ライフサイエンスコーパス: vagina

1 ents of the human gastrointestinal tract and vagina.

2 herniation of the uterus into or through the vagina.

3 five swabs from the lateral wall of the mid-vagina.

4 sity as physician collected swabs of the mid-vagina.

5 ivity on bone, plasma lipids, hot flush, and vagina.

6 precursor lesions in both the cervix and the vagina.

7 red the titers of the challenge virus in the vagina.

8 nized monkeys was minimal and limited to the vagina.

9 monads is preparatory to colonization of the vagina.

10 ated in milk and C. pecorum dominated in the vagina.

11 eficiency virus (SHIV) infection through the vagina.

12 appeared to be nonspecific in the uterus and vagina.

13 primordia of the oviducts, uterus and upper vagina.

14 ell as epithelia of the oviduct, cervix, and vagina.

15 for sustained long-term colonization of the vagina.

16 primary role in creating the acidity of the vagina.

17 ut did not entirely prevent infection of the vagina.

18 els after controlled topical delivery to the vagina.

19 lective homing of T and B lymphocytes to the vagina.

20 approximately 1% of the concentration in the vagina.

21 in mucosal fluids of the eye as well as the vagina.

22 unction was not entirely eliminated from the vagina.

23 ns were not detected in either the uterus or vagina.

24 elia such as the oral cavity, esophagus, and vagina.

25 intermediate state between normal uterus and vagina.

26 did not increase plasma cell numbers in the vagina.

27 and specific IgG in both the cervix and the vagina.

28 4) known bacteria formerly isolated from the vagina.

29 elatively little to immune protection of the vagina.

30 ucts and sinovaginal bulbs, give rise to the vagina.

31 eutrophil transepithelial migration into the vagina.

32 eral human niches such as the mouth, gut and vagina.

33 e from semen, 69 from urine, and 21 from the vagina.

34 factors and secreted proteins in the macaque vagina.

35 ations: caries lesions, the stomach, and the vagina.

36 ations through natural orifices, such as the vagina.

37 phonuclear neutrophil (PMN) migration to the vagina.

38 clinically without further treatment of the vagina.

39 actors that influence drug movement into the vagina.

40 alic acid-containing mucus components in the vagina.

41 ay be more likely to have involvement of the vagina.

42 persistent interdigital webs and imperforate vaginas.

43 he endocervix and by patients from their own vaginas.

44 ty, nares, skin, gastrointestinal tract, and vagina (15 specimens from men and 18 from women).

45 ce receiving recombinant IFN-alphaA (5-500 U/vagina) 24 h PI showed no significant survival in compar

46 highest in the skin (61.3%), followed by the vagina (41.5%), mouth (30%), and gut (17.3%).

47 ess common for cancers of the cervix (3.3%), vagina (8.3%), vulva (1.5%), and penis (8.3%).

48 docervix, 65 and 40%; urine, 72 and 24%; and vagina, 81 and 72%.

49 , cervix plus urine, 86 and 49%; cervix plus vagina, 91 and 93%; and vagina plus urine, 94 and 79%.

50 ory mice showed high in vivo CTL activity in vagina, a strong recall response, and robust protection

51 fic CD8(+) T cells in any tissues except the vagina after challenge.

52 Lymphocyte recruitment to the vagina after virus challenge appeared to involve memory

53 the intestine, oral cavity, nasopharynx, and vagina all have associated commensal flora.

54 The distal vagina also showed increased vascularization and perivas

55 nsenii, are common and abundant in the human vagina and absent from other habitats.

56 of nectin-1 in epithelial cells of the mouse vagina and also in neuronal cells of the central nervous

57 he detection of GBS is culture of the distal vagina and anorectum in a selective broth medium followe

58 main supportive structures of the uterus and vagina and are often attenuated in women with POP.

59 re part of the normal bacterial flora of the vagina and are typically considered contaminants when cu

60 to what was reported for studies of HSV-2 in vagina and brain and suggests that receptor requirements

61 EM is dispensable for HSV-2 infection of the vagina and brain, but is required for WT pathogenesis of

62 imary entry receptors for HSV-2 in the mouse vagina and brain.

