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1 that may favour its hepatotropism in the new intermediate host.
2 e species of snail (Helix aspersa) acting as intermediate host.
3 t have complex life cycles involving a snail intermediate host.
4 g that they represent an important potential intermediate host.
5 lonal expansion of larvae inside a molluscan intermediate host.
6 r snail Biomphalaria glabrata as its primary intermediate host.
7 nent that increases with size or time in the intermediate host.
8 sibly in the emergence of P. tenuis from the intermediate host.
9 lly transmitted by an invertebrate vector or intermediate host.
10 blue/white' screening, without the use of an intermediate host.
11 sion of MERS-CoV, either directly or through intermediate hosts.
12 ity- and trait-mediated effects on the snail intermediate hosts.
13 from the gut to exploit the tissues of their intermediate hosts.
14 of transmission-asexual transmission between intermediate hosts.
15 ies for disease control focused on gastropod intermediate hosts.
16 eventing the protozoan from overwhelming its intermediate hosts.
17 was most likely due to parasite reduction of intermediate host abundance (a density-mediated effect),
18 study also shows that whether coinfection of intermediate hosts affects the levels of drug resistance
19 f food; invertebrate vectors of disease; and intermediate hosts among birds, mammals, and nonhuman pr
20 o lifestages involved in the invasion of the intermediate host and transcripts ubiquitously expressed
21 ity to larval trematodes by augmenting snail intermediate hosts and suppressing amphibian immunity.
22 ity to deduce why there is sometimes growth (intermediate hosts) and sometimes no growth (paratenic h
23 ing bradyzoites during its life cycle in the intermediate host, and conversion can be induced in vitr
24                              Pigs can act as intermediate hosts by which reassorted influenza A virus
25 ation of drinking water, chemical control of intermediate hosts, case containment and, crucially, loc
26 o increased cercaria production by the snail intermediate hosts, causing opposing effects on tadpole
27 ed in more southeastern wetlands, and snail (intermediate host) community composition had strong effe
28    Opposite conditions favour growth in the (intermediate) host, either to GALM or until death withou
29  typically involves larval development in an intermediate host followed by maturation in the respirat
30                        Pigs are an important intermediate host for influenza; thus, we assessed the r
31 labrata is relevant because this snail is an intermediate host for Schistosoma mansoni, the most wide
32 ic felines, that are not commonly considered intermediate hosts for avian influenza viruses.IMPORTANC
33  and Biomphalaria alexandrina, are the major intermediate hosts for S. mansoni in sub-Saharan Africa,
34 i) that are voracious predators of the snail intermediate hosts for schistosomiasis.
35 d snails of the genus Biomphalaria are major intermediate hosts for the digenetic trematode parasite
36 A viruses, pigs are believed to be effective intermediate hosts for the spread and production of new
37 asites have complex life cycles that require intermediate hosts for their transmission, but little is
38 reby newly hatched larvae must find suitable intermediate hosts (freshwater snails) and mature larvae
39 dditionally, our clustering approach reveals intermediate host functional states between these extrem
40 a infective stages) and the parasite's snail intermediate host (growth and reproduction).
41 etle (Tribolium castaneum) that serves as an intermediate host in its transmission.
42         Although swine are believed to be an intermediate host in the emergence of new human influenz
43  possibility that chickens may be a possible intermediate host in zoonotic transmission.
44 ndicate that the parasite has found suitable intermediate hosts in Hawai'i, which are required for th
45 efly outline what is known about the role of intermediate hosts in influenza emergence, summarize our
46 omphalaria pfeifferi) that serve as obligate intermediate hosts in the complex life cycle of the para
47 uenza A viruses in two species thought to be intermediate hosts in the spread of influenza A viruses
48 rtant role in the ecology of AIVs, acting as intermediate hosts in which viruses become more adapted
49 ghlight the potential role of dogs to act as intermediate hosts in which viruses with zoonotic and/or
50 rval parasite controls its own growth in the intermediate host, in order that growth eventually arres
51       The original host typically becomes an intermediate host, in which reproduction is suppressed.
52           In 'downward incorporation', a new intermediate host is added at a lower trophic level; thi
53       Toxoplasma gondii transmission between intermediate hosts is dependent on the ingestion of wall
54       This model assumes that on entering an intermediate host, larval death rate initially has both
55 in a 'poised' chromatin state throughout the intermediate host life cycle in low passage strains.
