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1 r facilitates egg predation by conspecifics (cannibalism).
2 ntext of a novel tadpole behavior: predatory cannibalism.
3  within the same body, sometimes called cell cannibalism.
4 icrocephaly is produced through entotic cell cannibalism.
5 volution of the extreme selfish behaviour of cannibalism.
6 ed dispersal are selected for lower rates of cannibalism.
7 1-HD) in the eggshell's wax layer deters egg cannibalism.
8 -predator responses by promoting intraclutch cannibalism.
9              In addition, we did not observe cannibalism.
10 atives in the interpretation of Palaeolithic cannibalism.
11 l-defined clinical phenomenon of cancer cell cannibalism.
12 cally identical siblings in a process termed cannibalism.
13 lm against Gram-positive bacteria as well as cannibalism.
14 arisen to protect humans from the effects of cannibalism.
15  spider are possible during spider mating or cannibalism.
16  interpreted by some scholars as evidence of cannibalism.
17 ns from a site with osteological evidence of cannibalism.
18 nt could be facilitated by enhanced rates of cannibalism.
19                                           Is cannibalism a significant density-dependent factor in sp
20                             During bacterial cannibalism, a differentiated subpopulation harvests nut
21 mputational analyses, we uncovered cathepsin cannibalism, a novel mechanism by which cathepsins degra
22 ual-based evolutionary model, we reveal that cannibalism, a striking feature of locust ecology, could
23 nspecifics as well as a unique adaptation to cannibalism-a strong attraction to vulnerable hatchlings
24                                        Might cannibalism also increase in a novel environment to whic
25                                              Cannibalism among generalist predators has implications
26 mary literature to document the incidence of cannibalism among insects that typically are not carnivo
27                                      Whereas cannibalism and autophagy eliminate mtDNAs stochasticall
28 s an ideal mechanism for a toxin involved in cannibalism and biofilm defence, since this would incapa
29 play auxiliary roles in development, such as cannibalism and biofilm formation, are turned on and a l
30                                              Cannibalism and matrix formation are both triggered in r
31               The possible interplay between cannibalism and physiological adaptation to a new enviro
32 t can be extended to include transition into cannibalism and the role of colony organization.
33 briefly treats the different types of spider cannibalism and then focuses in more depth on evidence r
34  result in increased transmission of DWV via cannibalism and trophallaxis.
35 aspecific competition (IC) may cause stress, cannibalism, and affect survival and reproduction.
36 action terms of autodigestion, inactivation, cannibalism, and distraction, altering kinetic considera
37  examined birthweight, litter size, maternal cannibalism, and epigenetic modifications.
38 n fishes include clustered mutations, filial cannibalism, and local population size.
39 urs such as parental care, and that care and cannibalism are antagonistically linked.
40            Higher rates of density-dependent cannibalism are further supported by the results from ou
41  predation and self-limiting factors such as cannibalism are investigated.
42 es suggests an increase in density-dependent cannibalism as a result of increased intraspecific compe
43 listic tendencies, and that the emergence of cannibalism-avoidance behaviour depends strongly on assu
44 th population density including sporulation, cannibalism, biofilm formation and genetic competence.
45  they become contagious, showing that filial cannibalism both contains an otherwise lethal infection
46 s allocated to eggs exacerbating the risk of cannibalism but reducing the risk of interspecific preda
47                  Recently we found that cell cannibalism by entosis, a form of cell engulfment involv
48 nocyte death by cornification, and cell-cell cannibalism by entosis.
49  kin from nonkin, raise the possibility that cannibalism by guardian males is directed primarily or e
50 sed alloparental care after we simulated egg cannibalism by helpers, an effect not shown by related h
51               Is this a legacy of widespread cannibalism by our ancestors?
52 erns immunity to a protein toxin involved in cannibalism by the spore-forming bacterium Bacillus subt
53              In the study reported here, egg cannibalism by two strains of T. castaneum was significa
54                                              Cannibalism can be adaptive by improving growth rate, su
55                                          Egg cannibalism can be adaptive, wherein cannibals may benef
56 y, we investigate the extent to which sexual cannibalism can modulate mate-finding Allee effects, and
57  complex picture of galaxy genesis driven by cannibalism, collisions, bursts of star formation and ot
58                         We found that sexual cannibalism could lead to high extinction risk, particul
59                                         Does cannibalism dampen spider-initiated trophic cascades?
60                         We also analysed how cannibalism-derived female fecundity benefits affected e
61 , or potential for severe injury-even sexual cannibalism during MFA.
62 mparatively low nutritional value of hominin cannibalism episodes support more socially or culturally
63                                              Cannibalism evolved in the spadefoot genus Spea, where a
64  between phenotypes in either mate choice or cannibalism frequency.
65 tand the antitumor activity of MSCs and cell cannibalism further, and therefore open new therapeutic
66  sexual repertoire that predictably involves cannibalism, genital mutilation, male preference for ten
67 tation by males, to maximise paternity after cannibalism, has led to the evolution of an abdominal co
68                     Episodes of Palaeolithic cannibalism have frequently been defined as 'nutritional
69 ive cell engulfment programs, homotypic cell cannibalism (HoCC) and anti-CD47 antibody-mediated phago
70 lly test whether sodium limitation increases cannibalism in a gregarious lepidopteran herbivore, we h
71                        Here, we discuss cell cannibalism in cancer and other mechanisms that result i
72 cally associated with a dietary response and cannibalism in derived Spea.
