ライフサイエンスコーパス: vulgaris

1 na) and other plants such as bean (Phaseolus vulgaris).

2 tion in juvenile European starlings (Sturnus vulgaris).

3 l neostriatum of European starlings (Sturnus vulgaris).

4 based on synteny with common bean (Phaseolus vulgaris).

5 s and the distantly-related beet plant (Beta vulgaris).

6 biome can be useful as a biotherapy for acne vulgaris.

7 the defensin from the common bean Phaseolus vulgaris.

8 the flaky tail mouse, a model for ichthyosis vulgaris.

9 skin and can promote the common disease acne vulgaris.

10 at resembles the genetic disorder ichthyosis vulgaris.

11 oma, hidradenitis suppurativa, and pemphigus vulgaris.

12 to the dosing regimen approved for psoriasis vulgaris.

13 a history of condyloma acuminata or verruca vulgaris.

14 istory of condyloma acuminata and/or verruca vulgaris.

15 relevant studies of isotretinoin use in acne vulgaris.

16 ed as a dominant etiological factor for acne vulgaris.

17 well-tolerated, effective treatment for acne vulgaris.

18 al squamous papillomas and cutaneous verruca vulgaris.

19 are warranted in the treatment of pemphigus vulgaris.

20 is necessary for treating patients with acne vulgaris.

21 ssing an L-amino acid deaminase from Proteus vulgaris.

22 ntrally involved in the pathogenesis of acne vulgaris.

23 developed as an effective treatment for acne vulgaris.

24 urse distinct from pathogenesis of pemphigus vulgaris.

25 al tolerance in the phytoplankton, Chlorella vulgaris.

26 ntibiotic approved for the treatment of acne vulgaris.

27 studies for rare diseases, such as pemphigus vulgaris.

28 therapeutic agent for the treatment of acne vulgaris.

29 other blistering disorders such as pemphigus vulgaris.

30 yphenol composition of T. citriodorus and T. vulgaris.

31 gy in both pemphigus foliaceus and pemphigus vulgaris.

32 ribute to the common human skin disease acne vulgaris.

33 , and seborrheic dermatitis), 0.29% for acne vulgaris, 0.19% for psoriasis, 0.19% for urticaria, 0.16

34 nnic acid equivalents (TAE) g(-1) DW) and T. vulgaris (8.55mg quercetin equivalents (QE) g(-1) DW), r

35 Participants included 92 patients (pemphigus vulgaris, 84 [91%], and pemphigus foliaceus, 8 [9%]) who

36 eritance of PD in the common bean (Phaseolus vulgaris), a major domesticated grain legume.

37 H mutant was Fix(+) on common bean (Phaseoli vulgaris), a member of the phaseoloid clade of legumes,

38 Here we use the freshwater polyp Hydra vulgaris, a well-established model previously adopted to

39 Acne vulgaris (acne) is a common inflammatory disorder of the

40 les for cosmetic applications including acne vulgaris, acne scars, skin rejuvenation and hair growth,

41 order Intensity Score (ABSIS), and Pemphigus Vulgaris Activity Score (PVAS) were validated to correla

42 Psoriasis vulgaris, affecting the skin, is one of the most common

43 triggered stomatal closure in both Phaseolus vulgaris and Arabidopsis (Arabidopsis thaliana), which i

44 KP is associated clinically with ichthyosis vulgaris and atopic dermatitis and molecular genetically

45 i) and two fresh water microalgae (Chlorella vulgaris and Chlorella protothecoides) important for nut

46 tients with confirmed diagnoses of pemphigus vulgaris and clinical pemphigus lesions (mean [SD] age,

47 ut), Ulex europaeus (gorse, furze), Triticum vulgaris and Concanavalin A (ConA) was used for probes t

48 e food web consisting of the algae Chlorella vulgaris and daphnid Daphnia magna.

49 aeruginosa, Enterococcus aerogenes, Proteus vulgaris and Enterobacter sakazakii) bacteria, with deco

50 in different organs of Aruncus dioicus var. vulgaris and in aerial parts of A. dioicus var. aethusif

51 , fruiting body-forming amoeba Guttulinopsis vulgaris and its non-fruiting relatives Rosculus 'ithacu

52 The D. vulgaris and M. barkeri enzyme complexes both copurify w

53 f Desulfovibrio desulfuricans, Desulfovibrio vulgaris and Methanosarcina barkeri AhbA/B have been pro

54 that contributes to the development of acne vulgaris and other infections.

