ライフサイエンスコーパス: Mycoplasma hominis

1 FP29 could inhibit binding to HeLa cells by Mycoplasma hominis, a distinct human mycoplasma species

2 ducing lactobacillus, Gardnerella vaginalis, Mycoplasma hominis, anaerobic gram-negative rods, and, t

3 Mycoplasma hominis and Gardnerella vaginalis also stimul

4 %), fungi (10%) and Mycobacterium abscessus, Mycoplasma hominis and Lactobacillus sp. (one each).

5 One had high abundance of Mycoplasma hominis and other had high abundance of an un

6 ited sequence similarity with the adhesin of Mycoplasma hominis and the attachment protein of M. geni

7 R for Mycoplasma genitalium and cultured for Mycoplasma hominis and the ureaplasmas.

8 Mycoplasma hominis and Ureaplasma parvum do not appear t

9 Mycoplasma hominis and Ureaplasma species are urogenital

10 Mycoplasmas such as Mycoplasma hominis and Ureaplasma urealyticum have been

11 also used to detect Ureaplasma urealyticum, Mycoplasma hominis, and Candida albicans; bacterial vagi

12 an during the first--Ureaplasma urealyticum, Mycoplasma hominis, and Gardnerella/Bifidobacterium spec

13 aginae, Gardnerella vaginalis, lactobacilli, Mycoplasma hominis, and the human albumin gene (for qual

14 eptibility testing of Mycoplasma pneumoniae, Mycoplasma hominis, and Ureaplasma urealyticum using bro

15 Ureaplasma, spp. Mycoplasma genitalium, and Mycoplasma hominis are associated with infection of the

16 Mycoplasma hominis identification was confirmed using se

17 NA, lactobacilli, Gardnerella vaginalis, and Mycoplasma hominis in cervicovaginal lavage (CVL) sample

18 Lactobacilli, Gardnerella vaginalis, and Mycoplasma hominis in cervicovaginal lavage samples were

19 Invasive and disseminated Mycoplasma hominis infections are well recognized but un

20 Mycoplasma hominis is a commensal genitourinary tract or

21 Mycoplasma hominis is a commensal in the genital tract o

22 riable adherence-associated (Vaa) antigen of Mycoplasma hominis is an abundant surface lipoprotein ad

23 Among human mycoplasmas, Mycoplasma hominis is described as a commensal bacterium

24 r surface protein and a putative adhesin (of Mycoplasma hominis, is described.

25 Mycoplasma hominis isolates were subjected to whole-geno

26 We isolated a Mycoplasma hominis-like mycoplasma from a stock culture

27 n symbiosis with the intracellular bacterium Mycoplasma hominis (Mh), an opportunistic pathogen of th

28 ecies and could reliably detect <5 copies of Mycoplasma hominis, Mycoplasma fermentans, or a molecula

29 but not in 40 other species representing the Mycoplasma hominis, Mycoplasma pneumoniae, and Spiroplas

30 ardnerella vaginalis, Mycoplasma genitalium, Mycoplasma hominis, Neisseria gonorrhoeae, Streptococcus

31 ed colonization by Gardnerella vaginalis and Mycoplasma hominis, only metronidazole treatment resulte

32 to sterile media, lipopolysaccharide (LPS), Mycoplasma hominis, or Ureaplasma urealyticum.

33 significantly greater loss of viability for Mycoplasma hominis, Prevotella bivia, Prevotella corpori

34 illus iners, Peptoniphilus asaccharolyticus, Mycoplasma hominis, Prevotella bivia, Prevotella corpori

35 Mycoplasma hominis should be considered a cause of donor

36 ultures inoculated with clinical isolates of Mycoplasma hominis to determine whether liquid media of

37 d the ability of both viable and heat-killed Mycoplasma hominis to elicit type II epithelial cell pro

38 eisseria gonorrhoeae, Trichomonas vaginalis, Mycoplasma hominis, Ureaplasma species, and yeast.

39 d evidence supporting an association between Mycoplasma hominis, Ureaplasma urealyticum, and Ureaplas

40 Mycoplasma hominis was detected by culture and qPCR in 2

41 tutively expressed membrane protein (P56) of Mycoplasma hominis was subject to high-frequency phase v

42 Mycoplasma hominis was transmitted through amniotic tiss