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Titlebook: Biology of Spermatogenesis and Spermatozoa in Mammals; Sardul S. Guraya Book 1987 Springer-Verlag Berlin Heidelberg 1987 biochemistry.biol

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期刊全称Biology of Spermatogenesis and Spermatozoa in Mammals
影响因子2023Sardul S. Guraya
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图书封面Titlebook: Biology of Spermatogenesis and Spermatozoa in Mammals;  Sardul S. Guraya Book 1987 Springer-Verlag Berlin Heidelberg 1987 biochemistry.biol
Pindex Book 1987
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Spermatids and Spermiogenesisrmiogenesis which ends when the spermatozoa are released from the seminiferous epithelium. After the haploid round spermatids are formed, their nuclear and cytoplasmic components undergo a complex series of morphological, histochemical and biochemical changes ending with the production of highly dif
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Headammals including marsupials (Guraya 1965, 1971a, Phillips 1975a, Harding et al. 1979, Sarafis et al. 1981, Holstein and Roosen-Runge 1981, Heath et al. 1983, Gledhill 1986). The spermatozoa of various primate species show, more or less, the same basic configuration of the head, except for some minor
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Neckhe mid-piece (Figs. 55 and 61) (Fawcett and Ito 1965, Zamboni et al. 1971, Fawcett 1975b, Phillips 1975a, Holstein and Roosen-Runge 1981, Sato and Oura 1985). The neck differs clearly from both the head and the tail in certain morphological features of the plasmalemma, a sharp demarcation of its upp
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Tailcrotubules) surrounded by an inner row of nine evenly spaced doublet microtubules, each with two rows of arms that project towards the adjacent doublet tubule, one row of radial spokes that radiate inwards towards the central pair of microtubules, and an outer ring of nine coarse longitudinal fibres
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Plasma Membrane and its Surface Componentshe molecular character of its surface is an important determinant of the spermatozoon’s ability to recognize and fuse with the egg (Shapiro 1984, Monroy and Rosati 1983, Peterson et al. 1985, O’Rand et al. 1984) and is the primary determinant of species specificity in fertilization. Therefore, durin
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