55 nscripts in the invertebrate mollusk Octopus vulgaris and present evidence of their expression not on

56 ritability of cutaneous psoriasis, psoriasis vulgaris and psoriatic arthritis.

57 ly used algal strains, fresh-water Chlorella vulgaris and seawater Tetraselmis chuii, were selected.

58 , a form of vitamin B12 was identified in C. vulgaris and this finding enhances its use as a nutritio

59 rous plant (greater bladderwort, Utricularia vulgaris) and a vertebrate (bluegill, Lepomis macrochiru

60 the phytochemical profile of red beet (Beta vulgaris) and amaranth (Amaranthus sp.) microgreens.

61 us), and eggs of European starlings (Sturnus vulgaris) and American kestrels (Falco sparverius) at an

62 the betalain-producing plants red beet (Beta vulgaris) and four o'clocks (Mirabilis jalapa) to identi

63 reports the genome of common bean (Phaseolus vulgaris) and genome-wide resequencing data from both wi

64 riptomes to select common selfheal (Prunella vulgaris) and its highly unusual vulgarisin diterpenoids

65 s established between common bean (Phaseolus vulgaris) and Rhizobium etli.

66 issue in experiments with starlings (Sturnus vulgaris) and show that integrating normative and descri

67 s in the eggs of European starlings (Sturnus vulgaris) and three congeneric gull species (i.e., herri

68 uced from C3 plants such as sugar beet (Beta vulgaris) and wheat (Triticium vulgare).

69 inoin therapy for conditions other than acne vulgaris, and concomitant acne therapy.

70 m baseline in 46% of patients with psoriasis vulgaris, and it decreases epidermal thickness as well a

71 composition, favouring grasses over Calluna vulgaris, and led to a reduction in vegetation C stocks.

72 In the non-aging H. vulgaris animals, the blockade of autophagy by knocking

73 Desmoglein 3 (Dsg3), the pemphigus vulgaris antigen, has recently been shown to be upregula

74 phalopod molluscs, and in particular Octopus vulgaris, are well known for their capacity to regenerat

75 Using Desulfovibrio vulgaris as a model SRB organism, we compared the transc

76 ing Rhizobium tropici CIAT 899 and Phaseolus vulgaris as working models, we demonstrated that rhizoba

77 encapsulated in algae (Alg) cell (Chlorella vulgaris) as confirmed by fluorescence microscopy, therm

78 ries of batch tests on U(VI) reduction by D. vulgaris at a low initial biomass (10 to 20 mg/L of prot

79 Acne vulgaris (AV) affects most adolescents, and of those aff

80 lycine max) and black turtle bean (Phaseolus vulgaris), belonging to two different genera were used t

81 Vitamin B12 was extracted from Chlorella vulgaris biomass under aqueous conditions, partially pur

82 mediterraneus, Trachurus trachurus, Octopus vulgaris, Boops boops, Sarda sarda, Trisopterus capelanu

83 ce or in newborn individuals with ichthyosis vulgaris but is present in other forms of ichthyosis.

84 y developed to treat moderate to severe acne vulgaris by directly delivering the combination of the t

85 are formed during colonization of Phaseolus vulgaris by Pseudomonas syringae.

86 ovide evidence that nitrate inhibition of D. vulgaris can be independent of nitrite production.

87 We also show that D. vulgaris can use nitrite as a nitrogen source or termina

88 ch often manifests with concurrent psoriasis vulgaris, can have an acute systemic (generalized pustul

89 ibodies in pemphigus foliaceus and pemphigus vulgaris cause blisters through loss of desmosomal adhes

90 CAP 849/10 and a marine isolate of Chlorella vulgaris CCAP 211/21A as the best lipid producers.

91 n conclusion, the data proved that Chlorella vulgaris cell can be used as a new stable carrier for Cu

92 ording to their ability to degrade Chlorella vulgaris cell wall to access its valuable nutritional co

93 displays an effective capacity to degrade C. vulgaris cell wall.

