ライフサイエンスコーパス: vas

1 ine was recruited to the posterior pole in a vas-dependent manner and is itself a polar granule compo

2 The ryanodine receptor (RyR) in aortic and vas deferens smooth muscle was localized using immunoflu

3 the peripheral and central SR in aortic and vas deferens smooth muscle.

4 Native alpha1A-ARs from rat tail artery and vas deferens are also desensitized by OXY, but not by NE

5 mooth muscle was investigated in bladder and vas deferens of mice carrying a targeted mutation in bot

6 riole as the sperm transits to the cauda and vas deferens in preparation for its climactic release.

7 intestines, lungs, pancreas, sweat ducts and vas deferens, among others.

8 m in an immotile state in the epididymis and vas deferens (2,4-6).

9 Clear cells of the epididymis and vas deferens contain abundant V-ATPase in their apical p

10 Wolffian duct and formed the epididymis and vas deferens, but failed to elaborate the efferent ductu

11 prostate, coagulating gland, epididymis, and vas deferens.

12 s (orchitis), epididymis (epididymitis), and vas deferens (vasitis).

13 The bigenic ampullary glands and vas deferens were extremely cystic, hypertrophic and hyp

14 s the lungs, pancreas, liver, intestine, and vas deferens.

15 meconium ileus (MI); pancreatic, liver, and vas deferens disease; and a predisposition to lung infec

16 MYPT1 in phasic rabbit portal vein (PV) and vas deferens (VD) smooth muscles.

17 y cirrhosis), sweat glands (heat shock), and vas deferens (infertility).

18 ion in precapillary arterioles in ureter and vas deferens.

19 Cultures from aorta, vas deferens, seminal vesicle, and kidney tissue were ch

20 Expression of a C. floridanum homolog (Cf-vas) of the germ cell marker Vasa indicated that the B(4

21 havior and sperm counts, but abnormal distal vas deferens convolution resulting in complete and incom

22 60 s with electrical field stimulation (EFS; vas deferens), dimethylphenylpiperazinium (chromaffin ce

23 se in P2X1 protein expression in Entpd1(-/-) vas deferens with no variation in mRNA levels.

24 In vitro, Entpd1(-/-) vas deferens displayed an exacerbated contraction to ATP

25 As a result, the epididymis, vas deferens and efferent ductules were largely absent i

26 ation of Wolffian ducts into the epididymis, vas deferens and seminal vesicle.

27 specific structures such as the epididymis, vas deferens, and seminal vesicle from a straight Wolffi

28 ere detected in epithelia of the epididymis, vas deferens, coagulating gland, preputial gland and sal

29 3.7% versus 33.2% +/- 10.3% (P < 0.0001) for vas deferens sperm and 40.1% +/- 9.6% versus 33.2% +/- 7

30 Furthermore, vas transcript was detected in a novel pattern, localize

31 focal biliary cirrhosis, micro-gallbladder, vas deferens loss, airway disease, and meconium ileus.

32 ents in single cells from the Syrian hamster vas deferens cell line DDT1MF-2 were investigated using

33 m agonist exposure (0.5-4 hr) in the hamster vas deferens smooth muscle cell line (DDT1MF-2 cells).

34 structures (e.g., uterus in hermaphrodites, vas deferens in males).

35 ting revealed that zebrafish vasa homologue (vas) transcript is present in embryos just after fertili

36 dorsalize the egg chamber can accumulate in vas mutants, if fs(1)K10 is also mutant.

37 Mutations in vas homologs in other bacterial species have been report

38 ]Norepinephrine release studies performed in vas deferens confirmed these findings.

39 actile response to electrical stimulation in vas deferens from alpha2B-AR knockout, alpha2C-AR knocko

40 s, present on many excitable cells including vas deferens smooth muscle cells.

41 st functional activity in the mouse isolated vas deferens (MVD) and guinea pig isolated ileum (GPI) a

42 NCTs) in smooth muscle of the mouse isolated vas deferens has been used to detect the packeted releas

43 ly-evoked contractions of the mouse isolated vas deferens when administered at submicromolar concentr

44 c nerve terminals in the guinea-pig isolated vas deferens.

45 lpha2-AR function was tested in two isolated vas deferens preparations.

46 vity in the guinea pig ileum (GPI) and mouse vas deferens (MVD) functional bioassays were determined

47 dies in the guinea pig ileum (GPI) and mouse vas deferens (MVD) preparations.

48 itro on the guinea pig ileum (GPI) and mouse vas deferens (MVD) preparations.

49 ssays using guinea pig ileum (GPI) and mouse vas deferens (MVD) smooth muscle preparations.

50 ro (guinea pig ileum assay) and delta (mouse vas deferens assay) opioid receptors, respectively.

51 or-induced gene (FR-1) (80% identity), mouse vas deferens protein (MVDP) (76%), and human aldose redu

52 t Phe3 was required for bioactivity in mouse vas deferens but not for interaction with delta opioid r

53 ganglionic sympathetic axon bundles in mouse vas deferens have been characterized using confocal micr

54 e terminals and smooth muscle cells in mouse vas deferens were loaded with the Ca2+ indicator Oregon

55 he compounds described in the isolated mouse vas deferens and guinea pig ileum bioassays revealed tha

56 ctivity toward delta-opioid receptors (mouse vas deferens) and produced analgesia in mice in a naloxo

57 tional assays (electrically stimulated mouse vas deferens and guinea pig ileum).