63 ) and clear cell adenocarcinoma (CCA) of the vagina and cervix is well known, yet there has been no s

64 d in a multistage pathway exclusively in the vagina and cervix of K14-HPV16 transgenic mice.

65 me animals) of the SIV-infected cells in the vagina and cervix were Langerhans' cells.

66 ere preferentially found in the lower tract (vagina and cervix), whereas APCs and innate lymphoid cel

67 ased the number of viral target cells in the vagina and cervix, suggesting that the ratio of target c

68 was decreased in the laminae propriae of the vagina and cervix.

69 -fire endorectal probe was inserted into the vagina and directed toward the posterior vaginal wall.

70 message was invariantly expressed by normal vagina and ectocervix and inflamed fallopian tube, but v

71 lls and silence gene expression in the mouse vagina and ectocervix for at least nine days.

72 of the stratified squamous epithelium of the vagina and ectocervix, with the intensity of cellular st

73 he histologically comparable surfaces of the vagina and ectocervix.

74 e of Lactobacillus strains isolated from the vagina and enhances the color production of H(2)O(2)-pro

75 echanism that coordinates development of the vagina and feminization of the urethra, which may accoun

76 Two sites, the vagina and gastrointestinal tract, are highlighted to ex

77 were the least stable, whereas those in the vagina and gut were the most stable.

78 aginal development, including an imperforate vagina and hydrometrocolpos.

79 some females characterized by an imperforate vagina and hydrometrocolpos.

80 it is unknown whether ZIKV replicates in the vagina and impacts the unborn fetus.

81 reased the number of IgG plasma cells in the vagina and increased vaginal secretion/serum titer ratio

82 ell types in the oviduct, uterus, cervix and vagina and is dependent upon specific mesenchymal-epithe

83 oundary structure between the uterus and the vagina and is key for the maintenance of pregnancy and t

84 de (H(2)O(2))-producing species found in the vagina and is under development as a probiotic for the t

85 meters both into the posterior fornix of the vagina and on the skin at the beam entrance site.

86 These may be adapted to the vagina and possess characteristics enabling them to thri

87 tion defined as reduced bacterial numbers in vagina and prevention of pathological changes in the upp

88 Upon infection, pDCs are recruited to the vagina and produce large amounts of type I IFNs in a TLR

89 suggest that the mucosal environments of the vagina and rectum both impose a strong selection for the

90 Cocolonization of the vagina and rectum by H(2)O(2)-producing lactobacilli was

91 ctions of challenge virus replication in the vagina and reduced latent viral loads in dorsal root gan

92 of innervation of epithelium of the proximal vagina and reduced proportions of VIP, CGRP, and SP cont

93 that IgG viral antibody was produced in the vagina and released into vaginal secretions at 6 weeks a

94 including stratified squamous epithelia from vagina and skin, as well as cuboidal epithelium from lun

95 s, and can colonize the periurethral area or vagina and subsequently ascend through the urethra to th

96 essing high levels of CCR5 reside within the vagina and that these cells are preferentially targeted

97 acterised by an abnormal opening between the vagina and the bladder or rectum, which results in conti

98 he squamous epithelium of the ectocervix and vagina and the columnar epithelium of the endocervical c

99 tion of immune effector function between the vagina and the periphery.

100 hat telomerase activity, particularly in rat vagina and uterus, appears to be associated with a cell

101 avity and esophagus, gastrointestinal tract, vagina and vascular system of humans.

102 The small-cell carcinomas of the vagina and vulva need to be distinguished from Merkel ce

103 ecific concordance suggests that the cervix (vagina) and anus may serve as reservoirs for HPV infecti

104 cus, and groin) and their mothers (mouth and vagina) and were obtained from infants weekly until they

105 usly isolated from body sites other than the vagina, and (4) known bacteria formerly isolated from th

106 erforate anus with confluence of the rectum, vagina, and bladder in a urogenital sinus.

