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 One such example is the fertile XO female mouse.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

22 conditional genetic transsynaptic tracing in female mouse embryos.

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

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

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

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

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

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

29 Thus, female mouse germ cell clusters exhibit key characterist

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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