94 Andean beans (Phaseolus vulgaris) chemical compositions and cooking characterist

95 species such as European starlings (Sturnus vulgaris) cohabit urban neighborhoods and may serve as s

96 ne max (soybean), Lotus japonicus, Phaseolus vulgaris (common bean), Cicer arietinum (chickpea) and C

97 species, Glycine max (soybean) and Phaseolus vulgaris (common bean).

98 se genes from an Asteraceae species, Senecio vulgaris (common groundsel).

99 Psoriasis vulgaris concurrence was lowest in PPP (15.8% vs 54.4% i

100 commercially relevant micro algae (Chlorella vulgaris) cultivation using stable Synthetic Ecologies i

101 The pathophysiology of acne vulgaris depends on active sebaceous glands, implying th

102 dorsal petal elongation in Antirrhinum In S vulgaris, diversification of CYC genes has led to novel

103 rent microalgae samples, including Chlorella vulgaris, Dunaliella salina, and Phaeodactylum tricornut

104 strom resolution) of CODH from Desulfovibrio vulgaris (DvCODH) heterologously expressed in either the

105 Intriguingly, D. vulgaris encodes two sirohydrochlorin chelatases, CbiK(P

106 tion on the nutritional pattern of Chlorella vulgaris enriched breads.

107 (ECL), Sambucus nigra lectin, and Phaseolus vulgaris Erythroagglutinin (PHA-E) are used to identify

108 ylated N-glycans recognized by the Phaseolus Vulgaris erythroagglutinin lectin.

109 l and antiaflatoxigenic properties of Thymus vulgaris essential oil (TEO) were evaluated upon Aspergi

110 microemulsion (ME) characteristics of Thymus vulgaris essential oil (TVO).

111 cans, Desulfovibrio gigas, and Desulfovibrio vulgaris, exhibited significantly relaxed specificity to

112 Hydra vulgaris exhibits a remarkable capacity to reassemble it

113 positions of Thymus x citriodorus and Thymus vulgaris extracts as obtained by exhaustive hydroethanol

114 netic level to flavodoxin from Desulfovibrio vulgaris (FLD) to create the chimeric CYP2A6-FLD.

115 ssion of the downstream bolting repressor B. vulgaris flowering locus T1 (BvFT1) and activation of th

116 ients had a confirmed diagnosis of pemphigus vulgaris/foliaceus, bullous pemphigoid, epidermolysis bu

117 The phenol-chloroform extraction of C. vulgaris followed by ethanol precipitation of polyphosph

118 stinal tracts of European starlings (Sturnus vulgaris) found on concentrated animal feeding operation

119 e day, while appreciating a print of Primula vulgaris from William Curtis' Flora Londinensis, I was s

120 the split of the Mesoamerican and Andean P. vulgaris gene pools.

121 apoplast of the susceptible plant Phaseolus vulgaris Genes within the functional categories of amino

122 Transcripts mapped to the Phaseolus vulgaris genome-another phaseoloid legume with the same

123 D. vulgaris grew with U(VI) respiration alone, as well as w

124 and leaf mass in the common bean (Phaseolus vulgaris) grown in two contrasting environments.

125 podium podagraria L.) and mugwort (Artemisia vulgaris), grown in two Appalachian acid-mine soils (MS-

126 In these conditions, D. vulgaris had a maximum growth rate of 0.078 h(-1) and a

127 The green microalga Chlorella vulgaris has been widely recognized as a promising candi

128 ximate Bayesian Computation indicate that D. vulgaris has likely inhabited the Azores for approximate

129 Red squirrels in Great Britain (Sciurus vulgaris) have increasingly been observed with leprosy-l

130 inant inbred lines of common bean (Phaseolus vulgaris) having four distinct root phenotypes: long roo

131 oxin regulates the expression of the Proteus vulgaris higBA toxin-antitoxin operon from the Rts1 plas

132 ripts, causing a population of Desulfovibrio vulgaris Hildenborough (DvH) to collapse after repeatedl

133 rmate dehydrogenase (FDH) from Desulfovibrio vulgaris Hildenborough (DvH) to metal oxides for catalyt

134 om Rhodobacter sphaeroides and Desulfovibrio vulgaris Hildenborough cytochrome c(3)).