107 sentative UTI isolate present in the rectum, vagina, and bladder of a woman with UTI was chosen as th

108 Following analysis of primary cervix, vagina, and first-void female urine specimens for Chlamy

109 tices (cleaning with the fingers, wiping the vagina, and inserting traditional substances) are associ

110 aea have been isolated from the human colon, vagina, and oral cavity, but have not been established a

111 that can harmlessly colonize the human gut, vagina, and rectum but can also cause pneumonia, sepsis,

112 ains from the three body sites (oral cavity, vagina, and rectum), regardless of host conditions.

113 ntrations of bacteria present in the rectum, vagina, and small intestine.

114 cells of primitive neurons, the cervix, the vagina, and the endometrium in 5- to 400-fold higher num

115 cit functional and structural effects on the vagina, and therefore E4 appears promising as a therapeu

116 al tumor at all sites except paratesticular, vagina, and uterus, or with alveolar RMS were randomly a

117 ium, ovary, penis, prostate, rectum, testis, vagina, and vulva.

118 ell carcinomas of the cervix, ovary, uterus, vagina, and vulva.

119 ary lymphoid follicles in the ectocervix and vagina; and 3) concentrated on the path of virus entry b

120 carcinomas and premalignancies of the vulva, vagina, anus, and oropharynx.

121 e 16) can cause cancer of the cervix, vulva, vagina, anus, penis, and oropharynx.

122 outine Papanicolaou smears of cells from the vagina are commonly examined in women who have undergone

123 gulate development of the female urethra and vagina are largely unknown.

124 we demonstrated that these E4 effects on the vagina are mediated by nuclear ERalpha activation.

125 agement of cancers of the cervix, vulva, and vagina are reviewed.

126 Mucosal surfaces of the vagina are the portals for heterosexual transmission of

127 ns of peptide-containing nerves in the mouse vagina are unknown.

128 uding the oviducts, uterus, cervix and upper vagina, are derived from the Mullerian ducts, a pair of

129 innervate the distal urethra and the distal vagina, as well as the clitoris and perigenital skin and

130 f immunoglobulin G (IgG) plasma cells in the vagina at 6 weeks and 10 months after immunization, wher

131 hat vaginal lactobacilli could reacidify the vagina at the rate observed postcoitally following neutr

132 n serum and detectable levels of MAbs in the vagina at the time of infection, there was only modest p

133 rest in the vaginal stroma; as a result, the vagina becomes more vulnerable to pathogens.

134 HPV can be detected in the vagina before first sexual intercourse, highlighting the

135 have documented the detection of HPV in the vagina before first vaginal intercourse.

136 xynol 9 or a placebo film, inserted into the vagina before intercourse.

137 clear p63 protein was localized to the skin, vagina, bladder, urethra, and basal columnar cells of th

138 ation (> or =10(5) cfu/mL) of E. coli in the vagina (both, P<.001) and urine (all <10(5) cfu/mL; P=.0

139 duced a strong IgG response in the serum and vagina but was inefficient in generating a mucosal IgA r

140 rkedly reduced T cells in blood, spleen, and vagina, but major histocompatibility complex class II an

141 g sustained local drug concentrations in the vagina can be challenging, due to the high permeability

142 rgent epithelial cell differentiation in the vagina, cervix, and urinary tract.

143 lls were detected in the blood, lymph nodes, vagina, cervix, uterus, and fallopian tubes.

144 llenge with herpes simplex virus in skin and vagina challenge models, and were clearly superior to th

145 resulted in an inflammatory response in the vagina characterized by neutrophils and infiltrating sub

146 s significantly higher on CD4 cells from the vagina, compared with those from blood.

147 an initial elevation in myeloid cells in the vagina (day 3) and uterine horns (day 7), followed by a

148 Development of the vagina depends on sexual differentiation of the urogenit

149 Twenty-two patients had no discernible vagina (dimple or less).

150 estation and monthly after delivery from the vagina, distal gut, saliva, and tooth/gum.

