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1 atient with advanced serous carcinoma of the ovary.
2 ok kinase-dependent manner in the Drosophila ovary.
3 rge germ line-derived nurse cells within the ovary.
4 patients with papillary serous tumors of the ovary.
5 cking ovarian cancer cell recruitment to the ovary.
6 ughout the reproductive tract, from labia to ovary.
7 he overall nuclear level of actin within the ovary.
8 arachidonate 15-lipoxygenaseP< 0.05) in the ovary.
9 istic organogenetic fates, the testis or the ovary.
10 es with transposon suppression in Drosophila ovary.
11 ns of the various constituent tissues of the ovary.
12 on and bcd gene copy number expansion in the ovary.
13 line, indicating increased DNA damage in the ovary.
14 on progenitor development in the Drosophila ovary.
15 n HT suppressed plants, but not to reach the ovary.
16 vidual follicles and corpora lutea in intact ovaries.
17 wth and stimulates estrogen synthesis in the ovaries.
18 tients undergoing treatments that ablate the ovaries.
19 ter in the chromatin of embryonic testes and ovaries.
20 sociated with defective ovulation in treated ovaries.
21 eavage by cell wall invertases in developing ovaries.
22 arp), to the mitochondrial outer membrane in ovaries.
23 floridae, was especially intense in the ripe ovaries.
24 GLI1 was significantly higher in testis than ovaries.
25 oocyte cyclic AMP (cAMP) levels in perinatal ovaries.
26 ded the stigmas and styles, occasionally the ovaries.
27 -cadherin junctions between oocytes in mouse ovaries.
28 mordial follicle formation in cultured mouse ovaries.
29 ere highly expressed in oocytes in perinatal ovaries.
30 showed that miR160 is abundant in developing ovaries.
31 obably after the switch to abortion of these ovaries.
32 sis frequently found in postmenopausal human ovaries.
33 biogenesis pathways in developing Drosophila ovaries.
34 s of cancer cells present relative to intact ovaries.
35 in mitochondria of adrenal glands and gonads/ovaries.
36 regulates PF formation in developing hamster ovaries.
37 of the testes and somatic cells of embryonic ovaries.
38 temperature to estrogen causes it to develop ovaries.
39 future studies on normal and diseased human ovaries.
40 maintenance of the functional reconstructed ovaries.
41 cultured testes and increased Sox9 levels in ovaries.
42 duction in the uptake of vitellogenin by the ovaries.
43 %), nonmelanoma skin (43%; 95% CI, 26%-59%), ovary (39%; 95% CI, 23%-55%), kidney (38%; 95% CI, 21%-5
46 rstitial fibrosis and collagen deposition in ovaries, accompanied by a reduction in TGF-beta1 express
49 study, we found that deletion of Wt1 in the ovary after sex determination caused ectopic development
50 reased lung VACV titers and dissemination to ovaries and a significantly shorter mean time to death c
53 ced the protein and glycerin contents in the ovaries and fat bodies of JGM + dsAtgl females required
54 A sequencing to analyze the transcriptome of ovaries and fruit tissues of the wild tomato species Sol
55 which suppresses the development of workers' ovaries and if she is removed, workers can transition to
56 lar changes occurred in silks rather than in ovaries and involved genes affecting expansive growth ra
57 s-oocyte complexes derived from immature pig ovaries and provides a twofold increase in the efficienc
58 e development whereas F2 females had smaller ovaries and reduced follicle numbers during puberty/adul
60 tosoma mansoni in-depth we isolated complete ovaries and testes from paired and unpaired schistosomes
61 67 first trimester human embryonic and fetal ovaries and testis and confirmed by qPCR and immunohisto
66 , disseminate as carcinomas that involve the ovary and extraovarian sites, which probably accounts fo
68 two sources: Wt1(+) cells indigenous to the ovary and Gli1(+) mesenchymal cells that migrate from th
70 istinct expression patterns in the embryonic ovary and interact with each other and other oocyte-spec
71 itoes, it is essential for maturation of the ovary and normal male reproductive behavior, but how JH
