ライフサイエンスコーパス: female mouse

1 unctioning of the GnRH neuron network in the female mouse.

2 uronal network required for fertility in the female mouse.

3 he acquisition of uterine receptivity in the female mouse.

4 One such example is the fertile XO female mouse.

5 Here, we show that the female mouse ACL accrues more collagen matrix damage tha

6 rone receptor are essential for male but not female mouse aggression.

7 chromosomes may have a more critical role in female mouse aggression.

8 Here, shell Ox1R inhibition did not alter female mouse alcohol drinking, unlike in males.

9 al antibodies and protection from disease in female mouse and male ferret challenge models.

10 he acquisition of uterine receptivity in the female mouse, and disruption of such signaling results i

11 We tested whether primary female mouse aortic ECs could cross-present exogenous ma

12 l KO of the beta(1)-adrenergic receptor from female mouse astrocytes impairs gray matter astrocyte ma

13 gic levels of estradiol, in vitro, increased female mouse BEC (mBEC) IL-6 messenger RNA (mRNA) and pr

14 ng nicotinic PET ligands in vivo in male and female mouse brain and identifying the trapping brain or

15 neurons of NAc slices; and in either male or female mouse brain in a region-specific manner.

16 neurons of NAc slices; and in either male or female mouse brain in a region-specific manner.

17 ne dinucleotide (NAD(+)) levels in the adult female mouse brain in vivo and in human cortical neurons

18 analysis reveals that gene expression in the female mouse brain is remarkably stable during the estro

19 We identified a distributed network of female mouse brain regions for maternal behaviors that a

20 ectrophysiology and optogenetics in male and female mouse brain slices to examine cholinergic regulat

21 ltured mouse and rat neurons and in male and female mouse brain.

22 male-specific behaviours exist in the normal female mouse brain.

23 , we show by RNAseq from Irf8 (-/-) male and female mouse brains that several genes involved in regul

24 s EXC, PV, SST and VIP neurons from male and female mouse brains.

25 us excitatory (glutamatergic) neurons in the female mouse by selective ablation of the leptin recepto

26 nteractions in the Xist promoter region in a female mouse cell line (BMSL2), which has distinguishabl

27 Here, we use the male and female mouse cerebral cortex to show that a higher perce

28 we investigated CD8+ T cell responses in the female mouse cervicovaginal mucosa after intravaginal im

29 A novel female mouse chimera assay was developed and revealed th

30 ine release from single vesicles in male and female mouse chromaffin cells with altered levels of syp

31 tOn-inducible system in transfected male and female mouse cones in vivo, we show that the entry of na

32 elrhodopsins (ChR2) specifically in male and female mouse DCs and OPCs.

33 sly shown that estradiol administered to the female mouse decreases inward currents in fluorescently

34 The X-linked gene Rlim plays major roles in female mouse development and reproduction, where it is c

35 alcium microfluorimetry analysis of male and female mouse DRG neurons demonstrated that the cooling c

36 served increased PTGDS protein and PGD(2) in female mouse DRG.

37 mouse embryonic stem cells or in cells from female mouse E7.5 embryos.

38 mosome will be inactivated in the developing female mouse embryo.

39 Here, using female mouse embryonic stem cells (ES) and mouse embryon

40 Female mouse embryonic stem cells (mESCs) contain two ac

41 GSK-3 inhibition in differentiating female mouse embryonic stem cells and epiblast stem cell

42 F binding present initially in both male and female mouse embryonic stem cells is lost from the activ

43 ocalization to a Barr body-like structure in female mouse embryonic stem cells or in cells from femal

44 Using female mouse embryonic stem cells, we initiate XCI by in

45 Here, we discovered that female mouse embryos lacking Coup-tfII (chicken ovalbumi

46 7(3,4)-that cause genomic instability render female mouse embryos markedly more susceptible than male

47 In female mouse embryos, somatic cells undergo a random for

48 ey enzyme in estrogen synthesis, in male and female mouse embryos.

49 conditional genetic transsynaptic tracing in female mouse embryos.