135 e tested a deposited strain of Desulfovibrio vulgaris Hildenborough for its capacity to transform SMX

136 ansferase, showed increased levels in the D. vulgaris Hildenborough Rex (RexDvH) mutant relative to t

137 In Desulfovibrio vulgaris Hildenborough, a model bacterium for sulfate re

138 tion of the putative rex gene was made in D. vulgaris Hildenborough, and transcript expression studie

139 del sulfate-reducing bacterium Desulfovibrio vulgaris Hildenborough, but two copies in Desulfovibrio

140 ate-reducing microbes, such as Desulfovibrio vulgaris Hildenborough, cause "souring" of petroleum res

141 model sulfate-reducing microbe Desulfovibrio vulgaris Hildenborough, the gene DVU_0916 was observed t

142 is work, we studied FlxABCD of Desulfovibrio vulgaris Hildenborough.

143 on in the process of sulfate reduction in D. vulgaris Hildenborough.

144 evolving G20 cultures and in another SRM, D. vulgaris Hildenborough.

145 enesis of many skin conditions, such as acne vulgaris, hirsutism, and androgenic alopecia.

146 uously self-renew and prevent aging in Hydra vulgaris However, sexual animals from the H. oligactis c

147 trated that T. daenensis-3 (IC50=273.36), T. vulgaris (IC50=289.3), and T. fedtschenkoi-3 (IC50=339.2

148 ntified and added to the updated model of C. vulgaris, iCZ946, thus increasing our knowledgebase by 1

149 th the [NiFe]-hydrogenase from Desulfovibrio vulgaris immobilized on a functionalized electrode were

150 us foliaceus and six patients with pemphigus vulgaris in active disease and remission were compared,

151 del sulfate-reducing bacterium Desulfovibrio vulgaris in the absence of sulfate or a syntrophic partn

152 multiple (2 - 80+) Common starlings (Sturnus vulgaris) in Great Britain that appeared to be due to dr

153 etic variation of the common bean (Phaseolus vulgaris) in its centres of domestication.

154 vs. leaf mass for the common bean (Phaseolus vulgaris) in two different environments.

155 digm in European starling nestlings (Sturnus vulgaris), in which we separately manipulated nutritiona

156 of fellow legumes, Glycine max and Phaseolus vulgaris, in addition to the model plant Arabidopsis tha

157 ynamics of the invasive common wasp, Vespula vulgaris, in its native range in England and its invaded

158 ities of Fagioli di Sarconi beans (Phaseolus vulgaris), including 21 ecotypes protected by the Europe

159 G564 ortholog in the Common Bean (Phaseolus vulgaris), indicating that the regulation of G564 is evo

160 nthus annuus, Solanum lycopersicum, and Beta vulgaris) inoculated with the same strain of S. scleroti

161 Psoriasis vulgaris is a common T cell-mediated inflammatory skin d

162 the nonconventional H2-producing organism D. vulgaris is a good biocatalyst for converting formate to

163 Acne vulgaris is a nearly universal cutaneous disease charact

164 Acne vulgaris is a nearly universal cutaneous inflammatory di

165 Psoriasis vulgaris is an inflammatory skin disease caused by hyper

166 and highly prevalent skin disorder psoriasis vulgaris is characterized by a hyperproliferative epider

167 ent of the first-line treatment of pemphigus vulgaris is high doses of systemic corticosteroids, but

168 Psoriasis vulgaris is the best-understood and most accessible huma

169 Acne vulgaris is the most common skin disorder affecting mill

170 Sugar beet (Beta vulgaris) is a biennial root crop that grows vegetativel

171 as the common two-banded seabream (Diplodus vulgaris) is now relatively common along the coastline o

172 n mutations in the FLG gene cause ichthyosis vulgaris (IV) and represent the major predisposing genet

173 Proteus vulgaris L-amino acid deaminase (pvLAAD) belongs to a cl

174 the species Lens culinaris Medik., Phaseolus vulgaris L. and Cicer arietinum L. after soaking, boilin

175 from the skin and flesh of red beetroot Beta vulgaris L. cultivars Nochowski from 2012 and 2013 seaso

176 6 LEA protein from a common bean (Phaseolus vulgaris L.) (PvLEA6) by circular dichroism and nuclear

177 cyanus L., Matricaria chamomilla L., Thymus vulgaris L.) and dried fruit (currants, chokeberry), usi

178 tein extraction from sugar beet leaves (Beta vulgaris L.) by a traditional thermal extraction method

179 in the preparation of navy beans (Phaseolus vulgaris L.) for canning.