72 ecific growth of maturing oocytes within the ovary and permits the presence of sub-populations of ooc
73 ycopersicum pollen tubes to penetrate to the ovary and produce hybrids that, otherwise, would be diff
74 of luteinizing hormone (LH) that acts on the ovary and triggers the rupture of the preovulatory ovari
75 ign extraovarian lesions that implant on the ovary and which can subsequently undergo malignant trans
76 bryo sacs derived from nucellar cells of the ovary and, by parthenogenesis, the development of the un
77 duced oocytes ovulated (3.8 vs. 16.4 oocytes/ovary) and smaller litters (4.29 +/- l.02 vs. 8.50 pups/
78 get mutations in various somatic tissues and ovaries, and demonstrated that injection of zygotes with
80 stably colonizes the mosquito midgut, female ovaries, and male accessory glands and spreads rapidly t
81 anscript abundance of PsACS and PsACO in the ovaries, and PsACO in the pedicels was correlated with h
82 piroplasma density was higher in testes than ovaries, and was significantly higher density in live ve
83 nriched in embryos, exclusively expressed in ovaries, and when silenced, dramatically increased bug f
84 QuIC seeding activity in uterus, placentome, ovary, and amniotic fluid but not in allantoic fluids ha
85 denocarcinoma, and squamous cell carcinoma), ovary, and bladder, as well as leukemia, multiple myelom
90 fail to preserve the natural function of the ovaries as a source of hormones that regulate many aspec
94 e somatically male-biased, whereas autosomal ovary-biased miRNAs are female-biased, possibly due to b
97 vation of primordial follicles in artificial ovaries can result in further rapid loss of germ cells.
100 s, we have analyzed the relationship between ovary cell number and the final size of ovaries and berr
101 based on the comet assay for Chinese hamster ovary cells (assesses the level of DNA strand breaks).
102 zebrafish (Danio rerio) and Chinese hamster ovary cells (CHO) was investigated with specific emphasi
103 mologs that are expressed in Chinese hamster ovary cells (DPY19L1, DPY19L3, and DPY19L4) and compleme
104 s from channels expressed in Chinese Hamster Ovary Cells at different temperatures (32, 37, and 40 de
105 human receptors expressed in Chinese hamster ovary cells demonstrate that NDD-713 and -825 have nanom
106 a1-adrenoceptor expressed in Chinese hamster ovary cells revealed negative cooperative interactions b
109 Transport was measured in Chinese hamster ovary cells that stably expressed the human ortholog of
110 heterologously expressed in Chinese hamster ovary cells, supporting our findings in DRG neurons.
111 14 +/- 0.44 nM) expressed in Chinese hamster ovary cells, the binding being reversible and competitiv
113 trated from both E. coli and Chinese hamster ovaries (CHO) cell expression platforms; however, isotop
115 m to image endogenous H2S in Chinese hamster ovary (CHO) cells and use the developed constructs to re
116 urrent when transfected into Chinese hamster ovary (CHO) cells but, surprisingly, exerted "chaperone-
117 al mouse cardiac myocytes or Chinese hamster ovary (CHO) cells expressing the mouse or human subunits
118 valuated the genotoxicity to Chinese hamster ovary (CHO) cells induced by municipal secondary wastewa
120 Treatment of fibroblasts or Chinese hamster ovary (CHO) cells with 25OH caused a 50-70% reduction in
121 tosolic G protein by 350% in Chinese hamster ovary (CHO) cells with genetically induced expression of
122 ciferase reporter fusions in Chinese hamster ovary (CHO) cells, where the putative cis element requir
128 s inhibited proliferation of Chinese hamster ovary (CHO) sublines expressing folate receptors (FRs) a
129 rmed on mouse myeloma SP2/0, Chinese hamster ovary (CHO), and human embryonic kidney (HEK) cells in o
131 is linked to the differential development of ovary cohorts along the ear and to the timing of silk em
133 first silk emergence, simultaneously for all ovary cohorts, versus 7 to 8 d in well-watered plants.