50 ents.(1)(,)(2)(,)(3)(,)(4) We find that each female mouse exhibits a characteristic pattern of explor

51 hroughput in vivo screening in both male and female mouse eyes and identified the mouse gamma-synucle

52 acids that are variably excreted in male and female mouse faeces, and others respond to bile acids ab

53 ction but for correct meiotic progression in female mouse fetal germ cells.

54 excision of 21 kb from both Xist alleles in female mouse fibroblasts led to the appearance of two hi

55 structure consistent with the inactive X in female mouse fibroblasts.

56 s and distribution of ERbeta in the male and female mouse forebrain on the day of birth (P0), on post

57 mediated motor activity in ex vivo male and female mouse full length colon preparations.

58 metritis resulting in infertility by using a female mouse genital tract chlamydial infection model.

59 n their abilities to colonize and infect the female mouse genital tract.

60 Thus, female mouse germ cell clusters exhibit key characterist

61 Early female mouse germ cells are organized as cell clusters a

62 at affect oxidative phosphorylation into the female mouse germ line.

63 le-strand DNA break (DSB) is feasible in the female mouse germline.

64 stability in human cells and in the male and female mouse germlines.

65 l muscle precursor cells were implanted into female mouse hearts by direct intramuscular injection.

66 Isolated male and female mouse hearts from TNFR2 knockout, TNFR1/2 knockou

67 iling to define differences between male and female mouse hearts.

68 pathy caused by paclitaxel (PTX) in male and female mouse hindpaws and dorsal root ganglia (DRG).

69 tosterone administration altered prepubertal female mouse hippocampus-dependent memory, PV IN functio

70 methylomes and transcriptomes from male and female mouse hypothalamic arcuate nucleus, a key site fo

71 s expressing nNOS in the postnatal and adult female mouse hypothalamus using immunohistochemistry.

72 n 36-like 2, Zfp36l2, has been implicated in female mouse infertility, because an amino-terminal trun

73 and gene expression data from a cohort of F2 female mouse intercross.

74 eiotic failure, and the mammary gland of the female mouse is underdeveloped.

75 ed for the suppression of male mating when a female mouse is unhealthy.

76 le-cell RNA sequencing of the adult male and female mouse kidney with in situ expression studies and

77 iggers a metabolic shift in Ppif-/- male and female mouse kidneys towards glycolysis and Krebs cycle

78 fic differences between the Ppif-/- male and female mouse kidneys were observed including activation

79 and antisense RNA probes were hybridized to female mouse lacrimal gland frozen sections.

80 RP1 was expressed in the acinar cells of the female mouse lacrimal gland.

81 lar glands, and in ABPs secreted by male and female mouse lacrimal glands.

82 robe was hybridized to RNA blots of male and female mouse lacrimal, harderian, parotid, mandibular, s

83 ladder tumors at high exposure levels and on female mouse liver tumors.

84 nd lipidomics in response to DR and aging in female mouse liver.

85 tes inflammatory gene expression in male and female mouse liver.

86 pecific maps of regulatory sites in male and female mouse livers and in livers of male mice feminized

87 in B produced sensitization of male, but not female, mouse, macaque, and human dorsal root ganglion n

88 By the age of 4 months, 100% of female mouse mammary tumor virus-EZH2 virgin mice develo

89 hin different anatomical regions of male and female mouse masseters.

90 Cultured male and female mouse mechano- and polymodal nociceptor corneal n

91 gion unsynapsed during pachytene of male and female mouse meiosis is subject to transcriptional silen

92 igated the role of Kinesin 5b (Kif5b) during female mouse meiotic cell development and mitotic cell d

93 eneity in the preclinical Mecp2-heterozygous female mouse model (Het).

94 idarum genital tract infections, we used the female mouse model and evaluated infection in the presen

95 nemia in a dihydrotestosterone (DHT)-treated female mouse model induces whole body insulin resistance

96 of BAI1 in a male hNSC line in vivo using a female mouse model of acute spinal cord injury (SCI).