56 gest that behavioral thermoregulation by the intermediate host may buffer the larvae of indirectly tr
57 ration of a natural predator of a parasite's intermediate hosts may enhance drug-based schistosomiasi
58 emocytes of the snail Biomphalaria glabrata, intermediate host of the human blood fluke Schistosoma m
59 ne derived from Biomphalaria glabrata, snail intermediate host of the human blood fluke Schistosoma m
60         To elucidate the role of sparrows as intermediate hosts of highly pathogenic avian influenza
61 B. glabrata and B. pfeifferi, both important intermediate hosts of the human pathogen, Schistosoma ma
62 ed deer (Odocoileus virginianus) are natural intermediate hosts of the parasite demonstrate the exist
63 erborne diseases and a favorable habitat for intermediate hosts of tropical parasitic infections that
64                          Larval helminths in intermediate hosts often stop growing long before their
65 feeding arthropods transmitting the virus to intermediate hosts or humans during oral ingestion or en
66 f the fundamental biology of their gastropod intermediate hosts, or of the interactions occurring at
67 he complex life cycles of helminths, life in intermediate hosts poses special problems not covered by
68 phication help explain historical changes in intermediate host range and parasite transmission.
69 p, and cows, these form a potential MERS-CoV intermediate host reservoir species.
70 mon life history pattern of avoidance of the intermediate host's gut because the tissues offer a high
71 in particular why larval helminths avoid the intermediate host's gut, and adult helminths favour it.
72 ttle is known about the genetic basis of the intermediate host's susceptibility to these parasites.
73 mplex cycles occupy sites exclusively in the intermediate host's tissues or body spaces, and may or m
74 able of altering nutrient excretion in their intermediate host snails (dominant grazers).
75 oductive plants is therefore recovered at an intermediate host spacing.
76 rasite Toxoplasma gondii are associated with intermediate hosts such as humans: rapidly growing tachy
77 rstand the virulence determinants for IAV in intermediate hosts, such as swine and turkeys, and highl
78 d species that split from T. saginata via an intermediate host switch approximately 1.14 Myr ago.
79  protozoon Toxoplasma gondii for its natural intermediate host, the mouse, appears paradoxical from a
80 eceptors on the defence cells of their snail intermediate hosts, thus preventing host-cell activation
81 ry theory as to how larval helminths exploit intermediate host tissues and avoid the gut to maximise
82 parasite larvae are able to manipulate their intermediate host to increase ingestion probability by d
83          Warming of 3 degrees C caused snail intermediate hosts to release parasites 9 months earlier
84 ents of the biology and ecology of the snail intermediate hosts, together with an improved understand
85                                   Within its intermediate host, Toxoplasma gondii switches between tw
86                     During its life cycle in intermediate hosts, Toxoplasma gondii exists in two inte
87 facilitate survival and replication in their intermediate hosts, trematode parasites down regulate ho
88 restricted to larval stages within the snail intermediate host (Triodopsis sp.), beginning as early a
89  In complex cycles, helminth larvae in their intermediate hosts typically grow to a fixed size.
90 us maintaining a high titer of virus in this intermediate host used to produce virus inoculum for gra
91 y and habitat can increase their exposure to intermediate hosts via infected prey, altering their par
92 l size for the parasite larva at GALM in the intermediate host whether the evolutionary approach to t
93  arisen via a cross-species transfer from an intermediate host whose range overlaps those of both gib
94 f this uncharacterized snRNP included snoRNA intermediates hosted within ribosomal protein (RP) genes

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