151 yed bimodal (e.g., gut) or multimodal (e.g., vagina) distributions of sample abundances, but not all

152 r titers in the corneas, trigeminal ganglia, vaginas, dorsal root ganglia, spinal cords, and brains o

153 th contributing to the overall health of the vagina due to its direct and indirect effects on pathoge

154 applying antiseptic washes to the cervix and vagina during labor, are in progress.

155 es in elastic fiber homeostasis in the mouse vagina during pregnancy and parturition were determined.

156 In the adult vagina, E(2) induced expression of involucrin, a CCAAT/e

157 Epithelial cells derived from normal human vagina, ectocervix, and endocervix expressed mRNA for TL

158 the kidney and the epithelial layers of the vagina, ectocervix, endocervix, uterus, and fallopian tu

159 -related changes in innervation of the mouse vagina, effecting the distribution of neuropeptides with

160 lassical theory of Mullerian origin of upper vagina fails to explain complex urogenital malformations

161 ed body sites (gut, skin, oral, airways, and vagina), focusing on interpersonal and intrapersonal var

162 w outlines the anatomy and physiology of the vagina, focussing on areas relevant to drug delivery.

163 f K5-expressing tissues, including the skin, vagina, forestomach, and odontogenic epithelium.

164 omized rats (very low proliferation) than in vagina from ovariectomized and estradiol-treated rats (h

165 The high telomerase levels observed in vagina from ovariectomized rats indicates that the same

166 re compared from the lymph nodes, blood, and vagina from uninfected and simian immunodeficiency virus

167 ward nanoparticle-based drug delivery in the vagina has been focused on HIV prevention, strategies fo

168 anti-candida host defence mechanisms in the vagina has developed slowly and, despite a growing list

169 Epithelial delivery of medication across the vagina has proven successful for administration of small

170 Normal vaginas have stratified epithelium and normal uteri have

171 ccurs when semen temporarily neutralizes the vagina, HIV maintained its native surface charge and dif

172 se to the prostate in the male and the sinus vagina in the embryonic female.

173 We compared cervical and vulvar areas of the vagina in young nullipara and older multipara C57Bl/6 mi

174 le lower reproductive tracts (ie, cervix and vagina) in the human papillomavirus transgenic mouse mod

175 mmunolabeling of ganglia associated with the vagina indicated the likely origin of some peptidergic f

176 Entry of bacteria from the vagina into the uterus raises the question of uterine ep

177 areas in intravaginal drug delivery, but the vagina is a challenging route of administration, due to

178 In women, a healthy, patent vagina is important for the maintenance of a good qualit

179 The vagina is innervated by a complex arrangement of sensory

180 that a similar acute PMN migration into the vagina is mediated by chemotactic S100A8 and S100A9 alar

181 ermine the prevalence of each species in the vagina, its association with BV, and the utility of PCR

182 When disks were placed in the vagina, large amounts of III-174 (5 to 3,000 ng) were re

183 oliferation and indicators of cellularity in vagina, mammary gland, and uterus from virgin, pregnant,

184 The most common tumor sites were vagina (n = 7), pelvis/retroperitoneum (n = 6), and blad

185 sitive at the mouth, n = 26; positive at the vagina, n = 18; positive at both sites, n = 10) at the t

186 tivity was significantly higher (P=0.003) in vagina obtained from ovariectomized rats (very low proli

187 atients (4.6%), of which mesh erosion to the vagina occurred in 7 patients (1.3%).

188 t to establish a productive infection in the vagina of 75% +/- 17% and in the spinal cord of 71% +/-

189 s) is a commensal of the human intestine and vagina of adult women but is the leading cause of invasi

190 the controlled release of lactic acid in the vagina of BV-infected women.

191 f herpesvirus entry mediator nectin-1 in the vagina of human and mouse at different stages of their h

192 ological and functional impacts of E4 on the vagina of ovariectomized mice, and we determined the mol

193 Swab samples were obtained from the lower vagina of participants at admission for delivery and ino

194 the oviduct, uterus and upper region of the vagina of the female reproductive tract.

195 oduced no pregnancies because the uterus and vagina of the MOER female mice were extremely atrophic.

