ライフサイエンスコーパス: vulgaris

1 tion in juvenile European starlings (Sturnus vulgaris).

2 ent of halo blight in common bean (Phaseolus vulgaris).

3 male and female European starlings (Sturnus vulgaris).

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

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

6 ed as a dominant etiological factor for acne vulgaris.

7 well-tolerated, effective treatment for acne vulgaris.

8 al squamous papillomas and cutaneous verruca vulgaris.

9 are warranted in the treatment of pemphigus vulgaris.

10 is necessary for treating patients with acne vulgaris.

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

12 ntrally involved in the pathogenesis of acne vulgaris.

13 developed as an effective treatment for acne vulgaris.

14 urse distinct from pathogenesis of pemphigus vulgaris.

15 al tolerance in the phytoplankton, Chlorella vulgaris.

16 studies for rare diseases, such as pemphigus vulgaris.

17 therapeutic agent for the treatment of acne vulgaris.

18 other blistering disorders such as pemphigus vulgaris.

19 tor contributing to the pathogenesis of acne vulgaris.

20 tion of leaf and xylem function in Phaseolus vulgaris.

21 quently prescribed for the treatment of acne vulgaris.

22 of 7 patients with sarcoidosis and psoriasis vulgaris.

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

24 ablishing symbiosis with its host, Phaseolus vulgaris.

25 ial DNA sequence exists in angiosperm Silene vulgaris.

26 ociation with the common teenage malady acne vulgaris.

27 at resembles the genetic disorder ichthyosis vulgaris.

28 oma, hidradenitis suppurativa, and pemphigus vulgaris.

29 to the dosing regimen approved for psoriasis vulgaris.

30 a history of condyloma acuminata or verruca vulgaris.

31 istory of condyloma acuminata and/or verruca vulgaris.

32 relevant studies of isotretinoin use in 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 pping of S. latifolia sex-linked genes in S. vulgaris (a related hermaphrodite species without sex ch

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

38 In pemphigus vulgaris, a life-threatening autoimmune skin disease, ep

39 activated in two sequential steps: Phaseolus vulgaris ABI3-like factor (Pv-ALF)-dependent potentiatio

40 S. vulgaris accumulated more Cr when grown with Cr(VI) resu

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

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

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

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

45 the sulfate-reducing bacterium Desulfovibrio vulgaris, although it grows only poorly on CO.

46 a variation in gene flanking regions make S. vulgaris an excellent model for the study of mitochondri

47 diates tissue damage in autoimmune pemphigus vulgaris and "IgG4-related disease." Approximately half

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

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

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

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

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

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

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

55 enomes from the gynodioecious species Silene vulgaris and found unprecedented amounts of intraspecifi

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

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

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

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

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

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

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

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

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

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

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

67 ing the acetate moiety from sugar beet (Beta vulgaris) and potato (Solanum tuberosum) pectin in vitro

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

69 dy in closely related common bean (Phaseolus vulgaris) and soybean (Glycine max) reference genomes.

70 alis), nettle (Urtica dioica), linden (Tilia vulgaris) and St. John's wort (Hypericum calycinum).

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

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

73 ng seeds and seedlings of the bean Phaseolus vulgaris, and a smaller but consistently detectable amou

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

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

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

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

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

79 us terrestris) and a third of wasps (Vespula vulgaris), as well as all honey bees, were positive for

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

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

82 nfunctional hAT transposons (BvhAT), in a B. vulgaris BAC library as well as in whole genome sequenci

83 In comparison, acne vulgaris, bacterial skin diseases, urticaria, pruritus,

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

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

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

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

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

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

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

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

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

93 rehensive analysis of common bean (Phaseolus vulgaris) centromeric satellite DNA using genomic data,

94 elated species, showing a localization on B. vulgaris chromosomes predominantely in euchromatic regio

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

98 y the presence of selenocyanate in Chlorella vulgaris culture medium by electrospray mass spectrometr

99 plant defensins was purified from Phaseolus vulgaris cv. 'King Pole Bean' by anion-exchange chromato

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

101 latively constant level throughout Aquilegia vulgaris development, with the VEL PHD family and MSI1 e

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 enter, bacterial ferritin from Desulfovibrio vulgaris (DvFtn) and its E130A variant was loaded with s

105 ermined in fresh European starling ( Sturnus vulgaris ) eggs collected in 2009, 2010, and 2011 from n

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

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

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

109 xtracts from Thymus serpyllum (ExTs), Thymus vulgaris (ExTv), Majorana hortensis (ExMh), and Mentha p

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

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

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

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

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

115 ticated accessions of common bean (Phaseolus vulgaris) from Mesoamerica.

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

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

118 th the resistant and susceptible types of B. vulgaris glucosylate sapogenins and are not located in t

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

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

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

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

123 We conclude that S. vulgaris harbors an unusually large degree of variation

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

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

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

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

128 rophic cocultures, Dhc195 with Desulfovibrio vulgaris Hildenborough (-13.0 +/- 2.0 per thousand) and

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

130 doxin (Dtrx) from the anaerobe Desulfovibrio vulgaris Hildenborough has been identified as a new memb

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

132 odA and modBC genes by TunR in Desulfovibrio vulgaris Hildenborough was confirmed in vivo, and we dis

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

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

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

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

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

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

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

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

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

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

143 nthetic activity of the green alga Chlorella vulgaris in presence of different multiwalled CNT (indus

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

145 morphism in Mediterranean wild thyme (Thymus vulgaris) in association with modified extreme winter fr

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

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

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

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

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

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

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

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

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

155 Acne vulgaris is a nearly universal cutaneous disease charact

156 Acne vulgaris is a nearly universal cutaneous inflammatory di

157 Psoriasis vulgaris is an inflammatory skin disease caused by hyper

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

159 tion method for cellular lipids in Chlorella vulgaris is demonstrated in this study.

