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1 common component of the human skin microbial flora.
2 f different honey types belonging to Turkish flora.
3 ated with the presence of normal respiratory flora.
4 including terrestrial and aquatic fauna and flora.
5 ice in the presence or absence of intestinal flora.
6 matically detected in samples with anaerobic flora.
7 ther infectious bacteria, host and human gut flora.
8 nderstanding the nature of the earliest land flora.
9 f IAP (cIAP) rapidly restores the normal gut flora.
10 e important for the development of anaerobic flora.
11 drug targets that may also affect human gut flora.
12 heir expansion is regulated by commensal gut flora.
13 etrimental effect of its commensal bacterial flora.
14 ficant alteration from baseline conjunctival flora.
15 re highly affected by the resident microbial flora.
16 degradation pathway is present in human gut flora.
17 P </= .01), with most concordant for normal flora.
18 and symbiotic relationships with mycorrhizal flora.
19 ce mechanisms in response to the normal oral flora.
20 orrelated with patient's ocular conjunctival flora.
21 all samples, predominantly reflecting normal flora.
22 bly conserved low diversity of gut microbial flora.
23 ance or a discernible change in conjunctival flora.
24 gnized a substantial part of the neotropical flora.
25 at is permissive for the growth of competing flora.
26 ient absorption, and the effect of microbial flora.
27 ents (46%) had culture positive conjunctival flora.
28 y, by the host, and by other copathogens and flora.
29 acts but at the same affected the normal gut flora.
30 affect Escherichia coli of normal intestinal flora.
31 ntibiotics at the expense of other commensal flora.
32 ge of not generally perturbing the bacterial flora.
33 nd Th17 cells regulated by Ahr and commensal flora.
34 aused by food sensitivity or a change in gut flora.
35 ntially shape the composition of the natural flora.
36 ases antibiotic resistance of ocular surface flora.
37 from an exceptionally well-preserved fossil flora.
38 metabolic tradeoffs as the native understory flora.
39 c microorganisms and tolerate the endogenous flora.
40 d by differences in the intestinal bacterial flora.
41 eased rates of resistance among conjunctival flora.
42 han indiscriminately eliminating natural gut flora.
43 -locus barcode for 89.7% of the native Welsh flora.
44 alth by breeding resistance in the bacterial flora.
45 sceptible S. aureus (MSSA) as less prevalent flora.
46 l periurethral, vaginal, or gastrointestinal flora.
47 part of the normal oral and intestinal human flora.
48 n isolators and colonized with a defined gut flora.
49 ant impact on the gingival and oropharyngeal flora.
50 for colonization with the normal respiratory flora.
51 without harming healthy commensal microbial flora.
52 g' through the expansion in range of various flora.
53 nx, and vagina all have associated commensal flora.
54 CXCL2 expression similar to the normal oral flora.
55 ould not inhibit growth of natural bacterial flora.
56 rging pattern in the evolution of the global flora.
57 ct domestic agriculture and native fauna and flora.
58 al pathogen found as part of the normal oral flora.
59 re of the relatedness of the three medicinal floras.
60 has been used to reconstruct late-Quaternary floras.
61 ontribution to reconstructions of Quaternary floras.
62 lithocholic acid, a by-product of intestinal flora, activate pregnane X receptor (PXR) and subsequent
65 stinal tract, leading to a loss of commensal flora and an overgrowth of potentially pathogenic bacter
66 deposition in wild boars such as intestinal flora and anatomy, dietary composition, housing or genet
67 tobacillus spp. are part of the normal human flora and are generally assumed to be nonpathogenic.
