Oocyte

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    TPEN can result in egg stimulation. The oocyte itself also appears to play a crucial role in the activation mechanism, the exact facts of which are yet to be properly understood. The capability to produce suitable Ca oscillations is acquired following fruitful oocyte maturation and involves several cytoplasmic changes. Evidence for this includes the fact that fertilized immature mouse oocytes generate fewer Ca transients of lower amplitude than do oocytes fertilized at MII. During

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    Oocyte production and quality Recent experimental animal studies report that BPA exposure affects oocyte quality, fertilization, and maturation (overview in Table 1), which is consistent with the previous findings (Peretz, et al., 2014). Low-dose BPA (50 μg/kg) was given orally to adult C57BL/6J mice and significantly decreased the percentage of fertilized oocytes without any ovulation changes (Moore-Ambriz et al., 2015). In the in vitro studies, it was reported that BPA treatment decreased meiosis

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    What activity during oocyte activation prevents penetration by additional sperm? There are to methods consisting of an electrical block and mechanical block, which prevents penetration of additional sperms during oocyte activation. Electrical block involves the absences of fertilization (the oocyte contains a negative charge within and the sperm a positive charge). For instance, if an oocyte comes into contact with a sperm the negative charge within the oocyte changes to positive resulting any other

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    Mos, MAPK, and p90Rsk (Sagata, 1989; Haccard et al., 1993; Bhatt and Ferrell, 1999; Gross et al., 1999). An oocyte-specific protein kinase, c-mos, plays an important role in up-regulating the activity of MPF at various stages of final oocyte maturation. Several studies suggest that the proper function of the c-mos-MPF system is associated with important features of the last stages of oocyte maturation such as the resumption of meiotic maturation, inhibition of DNA replication between meiosis I and

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    cells including: granulosa cells, cumulus cells, oocytes, and early embryos (ref more;(65,79,80)). Because leptin contributes to follicular growth, steroidogenesis, oocyte maturation and embryo development, hyperleptinemia seen in obese women may disrupt these processes (30,58,70,75,78,81-96). Similarly, insulin resistance and or hyperinsulinemia, have been shown to alter ovarian morphology, ovarian insulin signaling, ovulation and maturation of oocytes (23,30,36,39,40,71,73,74,97-107). Obesity leads

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    research and continual attempts at success. Therapeutic cloning is a process in which the cells of one person are manipulated into becoming the stem cells for another person through Somatic Cell Nuclear Transfer (SCNT). This process involves taking oocytes, or immature female egg cells that are generated during ovulation, incubating them in in vivo culture, and extracting the nucleus of such cells and replacing them with the the nucleus of another cell. This produces a stem cell with a genetic make-up

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    FSH Case Study

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    Follicular waves of different cattle species will result in a significantly different number of oocytes per wave. It is well known that many Bos Indicus breeds will produce significantly more follicles and embryos per OPU when compared to Bos Taurus breeds (Pontes et al. 2010). And within a breed, there will be significant differences between individual donors. In 2006, we followed 94 Holstein donors over 5 years and reported that 90% of these donors were lower potential animals which were donors

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    Follicle Simulation

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    Before the oocyte retrieval, woman follows a hormonal therapy for 9-14 days in order to achieve the maturation of as many follicles as possible. In order to induce ovulation, woman will be injected with chorionic gonadotropin 36 hours prior to the normal ovulation which will also promote follicle maturation. Oocyte retrieval will start 36 hours after the injection and will last 15-20 minutes. The whole procedure takes place in the surgery room which is designed in a unique way in order to communicate

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    its allotetraploid. Its modest and simple to keep them in the lab. Cell-Free concentrate from Xenopus oocyte is ideal for studding sub-atomic biology.Function of all early embryonic cell is known. incipient organisms are vulnerable to control. Egg generation can be evoked (chorionic gonadotropin) There are numerous approaches to study Xenopus yet principally in 3 classification: Embryonic Oocyte sans cell remove. Embryonic studies is Tissue transplant, single cell and germ layer dismemberment is

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    Before fertilization, mammalian oocytes are arrested in M II by an activity of cytostatic factor (CSF). APC/C is inhibited by CSF to prevent metaphase-anaphase transition and complete of meiosis II. Cyclin B and CDK2 control the establishment of CSF and Mos signaling pathway and also involve

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