戻る
「早戻しボタン」を押すと検索画面に戻ります。 [閉じる]

コーパス検索結果 (１語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します
1  of the parasite's lysosomal compartment-the food vacuole.
2 t to target green fluorescent protein to the food vacuole.
3 -cell hemoglobin in an acidic organelle, the food vacuole.
4  to have additional distribution outside the food vacuole.
5 dicted accumulation into the acidic parasite food vacuole.
6 n of hemoglobin in the Plasmodium falciparum food vacuole.
7 des occurs in an acidic organelle called the food vacuole.
8 ynthetic path leading to mature PM II in the food vacuole.
9 1 through the parasitophorous vacuole to the food vacuole.
10 grades host cell hemoglobin within an acidic food vacuole.
11 acidic environment of the heme-rich parasite food vacuole.
12  inside a lysosome-like organelle called the food vacuole.
13 ystallization and compromised the parasite's food vacuole.
14 nce of MSP1(19)-containing vesicles with the food vacuole.
15 hibited their own digestion in the protozoan food vacuoles.
16  L272F), causing the development of enlarged food vacuoles.
17 moglobin binding domain in PfHDP resulted in food vacuole abnormalities similar to that seen with a c
18 isinins act by inhibiting PfATP6 outside the food vacuole after activation by iron.
19 PfAPP were evaluated at the acidic pH of the food vacuole and at the near-neutral pH of the cytosol.
20                      PfAPP is present in the food vacuole and cytosol of the parasite, a distribution
21 s support a catalytic role for PfA-M1 in the food vacuole and indicate the importance of evaluating t
22 d blood cell, where it is transferred to the food vacuole and persists until the end of the intracell
23 es confirm the location of falcilysin in the food vacuole and reveal association with vesicular struc
24  for PfAPP in peptide catabolism in both the food vacuole and the cytosol and suggest that PfAPP has
25 dase activity, falcilysin, was purified from food vacuoles and characterized.
26       In this study, we purified merozoites, food vacuoles, and parasite membrane fragments released
27 pressed in trophozoites, was concentrated in food vacuoles, and was responsible for at least 93% of t
28 nce of amino acid-generating pathways in the food vacuole as well as the cytosol.
29 falcipain-2 cleaves hemoglobin in the acidic food vacuole at the early trophozoite stage, whereas it
30 -erythrocytic developmental stages in acidic food vacuole compartments.
31 protease activity and swollen, dark staining food vacuoles, consistent with a block in hemoglobin hyd
32 icity driver; however, AgNPs internalized in food vacuoles contributed to the perturbation of amino a
33 owed that falcipain-2 is a major trophozoite food vacuole cysteine protease.
34 d to release undigested bacteria in expelled food vacuoles (EFVs) when feeding on some pathogens.
35  the four aminopeptidases (including the two food vacuole enzymes) for efficient parasite proliferati
36 eptides invokes peptide transport out of the food vacuole followed by hydrolysis to amino acids by cy
37 falciparum degrades hemoglobin in its acidic food vacuole for use as a major nutrient source.
38 digestion of RBC hemoglobin within an acidic food vacuole (FV) but lack a heme oxygenase to release p
39 The heme polymer hemozoin is produced in the food vacuole (fv) of the parasite after hemoglobin prote
40  lysosomal compartment, the malaria parasite food vacuole (FV), rather than to cytoplasmic endocytic
41                           Trafficking to the food vacuole has not been well characterized.
42 RP2-ferric heme complex at pH 5.5 (pH of the food vacuole) has the same heme spin state and coordinat
43 de, which is generated at high levels in the food vacuole, has been shown to stimulate the motion of
44              Falcipain-2 and falcipain-3 are food vacuole hemoglobinases that may have additional fun
45 the basic drug is concentrated in the acidic food vacuole in its membrane-impermeable diprotonated fo
46 rasites, and anti-DPAP1 antibody labeled the food vacuole in parasite cryosections.
47 roquine (CQ)-hematin binding in the parasite food vacuole leads to inhibition of hematin polymerizati
48                             At the pH of the food vacuole lumen (5.0-5.5), the catalytic efficiency o
49 th stable and active at the acidic pH of the food vacuole lumen.
50 e lower than the concentration found for the food vacuole of a parasitized erythrocyte.
51 ent protein fluorescence was observed in the food vacuole of live transgenic parasites, and anti-DPAP
52 n (HZ) is an insoluble crystal formed in the food vacuole of malaria parasites.
53    Four paralogous plasmepsins reside in the food vacuole of P. falciparum.
54                                   The acidic food vacuole of Plasmodium falciparum has been the subje
55  plasmepsins that has been identified in the food vacuole of Plasmodium falciparum.
56 n addition to these functions, the digestive food vacuole of the malaria parasite is a dynamic intern
57          These data imply that the digestive food vacuole of the malaria parasite is functionally aki
58  protease (HAP), have been identified in the food vacuole of the parasite.
59 rozooplankton themselves due to buffering of food vacuole pH, and ultimately the continued ability of
60                                  The swollen food vacuole phenotype of falcipain-2 knockout parasites
61 creased chloroquine sensitivity and enlarged food vacuole phenotype.
62 ous recombination has been employed to study food vacuole plasmepsin function in cultured parasites.
63 spartic protease encode hemoglobin-degrading food vacuole proteases.
64 nance of elevated free Ca2+ in the digestive food vacuole (relative to cytosolic levels) is achieved
65 oupled with biochemical analysis of enriched food vacuoles, revealed the presence of amino acid-gener
66 e pH and reducing conditions of the malarial food vacuole, suggesting that parasite enzymatic activit
67 approximately 200-kDa protein complex in the food vacuole that is required for Hb degradation and Hz
68 ge of native hemoglobin in the P. falciparum food vacuole, that, following initial cleavages, the pro
69 a-Asp repeats and is present in the parasite food vacuole, the site of hemoglobin degradation and hem
70 ia parasites degrade hemoglobin in an acidic food vacuole to acquire free amino acids and maintain pa
71 ance mechanism that acts specifically at the food vacuole to alter the binding of chloroquine to hema
72 alcipain-3 hydrolyze hemoglobin in an acidic food vacuole to provide amino acids for erythrocytic mal
73 ydrolyze erythrocyte hemoglobin in an acidic food vacuole to provide amino acids for parasite protein
74 es, and which gene products are found in the food vacuole where catabolism takes place.
75 d along with its substrate hemoglobin to the food vacuole where it is proteolytically processed to ma
76 al intraerythrocytic parasites; that is, the food vacuole, where the catabolism of host hemoglobin ta
77 CRT-mediated drug resistance, as well as the food vacuole, which is an important target of many antim