ライフサイエンスコーパス: microbial gene

1 oli and/or changes in expression of specific microbial genes.

2 ines incorporating tumor sequences linked to microbial genes.

3 o predicting the functions of new classes of microbial genes.

4 However, there was a wide array of shared microbial genes among sampled individuals, comprising an

5 ite the growing interest to explore untapped microbial gene and protein diversity, no single platform

6 explore the transport and transformation of microbial genes and cells through Earth's Critical Zone.

7 e positions of mononucleotide repeats within microbial genes and detect a pervasive bias in the locat

8 vertheless, associations between microbes or microbial genes and human genes have emerged that are co

9 systems to identify novel virulence-related microbial genes and immune-related host genes, many of w

10 ulted in the generation of vast data sets of microbial genes and pathways present in different body h

11 Large microbial gene clusters encode useful functions, includi

12 ssociated with differences in both predicted microbial gene content and endogenous metabolite profile

13 ed tools for quantifying absolute numbers of microbial gene copies in test samples.

14 he amount of carbon/energy resources driving microbial gene diversity was identified to be the critic

15 Microbial genes encoding for secondary bile acid product

16 Induction of microbial genes encoding HSPs might provide a novel stra

17 If homologous microbial genes exist-and about one-half the genes encod

18 research groups has developed BmuG@Sbase, a microbial gene expression and comparative genomic databa

19 estricts our ability to study time-dependent microbial gene expression in one of the Earth's largest,

20 Microbial gene expression in the context of persistent i

21 Microbial gene expression in the environment has recentl

22 as markedly advanced the capacity to examine microbial gene expression in vivo.

23 s, among other things, detailed knowledge of microbial gene expression in vivo.

24 c mice, and changes in species abundance and microbial gene expression were measured in response to r

25 and talented microbiologists in the area of microbial gene expression, regulation, biogenesis, patho

26 rter bacteria and community-wide analysis of microbial gene expression.

27 d overwhelms inter-individual differences in microbial gene expression.

28 e as a common mechanism in the regulation of microbial gene expression.

29 roarrays are becoming the tool of choice for microbial gene-expression profiling and genotypic analys

30 The diversity of C-degradation microbial genes generally declined with time during the

31 The GLIMMER system for microbial gene identification finds approximately 97-98%

32 e scientific literature contains millions of microbial gene identifiers within the full text and tabl

33 erobacteriaceae and alters a small subset of microbial genes important for tumour development.

34 GeoChip analysis of microbial genes in a Bangladeshi paddy soil showed the p

35 presence of I2, a Crohn's disease-associated microbial gene, in the murine intestine.

36 Here we show that microbial genes involved in cellular iron uptake are hig

37 ficant increase in the signal intensities of microbial genes involved in degrading complex organic co

38 In many cases, microbial genes known to be important for full virulence

39 d tumor necrosis factor (TNF)-alpha and anti-microbial genes Lysozyme M and SLPI in the colon of Muc4

40 sults reveal two sharply distinct classes of microbial genes, one of which is characterized by effect

41 ently want to know how abundant a particular microbial gene or pathway is across different human host

42 a microbial group, (iii) the enrichment of a microbial gene or sequence and (iv) enrichment of a func

43 f their ability to invade and proliferate in microbial gene pools and like symbionts when they coevol

44 cellular signaling pathways, often involving microbial gene products that mimic the functions of the

45 a type III secretion system to inject these microbial gene products, referred to as Yersinia effecto

46 plex interplay between endothelial cells and microbial gene products.

47 s allows us to conduct systematic studies on microbial gene regulatory systems.

48 unctional genomics technique that identifies microbial genes required for infection within an animal

49 al microbiome, functional analyses of common microbial gene sets are required.

50 ved in disease and the elucidation of entire microbial gene sets.

51 in model organisms are now being extended to microbial genes, species, and communities from the human

52 cs and the evolutionary dynamics of a social microbial gene, SUC2, in laboratory yeast populations wh

53 The distributional patterns of microbial genes suggested depth-variable community trend

54 wever, several recent studies have described microbial genes that affect social traits, thereby bring

55 ere we describe one approach for identifying microbial genes that affect the magnitude of host respon

56 mphasised regularities in the positioning of microbial genes that are co-regulated, co-expressed or e

57 f anaerobic microbiology and is now yielding microbial genes that have potential in biotechnology.

58 Cytosine deaminase (CD) is a microbial gene undergoing clinical trials in gene-direct

59 However, only 4.0% of the mouse gut microbial genes were shared (95% identity, 90% coverage)