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1 n hormone receptor type 2 (Amhr2)-Cre causes oviductal and myometrial defects.
2                        The meiotic status of oviductal and remaining follicular oocytes was evaluated
3 strated in the oviduct epithelium and in the oviductal and uterine fluids in different stages of the
4 y Western-blot and proteomic analyses of the oviductal and uterine fluids.
5      Using cryopreserved semen, laparoscopic oviductal artificial insemination was performed on three
6 tudy, we assessed the effect of E(2) on each oviductal cell type, using an ovariectomized-hormone-rep
7               In summary, we have shown that oviductal cell types, including epithelial, stromal, and
8 luate embryo location along the longitudinal oviductal-cervical axis of murine uteri.
9 wever, selective ablation of CTNNB1 from the oviductal ciliated cells did not affect embryo transport
10                                    Defective oviductal embryo transport arising from aberrant endocan
11                                     Impaired oviductal embryo transport is also observed in wild-type
12 contraction and relaxation crucial to normal oviductal embryo transport.
13 es of the female reproductive tract, such as oviductal, endometrial and cervical epithelia, and show
14 evelopment; hence, accelerated ageing of the oviductal environment could have important implications
15 completely understood how E(2) regulates the oviductal environment in vivo.
16 ture anaphase II onset upon removal from the oviductal environment.
17 PR-Cas9 to knock out the oncogene p53 in dog oviductal epithelia cultured in a dynamic microfluidic c
18 on of the R273H p53 mutant protein in murine oviductal epithelial (MOE) cells enhanced proliferation
19 and was also increased in FT explants and in oviductal epithelial cell line OE-E6/E7 infected with C.
20    We tested that hypothesis by infecting an oviductal epithelial cell line with C muridarum, followe
21                        FT explants (n=4) and oviductal epithelial cells (cell line OE-E6/E7) were tre
22 ted that disruption of estrogen signaling in oviductal epithelial cells alters ciliary function and i
23 hat ciliary length and beat frequency of the oviductal epithelial cells are regulated through estroge
24 the classical progesterone receptor (Pgr) in oviductal epithelial cells, called the Pgr(d/d) mouse mo
25                   Adgrd1 is expressed on the oviductal epithelium and the post-ovulatory attenuation
26 ype showed significantly enhanced binding to oviductal epithelium.
27 e the promotion of flagellar detachment from oviductal epithelium.
28 -head agglutination and lack affinity to the oviductal epithelium.
29 area between the OSE, mesothelium and tubal (oviductal) epithelium, as a previously unrecognized stem
30                These findings indicated that oviductal EVs mediate sperm function and fertilization i
31           Here, we examined the influence of oviductal EVs on sperm function in the domestic cat.
32                                              Oviductal extracellular vesicle proteins from pregnant s
33                              The presence of oviductal extracellular vesicles (oEVs, also called ovid
34 vine oocytes by examining the role of bovine oviductal fluid and species-specific oviductal glycoprot
35     In this study, we isolated oEVs from the oviductal fluid at estrus and different stages of early
36     Our findings demonstrate that regulating oviductal fluid flow by Adgrd1 controls embryo transit a
37                        However, contact with oviductal fluid or bovine, murine, or human OVGP1, confe
38 port, the other relatively simple (synthetic oviductal fluid plus albumin).
39 d coitus in female mice; prolactin-triggered oviductal fluid secretion clears the oviduct of debris,
40                     Abundant proteins in the oviductal fluid were differentially observed between nat
41 h contains 5.5 mM d-glucose, or in synthetic oviductal fluid, in the presence but not in the absence
42 ased on the electrolyte concentration of the oviductal fluid.
43                                              Oviductal gene expression was assayed at the RNA (quanti
44         Evidence suggests that gametes alter oviductal gene expression.
45                        Sperm lectins bind to oviductal glycans to form the reservoir.
46  bovine oviductal fluid and species-specific oviductal glycoprotein (OVGP1 or oviductin) from bovine,
47 -40, followed by macrophage chitotriosidase, oviductal glycoprotein, and macrophage YM-1.
48 sed integrated molecular characterization of oviductal HGSCs arising in the context of Brca1, Trp53,
49 e and humans produces uterine, cervical, and oviductal malformations.
50 ration with adrenergic receptors coordinates oviductal motility for normal journey of embryos into th
51 pendent technique, called Genome-editing via Oviductal Nucleic Acids Delivery (GONAD).
52 ped a method named GONAD (genome editing via oviductal nucleic acids delivery), which bypasses these
53                          Ovulation sites and oviductal oocytes were routinely observed in controls.
54 d by counting ovulation sites and collecting oviductal oocytes.
55  antimicrobial and antiinflammatory drugs on oviductal pathology in chronic chlamydial upper genital
56                         Thus, suppression of oviductal protease activity mediated by estrogen-epithel
57 rough cervical mucus, formation of the sperm oviductal reservoir, and sperm capacitation.
58 a multi-layered egg resulting from prolonged oviductal retention.
59  cell-tumor axis changes in a mouse model of oviductal serous carcinoma closely mirror those of human
60 nt cannabinoid signaling impedes coordinated oviductal smooth muscle contraction and relaxation cruci
61 ation, adenomyosis, and fibrosis, as well as oviductal smooth muscle hypertrophy.
62                                              Oviductal telomere length was assayed using Southern blo
63                                              Oviductal telomere length was reduced in the gestational
64  performed a multi-omics characterization of oviductal tissues utilizing bulk RNA-sequencing (RNA-seq
65 e infertility, in part because of defects in oviductal transport and reduced numbers of follicles.
66      Estrogen receptor alpha is required for oviductal transport of embryos.
67 one" required for normal embryo development, oviductal transport, implantation, and pregnancy (see th
68 h-/- mice rescued developmental defects, not oviductal transport, implying that embryonic and materna
69  for normal development of embryos and their oviductal transport.
70 -expression in HGSC cells and PTEN-deficient oviductal tumors may have the potential to induce apopto