ライフサイエンスコーパス: sperm motility

1 unction is impaired through gross defects in sperm motility.

2 m tail suggest that CABYR may be involved in sperm motility.

3 mammalian sperm tail and it is essential for sperm motility.

4 ed to male sterility resulting from aberrant sperm motility.

5 An inhibitor blocks the suNCKX activity and sperm motility.

6 llum, suggesting a role in the regulation of sperm motility.

7 other known voltage-gated channels, regulate sperm motility.

8 evealing a critical role for this isoform in sperm motility.

9 lt of significantly reduced sperm output and sperm motility.

10 inhibition of this isoform alone eliminates sperm motility.

11 wever, sperm competition does require normal sperm motility.

12 e fertile and have no significant changes in sperm motility.

13 in the sperm flagellum believed to modulate sperm motility.

14 ture of the fibrous sheath or participate in sperm motility.

15 is important for the initiation of mammalian sperm motility.

16 CO3 (-) is a key factor in the regulation of sperm motility.

17 ncidence of retained nipples and compromised sperm motility.

18 able to fertilize oocytes and exhibited poor sperm motility.

19 onment within the oviduct, thereby affecting sperm motility.

20 paratus have strikingly different effects on sperm motility.

21 1 may play a role in acrosome biogenesis and sperm motility.

22 ility associated with defects in progressive sperm motility.

23 n between superoxide production and enhanced sperm motility.

24 additional cryoprotectants and CAT on fresh sperm motility.

25 exposure for cellular repair and increasing sperm motility.

26 and the brain, and flagella are required for sperm motility.

27 be critical for normal sperm morphology and sperm motility.

28 along the length of the flagellum to support sperm motility.

29 fertility associated with a complete loss of sperm motility.

30 round-headed sperm morphology and no forward sperm motility.

31 to play essential roles in the mechanics of sperm motility.

32 fy lipid regulators required for directional sperm motility.

33 ra block the activity of suPDE5 and increase sperm motility.

34 ed in the mitochondrial capsule and enhances sperm motility.

35 regulation and a novel cellular function in sperm motility.

36 cGMP levels in sperm, which in turn modulate sperm motility.

37 n species known to have cyclic AMP-dependent sperm motility.

38 he major Ca2+ channel (CatSper) required for sperm motility.

39 m cells, reduced sperm counts, and decreased sperm motility.

40 f the coagulum, semenogelin I, also inhibits sperm motility.

41 of a complex series of events that triggers sperm motility (2,7,8).

42 on of the CATSPER1 channel, which can affect sperm motility, an important determinant in sperm compet

43 ar function driven by selective pressures on sperm motility, an important determinant of male reprodu

44 The HCO3(-) anion activates sperm motility, an important early step in capacitation,

45 vating factor (PAF) has been shown to affect sperm motility and acrosomal function, thereby altering

46 s have revealed a wide range of variation in sperm motility and ATP production and that the laborator

47 inase A is thought to play a pivotal role in sperm motility and capacitation, the distinctive biochem

48 ion of decreased spermatozoa number, reduced sperm motility and defective acrosome formation.

49 2) male mutants are sterile and show reduced sperm motility and epididymal sperm counts.

50 s to examine the role of PKA localization in sperm motility and fertility.

51 perm membrane is modified, which facilitates sperm motility and fertility.

52 ermatozoa has been shown to be essential for sperm motility and fertility.

53 vity of the CHDH enzyme could have decreased sperm motility and fertility.

54 uid and in a dramatic but incomplete loss of sperm motility and fertilization capacity, raising the p

55 : 1) cryopreservation of coral sperm reduced sperm motility and fertilization success in half, thus f

56 vital to cAMP-mediated Ca2+ influx in sperm, sperm motility and fertilization.

57 pha4 deletion results in severe reduction in sperm motility and hyperactivation typical of sperm capa

58 ts also displayed a substantial reduction in sperm motility and infertility, whereas those carrying m

59 It is required for sperm motility and may reduce the risk of miscarriage.

60 h, focal spermatogenic anomalies, diminished sperm motility and subfertility.

61 y provide help to uncover the causes of poor sperm motility and suggest new approaches for novel trea

62 KA catalytic activity, is a key regulator of sperm motility and that disruption of this interaction u

63 indicates that its role may be conserved in sperm motility and that JAM-A may be a candidate gene fo

64 Here, we evaluate sperm motility and the proportion of sperm expressing PL

65 ycerol monolaurate (GML) to potently inhibit sperm motility and viability.

66 cell apoptosis and reduced sperm production, sperm motility, and fertility.

67 processes are important in the regulation of sperm motility, and gene targeting was used here to test

68 y lowered daily sperm production, in reduced sperm motility, and in several animals, in sloughing of

69 to inhibit protein kinase A phosphorylation, sperm motility, and in vitro fertilization.

70 ses including left-right axis determination, sperm motility, and photoreceptor maintenance.

71 Sperm counts, sperm motility, and sperm morphology were normal, as was

72 including the phagocytic respiratory burst, sperm motility, apoptosis, and metastatic cancer.

73 hat previously observed effects of microG on sperm motility are coupled to changes in phosphorylation

74 aphase II, cellular components essential for sperm motility are partitioned almost exclusively to the

75 es comprising the Ca2+-permeation pathway in sperm motility are poorly understood.