196 S. pneumoniae was recovered from the vagina of the mother on a swab culture collected prior t

197 quences were also found within the colon and vagina of the same animal, and within the peripheral blo

198 entical to the E. coli found in the urine or vagina of their sex partner.

199 gens isolated from the rectum, urine, and/or vagina of women with UTIs and 54 E. coli isolates from t

200 he three MAbs and were used to inoculate the vaginas of C3H/HeJ mice which had been pretreated with p

201 the amount of chlamydiae recovered from the vaginas of mice that had received the two IgG2b MAbs, E4

202 hydrogenase-C4 antibodies were placed in the vaginas of mice.

203 , activated mononuclear blood cells into the vaginas of mice; four hours later, numerous double-stain

204 ols used a pressure device placed within the vagina or anal canal, or electromyographic (EMG) sensors

205 ty of virus transmission when applied to the vagina or rectum of a person at risk of sexually acquiri

206 he vaginal apex below the upper third of the vagina, or anterior or posterior vaginal wall prolapse b

207 s in at least one of three body sites (nose, vagina, or anus), with approximately 9% colonized vagina

208 omplex, connective-tissue attachments of the vagina, or both, resulting in prolapse.

209 on the cervix, and distention of the uterus, vagina, or colon.

210 sites of keratinized epithelium, such as the vagina, or for adherence of these bacteria to damaged ep

211 cally and/or mucosally into the nose, mouth, vagina, or rectum in a 4-dose schedule, followed by 2 do

212 risk types to be first detected in the vulva/vagina (P = .03).

213 oof that Langerhans cells (LCs) in the human vagina participate in dissemination of infectious human

214 letion of CD4(+) T cells was observed in the vagina, particularly among the CCR5(+)CD4(+) subset.

215 ions obtained through the middle part of the vagina, perineal body, and anal canal.

216 ge seen in the Lactobacillus-dominated human vagina (pH 3.6 to 4.5 in most women).

217 and 49%; cervix plus vagina, 91 and 93%; and vagina plus urine, 94 and 79%.

218 ) were present at high concentrations in the vagina prior to treatment.

219 tious organisms (3 log(10)) from the cervico-vagina, produced a minimal inflammatory response in urog

220 ption factor for BMP4 signaling, was high in vagina-projecting sensory neurons after ovariectomy and

221 ry responses to infection in both cervix and vagina, recruits CD4(+) T cells to fuel this obligate ex

222 vical stroma, parametria and/or adnexae, and vagina, respectively, were 72%, 69%, 74%, and 85% for re

223 Specifically, HA depletion in the cervix and vagina resulted in inappropriate differentiation of epit

224 opening forms between a woman's bladder and vagina, resulting in urinary incontinence.

225 g single specimens, with the combined cervix-vagina results identifying the highest number of positiv

226 in sectioned murine lymph nodes draining the vagina revealed a profound cellular reorganization with

227 mmunocompartments matching blood, colon, and vagina samples from rhesus macaques were investigated.

228 or alpha, CXCL1, CCL2, CCL3, and CCL5 in the vagina, spinal cord, and/or brain stem than did wild-typ

229 lastin protein, and desmosine content in the vagina suggest that a burst of elastic fiber assembly an

230 e of the total number of lactobacilli in the vagina, suggest that vaginal lactobacilli could reacidif

231 quently identified in the cervix than in the vagina, suggesting that the expression levels of corecep

232 s and detectable levels of hemoglobin in the vagina, suggesting that the presence of hemoglobin in in

233 se (seeing/feeling a bulge in or outside the vagina) symptoms were assessed.

234 nsins (human neutrophil peptides 1-3) in the vagina than did uninfected women.

235 were more likely to be detected in the vulva/vagina than in the cervix (odds ratio, 4.38 [95% confide

236 significantly more T regulatory cells in the vagina than the unimmunized RM.

