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1 localisation patterns of PLCzeta within the sperm head.
2 -ribosylation to show the Gs presence in the sperm head.
3 ess is known about the source of cAMP in the sperm head.
4 odeling of the chromatin architecture of the sperm head.
5 lsations of the protrusion forming above the sperm head.
6 ing and condensation of the nucleus into the sperm head.
7 usters in the region of the membranes of the sperm head.
8 ound exclusively on the apical region of the sperm head.
9 and the shedding of binding proteins on the sperm head.
10 rs synchronously at a distinct region on the sperm head.
11 ocalization at the equatorial segment of the sperm head.
12 oplasmic structures required to elongate the sperm head.
13 ne-rich protamines to densely compact DNA in sperm heads.
14 implications for protamine-DNA packaging in sperm heads.
15 o rationalize the forces that package DNA in sperm heads.
16 anated sucrose gradient fractionated (Cs/Tx) sperm heads.
17 9 +/- 0.9 (n = 12) in eggs with four or more sperm heads.
18 FABP9(-/-) mice had significant increases in sperm head abnormalities (~8% greater than their WT coho
19 CNV in Y chromosome multicopy genes exhibit sperm head abnormalities and female-biased sex ratio.
20 enic males with, respectively, green and red sperm heads allowed us to unambiguously discriminate amo
21 logically abnormal with frequent loss of the sperm head and disorganization of flagellar structures,
22 ette, a microtubular organelle essential for sperm head and flagellar formation was disrupted in sper
23 sed on their identities and localizations in sperm head and flagellum, the putative functions of thes
24 specific interaction between (KDN)GM3 on the sperm head and Gg3 epitope (GalNAcbeta4Galbeta1-->) expr
25 ne and the nuclear envelope of the mammalian sperm head and is important for spermiogenesis and stabi
28 chanically obstruct the straightening of the sperm head and the stretching of the growing tail, leadi
29 e compaction of the paternal genome into the sperm head and to protect the DNA from damaging agents.
31 ot necessary for the initial swelling of the sperm heads and acquisition of Pol II but was required f
32 injection of unfertilized mouse oocytes with sperm heads and exogenous DNA encoding either a green fl
33 a urchin sperm is located at the base of the sperm head, and the flagellum extends from the mitochond
34 mbers of the PDI family were detected on the sperm head, and use of specific antibodies and substrate
38 alized to the equatorial region of wild-type sperm heads but was undetectable in sperm from patients
39 buted on the plasma membrane over the entire sperm head, but is found only on the posterior head once
40 d was shown to be present prominently at the sperm head by immunochemical staining with its specific
41 a negative regulator of capacitation in the sperm head by suppressing intracellular signaling pathwa
42 a male reproductive protein localized on the sperm head, comprising many domains known to be involved
43 -intact sperm on the anterior portion of the sperm head, concentrated in a thin band over the acrosom
44 an sperm resulted in a wave-like increase in sperm head cytosolic [Ca2+]i that appears to increase fa
45 lagellar bending and lateral movement of the sperm head during [Ca(2+)](i) peaks were markedly increa
46 The Ca2+ increase occurring in the human sperm head during the AR initiated by progesterone, a pu
47 reted into the epididymal lumen and binds to sperm heads during their transit through the epididymis.
48 ly, the number of annotated RNAs in the CsTx sperm heads exhibiting reduced peripheral enrichment was
49 Embryos derived after injecting oocytes with sperm heads from rehydrated freeze-dried and from thawed
50 termolecular disulfide bond formation in the sperm head generates multiple forms of zonadhesin with d
51 sidered and, in particular, cells with human sperm head geometries are well approximated by those wit
52 te oscillations increases with the number of sperm heads incorporated: 5.2 +/- 0.3 spikes per hour (m
54 e now report that injection of demembranated sperm heads into mouse oocytes efficiently induced Ca(2+
55 ys only a minor role in providing the murine sperm head its characteristic shape and is not absolutel
57 iodic oscillations; [Ca2+]i increases in the sperm head lag those in the tail and appear to result fr
58 in a complex breeding experiment showed that sperm head, mid-piece and flagellum length are heritable
60 is little sensitivity to the details of the sperm head morphologies considered and, in particular, c
62 iral ribbons', where the planar swing of the sperm head occurs on an osculating plane creating in som
63 uctive isolation, we expressed GFP or RFP in sperm heads of recently diverged sister species, Drosoph
64 Other heterologous injections, including sperm heads of the frog Rana pipiens and the zebrafish D
65 crescent, but are present elsewhere over the sperm head, often at the apical tip and equatorial segme
66 tivity and tmAC activity are detected in the sperm head, PKA is only found in the tail, where Adcy10
68 ue sperm motion, which we quantify using the sperm head's rolling rate, reflects sperm rotation that
69 t mouse, characterized by abnormal spermatid/sperm head shaping, we have determined that a deformity
72 t with green- and the second with red-tagged sperm heads) to demonstrate heritable variation in femal
73 e progesterone-mediated Ca2+ increase in the sperm head was strongly inhibited and the wave eliminate
75 have examined the behavior of demembranated sperm heads when injected into the germinal vesicle (GV)
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