76 tics of protein tyrosine phosphorylation and sperm motility are unaltered in mutant sperm relative to

77 Male nipple retention and compromised sperm motility at 2,000x may have been secondary to redu

78 oxidative phosphorylation as ATP sources for sperm motility between mouse species that exhibit signif

79 4-Aminopyridine, a powerful modulator of sperm motility, both raised pHi and mobilized Ca(2+) sto

80 t functional terms, including fertilization, sperm motility, calcium channel regulation, and SNARE pr

81 n of IL17BR, rs1025689, is linked to altered sperm motility characteristics and changes in choline me

82 f sperm intracellular pH and Ca(2+) regulate sperm motility, chemotaxis, capacitation and the acrosom

83 Although Ascaris sperm motility closely resembles that seen in many other

84 Both the sperm motility defect and the lack of induced protein ty

85 andidate gene for the analysis of idiopathic sperm motility defects resulting in male subfertility in

86 Tpst2-deficient mice have male infertility, sperm motility defects, and possible abnormalities in sp

87 Coupling between protein phosphorylation and sperm motility during activation in microG and at 1 G wa

88 [Ca(2+)]i signaling regulates sperm motility, enabling switching between functionally

89 s were infertile and had profound defects in sperm motility, exhibiting sluggish movement without for

90 ins are implicated in Caenorhabditis elegans sperm motility (Fer-1), mammalian skeletal muscle develo

91 ever, there were significant improvements in sperm motility for men with study entry CD4 cell counts

92 r sperm concentration, increased progressive sperm motility generated more pyruvate conversion to lac

93 Both in humans and in animals, sperm motility has been used as a metric for the viabili

94 ess reaction in zebrafish sperm reducing its sperm motility in a concentration dependent manner (P<0.

95 Cyclic AMP stimulates sperm motility in a variety of mammalian species, but th

96 Studies of both survival after sepsis and sperm motility in human populations have shown significa

97 icular histology, daily sperm production and sperm motility in knock-out and wild-type mice.

98 the impaired fertility was due to diminished sperm motility in the Chdh(-/-) males.

99 Adenosine is a candidate modulator of sperm motility in the female reproductive tract that inc

100 ns the way for convenient bioassays based on sperm motility including at-home motile sperm tests.

101 studies suggest several roles for hAKAP82 in sperm motility, including the regulation of signal trans

102 Sperm motility initiation by SMIF depended on decreased

103 An egg chorion ligand termed "sperm motility initiation factor" (SMIF) induces motilit

104 Poor sperm motility is a common cause of male infertility for

105 Sperm motility is decreased markedly in CatSper-/- mice,

106 s imply that most of the energy required for sperm motility is generated by glycolysis rather than ox

107 ity of the fibrous sheath and that effective sperm motility is lost in the absence of AKAP4 because s

108 Sea urchin sperm motility is modulated by sperm-activating peptides

109 Sperm motility is powered by adenosine triphosphate but

110 Mammalian sperm motility is regulated by a cascade of cAMP-depende

111 en identified as a fusion gene formed from a sperm motility kinase and a ribosomal S6 kinase.

112 omains and also with other components of the sperm motility machinery.

113 he major sperm protein (MSP) -based nematode sperm-motility machinery resembles that observed with ri

114 (as shown in mouse) that susAC has a role in sperm motility, most probably through axonemal protein p

115 les and decreased the acrosome integrity and sperm motility of males.

116 in intermediate chain presumably involved in sperm motility, originated from complex genetic rearrang

117 itigated stress and maintained viability and sperm motility (P>0.05), whereas superoxide dismutase (S

118 Methanol (8%) reduced viability and sperm motility (P<0.05), but the addition of CAT mitigat

119 icient in these sensory neurons to influence sperm motility parameters.

120 hat this SNP is also associated with altered sperm motility patterns and dysmorphic mitochondrial str

121 The gene encodes a novel sperm motility protein.

122 en-quality endpoints, except between DFI and sperm motility (r = -0.65, P < 0.001).

123 rol of sAC and sNHE activities to facilitate sperm motility regulation.

124 ust penetrate both layers in steps requiring sperm motility, sperm surface enzymes, and probably sper

125 n decreased male fertility due to diminished sperm motility; sperm from Chdh(-/-) males have decrease

126 lated and other experiments revealed reduced sperm motility, survival time, and sperm count also cont

127 eostasis, resulting in substantially reduced sperm motility, swimming speed, and HCO3 (-)-enhanced be

128 A concentration was positively correlated to sperm motility, to sperm count, and to the desmosterol-t

129 ffect of 633 nm coherent, red laser light on sperm motility using a novel wavelet-based algorithm tha

130 Sperm motility, viability, fertilization and blastocyst

131 Sperm motility was negatively affected by both OA and co

132 Sperm motility was reduced severely, and approximately 6

133 lox15(-/-)) showed normalized fertility, and sperm motility was reimproved to wild-type levels.

134 Sperm motility was significantly reduced, and Taf7l(-/Y)

135 e relationship between energy metabolism and sperm motility we used dissolution Dynamic Nuclear Polar

136 Given the critical role of Ca(2+) for sperm motility, we propose a novel CRISP1-mediated fine-

137 role in acquisition of normal morphology and sperm motility when faced with hyperosmotic challenges,

138 nderstanding of the link between [Ca2+]i and sperm motility will only be gained by analysis of [Ca2+]

139 , function in oocytes to control directional sperm motility within the uterus.