ライフサイエンスコーパス: cannibalism

1 l-defined clinical phenomenon of cancer cell cannibalism.

2 cally identical siblings in a process termed cannibalism.

3 lm against Gram-positive bacteria as well as cannibalism.

4 -predator responses by promoting intraclutch cannibalism.

5 arisen to protect humans from the effects of cannibalism.

6 spider are possible during spider mating or cannibalism.

7 In addition, we did not observe cannibalism.

8 interpreted by some scholars as evidence of cannibalism.

9 ns from a site with osteological evidence of cannibalism.

10 nt could be facilitated by enhanced rates of cannibalism.

11 atives in the interpretation of Palaeolithic cannibalism.

12 Is cannibalism a significant density-dependent factor in sp

13 During bacterial cannibalism, a differentiated subpopulation harvests nut

14 mputational analyses, we uncovered cathepsin cannibalism, a novel mechanism by which cathepsins degra

15 ual-based evolutionary model, we reveal that cannibalism, a striking feature of locust ecology, could

16 Might cannibalism also increase in a novel environment to whic

17 Cannibalism among generalist predators has implications

18 mary literature to document the incidence of cannibalism among insects that typically are not carnivo

19 s an ideal mechanism for a toxin involved in cannibalism and biofilm defence, since this would incapa

20 play auxiliary roles in development, such as cannibalism and biofilm formation, are turned on and a l

21 Cannibalism and matrix formation are both triggered in r

22 The possible interplay between cannibalism and physiological adaptation to a new enviro

23 t can be extended to include transition into cannibalism and the role of colony organization.

24 briefly treats the different types of spider cannibalism and then focuses in more depth on evidence r

25 examined birthweight, litter size, maternal cannibalism, and epigenetic modifications.

26 n fishes include clustered mutations, filial cannibalism, and local population size.

27 urs such as parental care, and that care and cannibalism are antagonistically linked.

28 predation and self-limiting factors such as cannibalism are investigated.

29 listic tendencies, and that the emergence of cannibalism-avoidance behaviour depends strongly on assu

30 th population density including sporulation, cannibalism, biofilm formation and genetic competence.

31 Recently we found that cell cannibalism by entosis, a form of cell engulfment involv

32 nocyte death by cornification, and cell-cell cannibalism by entosis.

33 kin from nonkin, raise the possibility that cannibalism by guardian males is directed primarily or e

34 sed alloparental care after we simulated egg cannibalism by helpers, an effect not shown by related h

35 Is this a legacy of widespread cannibalism by our ancestors?

36 erns immunity to a protein toxin involved in cannibalism by the spore-forming bacterium Bacillus subt

37 In the study reported here, egg cannibalism by two strains of T. castaneum was significa

38 Cannibalism can be adaptive by improving growth rate, su

39 complex picture of galaxy genesis driven by cannibalism, collisions, bursts of star formation and ot

40 Does cannibalism dampen spider-initiated trophic cascades?

41 , or potential for severe injury-even sexual cannibalism during MFA.

42 mparatively low nutritional value of hominin cannibalism episodes support more socially or culturally

43 between phenotypes in either mate choice or cannibalism frequency.

44 tand the antitumor activity of MSCs and cell cannibalism further, and therefore open new therapeutic

45 sexual repertoire that predictably involves cannibalism, genital mutilation, male preference for ten

46 tation by males, to maximise paternity after cannibalism, has led to the evolution of an abdominal co

47 Episodes of Palaeolithic cannibalism have frequently been defined as 'nutritional

48 Here, we discuss cell cannibalism in cancer and other mechanisms that result i

49 Intraclutch cannibalism in herbivorous insects might be a ubiquitous

50 data provide genetic documentation of filial cannibalism in nature.

51 the first unambiguous evidence of Neandertal cannibalism in Northern Europe, but also highlights cons

52 lines and mitotic index correlates with cell cannibalism in primary human breast tumours.

53 tions to address the following questions: Is cannibalism in spiders a foraging strategy that helps to

54 Does cannibalism in spiders reduce competition for prey?

55 l patients were born before the cessation of cannibalism in the late 1950s.

56 It is thought that BSE is a result of cannibalism in which faulty industrial practices produce

57 Cannibalism is a common ecological strategy among extant

58 Cannibalism is a mechanism to delay sporulation in Bacil

59 The existence of cannibalism is one of the most controversial issues in t

60 Cannibalism is well known to affect both the population

61 Cannibalism is widespread in natural populations of fish

62 Sexual cannibalism occurs in several arthropod taxa, but its ev

63 Notably, cannibalism of MSCs enhanced survival of BCCs deprived o

64 an intriguing link between cell division and cannibalism, of significance to both cancer and chemothe

65 Cannibalism often was favored by density-dependent facto

66 ty and food-chain length, and the degrees of cannibalism, omnivory, looping and trophic similarity.

67 for extreme sexual behaviors such as sexual cannibalism, opportunistic mating, mate-binding, genital

68 rulation, such as the skf- and sdp-dependent cannibalism pathways, were eliminated as potential targe

69 a mutant of which has been known to cause a cannibalism phenotype.

70 ext, we experimentally demonstrated that egg cannibalism reduces L. decemlineata vulnerability to pre

71 ales actually appear to facilitate their own cannibalism (reviewed in [3]).

72 fy metabolites active in a Bacillus subtilis cannibalism system in which sporulating cells lyse nonsp

73 Entosis is a form of epithelial cell cannibalism that is prevalent in human cancer, typically

74 t effects (for example, food competition and cannibalism) through prolonged overlap with prey and imp

75 Thus, the relationship of spider cannibalism to food limitation, competition, and populat

76 n focuses in more depth on evidence relating cannibalism to population dynamics and food web interact

77 umber and matrix production is enhanced when cannibalism toxins are produced.

78 to evolve when high rates of postcopulatory cannibalism trap males into investing in their first mat

79 n the presence of victim eggs, the extent of cannibalism was genetically variable, so that this trait

80 their territory, but immediately switched to cannibalism when establishing a new territory.

81 ion of two operons (sdp and skf) involved in cannibalism whose transcription is known to depend on Sp