97 fe-threatening acute allergic reactions in a female mouse model of anaphylaxis via a multi-burst deli

98 ling in a cell-based assay and in an in vivo female mouse model of asthma.

99 significantly reduces bacterial titers in a female mouse model of CAUTI.

100 Here, we use a female mouse model of coronavirus disease to evaluate in

101 Here, we establish a female mouse model of RSDS by inducing male aggression t

102 Both antibodies offer protection in a female mouse model via neutralization activity and Fc-me

103 In a female mouse model with critical-size cranial defects, n

104 In an immunodeficient female mouse model, transplanted cells edited with the n

105 odistribution throughout the whole lung in a female mouse model.

106 oses up to 1,000,000-fold lower than mRNA in female mouse models of influenza and rabies.

107 TAF4b deficiency in adult female mouse models results in hallmarks of POI includin

108 Here, we leverage both male and female mouse models, single-cell labeling and imaging ap

109 In multiple female mouse models, we show that pyroptosis-triggering

110 ar carcinoma in the absence of microbiota in female mouse models.

111 the anti-tumor activity of PD-1 blockade in female mouse models.

112 sly shown that estradiol administered to the female mouse modulates sodium currents in fluorescently-

113 ise in [Ca(2+)](i) during MI in male than in female mouse myocytes.

114 mixtures at four concentrations in male and female mouse neuronal cultures.

115 a major sex-specific epigenetic regulator of female mouse nurturing tissues.

116 genesis, and increased lipid peroxidation in female mouse offspring exposed to an obesogenic maternal

117 , we subtracted a phage display library with female mouse peritoneum tissue and selected phage clones

118 sion, distribution, and function at male and female mouse photoreceptor ribbon synapses.

119 clone were hybridized to a blot of male and female mouse poly(A)+ RNA isolated from harderian, lacri

120 combination with H7.HK2 moderately augments female mouse protection.

121 function, experiments were designed to test female mouse reproductive behaviors in the cold.

122 When memory CD8(+) T cells residing in the female mouse reproductive tract encountered cognate anti

123 ogenitor cells (MGPCs) in the adult male and female mouse retina.

124 t that are known to drive DSGCs, in male and female mouse retinas.

125 ve firing rates in identified adult male and female mouse SCN neurons: vasoactive intestinal peptide-

126 ivity is reduced in Ube3a deficient male and female mouse sensory neurons, a human Merkel cell carcin

127 Specifically, in the female mouse, short-term, low-dose exposure during the f

128 ression is higher in male mouse skin than in female mouse skin.

129 se = 5.4 +/- 0.4 and 4.0 +/- 0.4 in male and female mouse striatum).

130 te cold-induced adipocyte UCP1 expression in female mouse subcutaneous white adipose tissue (scWAT).

131 PLRP1 mRNA was also expressed in male and female mouse sublingual gland and pancreas.

132 cible Treg-cell-specific SRC-3 knockout (KO) female mouse that does not possess a systemic autoimmune

133 Neurons in the brain of a female mouse that respond to the scent of a given male b

134 from both sexes and whole-cell recordings on female mouse TIDA neurons in vitro to examine whether th

135 variability between SCFA levels in male and female mouse tissue explants cultured in the MOD system

136 es, we screened chromatographic fractions of female mouse urine for their ability to cause reproducib

137 Glomerular activity maps for sexually mature female mouse urine overlapped maps for juvenile and/or g

138 e found that conspecific chemosignals (male, female mouse urine) increased immediate early gene-prote

139 s were strongly selective for either male or female mouse urine, with the effective concentrations di

140 ensing neurons of the vomeronasal organ from female mouse urine.

141 compounds are the predominant VSN ligands in female mouse urine.

142 acts with estrogens to enhance production of female mouse urogenital cancers.

143 nt probes were imaged in the cerebellum of a female mouse, using confocal microscopy with spectral un

144 sparity selectivity of neurons from male and female mouse V1 following MD.

145 Here, we show that female mouse vomeronasal sensory neurons (VSNs) are temp

146 adically different conformations for the two female mouse X chromosomes.