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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

30 In male mouse fetuses, both ethinylestradiol and bisphenol

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

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

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

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

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

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

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

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

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

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

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

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

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

44 Adult male mouse submaxillary glands served as the preferred s

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

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

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

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

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

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

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

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