180 experimental plots of common bean (Phaseolus vulgaris L.) in Nicaragua, durum wheat (Triticum durum D

181 the drying conditions on red beetroot (Beta vulgaris L.) in terms of betalain variance, and polyphen

182 vements of shoots of common beans (Phaseolus vulgaris L.) in two conditions: with and without a suppo

183 Common bean (Phaseolus vulgaris L.) is the most important grain legume for huma

184 ng cultivated plants, common bean (Phaseolus vulgaris L.) is the most important grain legume.

185 ing the effect of red thyme oil (RTO, Thymus vulgaris L.) on the shelf-life and Penicillium decay of

186 erformances of 25 edible dry bean (Phaseolus vulgaris L.) varieties and to investigate correlations a

187 Common beans (Phaseolus vulgaris L.), represent the most consumed legume worldwi

188 ed storage protein of common bean, Phaseolus vulgaris L., accounting for up to 50 % of the total seed

189 oamerican genotype of common bean (Phaseolus vulgaris L., BAT93).

190 upland Atlantic heath, dominated by Calluna vulgaris (L.) Hull.

191 Importance: Cutaneous verruca vulgaris lesions (warts) and oral squamous cell papillom

192 jections of the anterograde tracer Phaseolus vulgaris leucoagglutinin into the LHb or the RMTg.

193 s, biotinylated dextran amine, and Phaseolus vulgaris leucoagglutinin were injected into the entorhin

194 Thus, the present study used Phaseolus vulgaris-leucoagglutinin (PHAL) anterograde tracing and

195 jections of the anterograde tracer Phaseolus vulgaris-leucoagglutinin (PHAL) in the perirhinal cortex

196 vegetative growth, biennial sugar beet (Beta vulgaris) maintains a steep Suc concentration gradient b

197 ots of Aruncus dioicus (Walter) Fernald var. vulgaris (Maxim.) H.Hara (Rosaceae), collected from the

198 led fully reduced Ni-R form of Desulfovibrio vulgaris Miyazaki F [NiFe]-hydrogenase.

199 Eurasian distribution, onto heather (Calluna vulgaris) moorland with podzolic and peaty podzolic soil

200 vels of endotoxin were detected on Artemisia vulgaris (mugwort) pollen, with little on other pollen.

201 acterized anthocyanin MYB-like protein, Beta vulgaris MYB1 (BvMYB1), regulates the betalain pathway i

202 A total of 116 patients with pemphigus vulgaris (n = 84) or pemphigus foliaceus (n = 32) were i

203 ree varieties of red kidney beans (Phaseolus vulgaris) namely Kashmiri red, Sharmili and Chitra were

204 1 diabetes (T1D; ncases = 5,567), psoriasis vulgaris (ncases = 3,089), idiopathic achalasia (ncases

205 pm) were similar to concentrations in Thymus vulgaris nectar (mean 5.2 ppm).

206 rmed in planta by the common bean (Phaseolus vulgaris) NF-Y subunits, revealing the existence of evol

207 or requires nitrite reductase (nrfA) as a D. vulgaris nrfA mutant cannot respire nitrite but remains

208 pproach to improve the bioavailability of C. vulgaris nutrients for monogastric diets, in particular,

209 (20%), multiple facial scars (20%), verruca vulgaris on the face (20%), and rhinophyma (10%).

210 r IgE levels, and 30 controls with pemphigus vulgaris or pemphigus foliaceus were included for compar

211 strain isolated from a red squirrel (Sciurus vulgaris orientis) from China.