73                                  Intraclutch cannibalism in herbivorous insects might be a ubiquitous
74 data provide genetic documentation of filial cannibalism in nature.
75 the first unambiguous evidence of Neandertal cannibalism in Northern Europe, but also highlights cons
76 lines and mitotic index correlates with cell cannibalism in primary human breast tumours.
77 tions to address the following questions: Is cannibalism in spiders a foraging strategy that helps to
78                                         Does cannibalism in spiders reduce competition for prey?
79 l patients were born before the cessation of cannibalism in the late 1950s.
80        It is thought that BSE is a result of cannibalism in which faulty industrial practices produce
81 tory cannibalism reduced extinction risk, if cannibalism increased female fecundity enough.
82 n gene expression plasticity associated with cannibalism-inducing cues.
83                                              Cannibalism is a common ecological strategy among extant
84                                              Cannibalism is a mechanism to delay sporulation in Bacil
85                         We propose that cell cannibalism is a result of aberrant phagocytosis, where
86 fects, and the conditions under which sexual cannibalism is likely to be particularly detrimental to
87                          We find that sexual cannibalism is likely to negatively impact population su
88                             The existence of cannibalism is one of the most controversial issues in t
89                                              Cannibalism is one such strategy; by killing and consumi
90                                              Cannibalism is well known to affect both the population
91                                              Cannibalism is widespread in natural populations of fish
92 act of pathogens on the expression of filial cannibalism is, in particular, poorly understood.
93            We propose that Rac-mediated cell cannibalism may contribute to Rac2(+/E62K) human immunod
94 d to high extinction risk, particularly when cannibalism occurred before copulation, founder populati
95                                       Sexual cannibalism occurs in several arthropod taxa, but its ev
96                     Although disease-induced cannibalism of eggs has been reported in fish(2), the be
97                                     Notably, cannibalism of MSCs enhanced survival of BCCs deprived o
98    Mesocosm experiments confirmed that adult cannibalism of recruits was size-dependent and could con
99 e-borne vibrations to induce the killing and cannibalism of young queens when the colony is starved,
100 an intriguing link between cell division and cannibalism, of significance to both cancer and chemothe
101                                              Cannibalism often was favored by density-dependent facto
102 ty and food-chain length, and the degrees of cannibalism, omnivory, looping and trophic similarity.
103  for extreme sexual behaviors such as sexual cannibalism, opportunistic mating, mate-binding, genital
104  advantage in environments where injury from cannibalism or predation is common.
105 e enzymes when co-incubated, indicating that cannibalism, or protease-on-protease degradation between
106 rulation, such as the skf- and sdp-dependent cannibalism pathways, were eliminated as potential targe
107 crophage-related genes that engender a novel cannibalism phenotype.
108  a mutant of which has been known to cause a cannibalism phenotype.
109 ts of neighboring cells, is an intercellular cannibalism process conserved from protozoa to mammals.
110 death that has been called phagotrophy, cell cannibalism, programmed cell removal and primary phagocy
111                     However, post-copulatory cannibalism reduced extinction risk, if cannibalism incr
112 ext, we experimentally demonstrated that egg cannibalism reduces L. decemlineata vulnerability to pre
113 s an explanation for the evolution of filial cannibalism - remain largely unexplored.
114 ales actually appear to facilitate their own cannibalism (reviewed in [3]).
115 fy metabolites active in a Bacillus subtilis cannibalism system in which sporulating cells lyse nonsp
116         Entosis is a form of epithelial cell cannibalism that is prevalent in human cancer, typically
117 ced the control of recruitment by adults via cannibalism, thereby facilitating the population explosi
118 t effects (for example, food competition and cannibalism) through prolonged overlap with prey and imp
119             Thus, the relationship of spider cannibalism to food limitation, competition, and populat
120 n focuses in more depth on evidence relating cannibalism to population dynamics and food web interact
121 umber and matrix production is enhanced when cannibalism toxins are produced.
122  to evolve when high rates of postcopulatory cannibalism trap males into investing in their first mat
123                              Entosis is cell cannibalism utilized by tumor cells to engulf live neigh
124                                     Although cannibalism was almost non-existent when sodium concentr
125 n the presence of victim eggs, the extent of cannibalism was genetically variable, so that this trait
126 te features that promote microglia death and cannibalism, we used time-lapse imaging and fate-mapping
127 their territory, but immediately switched to cannibalism when establishing a new territory.
128 athepsins are proteases capable of cathepsin cannibalism, where one cathepsin hydrolyzes another with
129                                       Filial cannibalism, where parents eat their own offspring, is a
130 nition system enables this nematode to avoid cannibalism while promoting the killing of competing nem
131 ion of two operons (sdp and skf) involved in cannibalism whose transcription is known to depend on Sp

 
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