68 inflammatory signals induced by both the gut flora and arthritis, Breg cells increase in number and r
70 contain smaller quantities of oropharyngeal flora and be more likely to have a predominance of poten
73 imal development is dependent upon commensal flora and expression of the nonpolymorphic MHC class I-l
74 on for the International Trade of Endangered Flora and Fauna (CITES) treaty; (2) assess the origin an
76 to more and more remote regions, much of the flora and fauna of the world are experiencing evolutiona
79 how that climate change forced a turnover of flora and fauna, suggesting there was a change from larg
83 isolation of low quantities of oropharyngeal flora and higher prevalence of potential pathogens as ma
84 l infection of the midgut requires bacterial flora and is inhibited by the activities of immune defic
85 Studies have shown that probiotics alter gut flora and lead to elaboration of flora metabolites that
86 t-brain axis and an impact of the intestinal flora and meningeal IL-17(+) gammadelta T cells on ische
87 a mechanism independent both of the enteric flora and of interferon gamma, a key cytokine for the re
89 isms or mixed outgrowth of upper respiratory flora and provided quantitative data on relative abundan
90 nce of a group of bacteria in the intestinal flora and relapse/progression of disease after allo-HCT.
91 y, the bacterial diversity of the intestinal flora and the diversity of various environmental factors
92 that provides the habitat for the commensal flora and the inner mucous layer that protects the epith
93 active physiologic dynamics of the salivary flora and the possible reservoir function associated wit
94 omic similarity between the native and alien flora and the total number of recorded associations (a m
95 levels were dependent on the local microbial flora and were not detectable under germ-free conditions
96 nection of previously independently evolving floras and faunas is thought to be one of the key factor
97 s the most complete coverage of any national flora, and offers a valuable platform for a wide range o
99 h human is colonized by a distinct bacterial flora, and that the microbiota can be manipulated to red
101 an health, and alterations of the normal gut flora are associated with a variety of distinct disease
102 reviously that alterations in the intestinal flora are associated with GVHD, bacteremia, and reduced
103 he diversity and stability of the intestinal flora are disrupted, resulting in domination by bacteria
104 redicts that invaders less related to native flora are more likely to be successful than those that a
105 nt species comprising the present-day Arctic flora are thought to have originated in the high mountai
108 a and then inoculated with altered Schaedler flora (ASF), a defined consortium of 8 bacteria with min
110 ommon polymicrobial imbalance of the vaginal flora associated with a wide variety of obstetric and gy
113 gut microbes, longitudinal studies of human flora before initial onset of intestinal inflammation ha
114 scar is well known for its diverse fauna and flora, being home to many species not found anywhere els
116 niae forms part of the normal nasopharyngeal flora but can also cause a broad spectrum of inflammator
117 imprints of these processes on the Galapagos flora by analysing a comprehensive regional phylogeny fo
120 gether, these data demonstrate regulation of flora by intestinal inflammation and suggest that flora
123 y enhances butyrate production by normal gut flora can influence the outcome of an E. coli O157 infec
124 n, mostly harmless member of the human viral flora can initiate cancer if it acquires a precise set o
126 is arid environment has favoured a resilient flora capable of large fluctuations in photosynthetic pr
127 morsus, a commensal bacterium of dog's mouth flora causing severe infections in humans after dog bite
128 vaginosis (BV) is a perturbation of vaginal flora characterized by reduced levels of lactobacilli an
129 nal Trade in Endangered Species of Fauna and Flora (CITES), including the whale shark (Rhincodon typu
132 ion on a healthy vaginal environment (normal flora confirmed by Gram stain with no candidiasis or tri
134 moniae can become part of the nasopharyngeal flora, contributing to the severity of respiratory disea
136 assemblages with other encrusting fauna and flora (corraline algae), and are highly abundant across
137 pothesized that components of the intestinal flora could be associated with relapse after allo-HCT.