58 was devoid of agonist activity in the mouse vas deferens (MVD) and guinea pig ileum (GPI) preparatio

59 of the guinea pig ileum (GPI) and the mouse vas deferens (MVD) with EC50 values of 1.82 +/- 0.16 and

60 Evaluation of the ligands in the mouse vas deferens and guinea pig ileum preparations revealed

61 MH side chain exchange was seen in the mouse vas deferens assay.

62 t the CB1 and CB2 receptors and in the mouse vas deferens in vitro assay and the mouse tetrad in vivo

63 sensitization than those found in the native vas deferens tissue, in agreement with previous reports.

64 lene mesh with either trapped or obliterated vas in all patients.

65 2 signaling and is involved in the occlusive vas cular remodeling of PAH, findings that may have ther

66 sulfonate-induced, female sterile alleles of vas have been isolated.

67 cal-uterine junction, and the development of vas deferens-proctodeal connection in the male.

68 The maximal inhibition of vas deferens contraction by the alpha2 agonist in alpha2

69 Immunoelectron microscopy of vas deferens smooth muscle showed anti-RyR antibodies lo

70 n, we investigated the expression pattern of vas RNA in zebrafish embryos from the 1-cell stage to 10

71 cellular CPI-17 concentration of the phasic vas deferens.

72 of neurogenic contractions in the guinea pig vas deferens (n = 4-5).

73 rkedly reduced contraction of the guinea pig vas deferens to electrical field stimulation (EFS) and n

74 -smooth muscle preparation of the guinea-pig vas deferens and from isolated bovine adrenal chromaffin

75 ympathetic nerves innervating the guinea-pig vas deferens releases not only neuronal ATP, but also so

76 ow of NA and the purines from the guniea-pig vas deferens preparation was examined after treatment wi

77 D) (rat aorta), and alpha(2A) (rat prostatic vas deferens) was also evaluated.

78 determined from functional assays in rabbit vas deferens and inhibition constant (Ki) of 0.02 nM mea

79 P2X1 currents recorded from dissociated rat vas deferens smooth muscle cells.

80 d non-selective cation channels from the rat vas deferens (P2X1 receptors) were stably expressed in H

81 loned; of these, one was cloned from the rat vas deferens (P2X1) and another from pheochromocytoma (P

82 Phasic SMCs (vas deferens, uterus and bladder) rely on membrane depol

83 ion of the testis and associated structures (vas deferens, testicular vessels) and subsequent treatme

84 Here we present evidence that vas RNA is a germ-cell-specific marker, allowing a descr

85 We show that vas genes are required for cytotoxicity of V. cholerae c

86 uterus anteriorized towards oviduct and the vas deferens anteriorized towards epididymis.

87 of principal cells of the epididymis and the vas deferens, and that both NHERF1 and CFTR co-immunopre

88 cer Fluorogold into the junction between the vas deferens and the cauda labeled a population of neuro

89 w of purines and noradrenaline (NA) from the vas deferens preparation differed from the pattern of ov

90 in normal P2X1 receptor functionality in the vas deferens and that its absence leads to impaired peri

91 In the vas deferens and the ileal submucosa, P2X1 immunoreactiv

92 Up to 80% of the net proton secretion in the vas deferens is inhibited by bafilomycin, consistent wit

93 om postganglionic sympathetic neurons in the vas deferens of mice injected with IgG from LEMS patient

94 w that similar cells are also present in the vas deferens, and that a bafilomycin-sensitive proton fl

95 d predominantly to the cell periphery in the vas deferens.

96 bnormal escape reflex, mispositioning of the vas deferens and uterus, and mitotic chromosome loss and

97 (15.6%) patients; unilateral absence of the vas deferens in 31 (11.2%) patients; obstructing cysts o

98 included congenital bilateral absence of the vas deferens in 94 (34.1%) patients; bilateral occlusion

99 well as congenital bilateral absence of the vas deferens in males.

100 y due to congenital bilateral absence of the vas deferens or nonclassic cystic fibrosis.

101 -receptor-deficient mice, contraction of the vas deferens to sympathetic nerve stimulation is reduced

102 component of the contractile response of the vas deferens to sympathetic nerve stimulation, which pro

103 Superfusion of the vas deferens with exogenous epsilon-ATP, a fluorescent d

104 infertility due to congenital absence of the vas deferens, 9 patients with nonclassic CF, and 27 unaf

105 enotype, congenital bilateral absence of the vas deferens, and determined whether mutant CFTR could r

106 rly evident within sympathetic fibers of the vas deferens, reflecting a high degree of spatial organi

107 (34.1%) patients; bilateral occlusion of the vas deferens, seminal vesicles, and ejaculatory ducts by

108 s tubule and collected by cannulation of the vas deferens.

109 fluorescence in the tunica muscularis of the vas deferens.

110 y due to congenital bilateral absence of the vas deferens.

111 Microsurgical reconstruction of the vas has remained a cost-effective, reliable and effectiv

112 erm effects of the polypropylene mesh on the vas deferens, especially with regard to fertility.

113 of the spicule-associated muscles pinch the vas deferens opening, thus blocking sperm release.

114 tically mediated sperm transport through the vas deferens during the emission phase of ejaculation.

115 al tract, including the seminal vesicle, the vas deferens and the prostate.

116 ior end of the oocyte, is epistatic to these vas alleles.

117 old greater in femoral artery as compared to vas deferens.

118 acterial pathogens carry genes homologous to vas genes and potential effector proteins secreted by th

119 +/- 0.4 million for Entpd1(+/+)) pointed to vas deferens dysfunction.

120 aging of the distal male reproductive tract (vas deferens, seminal vesicles, ejaculatory ducts).

121 encoded by the "posterior" group gene vasa (vas) in control of localization of the mRNA encoded by t

122 ; obstructing cysts of the seminal vesicles, vas deferens, ejaculatory ducts, or prostate in 26 (9.4%