212 In Primula vulgaris outcrossing is promoted through reciprocal herk

213 ockade of desmoglein 3 function in pemphigus vulgaris patients leads to skin blistering (acantholysis

214 men in their 50s, 60s, or 70s with pemphigus vulgaris (Pemphigus Disease Area Index score, 15-84 at d

215 ed down-regulation of common bean (Phaseolus vulgaris) PI3K severely impaired symbiosis in composite

216 severely impaired symbiosis in composite P. vulgaris plants with endosymbionts such as Rhizobium tro

217 Beetroot (Beta vulgaris) pomace extract is a rich source of betalain, p

218 ibition of photosynthesis indicating that S. vulgaris possess tolerance mechanisms that allows it to

219 Experiments with the green alga Chlorella vulgaris presented here compared polyphosphate extractio

220 The model organism Nitrobacter vulgaris produced only trace amounts of 2-methylhopanoid

221 e (62.5-500 mg/kg) on kidney bean (Phaseolus vulgaris) productivity and seed quality as a function of

222 yzed resulting data: eczema, psoriasis, acne vulgaris, pruritus, alopecia areata, decubitus ulcer, ur

223 Psoriasis vulgaris (PsV) is a common inflammatory and hyperprolife

224 Psoriasis vulgaris (PsV) risk is strongly associated with variatio

225 en documented in familial forms of psoriasis vulgaris (PV) and pityriasis rubra pilaris (PRP).

226 cells (DSG3-CAART) expressing the pemphigus vulgaris (PV) autoantigen DSG3 fused to CD137-CD3zeta si

227 Patients with pemphigus vulgaris (PV) harbor antibodies reactive against self-an

228 s with the blistering skin disease pemphigus vulgaris (PV) IgG is reduced in maturated desmosomes and

229 IMPORTANCE Pemphigus vulgaris (PV) is a disease that features blistering of t

230 Pemphigus vulgaris (PV) is a life-long, potentially fatal IgG auto

231 Pemphigus vulgaris (PV) is a potentially fatal blistering disease

232 Pemphigus vulgaris (PV) is a potentially lethal mucocutaneous blis

233 Pemphigus vulgaris (PV) is a prototypic tissue-specific autoantibo

234 Pemphigus vulgaris (PV) is an autoimmune blistering disease charac

235 Pemphigus vulgaris (PV) is an autoimmune epidermal blistering dise

236 3 (Dsg3) in the autoimmune disease pemphigus vulgaris (PV), as well as B cells responding to rotaviru

237 autoimmune skin-blistering disease pemphigus vulgaris (PV), autoantibodies (IgG) target the desmosoma

238 tibody-mediated autoimmune disease pemphigus vulgaris (PV), autoantigen-based chimeric immunoreceptor

239 videnced by the autoimmune disease pemphigus vulgaris (PV), in which autoantibodies against the extra

240 y-mediated blistering skin disease pemphigus vulgaris (PV), we applied antibody fractions of PV patie

241 s with the blistering skin disease pemphigus vulgaris (PV), which is caused by autoantibodies against

242 are two major clinical subsets of pemphigus vulgaris (PV)-mucosal PV (mPV) and mucocutaneous PV (mcP

243 expression in patients with severe psoriasis vulgaris (PV).

244 the structure and expression of all eight P. vulgaris PvKNOX genes in both wild-type and Oakleaf plan

245 rom four botanical origins: heather (Calluna vulgaris), raspberry (Rubus idaeus), rape (Brassica napu

246 ot indicates that, in common bean (Phaseolus vulgaris), reduced root secondary growth reduces root me

247 , 3 mg/kg/d, and a young girl with pemphigus vulgaris responded to treatment with voriconazole, 8 mg/

248 ription factor in the common bean (Phaseolus vulgaris)-Rhizobium etli symbiosis.

249 d the role of TOR during the bean (Phaseolus vulgaris)-Rhizobium tropici (Rhizobium) symbiotic intera

250 species spanning the Pentapetalae (Phaseolus vulgaris, Ricinus communis, Arabidopsis [Arabidopsis tha

251 associated changes in common bean (Phaseolus vulgaris) roots were due to direct selection for some ab

252 us x giganteus, and notably sugar beet (Beta vulgaris) roots where phloem identification is an import

253 rated genetic and physical map across the P. vulgaris S locus flanked by phenotypic and DNA sequence

254 mutant phenotypes to create a map of the P. vulgaris S locus region that will facilitate the identif

255 A total of 39% (24/62) of red squirrel (S. vulgaris) samples from the Netherlands were positive for

256 n the market including Se-enriched Chlorella vulgaris (Se-Chlorella) which accumulates Se in the form

257 ean (Glycine max) and common bean (Phaseolus vulgaris) share a paleopolyploidy (whole-genome duplicat

258 inocycline 200mg daily for treatment of acne vulgaris since 16 years old.

