ライフサイエンスコーパス: M. arthritidis

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1 oiety from a culture of a virulent strain of M. arthritidis.

2 genome sequence and a transposon library of M. arthritidis.

3 oduct) predicted from the genome sequence of M. arthritidis.

4 poprotein designated MAA1 in cytadherence of M. arthritidis.

5 ed in M. pulmonis, and Tn4001T transposed in M. arthritidis.

6 by the lack of genetic systems for use with M. arthritidis.

7 nsfer of Tn916 from an enterococcal donor to M. arthritidis.

8 h the recently described MlpD lipoprotein of M. arthritidis.

9 n (MAM) is a potent superantigen secreted by M. arthritidis, an agent of murine arthritis.

10 are procedures for genetic transformation of M. arthritidis and conjugal transfer of Tn916 from an en

11 from a 41-kDa known bioactive lipoprotein of M. arthritidis, avidly bound to purified apoA-1 that sep

12 and upstream DNA sequences were cloned from M. arthritidis clonal variants differing in MAA2 express

13 We suggest that macrophage activation by M. arthritidis could play a significant role in the infl

14 , the process of obtaining purified MAM from M. arthritidis culture supernatants is extremely time-co

15 ge-activating lipopeptide-2, activity of the M. arthritidis-derived 28-kDa component was dependent up

16 The presence of M. arthritidis glycoproteins was confirmed by high-resol

17 ed that bioactive lipopeptides prepared from M. arthritidis grown in serum-free medium and also from

18 ritis in C3H/HeJ mice following injection of M. arthritidis in comparison to the mild disease seen in

19 M. arthritidis-induced arthritis serves as a model for a

20 The M. arthritidis lipoproteins exhibited infrared absorbanc

21 The M. arthritidis mitogen (MAM) superantigen has long been

22 To study the pathogenic significance of MAM, M. arthritidis mutants that overproduced or failed to pr

23 ith C3H/HeSnJ mice after injection with live M. arthritidis organisms.

24 M. arthritidis strain 158-1 is a spontaneous mutant of s

25 hought to be associated with cytadherence of M. arthritidis strain 158p10p9.

26 observation that Maa1 is a major adhesin for M. arthritidis strain 158p10p9.

27 ing and sequencing of the maa2 gene from two M. arthritidis strains, 158p10p9 and H606, expressing tw

28 extracts derived from avirulent and virulent M. arthritidis strains.

29 serum-free medium supplemented with starch, M. arthritidis synthesized higher levels of rhamnose, wi

30 examining the role of the superantigen MAM (M. arthritidis T-cell mitogen) in the development of aut

31 The preparations from the virulent strain of M. arthritidis were also more potent in activating dendr

32 Several strains of M. arthritidis were examined for their ability to suppor

33 riton X-114 extracts of a virulent strain of M. arthritidis were found to be more potent in activatin

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