135 ndergoing surgery for cancer of the bladder, ovary, colon and/or rectum, pancreas, or stomach (P < .0
136 menopause (NM), hysterectomy with at least 1 ovary conserved (HOC), or hysterectomy with bilateral oo
138 Multiple labs have reported that mammalian ovaries contain oogonial stem cells (OSCs), which can di
141 e at the tip of the ovariole of a Drosophila ovary, contains two follicle stem cells (FSCs) that unde
142 ell lines (OVCAR3 and A2780), normal hamster ovary control cells (CHOK1) and alphavbeta3-deficient or
143 Further progress is needed before whole-ovary cryopreservation can be considered an option for s
144 n of biophysical methods as well as cell and ovary culture experiments we explain how TAp63alpha is k
146 A polymerase II in wild-type and piwi mutant ovaries demonstrates that Piwi binds a conserved DNA mot
147 iCre conditional knockout (Setd1b(Gdf9) cKO) ovaries develop through all stages; however, follicular
148 may be invented for non-lethal prediction of ovary development and sex because only a small amount of
149 resent work, we developed regression between ovary development and three ribosome RNA (rRNA) indexes,
150 nstrating species-specific quantification of ovary development can be established in species with eit
155 novel regulator of tissue remodeling in the ovary during oocyte cyst breakdown and folliculogenesis.
156 essed protein expression and localisation in ovaries, embryos, pupae or adults by stainings and live
157 follicle stem cells (FSCs) of the Drosophila ovary, Epidermal Growth Factor Receptor (EGFR) signaling
160 somatic cells and showed that reconstituted ovaries exhibited folliculogenesis after transplantation
161 y active, oestrogen-secreting tumours of the ovary existing in two forms: the adult form and the even
162 nt with defective RLC assembly in taf11(-/-) ovary extract, we reconstituted the RLC in vitro using t
164 ndocrine loops between organ modules for the ovary, fallopian tube, uterus, cervix and liver, with a
166 se infection of flower organs and mimicry of ovary fertilization unveiled in this study guided the ri
167 are slow freezing and vitrification of whole ovary for fertility preservation purposes, in an ewe mod
168 rian insufficiency, which includes a lack of ovary formation, primary and secondary amenorrhoea as we
169 curve [AUC]) of the number of follicles per ovary (FPO) measuring 9 mm or smaller (FPO-9) and FPO me
171 that Notch signaling activity was altered in ovaries from Gas2 null mice around the time of birth and
172 Histopathological and functional analysis of ovaries from these mutant mice (Ctnnb1(ex3)cko) showed n
173 We demonstrate herein that, in the mouse ovary, GAS2 is expressed in the stromal cells surroundin
174 dge bases, and analysis of the covariance of ovary gene expression with surface water chemistry.
176 of adult, fertile Sox8(-/-) mice, testis-to-ovary genetic reprogramming occurs and Sertoli cells tra
181 or radiation, with potential exposure of the ovaries, have an increased risk of premature ovarian ins
183 ic and sex steroid hormones, small testes or ovaries, impaired spermatogenesis, and lack of ovulation
186 rhagic content was associated with nonviable ovaries in seven of 10 patients (70%) and with viable ov
187 lated the percentage of PFs in hamster fetal ovaries in vitro compared with either of the treatments
188 01915 was primarily detected in the mosquito ovary in association with follicular epithelial cells.
189 Hrp38-associated gene transcripts in the fly ovary, including mRNA of the translational repressor Nan
190 ve demonstrated that fragmentation of murine ovaries increases actin polymerization and disrupts Hipp
193 dy offers weight to the dogma that the adult ovary is populated by a fixed number of oocytes and that
194 Choriocarcinoma arising de novo from the ovary is very rare and only occasionally reported in the
195 rrestin recruitment assay in Chinese hamster ovary-K(1) cells expressing the long isoform of D(2)R (D
196 tion; however, in HEK293T or Chinese hamster ovary-K1 cells overexpressing M3R, pilocarpine induces C
202 female rainbow trout hypothalamus-pituitary-ovary-liver axis to use as a tool to help understand the
203 tissues, we detect ERbeta protein in testis, ovary, lymphoid cells, granulosa cell tumours, and a sub