259 sing volume of genomic data on the Phaseolus vulgaris species have contributed to its importance as a

260 igna unguiculata) and common bean (Phaseolus vulgaris), specifically respond to OS via recognition of

261 These mechanisms make S. vulgaris suitable for in situ remediation of Cr polluted

262 Common bean (Phaseolus vulgaris) symbiotically associates with its partner Rhiz

263 two x-ray crystal structures of the Proteus vulgaris tetrameric HigB-(HigA)2-HigB TA complex and fou

264 xclosures dominated by dwarf shrubs (Calluna vulgaris) than by grasses (Molinia caerulea).

265 ly uncharacterized metabolic abilities of D. vulgaris that may allow niche expansion in low-sulfate e

266 fied 2,606 genes from common bean (Phaseolus vulgaris) that are differentially regulated at early sta

267 most bioactive species was heather (Calluna vulgaris), the second most productive UK nectar plant [1

268 Our results show that in D. vulgaris, the FlxABCD-HdrABC proteins are essential for

269 re, we show that in the common wasp, Vespula vulgaris, the pheromone that signals egg maternity and e

270 The capacity of Desulfovibrio vulgaris to reduce U(VI) was studied previously with non

271 his study investigated the ability of Silene vulgaris to take up Cr(III) and Cr(VI) with special atte

272 rain function in European Starlings (Sturnus vulgaris), trained to fly in a wind tunnel while metabol

273 ution cryo-EM structure of the Desulfovibrio vulgaris type I-C Cascade, revealing the molecular mecha

274 nteraction with negatively charged Chlorella vulgaris upon CO2-treatment.

275 of songbird, the European Starling (Sturnus vulgaris), using tone sequences that vary in both pitch

276 have achieved this with the cnidarian Hydra vulgaris, using calcium imaging of genetically engineere

277 a genome-scale metabolic model of Chlorella vulgaris UTEX 395 over time.

278 ion of a genome-scale metabolic model for C. vulgaris UTEX 395, iCZ843.

279 Vitexin-2-O-xyloside (XVX) from Beta vulgaris var. (BVc) seeds, betaxanthin (R1) and betacyan

280 (R1) and betacyanin (R2) fractions from Beta vulgaris var. (BVr) roots were combined and tested for c

281 Vitexin-2-O-xyloside (XVX) from Beta vulgaris var. cicla L. (BVc) seeds, betaxanthin (R1) and

282 Kidney bean plants (Phaseolus vulgaris var. red hawk) grown in soil contaminated with

283 (R1) and betacyanin (R2) fractions from Beta vulgaris var. rubra L. (BVr) roots were combined and tes

284 accuracy of a model developed for Chlorella vulgaris was assessed against data collected from photob

285 etection of individual algal cell (Chlorella vulgaris) was performed at the SERS substrate as fabrica

286 um antibodies cross-reactive against Proteus vulgaris (Weil-Felix reaction).

287 erties of a beta-class CA from Desulfovibrio vulgaris were dramatically enhanced.

288 strains, 45 adult smooth newts (Lissotriton vulgaris) were challenged via bath exposure with these r

289 European starlings (Sturnus vulgaris) were collected from feedlots within multiple g

290 Adult European starlings (Sturnus vulgaris) were exposed to vehicle emissions, with combin

291 ormerly considered the "wild ancestor" of P. vulgaris, which diverged before the split of the Mesoame

292 he two main pemphigus variants are pemphigus vulgaris, which often originates with painful oral erosi

293 We found that Beta vulgaris, which produces high concentrations of betalain

294 seudokirchneriella subcapitata and Chlorella vulgaris while dealing with photosynthesis, the multi-mi

295 us and eight patients with mucosal pemphigus vulgaris with active disease inhibited the adhesion of D

296 ucial for the mutualistic interactions of P. vulgaris with beneficial microorganisms.

297 ve as a linear proxy for polyphosphate in C. vulgaris with R(2) up to 0.956.

298 cospora beticola, is a major disease of Beta vulgaris worldwide.

299 activity of hydrogenase demonstrate that C. vulgaris YSL01 and YSL16 enzymatically produce hydrogen,

300 how that novel microalgal strains (Chlorella vulgaris YSL01 and YSL16) upregulate the expression of t