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1 the nervous system of the parasitic nematode Ascaris suum.
2  in the nematodes Caenorhabditis elegans and Ascaris suum.
3 l acid residues of the NAD-malic enzyme from Ascaris suum.
4 mintic properties against the swine nematode Ascaris suum.
5 mplex (PDC) of the adult parasitic nematode, Ascaris suum.
6 otonin-like immunoreactivity in the nematode Ascaris suum.
7                    Mice were inoculated with Ascaris suum (A. suum) eggs concurrent with ragweed (RW)
8                          The hemoglobin from Ascaris suum, a parasitic nematode, has a spontaneous di
9 emodeling after chronic antigen challenge in Ascaris suum (AA)-sensitized cats.
10  as 4 and 24 h after inhalation challenge by Ascaris suum) abolished both late-phase bronchoconstrict
11 rotected mice recovering from infection with Ascaris suum against subsequent infection with the phylo
12 r macrophages, and airway-derived cells from Ascaris suum-allergic cynomolgus monkeys did not produce
13 ptides in the nervous system of the nematode Ascaris suum, AMRNALVRFamide (AF21), NGAPQPFVRFamide (AF
14 embryo development in the parasitic nematode Ascaris suum and compared them with known small RNAs of
15  were also found in two parasitic nematodes, Ascaris suum and Oesophagostomum dentatum.
16 f the DNA eliminating pig parasitic nematode Ascaris suum and the horse parasite Parascaris univalens
17  two such hemoglobins, one from the nematode Ascaris suum and the other from the sulfide-fixing clam
18 y important parasites, Toxoplasma gondii and Ascaris suum, and gene expression in 11 different tissue
19 ester (L-NAME) before aerosol challenge with Ascaris suum, and the effect on antigen-induced airway r
20 4.5%, respectively, 4 h after challenge with Ascaris suum antigen (Ag).
21 ore and serially after airway challenge with Ascaris suum antigen alone, or after pretreatment with a
22 before and 24 h after aerosol challenge with Ascaris suum antigen in seven sheep hypersensitive to th
23 r as long as 2 h after airway challenge with Ascaris suum antigen, without and after pretreatment wit
24 ergic sheep undergoing airway challenge with Ascaris suum antigen.
25 ly after, and up to 2 h after challenge with Ascaris suum antigen.
26 to six sheep with airway hypersensitivity to Ascaris suum antigen.
27 acute responses or dual responses to inhaled Ascaris suum antigen.
28 e, it is shown that the CCA-adding enzyme of Ascaris suum carries such a specific adaptation in form
29                    The NAD-malic enzyme from Ascaris suum catalyzes the divalent metal ion-dependent
30                           The parasitic worm Ascaris suum contains the opiate alkaloid morphine as de
31 onance (NMR) data indicate that the nematode Ascaris suum eIF4E binds the two different caps in a sim
32 -avid hemoglobin from the parasitic nematode Ascaris suum exhibits one of the slowest known O(2) off
33 ties of pseudocoelomic body fluid from adult Ascaris suum gastrointestinal helminths (ABF) and its de
34 AD-malic enzyme from the parasitic roundworm Ascaris suum has been studied using a steady-state kinet
35 he AF8 and AF2 neuropeptides of the nematode Ascaris suum have been identified, cloned, and sequenced
36               Pharmacological experiments on Ascaris suum have demonstrated the presence of three (N-
37 ecular studies in Caenorhabditis elegans and Ascaris suum have identified key steps and factors invol
38 er distribution in the distal heme pocket of Ascaris suum hemoglobin (Hb) studied by resonance Raman
39 n Fe-CO stretching mode in the CO complex of Ascaris suum hemoglobin as compared to vertebrate hemogl
40  during infection with the helminth parasite Ascaris suum in pigs.
41 e of the mitochondrial NAD-malic enzyme from Ascaris suum, in a quaternary complex with NADH, tartron
42                                        In an Ascaris suum infection model in pigs, it was found that,
43 hat protection from allergic inflammation by Ascaris suum infection was characterized by a global inc
44 es infects 0.8 billion people worldwide, and Ascaris suum infects innumerable pigs across the globe.
45 in vitro in cell-free extracts of sperm from Ascaris suum: inside-out vesicles derived from the plasm
46        Using PCR techniques, we detected, in Ascaris suum intestine, message for: Asu-trp-2, Asu-gon-
47 ing edge protrusion in the amoeboid sperm of Ascaris suum is driven by the localized assembly of the
48 fected mice were more resistant to migrating Ascaris suum larvae in the lungs.
49             The major sperm protein (MSP) of Ascaris suum mediates amoeboid motility by forming an ex
50             The major sperm protein (MSP) of Ascaris suum mediates amoeboid motility by forming an ex
51                         The structure of the Ascaris suum mitochondrial NAD-malic enzyme in binary co
52 ectrophysiological and anatomical studies of Ascaris suum motor neurons demonstrated a strong correla
53 ructures of dimers and helical assemblies of Ascaris suum MSP has identified five conserved interacti
54              In vivo and in vitro studies of Ascaris suum MSP have demonstrated that motility occurs
55 d mutagenesis was used to change K199 in the Ascaris suum NAD-malic enzyme to A and R and Y126 to F.
56 meters of several active site mutants of the Ascaris suum NAD-malic enzyme was investigated to determ
57 carcinoma cell culture, raw bovine milk, and Ascaris suum nematode excretions), recovering size and s
58 al antibody, AF1-003, highly specific to the Ascaris suum neuropeptide AF1 (KNEFIRFamide), was genera
59                   Diminution in the nematode Ascaris suum occurs during early embryonic cleavages and
60 Early development of the parasitic nematode, Ascaris suum, occurs inside a highly resistant eggshell,
61                           Pigs infected with Ascaris suum or controls were given 100 microg (low-dose
62 no significant difference in inactivation of Ascaris suum ova in digesters operated at different soli
63 ed the fate of embryonated and unembryonated Ascaris suum ova in six laboratory-scale mesophilic (35
64  been used to study the kinetic mechanism of Ascaris suum phosphofructokinase (PFK) at pH 8.0 for the
65                                 The nematode Ascaris suum primarily infects pigs, but also causes dis
66 hes in the genome of the parasitic nematode, Ascaris suum, revealed a chimeric protein that is simila
67 erm protein (MSP)-based amoeboid motility of Ascaris suum sperm requires coordinated lamellipodial pr
68  extracts from spermatozoa from the nematode Ascaris suum suggest that retraction forces are generate
69 oduction of branched acids in the roundworm, Ascaris suum, that demonstrates selectivity for forming
70 racted development of the parasitic nematode Ascaris suum to provide a comprehensive time course of m
71 lecular weight SPIs originally isolated from Ascaris suum where they are believed to protect the para
72 two closely related parasites, the nematodes Ascaris suum, which infects pigs, and Ascaris lumbicoide
73                    The NAD-malic enzyme from Ascaris suum will utilize L-aspartate, (2S,3R)-tartrate,