ライフサイエンスコーパス: male mouse

1 ure of the PVH in the commonly used C57BL/6J male mouse.

2 participate in the GnRH/LH secretion in the male mouse.

3 of testis selenium and for fertility of the male mouse.

4 the reward salience of this stimulus for the male mouse.

5 that identifies individual autosomes in the male mouse.

6 mediating female pheromone signaling in the male mouse.

7 d in descendents of a chemically mutagenized male mouse.

8 l phenotypic abnormalities present in the Gy male mouse.

9 rimary auditory cortex neurons from a single male mouse.

10 rylation, P) of MAPK in the VN system of the male mouse?

11 A digital color brain atlas of the C57BL/6J male mouse, 2007).

12 l hypothalamus (VMHvl)-a region required for male mouse aggression.

13 n competition experiments on both female and male mouse and rats hippocampal slices.

14 osolic-nuclear estrogen receptors in control male mouse aortas.

15 rtic rings without endothelium and in intact male mouse aortic rings treated with NG-nitro-L-arginine

16 icroglia within the context of an Mecp2-null male mouse arrested numerous facets of disease pathology

17 clude that achiasmate bivalents arise in the male mouse at a frequency of 0.1%.

18 Kcne4 deletion also reduced Kv currents in male mouse atrial myocytes, by >45% (P < 0.001).

19 to repeated tones pyramidal (Pyr) neurons in male mouse auditory cortex (A1) exhibit facilitating and

20 ostimulation we investigated whether L2/3 of male mouse auditory cortex contains discrete subpopulati

21 single-cell transcriptomic profiling of the male mouse brain during the first week of injury.

22 d functional plasticity of the rescued adult male mouse brain.

23 igital atlas of gene expression in the adult male mouse brain.

24 nt mitochondrial phenotypes exist across the male mouse brain.

25 cid cycle, was decreased in CHCHD2-deficient male mouse brains and human dopaminergic neurons.

26 hown to promote NAM effects in both isolated male mouse cardiomyocytes and failing human heart left v

27 te a targeted deletion of Tsix in female and male mouse cells.

28 a platform to analyze diurnal variations in male mouse ChP and CSF.

29 on ex vivo sorted microglia from ipsilateral male mouse cortex after a transient in vivo ischemic pul

30 s (cystocytes), and under certain conditions male mouse cystocytes have been postulated to revert int

31 show that astrocytes bidirectionally control male mouse dominance behavior, affecting social rank.

32 h the entire somatodendritic domain of adult male mouse dopaminergic neurons, previously recorded in

33 DAT/retromer colocalization was observed in male mouse dopaminergic somatodendritic and terminal reg

34 of Nr4a1, Nr4a2, or both transcripts in the male mouse dorsal hippocampus can ameliorate age-related

35 ptor 2 expression was observed in female and male mouse dorsal root ganglia, respectively.

36 utics; MET-1) can affect the excitability of male mouse DRG neurons.

37 se on male gonad development that covers six male mouse embryonic gonad stages, including E10.5, E11.

38 e of MeCP2, the X-linked gene was mutated in male mouse embryonic stem (ES) cells using a promoterles

39 the Y-linked homolog KDM5D, induces Xist in male mouse embryonic stem cells (mESCs).

40 Using global quantitative proteomics in male mouse embryonic stem cells, we identified the deubi

41 Here we show that prolonged culture of male mouse ES cells in 2i/L results in irreversible epig

42 ences on human X chromosomes, we transfected male mouse ES cells with a YAC transgene containing 480

43 of sperm quality and can accurately predict male mouse fertility.

44 ntial for piRNA-directed DNA methylation and male mouse fertility.

45 at a 50% increase in free-serum estradiol in male mouse fetuses (released by a maternal Silastic estr

46 In male mouse fetuses, both ethinylestradiol and bisphenol

47 c2d1a exclusively from excitatory neurons of male mouse forebrain to examine its role in hippocampal

48 y (IR) in the brain of the hypogonadal (hpg) male mouse, genetically deficient in GnRH.

49 the hottest segment for DSB formation in the male mouse genome.

50 led translation and transcription in haploid male mouse germ cells.

51 In the male mouse germ line, PIWI-interacting RNAs (piRNAs), bo

52 e wild-type (WT) male mouse, the Cyp2a5-null male mouse had intact capability to metabolize APAP to r

53 ce of Sry, we constructed an XY(Sry(-))Ods/+ male mouse, in which the male phenotype is controlled au

54 forms, we analyze over a million cells on 12 male mouse kidneys across six stages of renal injury and

55 subunits of ABP were expressed primarily in male mouse lacrimal gland.

