rhodiumcarbonyl-Katalysatoren, II. Einfluß der Olefinstruktur auf die Reaktionsgeschwindigkeit. Chem. Ber. 102, 2238–2240 (1969).

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;

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In this work, the latest improved version of the genomic assembly [ 18] allowed us to fill the gap in our knowledge [ 5] regarding the genomic organisation of the dromedary TRA/TRD locus, which represents the most complex among the TR loci. Clar, E. Aromatische Kohlenwasserstoffe, 2nd ed., Berlin, 1952; Badger, G. M., Pearce, R. S. and Pettit, R. J. chem. Soc. (1951) 3199V a) Angyal, G. L. and Werner, R. L. J. chem. Soc. (1952) 2911; ( b) Goulden, J. D. S. (1952) 2939; ( c) Mason, S. F. (1958) 3619; (1959) 1281

This updated edition includes expanded coverage on the Second World War, as well as new sections on Finns in America and Russia, the centenary of the republic, and Finland’s battle with COVID-19, right up to its historic application to join NATO. Due to several sequencing errors between nucleotides 1 and 30, this part of the sequence is not annotated and FR1-IMGT and CDR1-IMGT have not been assigned. As a consequence, V-REGION is partial. V-REGION is partial: AA 1 is missing (partial FR1-IMGT), and only amino acid 105 is present (CDR3-IMGT partial). a) Jones, R. A. and Katritzky, A. R. J. chem. Soc. (1958) 3610; ( b) Albert, A. and Barlin, G. B. (1959) 2384 Clegg, W. et al. Characterization and Dynamics of [Pd(L−L)H(solv)]+, [Pd(L−L)(CH2CH3)]+, and [Pd(L−L)(C(O)Et)(THF)]+ (L−L=1,2-(CH2PBut2)2C6H4): Key Intermediates in the Catalytic Methoxycarbonylation of Ethene to Methylpropanoate. Organometallics 21, 1832–1840 (2002).

The Auctioneer will be pleased to execute bids free of charge for anyone unable to attend the sale on receipt of written instructions. Bids by telephone are accepted only at the senders risk and should be confirmed by letter or fax. DeTar, D. F., with Ballentine, A. R. J. Am. chem. Soc. 78 (1956) 3916; with Sagmanli, S. V. 72 (1950) 965