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1 evidence to bear on these questions and find the split between A. thaliana and Arabidopsis lyrata occ

2 many of the features of rods emerged before the split between agnatha and gnathostomata, and a rod-l

3 continued to diversity at a high rate after the split between anthozoans and hydrozoans.

4 opsis lyrata occurred about 13 Mya, and that the split between Arabidopsis and the Brassica complex (

5 bidopsis, WGD occurred more than once before the split between Arabidopsis thaliana and Arabidopsis a

6 The RIO kinases existed before the split between Archaea and Eubacteria and are essenti

7 Our data suggest that the split between C5aR and C3aR from a common ancestral

8 nce estimates of approximately 25-30 Myr for the split between Cercopithecoidea (Old World monkeys) a

9 origin of this pattern is at least as old as the split between crocodilians and birds, which occurred

10 s indicates that TPR Mps1 was acquired after the split between deutorostomes and protostomes, as it i

11 hese elements are very old and might predate the split between Escherichia coli and Salmonella enteri

12 postulated a relatively sudden change, after the split between extant lobe-finned fish and tetrapods,

13 xciting into the e(g) (sigma*) orbitals, and the splitting between final states of different symmetry

14 ignificant divergence in Nrf2 is seen during the split between fungi and the Metazoa approximately 1.

15 The split between G. chilensis and the Galapagos lineage

16 Our phylogenetic analysis though places the split between GatE and GatB, prior to the phylogenet

17 f PEPP genes has significantly changed since the split between hominids and rodents.

18 nonsaline split in environmental samples and the split between host-associated and free-living commun

19 al importin alpha gene family arose prior to the split between invertebrates and vertebrates.

20 eV for 1(powder) and ~2.0 eV for 1', and (3) the splitting between iron d(z(2)) and d(x(2)-y(2)) leve

21 lymorphism at this locus, possibly predating the split between L. stylosa and its two inbreeding sist

22 r-toothed and modern cats, the other marking the split between large and small-medium cats.

23 tion within the Rosid I clade, clearly after the split between legumes and Salicaceae (poplar).

24 ility interval, 56.64-77.83 Ma) obtained for the split between Macrauchenia and other Panperissodacty

25 symptoms in the same episode do not support the splitting between mania/hypomania and depression); f

26 or K222 infected the primate germ line after the split between New and Old World monkeys.

27 A phylogenetic analysis placed the split between Plasmodium GatB, archaeal GatE, and ba

28 the Metazoan lineage, both occurring before the split between the Bilateria and Cnidarians.

29 This ancestral DSR was either present before the split between the domains Bacteria, Archaea, and Euc

30 iversification of MHC genes took place after the split between the Equidae and the Rhinocerotidae yet

31 icates that many of these genes arose before the split between the New and Old World monkeys, but the

32 We date the split between the two ancestral populations to appro

33 ort neochromes diverging 179 Mya, long after the split between the two plant lineages (at least 400 M

34 re ancient than generally thought and places the split between the two strepsirrhine lineages well be

35 Intriguingly, the split between the two subpopulations is clearest in

36 superimposed on the experimental PIE curves, the splitting between the ground state singlet and excit

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