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Titlebook: Germ Cell Protocols; Volume 1: Sperm and Heide Schatten Book 2004 Humana Press 2004 Activation.DNA.cryopreservation.electron microscopy.ge

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發(fā)表于 2025-3-21 17:59:56 | 只看該作者 |倒序瀏覽 |閱讀模式
書目名稱Germ Cell Protocols
副標題Volume 1: Sperm and
編輯Heide Schatten
視頻videohttp://file.papertrans.cn/385/384310/384310.mp4
概述Includes supplementary material:
叢書名稱Methods in Molecular Biology
圖書封面Titlebook: Germ Cell Protocols; Volume 1: Sperm and  Heide Schatten Book 2004 Humana Press 2004 Activation.DNA.cryopreservation.electron microscopy.ge
描述All sexually reproducing organisms produce primordial germ cells, a small population of cells that differentiate into gametes of either sex and carry to- potency, an ability to develop into an entire new organism. The study of germ cells has undergone enormous advances in recent years and has entered into an explosive phase of new discoveries with the introduction of transgenic te- nologies and nuclear cloning. Basic knowledge and techniques developed for lower vertebrate and invertebrate systems have facilitated the study of higher vertebrates, including humans. Many experiments that have first been performed on lower vertebrates provided the tools and strategies that could later be applied to other less readily available mammalian systems. The discovery of centrosomes in ascidians and sea urchin eggs now benefits studies of fertility and infertility in mammals. External in vitro fertilization, now a common technique in assisted fertilization, has only been possible as a result of numerous studies in lower systems in which external fertilization is natural. Egg activation, first explored in sea urchin and ascidian eggs, now benefits techniques designed to increase cl- ing efficien
出版日期Book 2004
關鍵詞Activation; DNA; cryopreservation; electron microscopy; genes; mammalian oocytes; reproducible techniques
版次1
doihttps://doi.org/10.1385/1592597440
isbn_softcover978-1-61737-374-9
isbn_ebook978-1-59259-744-4Series ISSN 1064-3745 Series E-ISSN 1940-6029
issn_series 1064-3745
copyrightHumana Press 2004
The information of publication is updating

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Stallion Spermatozoa Viability,ong ejaculates collected from the same stallion (.,.). Spermatozoa concentration, total volume, motility, percent live spermatozoa, and percent normal spermatozoa can range greatly (.), and any or all may have an effect on the ability of the ejaculate to fertilize. Cryopreservation of semen results
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Visualization of Sperm Accessory Structures in the Mammalian Spermatids, Spermatozoa, and Zygotes bosomes into the fertile environment of oocyte cytoplasm. Much less attention has been paid to the events that occur between gamete fusion and first embryonic cleavage. The interaction of the mammalian spermatozoa with the oocyte during and after gamete fusion is a complex and meticulously orchestrat
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Detection of Human Papillomavirus DNA in Sperm Using Polymerase Chain Reaction,ased risk of genital tract neoplasia in women (.,.). Nucleic acid amplification techniques such as the polymerase chain reaction (PCR) have enabled the sensitive and specific detection of HPV DNA in many different bodily fluids and tissues (.–.). Although HPVs were first detected in semen in 1986 (.
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