237 bition of challenge virus replication in the vagina than when the virus was used to vaccinate mice in

238 her E. coli to the urethra, periurethra, and vagina, the authors reasoned that uropathogenic E. coli

239 Of the 44 patients with a vagina, the mean length was 2.0 cm (range, 1.0-6.5 cm).

240 highly expressed in the epithelium of human vagina throughout the menstrual cycle, whereas the mouse

241 ions of the RT, persisting in the cervix and vagina throughout the menstrual cycle.

242 thmic anastomosis enabling continuity of the vagina to be preserved following insertion of an isthmic

243 emselves and/or by vaginal flora, causes the vagina to become acidic (pH approximately 4).

244 rom normal human endocervix, ectocervix, and vagina to characterize gonococcal epithelial interaction

245 sport of microbicides or immunogens from the vagina to local lymph organs is feasible.

246 Ascending infection from the colonized vagina to the normally sterile intrauterine cavity is a

247 osa explant model (endocervix and ectocervix/vagina) to mimic genital herpes infections caused by her

248 generally taught that LS does not affect the vagina, unlike lichen planus.

249 by-site, for primary melanomas of the vulva, vagina, urethra, ovary, and the uterine cervix.

250 nt mucosal antibody responses in the rectum, vagina, urine, seminal fluid, and blood.

251 report here the construction of a functional vagina using autologous cells expanded from a small vagi

252 nically significant anaerobes from the human vagina using conventional approaches with systematic mol

253 ells expressing viral RNA and protein in the vagina, uterus, and pelvic and mesenteric lymph nodes in

254 large bowel, resulting in protrusion of the vagina, uterus, or both.

255 rinary tract with adjacent organs namely the vagina, uterus, rectum and colon.

256 rinary tract with adjacent organs namely the vagina, uterus, rectum and colon.

257 strated tissue selectivity toward uterus and vagina versus breasts in a rodent model after oral admin

258 nd not seen in HPV-related precursors of the vagina, vulva, and penis further support the notion that

259 ral and nasal cavities, small intestine, and vagina was carried out in female rhesus macaques to dete

260 Fungal CFU in each vagina was determined to assess the severity of infectio

261 activity in the keratinized (differentiated) vagina was probably due to dilution of the number of tel

262 ound in human clitoral corpus cavernosum and vagina, we hypothesized that human arginase II is simila

263 cluding stool, oral gingiva, nares, skin and vagina were collected for each maternal-infant dyad.

264 s 14 days postinfection, both the uterus and vagina were found to be positive compared to those of sa

265 dermal LCs, the DCs in the epithelium of the vagina were found to be repopulated mainly by nonmonocyt

266 Also, lymphocyte numbers in the vagina were markedly but similarly increased by vaginal

267 s, the numbers of T and B lymphocytes in the vagina were similar in vaginally and parenterally immuni

268 Quantum dots instilled into the mouse vagina were transported across the vaginal mucosa into d

269 lamina propria of the cervical region of the vagina, where a higher number of fibers containing immun

270 ure downregulated RUNX1 in the fornix of the vagina, where DES-associated adenosis is frequently foun

271 iking homeotic transformation towards cervix/vagina, where Hoxa13 is normally expressed.

272 were pure NOTES, through a SILS port in the vagina, whereas TV cholecystectomies were hybrid procedu

273 p into the oviduct, uterus, cervix and upper vagina, whereas Wolffian ducts regress.

274 the Acien's hypothesis of Wolffian origin of vagina which explains the development of OHVIRA syndrome

275 s induced adenosis in the cranial portion of vagina, which mimicked the effect of developmental DES-e

276 bulin A chlamydia-specific antibodies in the vagina, while mice immunized with the detergent-extracte

277 igh levels of effector memory CD8 T cells in vagina, while the pool of memory T cells in spleen assum

278 aces of the oral cavity, rectum, cervix, and vagina with absorbent wicks.

279 and cytobrushes and from the ectocervix and vagina with cervicovaginal lavage.

280 he immune response was reoriented toward the vagina with strikingly higher CD8 T cell responses in th

281 communities in oral, nasal, stool, skin, and vagina, with Proteobacteria as the dominant phylum (60 %