138 well recognized, components of the human gut flora critical for colonization resistance are not known
139 Discovery of a relationship between gut-flora-dependent metabolism of dietary phosphatidylcholin
141 control BM monocytes, BM monocytes from gut flora-depleted mice had decreased migratory capacity tow
143 rize differential contributions of dysbiotic flora during eczema formation, and highlight the microbi
144 that in avoiding exposure to maternal bowel flora during labour or vaginal birth, offspring delivere
145 ria, mainly lactococci, were the predominant flora during the early stages of ripening, gradually bei
146 ichness reveals a significantly more diverse flora during the late Miocene than today at the same lat
147 ammatory cytokines elicited by the commensal flora dynamically enhanced the antigen responsiveness of
148 , which alters the balance of the intestinal flora, enabling C. difficile to proliferate in the colon
149 erstand why, among the vast diversity of gut flora, enterococci are so well adapted to the modern hos
152 We show that a hyperdiverse sclerophyll flora existed under high-rainfall, summer-wet climates i
153 ifold evidence for a synchronous turnover of flora, fauna and climate at the Eocene-Oligocene Boundar
154 ment of the future risks to the African palm flora, finding that African palm species on average may
156 ssessment and manipulation of the intestinal flora for prevention and treatment of radiation, enterop
158 corrhizal fungi, epiphytic lichen and ground flora); for ecological condition (e.g. sward height, pal
159 pid transition among Mesozoic ecosystems and floras formerly dominated by ferns, conifers, and cycads
160 nabantidae) and a diverse subtropical fossil flora from the Chattian (late Oligocene) of central Tibe
162 ense competition for light, as vascular land floras grew taller in the Palaeozoic, but also markedly
163 stablished that seaweed-affiliated bacterial flora had a wide-ranging antibacterial activities and po
165 , on the interaction between these fauna and flora has not been identified or elucidated, yet influen
166 sis (BV), a disruption of the normal vaginal flora, has been associated with a 60% increased risk of
168 pproximately the size of the native European flora, have become naturalized somewhere on the globe as
170 f intensive exploitation of certain types of flora helped Paleolithic people understand the propertie
171 s heavily influenced by the normal microbial flora, highlighting the complex interplay among harmless
172 that are inherently incompatible with native flora, highlighting the importance of maintaining commen
173 e the important contribution of host enteric flora in B. thuringiensis-killing activity and provide a
174 ifference in response towards the intestinal flora in dectin-1 deficient macrophages, during intestin
177 icance, since manipulation of the intestinal flora in individuals with congenital biopterin deficienc
181 ings define a key role for the gut commensal flora in sustaining ongoing autoimmune responses through
183 results support a vital role for intestinal flora in the maturation of intestinal barrier function.
184 a critical role for dietary choline and gut flora in TMAO production, augmented macrophage cholester
188 influenced by the presence of commensal gut flora, in particular increased colonization with segment
189 oted, (ii) infected sutures harbored a mixed flora, including multidrug-resistant health care-associa
191 nstrated that the diversity of the microbial flora involved in these infections was underestimated.
192 hough it is generally agreed that the Arctic flora is among the youngest and least diverse on Earth,
193 wth (SIBO) or other abnormalities in the gut flora is believed to contribute to the development of a
194 tantly, the presence of the midgut bacterial flora is required for full viral infectivity to Anophele
195 , where the presence of the midgut bacterial flora is required for protection against infection.
198 ptococcus mutans, a member of the human oral flora, is a widely recognized etiological agent of denta
199 occus epidermidis, a major component of skin flora, is an opportunist, often causing prosthetic devic
200 on driven by dysbiotic subgingival bacterial flora, is linked on clinical levels to the development o
201 int of Primula vulgaris from William Curtis' Flora Londinensis, I was struck by the fact that I was l
202 by intestinal inflammation and suggest that flora manipulation may reduce intestinal inflammation an
203 factors, cross seeding and recolonization of flora may affect the outcome of periodontal therapy.
