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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 the LUC7L2/LUC7L3 subfamilies evolved before the split between animals and plants.
4  continued to diversity at a high rate after the split between anthozoans and hydrozoans.
5 opsis lyrata occurred about 13 Mya, and that the split between Arabidopsis and the Brassica complex (
6 bidopsis, WGD occurred more than once before the split between Arabidopsis thaliana and Arabidopsis a
7               The RIO kinases existed before the split between Archaea and Eubacteria and are essenti
8                        Our data suggest that the split between C5aR and C3aR from a common ancestral
9 nce estimates of approximately 25-30 Myr for the split between Cercopithecoidea (Old World monkeys) a
10 ent on recombination (54% of the genome) and the split between clades A and B was estimated to have o
11   Hierarchies in nursing practice underlined the split between critical thinking and hands-on approac
12 origin of this pattern is at least as old as the split between crocodilians and birds, which occurred
13 s indicates that TPR Mps1 was acquired after the split between deutorostomes and protostomes, as it i
14 of a modern human population that, following the split between East and West Eurasians, experienced s
15 hese elements are very old and might predate the split between Escherichia coli and Salmonella enteri
16 c SNP rs62436463 that must have arisen after the split between European and Asian populations.
17 postulated a relatively sudden change, after the split between extant lobe-finned fish and tetrapods,
18 xciting into the e(g) (sigma*) orbitals, and the splitting between final states of different symmetry
19 ignificant divergence in Nrf2 is seen during the split between fungi and the Metazoa approximately 1.
20                                              The split between G. chilensis and the Galapagos lineage
21      Our phylogenetic analysis though places the split between GatE and GatB, prior to the phylogenet
22 f PEPP genes has significantly changed since the split between hominids and rodents.
23 and the use of stone tools probably predated the split between hominins and panins.(2) Using tools (h
24 nonsaline split in environmental samples and the split between host-associated and free-living commun
25  and become fixed in human populations since the split between humans and chimpanzees; the former are
26 al importin alpha gene family arose prior to the split between invertebrates and vertebrates.
27 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
28 lymorphism at this locus, possibly predating the split between L. stylosa and its two inbreeding sist
29 r-toothed and modern cats, the other marking the split between large and small-medium cats.
30 tion within the Rosid I clade, clearly after the split between legumes and Salicaceae (poplar).
31 ility interval, 56.64-77.83 Ma) obtained for the split between Macrauchenia and other Panperissodacty
32  symptoms in the same episode do not support the splitting between mania/hypomania and depression); f
33 ements with ancient sequence age (older than the split between marsupial and placental mammals) were
34 an unusually large momentum dependence, with the splitting between moire bands at the Gamma point mor
35 or K222 infected the primate germ line after the split between New and Old World monkeys.
36 methylglyoxal bypass, acetate metabolism and the split between pentose phosphate and Entner-Doudoroff
37               A phylogenetic analysis placed the split between Plasmodium GatB, archaeal GatE, and ba
38  old inversions (>1 MY), albeit formed after the split between the Atlantic herring and its sister sp
39  the Metazoan lineage, both occurring before the split between the Bilateria and Cnidarians.
40 This ancestral DSR was either present before the split between the domains Bacteria, Archaea, and Euc
41 iversification of MHC genes took place after the split between the Equidae and the Rhinocerotidae yet
42  a potential ancient origin concomitant with the split between the hard and soft corals.
43 icates that many of these genes arose before the split between the New and Old World monkeys, but the
44                                      We date the split between the two ancestral populations to appro
45 ort neochromes diverging 179 Mya, long after the split between the two plant lineages (at least 400 M
46 re ancient than generally thought and places the split between the two strepsirrhine lineages well be
47                                Intriguingly, the split between the two subpopulations is clearest in
48 superimposed on the experimental PIE curves, the splitting between the ground state singlet and excit
49 -soft interaction in (t)Bu-ZnP/CNT increases the splitting between the highest occupied orbitals of t
50        A 4.6 tesla field was applied to tune the splitting between two members of the triplet excited