56 Female, but not male, mouse lacrimal gland expressed PLRPI mRNA.

57 at PLRP1 was expressed in female, but not in male, mouse lacrimal gland.

58 or constitutive expression in female but not male mouse liver of certain GH-regulated CYP steroid hyd

59 , sequence analysis of the lacZ mutants from male mouse liver showed that the principal sequence alte

60 thway both in cultured C2C12 myotubes and in male mouse liver, brown adipose tissue and muscle, even

61 Androgen-dependent male mouse mammary carcinoma (Shionogi) was implanted in

62 in chemotherapy, induces DNA lesions during male mouse meiosis that persist unrepaired as germ cells

63 We show TUBD1 stabilizes kinetochores during male mouse meiosis, enabling meiotic progression, and th

64 , we show that cholesterol esterification in male mouse microglia/macrophages is a necessary adaptive

65 es mitochondrial dysfunction in vitro and in male mouse model of ALD.

66 To address this issue, we used a male mouse model of androgen-dependent salivary gland mo

67 idbrain dopamine neurons in the MPTP-induced male mouse model of PD and improves both motor and non-m

68 nt of ASD-relevant behaviors in a cerebellar male mouse model of tuberous sclerosis complex (TSC), by

69 Here, we show, in a male mouse model, that mWAKE/ANKFN1 labels a subpopulati

70 Most studies have focused on male mouse models because of the shorter latency to and

71 proved cognition in healthy male mice and in male mouse models of Alzheimer's disease and aging.

72 Here we refine two male mouse models of human chronic and acute liver disea

73 Together, this study using male mouse models reveals a role for microglial COX1 in

74 In both cell studies and male mouse models, sequentially irradiated groups (RC fo

75 In male mouse models, we show that this TYR-catalyzed thera

76 AAV2-mediated alpha-synuclein-overexpressing male mouse models.

77 Housed with a castrated male mouse, most intact resident CFW females readily att

78 D2 medium spiny neurons (MSNs) in the adult male mouse NAc core.

79 d fast in vivo two-photon calcium imaging in male mouse neocortex to reconstruct, with single-cell re

80 logs of open chromatin regions of female and male mouse neuronal subtypes: cortical excitatory, D1, D

81 ctional study found neurotransmission at the male mouse NMJ to be biphasic, displaying an early incre

82 otransmission over the ageing time course at male mouse NMJs.

83 ern diet, named CL-HFS, successfully induces male mouse non-alcoholic steatohepatitis with some featu

84 diet results in platelet hyperactivation in male mouse offspring, suggesting a novel 'double-hit' ef

85 In male mouse osteoblasts and human prostate cancer cells,

86 -cell patch-clamp recordings of neurons from male mouse ovBNST in vitro showed that the BDNF/TrkB int

87 s, but not other cell lineages, in the adult male mouse pituitary.

88 Activation of Map1b in adult male mouse prefrontal cortex excitatory neurons impairs

89 framework by quantifying the projections of male mouse primary motor cortex to the primary and secon

90 ent from P1, P7, P14, P20, P42, P56 to adult male mouse prostate and urethral tube.

91 nsures efficient nebulization in preclinical male mouse, pup rat, and male dog models.

92 ss this gap, in the diabetic and nondiabetic male mouse retina, we combined an unbiased longitudinal

93 tion, as being a protective agent in various male mouse SAP models.

94 Unlike Scd1, Scd3 expression is higher in male mouse skin than in female mouse skin.

95 we found 11 distinct macrophage clusters in male mouse SKM with enriched gene expression programs li

96 ice that experienced pre-exposure to a rival male mouse ("social instigation") resulting in heightene

97 we identify increased CD38 expression in the male mouse spinal cord following chronic high fat consum

98 nd nucleus accumbens (NAc) core and shell in male mouse striatal slices, and also an increase in the

99 Adult male mouse submaxillary glands served as the preferred s

100 Compared with the wild-type (WT) male mouse, the Cyp2a5-null male mouse had intact capabi

101 lts in the complete regeneration of the aged male mouse thymus, restoration of peripheral T cell phen

102 to address dopamine release dynamics in the male mouse TIDA system.

103 ression across numerous brain regions in the male mouse to test the potential impact of such compound

104 rcin, an involatile protein sex pheromone in male mouse urine, can rapidly condition preference for i

105 mice and during investigation of a source of male mouse urine.

106 re we studied dopaminoceptive neurons in the male mouse ventral hippocampus (vHipp), molecularly dist

107 er lysolecithin-induced demyelination of the male mouse ventral spinal cord white matter, the recruit

108 xperiment in which whole marrow cells from a male mouse were infused into a female immunodeficient ra

109 e detect a similar high level of Me(K9)H3 in male mouse XY bodies, suggesting an evolutionarily conse