205 S. aureus and other members of the bacterial flora may determine colonization and have been inferred
209 ce mechanisms in response to the normal oral flora, mediating catabolic alveolar bone homeostasis in
210 s alter gut flora and lead to elaboration of flora metabolites that influence health through 1 of 3 g
211 pecies combined with conventional intestinal flora obtained from the gastrointestinal tract of health
214 thirty volumes of Flora of North America and Flora of China combined, in addition to some smaller dat
218 l water, irrigated farmland, and human fecal flora of local villagers within a pharmaceutical industr
223 e the terms extracted from thirty volumes of Flora of North America and Flora of China combined, in a
228 ungal pathogen and a component of the normal flora of the gastrointestinal tract, is a frequent colon
229 stent with the hypothesis that the bacterial flora of the newborn plays a role in the development of
232 This is the first report of gut bacterial flora of wild-caught P. papatasi collected in an endemic
233 senting three of the most complete digitized floras of the world: Australia (AU), South Africa (SA),
234 representing the 20,000 species found in the floras of three disparate biodiversity hotspots: Nepal,
238 orts to fully digitize and mobilize regional floras online offer a timely opportunity to assess commo
239 trains, which has changed the nasopharyngeal flora, opening the niche for entry of other virulent pat
241 onding to 3.9% of the extant global vascular flora, or approximately the size of the native European
242 cated by the presence of a diverse bacterial flora, or by differences in the relative nucleic acid yi
244 n-utero infection, acquisition from maternal flora, or postnatal acquisition from the hospital or com
245 mostly originated from the buccal or sinusal floras (P < 10(-2)) and were found in polymicrobial spec
248 In the complete absence of gut microbial flora PP is normal, but experimental PH is significantly
250 0, 1920, and 1980, which are associated with flora projects and the establishment of inventory plots.
252 biotic-induced alterations in the intestinal flora reduce ischemic brain injury in mice, an effect tr
253 ns by which the vast majority of the world's flora regenerate naturally, a framework for accurately p
254 rate shared phylogenetic patterns across the floras: related plants from these regions are used to tr
255 urthermore, maintenance of the gut microbial flora relies on the expression of mosGCTLs in A. aegypti
256 mpounds, and fermentability by the human gut flora, SCFAs production, nitric oxide and cytokine expre
257 mblages between the two periods, with native flora significantly decreasing (-10.7%) and alien flora
259 However, its application to a continental flora, spanning large climate gradients, has been hamper
261 lture and clarified whether a cultured "oral flora" species represented a state of acute infection.
262 gue that the functional traits of each woody flora, specifically the N-fixing ability and architectur
263 is contained by invasive isolates and normal-flora strains in a region that contains genes involved i
264 e early colonizing species of the human oral flora (Streptococcus mutans, Streptococcus gordonii and
265 trends for weedy plants reported from other floras, suggest that native and introduced weeds have di
267 indings demonstrate in neonatal mice how gut flora synergizes with poly(I:C) to elicit protective int
269 ction in the number of members of the normal flora that interfere with the growth of pathogens and th
270 rvention to affect this process - on the gut flora, the 'leaky' mucosal membrane and endotoxin couple
271 he normal human gastrointestinal and vaginal flora, they can also be occasional human pathogens.
274 s derived from dietary tryptophan by the gut flora to activate AHR signaling in astrocytes and suppre
276 arcode sequences was generated for the local flora to determine the taxonomic composition of honey.
279 ing signals from the diet and the intestinal flora to modulate ongoing inflammation in the central ne
281 elial tight junctions, allowing resident gut flora to promote chronic increases in antimicrobial pept
282 ctions become loose, enabling the intestinal flora to trigger a constitutive activation of the anteri
285 ct of diosgenin on the density of intestinal flora was examined in a murine model of food allergy.
286 experiments where only the natural bacterial flora was manipulated, the addition of kanamycin did not
288 utum specimens and quantity of oropharyngeal flora were compared for different quantities of SECs and
293 may induce an extinction debt in the native flora, where persistence over the short term masks deter
297 ert highly selective effects on resident gut flora, which, in turn, lead to very specific alterations
298 n (FMT) re-establishes a balanced intestinal flora with resultant cure of recurrent Clostridium diffi
299 ty based on the composition of fossil diatom floras with organic carbon burial off Oregon in the Nort
300 of concept study demonstrates that bacterial flora within the neonatal feeding tubes may influence th
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