蛻膜的 的英文怎麼說
中文拼音 [tuìmóde]
蛻膜的
英文
decidual-
Especially, at the site of implantation of day 5, 6, uterine stroma cell apposing the preimplantation blastocyst changed into the decidual cells and displayed a distinct immunostaining of phospho mapk. western - blot results showed p44 express stronger than p42 did, with both their peak expression were observed on day 5, during the period of uterine decidualization
上述結果表明, ma衛k的激活與子宮內膜的接受性及蛻膜的形成有密切關系,推測mapk級聯通路激活對蛻膜化十分重要,蛻膜化可能與egf尼gfr直接或間接激活erk有關。Quantitative determine of real - time fluorescent pcr on the expression of leukemia inhibitory factor in early pregnant decidua
測定早孕子宮蛻膜白血病抑制因子的研究Ppar8 was expressed in the decidua under artificial decidualization, while was not detected in the luminal epithelium of control uterus horn
未蛻膜化的子宮腔上皮中ppar弱表達,而在人工誘導蛻膜化的子宮蛻膜中強表達。More recently, the laboratory has focused on natural killer cells and their roles in peripheral blood and in the pregnant uterine decidua
最近,實驗室已經把目光投向了自然殺傷細胞以及它們在外周血和懷孕時子宮蛻膜中的作用。In contrast, ep2 immunostaining was strong in the luminal epithelium and glandular epithelium under delayed implantation and reinitiation of implantation
在第6 - 9天的子宮蛻膜區和胚胎上, ep2免疫染色較弱或檢測不到。The aim of this study is to examine stat3 expression and activation in mouse uterus during early pregnancy, pseudopregnancy, delayed implantation, artificial decidualization and steroid hormonal treatments by situ hybridization and immunohistochemistry
本實驗以小鼠為材料,利用原位雜交和免疫組化等方法,並採用假孕、延遲著床、人工蛻膜化及激素處理等模型,研究了stat3基因在早期妊娠子宮中的表達與調節。The aim of this study was to examine ppar5 expression in rat and mouse uterus during early pregnancy, pseudopregnancy, delayed implanation, artificial decidualization and regulation by steroid hormone treatment by in situ hybridization and inununohistochemisny the expression of ppar gene in preimplanation embryo was also determined by rt - pcr
本實驗以大鼠和小鼠為材料,利用原位雜交和免疫組化方法檢測了ppar基因在早期妊娠子宮中的表達,並利用假孕、延遲著床、人工蛻膜化及激素處理等模型研究ppar基因在子宮中的表達與調節。There was a strong level of both cpges mrna signal and immunostaining in the decidualized cells under artificial decidualization, while only a basal level of cpges mrna signal and immunostaining was seen in the control
在人工誘導蛻膜化的子宮中, cpges蛋白和mana在蛻膜中表達很強,而在對照組的子宮中, cpges蛋白和mrna在腔上皮中僅有微弱的表達。In conclusion, these results suggest that ppar8 expression is closely related to embryo implantation and decidualization
這些結果表明, ppar基因的表達與大鼠和小鼠胚胎著床及蛻膜化過程緊密相關。In conclusion, these results suggest that the expression and activation of stat3 may play an important role during embryo implantation and decidualization
總之, staf3的表達及激活可能在小鼠的胚胎著床和蛻膜化過積中起巫要作川。In summary, the specifical expression of both mpges and cpges at the implantation site and in the decidual cells suggests that mpges and cpges might play an important role during mouse implantation and decidualization. ph. d. student : ni hua major : animal histology and embryology supervisor : professor yang zeng - ming
Mpges和cpges在小鼠子宮胚胎著床點處的特異性表達以及在蛻膜中的高水平表達說明, mpges和cpges在小鼠胚胎著床和蛻膜化過程中可能具有重要作用。Change of decidual tissue lymphocyte transforming ratio and activity of cytokines
妊高征患者蛻膜組織中淋巴細胞轉化率及細胞因子活性的變化There were detectable expression and tyrosine - phosphorylation of stat3 in the decidual cells on days 5 and 6 of pregnancy
在妊娠第5 6天的蛻膜化基質細胞中可檢測到stat3表達及酪氨酸磷酸化。The aim of this study was to investigate the differential expression of mpges and cpges in mouse uterus during early pregnancy and its regulation under different conditions by in situ hybridization and immunohistochemistry. mpges expression in the preimplantation mouse embryos was also performed by reverse transcription pcr ( rt - pcr )
本實驗首先利用原位雜交和免疫細胞化學的方法,檢測小鼠正常妊娠1 - 8天子宮中mpges和cpges的表達情況,並利用假孕、延遲著床和人工誘導蛻膜化等模型研究mpges和cpges的表達及其調節。Expression of matrix metalloproteinase by luminex xmap in co - cultured system of decidual cells and cytotrophoblasts
液相蛋白晶元法測蛻膜細胞與滋養層細胞共培養體系中基質金屬蛋白酶的表達Is important for implantation and decidualization. the aim of this study was to examine the expression and regulation of ep2 gene in rat uterus during early pregnancy, and under delayed implantation and artificial decidualization by in situ hybridization and immunohistochemistry
本實驗利用原位雜交和免疫細胞化學方法,檢測了ep2基因在大鼠早期妊娠子宮中的表達,並利用延遲著床和人工蛻膜化模型研究了ep _ 2基因在子宮中的表達與調節。The signals for both cpges mrna and immunostaining were strongly detected in the decidualized cells from days 6 - 8 of pregnancy
在妊娠7 - 8天的次級蛻膜和胚胎上有較強的cpgesmrna表達。However, mpges mrna and protein were highly expressed in the stroma immediately surrounding the blastocyst, but not in the luminal epithelium on day 5 of pregnancy
Mpgesmrna在妊娠6 - 8天的蛻膜中表達,並且隨著蛻膜化程度的加強, mpgesmrna的表達也加強。The expression and tyrosine - phosphorylation of stat3 in the uterus of artificial decidualization were similar to that in day 8 uterus, implying that stat3 is closely related to decidualization
人工誘導蛻膜化的子宮中, stat3的表達及酪氨酸磷酸化形式與妊娠第8天的子宮中相似,表明stat3與小鼠的蛻膜化過程密切相關。From days 6 to 8 of pregnancy, the signals for mpges mrna and protein were strongly detected in the decidualized cells. mpges mrna and protein were also highly expressed in the artificially decidualized cells, but not in the control horn
在人工誘導蛻膜化的子宮中, mpges蛋白和mrna在蛻膜中表達很強,但在對照組的子宮中,沒有檢測到mpges蛋白和mrna的表達。分享友人