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

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

162 Acne vulgaris is the most common skin disorder affecting mill

163 Barbarea vulgaris is the only crucifer known to produce saponins.

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

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

166 ajor seed storage protein in bean (Phaseolus vulgaris), is activated in two sequential steps: Phaseol

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

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

169 henolic composition of dark beans (Phaseolus vulgaris L. c.v. Tolosana) and their effect on their ant

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

171 6 LEA protein from a common bean (Phaseolus vulgaris L.) (PvLEA6) by circular dichroism and nuclear

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

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

174 Wild common bean (Phaseolus vulgaris L.) is distributed throughout the Americas from

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

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

177 ect of germination of black beans (Phaseolus vulgaris L.) on the antioxidant capacity and antiprolife

178 ons and seed coats of black beans (Phaseolus vulgaris L.) subjected to germination over five days.

179 Common bean (Phaseolus vulgaris L.), the staple crop of Nicaragua, provides pro

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

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

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

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

184 erogradely following injections of Phaseolus vulgaris leucoagglutinin into the basolateral nucleus of

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

186 jections of the anterograde tracer Phaseolus vulgaris leucoagglutinin were aimed at different subdivi

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

188 otinylated dextran amine (BDA) and Phaseolus vulgaris-leucoagglutinin (PHA-L), into four subdivisions

189 oretic co-injection of the tracers Phaseolus vulgaris-leucoagglutinin (PHA-L; for outputs) and choler

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

191 jections of the anterograde tracer Phaseolus vulgaris-leucoagglutinin (PHAL) were performed at differ

192 s in S. latifolia are located on a single S. vulgaris linkage group and were probably inherited from

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

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

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

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

197 1 diabetes (T1D; ncases = 5,567), psoriasis vulgaris (ncases = 3,089), idiopathic achalasia (ncases

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

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

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

201 (20%), multiple facial scars (20%), verruca vulgaris on the face (20%), and rhinophyma (10%).

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

203 gist for a primary initial diagnosis of acne vulgaris or rosacea in 2010.

204 In Primula vulgaris outcrossing is promoted through reciprocal herk

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

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

207 ion of a heterologous French bean (Phaseolus vulgaris) peroxidase (FBP1) cDNA in Arabidopsis thaliana

208 ion of a heterologous French bean (Phaseolus vulgaris) peroxidase cDNA construct.

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

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

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

212 ript profile of this gene observed across S. vulgaris populations.

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

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

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

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

217 two genomes from each domain: Desulfovibrio vulgaris, Pseudomonas aeruginosa, Archaeoglobus fulgidus

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

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

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

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

222 opment of nonhormonal treatment of pemphigus vulgaris (PV) has been hampered by a lack of clear under

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

224 ptor (EGFR) is activated following pemphigus vulgaris (PV) IgG treatment of primary human keratinocyt

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

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

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

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

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

230 Pemphigus vulgaris (PV) is an autoimmune blistering disease of ski

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

232 Pemphigus vulgaris (PV) is considered as a model for an autoantibo

233 rituximab is highly effective for pemphigus vulgaris (PV) treatment.

234 3 (Dsg3) in the autoimmune disease pemphigus vulgaris (PV), as well as B cells responding to rotaviru

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

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

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

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

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

240 cases presenting with concomitant psoriasis vulgaris (PV; common or typical psoriasis).

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

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

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

244 , 3 mg/kg/d, and a young girl with pemphigus vulgaris responded to treatment with voriconazole, 8 mg/

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

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

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

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

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

250 A Beta vulgaris serine proteinase inhibitor gene (BvSTI) was fu

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

252 Calluna vulgaris showed a preference for higher N doses as ammon

253 The F. vulgaris showed high content of carvacrol (29.8%) as mai

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

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

256 In gynodioecious Beta vulgaris ssp. maritima, sex determination involves cytop

257 emoval from the water column was a Chlorella vulgaris strain (designated Cv).

258 brio alaskensis strain G20 and Desulfovibrio vulgaris strain Hildenborough growing syntrophically wit

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

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

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

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

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

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

265 ean (Glycine max) and common bean (Phaseolus vulgaris) that is associated with several disease resist

266 models for the equivalent of miR159.2, in P. vulgaris, the accumulation of miR159.2 is easily detecta

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

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

269 ggrin (FLG) gene are the cause of ichthyosis vulgaris-the most common disorder of keratinization-and

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 stem, we trained European starlings (Sturnus vulgaris) to differentially recognize sets of songs, the

273 cies (Arabidopsis thaliana, sugar beet [Beta vulgaris], tobacco [Nicotiana tabacum], and maize [Zea m

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

275 Salvia officinalis (SO) and Thymus vulgaris (TV) are medicinal plants well known for their

276 weight protein, the hemocyanin from Octopus vulgaris, under solution conditions that stabilize the d

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

278 atalase (HvCatalase) was isolated from Hydra vulgaris using 3'- and 5'- (RLM) RACE approaches.

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

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

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

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

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

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

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

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

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

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

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

290 water on the Raman spectrogram of Chlorella vulgaris were also addressed.

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

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

293 auriculata, Fumaria vaillantii and Falcaria vulgaris) were extracted with three different solvents t

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

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

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