204 RAME expression is limited to the testes and ovaries, making it a highly attractive cancer target.
205 n H. doenitzi, and that it is distributed in ovaries, malpighian tubules, salivary glands and midguts
206 cular transplantation of cryopreserved whole ovary may allow immediate revascularization, ensuring be
208 poptotic developmental PCD in the Drosophila ovary occurs by an alternative cell death program where
209 f reddish to "purple" discolored eggs in the ovaries of adult female blue catfish (Ictalurus furcatus
210 quential emergence of silks originating from ovaries of different cohorts along the ear with (2) one
215 hway in arthropods is best understood in the ovary of Drosophila melanogaster, where it acts to silen
221 ine with this, its down-regulation perturbed ovary patterning as indicated by the excessive elongatio
222 target, sly-miR160 regulates auxin-mediated ovary patterning as well as floral organ abscission and
224 erent human cancers, including human breast, ovary, prostate and brain cancer, due to amplification o
225 Germline stem cells (GSCs) in the Drosophila ovary provide an attractive model in which to study both
227 dysfunctional ovulation, classic polycystic ovaries, reduced large antral follicle health, and sever
230 it remains unclear how hysterectomy without ovary removal affects risk, whether menopausal hormone t
231 Premenopausal hysterectomy, even without ovary removal, may reduce the long-term risk of hormone
234 pment and sex because only a small amount of ovary sample (<50 mg) is needed for the approach establi
236 orrelated with higher ethylene evolution and ovary senescence and pedicel abscission in fruits that w
238 duced JH levels and consequent reductions of ovary size, egg production, and yolk deposition in matur
241 ation dynamics of FLEs-Hd appeared in female ovaries, suggesting that the symbiont may provide necess
242 assessment [HOMA]) in women with polycystic ovary syndrome (PCOS) and chronic periodontitis (CP).
243 1 (TIMP)-1 ratio in patients with polycystic ovary syndrome (PCOS) and systemically healthy controls
254 This would suggest that maternal polycystic ovary syndrome (PCOS), a condition associated with exces
255 stress, in the pathophysiology of polycystic ovary syndrome (PCOS), the most common endocrine disorde
260 ity of California, San Francisco, Polycystic Ovary Syndrome Multidisciplinary Clinic over a 6-year pe
262 adjustment for education, parity, polycystic ovary syndrome, energy intake, and physical activity.
263 ional qualification, nulliparity, polycystic ovary syndrome, physical activity, and body mass index.
264 d using a string of variations of polycystic ovary syndrome, therapy/treatment, and adolescence, and
265 was detected in mouse reproductive tissues (ovary, testis, and prostate) and lung and colon tissues
267 zymes of sugar metabolism occurred in apical ovaries that eventually aborted, but probably after the
268 cterium strain (AS1) isolated from Anopheles ovaries that stably colonizes the mosquito midgut, femal
269 e development of the Drosophila melanogaster ovary, the Hedgehog (Hh) gradient sets differential cell
271 essed in and have in vivo roles in postnatal ovaries, their expression and function in the embryonic
273 tegrity in late germ cells of the Drosophila ovary through Piwi-associated RNA-mediated repression of
274 cated the presence of Rickettsia bacteria in ovary tissue, indicating their maternal inheritance.
275 d significant deformation and degradation of ovary tissues and associated vitellogenin by the fungal
276 al temporal sensitivity of the fetus and its ovaries to EC mixtures has implications for adult ovaria
277 noclonal and unidirectional seeding from the ovary to intraperitoneal sites, and two patients demonst
279 iption factor can switch organ fate from the ovary to testis in mammals and represents the first miss
280 on, ovariectomized ARKO hosts with wild-type ovary transplants displayed normal estrous cycles and co
281 ough OSC-like cells can be isolated from the ovary using an antibody to DDX4, there is no good in sil
284 ived from receptacle tissues rather than the ovary wall which is more typical of fruiting plants.
285 Inhibition of mTORC1 or mTORC1/2 within ovaries was achieved during chemotherapy cotreatment, co
286 osynthesis gene expression in pre-pollinated ovaries was also associated with higher ethylene evoluti
287 Higher Spiroplasma density in testes than in ovaries was also detected by fluorescent in situ hybridi
288 he main portion of the gravid uterus and the ovaries was not seen on these images, but the parts that
291 month, the right ovary was removed, the left ovary was thawed/warmed, and its vessels were anastomose
292 ddress the role of Rspo1 expression in adult ovaries, we generated an Rspo1 gain-of-function mouse mo
293 Ovarian follicles in native and transplanted ovaries were counted and compared at study completion.
294 s striking phenotype originates in the pupal ovary, where the developing germarium is shaped by the b
295 ock of quiescent primordial follicles in the ovary which is gradually depleted during a woman's repro
296 Lack of MDI abolishes mtDNA replication in ovaries, which leads to mtDNA deficiency in mature eggs.
298 n, as judged by continuous anestrus, smaller ovaries with a decreased number of corpus luteum, and an
299 re is a rapid loss of oocytes postnatally in ovaries with combined loss of Sohlh1 and Sohlh2, meiosis
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