ライフサイエンスコーパス: Tritrichomonas foetus

1 ) and its analogue in the protozoan parasite Tritrichomonas foetus.

2 e salvage pathway of the parasitic protozoan Tritrichomonas foetus.

3 ite Trichomonas gallinae and cattle parasite Tritrichomonas foetus.

4 Tritrichomonas foetus, a venereal pathogen of cattle, wa

5 Tritrichomonas foetus, an anaerobic flagellated protozoa

6 is a sexually transmitted disease caused by Tritrichomonas foetus and characterized by early embryo

7 amine prevalence and risk factors for feline Tritrichomonas foetus and Giardia infection.

8 rmed multiple inhibitor experiments with the Tritrichomonas foetus and human type 2 IMPDHs using tiaz

9 loped to study the cytopathogenic effects of Tritrichomonas foetus and the role of lipophosphoglycan

10 richomonad highly similar to bovine venereal Tritrichomonas foetus but having a unique tropism for th

11 complex of this protozoan, and the costa of Tritrichomonas foetus; c) the flagellulm of trypanosomat

12 ae) formed one, while Monocercomonas sp. and Tritrichomonas foetus formed the other.

13 Likewise, the bovine parasite Tritrichomonas foetus had no cytotoxic effects on hVECs.

14 e phosphoribosyltransferase (HGXPRTase) from Tritrichomonas foetus has been determined and refined ag

15 e phosphoribosyltransferase (HGXPRTase) from Tritrichomonas foetus has been proven to be a target for

16 mplexes of IMPDH from the protozoan parasite Tritrichomonas foetus have been solved: with its substra

17 with the high K(m) for PPi (165.5 microM) in Tritrichomonas foetus HGXPRTase-catalyzed reverse reacti

18 butane-2,3-dione irreversibly inactivate the Tritrichomonas foetus hypoxanthine-guanine-xanthine phos

19 crystal structures of the protozoan parasite Tritrichomonas foetus IMPDH complexed with the inhibitor

20 al structure of the catalytic core domain of Tritrichomonas foetus IMPDH in complex with IMP and beta

21 An X-ray crystal structure of Tritrichomonas foetus IMPDH with mizoribine monophosphat

22 uctures of IMPDH from the protozoan parasite Tritrichomonas foetus in the apo form at 2.3 A resolutio

23 sferase (HGXPRT) from the protozoan parasite Tritrichomonas foetus is a rational target for antiparas

24 Tritrichomonas foetus is a serious veterinary pathogen,

25 ansferase (HGXPRTase), a type I PRTase, from Tritrichomonas foetus, is a potential target for antitri

26 One reason is because inhibition of Tritrichomonas foetus ODC results in growth arrest, dest

27 s in the previously characterized IMPDH from Tritrichomonas foetus ( TfIMPDH).

28 thermore, T. vaginalis LPG (but not LPG from Tritrichomonas foetus, the causative agent of bovine tri

29 ed by the genome of the trichomonad parasite Tritrichomonas foetus, this otherwise highly conserved h

30 he complete kinetic mechanism for IMPDH from Tritrichomonas foetus using ligand binding, isotope effe

31 ine phosphoribosyltransferase (HGXPRTase) of Tritrichomonas foetus was inactivated by the thiol reage