ライフサイエンスコーパス: higher animal

1 mark of living systems, from single cells to higher animals.

2 or slow recovery from acute seizures also in higher animals.

3 abundance are important for the survival of higher animals.

4 elopment, and restores the nervous system in higher animals.

5 releasable reservoir of thrombospondin-1 in higher animals.

6 ules play an analogous role to antibodies in higher animals.

7 has not been identified in Drosophila or in higher animals.

8 lmarks of zinc deficiency (ZD) in humans and higher animals.

9 tentions and expectations in the behavior of higher animals.

10 ial for eye development in invertebrates and higher animals.

11 ound in any integrin beta-subunit genes from higher animals.

12 ification and susceptibility to arthritis in higher animals.

13 are characteristically found in Sec tRNA of higher animals.

14 tenance of the female reproductive system of higher animals.

15 chromes c from fungi and plants but not from higher animals.

16 genetic approaches that are not possible in higher animals.

17 ntaining cholesterol homeostasis in cells of higher animals.

18 on is critical to goal-oriented behaviors in higher animals.

19 zymatic production of beta-apocarotenoids in higher animals; 2) the occurrence of beta-apocarotenoids

20 In higher animals, a centrally located system has evolved t

21 e-binding proteins (MBP) are both present in higher animals and both are composed of a carbohydrate-r

22 w methods for controlling gene expression in higher animals and in studying the interactions between

23 hosphorylation provides most of the ATP that higher animals and plants use to support life and is res

24 tionary connection between the leukocytes of higher animals and their unicellular, protozoan ancestor

25 Scarring is a long-lasting problem in higher animals, and reductionist approaches could aid in

26 onan is an essential polysaccharide found in higher animals as well as in a few pathogenic bacteria.

27 luding mammals, raising the possibility that higher animals can communicate gene-specific silencing i

28 g of lipid phosphate phosphatase 3, which in higher animals can dephosphorylate a range of phospholip

29 Cytochromes c from plants and fungi, but not higher animals, contain methylated lysine residues at sp

30 Complexity in higher animals derives in part from various modalities o

31 homology in smell and taste pathways in all higher animals, experimental approaches in Drosophila wi

32 Higher animal fat and cholesterol intakes were significa

33 subjects may have an impaired adaptation to higher animal fat diets that could result in higher card

34 is more deviant from muscle actin than other higher animal forms, the generality of glycolytic enzyme

35 tor family transporter, homologs of which in higher animals have been shown to transport S1P) can als

36 Many higher animals have evolved the ability to use the Earth

37 Antibiotic peptides of higher animals include the defensins, first discovered i

38 accumulate in various organs and tissues of higher animals, including humans, mice, and flies.

39 Adult body size in higher animals is dependent on the amount of growth that

40 redominant theme seen in the homologues from higher animals is extensive intron loss.

41 (vitamin A) serve two distinct functions in higher animals: light absorption for vision and gene reg

42 coordination of physiological sub-systems in higher animals may be through the direct entrainment of

43 n increased phospholipid unsaturation, as in higher animal models.

44 slices led to faster dilative remodeling and higher animal mortality.

45 The higher rates are associated with higher animal protein and fat, and lower fibre consumpti

46 ry fat intakes and girls aged 6-8 years with higher animal protein intakes became adolescents with ea

47 nce, resemble those of both MAO A and B from higher animals, raising the possibility that it may be a

48 Propagation in higher animals requires the efficient and accurate displ

49 umber of introns found in only one phylum of higher animals result from frequent intron loss, as oppo

50 In addition, reduced insulin signaling in higher animals-rodents and humans-causes glucose intoler

51 iological basis of information processing in higher animals, spiking neural networks must be able to

52 In all higher animals studied, we have found many fewer genes t

53 In higher animals, the structural integrity and functional

54 In higher animals, these membrane proteins participate in a

55 Higher animals typically rely on calcification to harden

56 a soluble cytoplasmic protein, analogous to higher animal visual pigments.