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1 th grey and white matter, suggesting neural 'masculinization'.
2 red a concomitant development to ensure male masculinization.
3  conditional deletion of Ihh inhibits penile masculinization.
4 nce testosterone production for hypothalamic masculinization.
5 rogramming by fetal androgen exposure during masculinization.
6 POA and whether they influence developmental masculinization.
7 testosterone production by fetal LC to drive masculinization.
8 is ultimately determined by androgen-induced masculinization.
9 ing the pathway of steroid-independent brain masculinization.
10 tivity lead to varying degrees of defects in masculinization.
11 ed that increased GABA neonatally results in masculinization.
12 to C. elegans caused only very weak, if any, masculinization.
13 n is essential for normal reproductive tract masculinization and has highlighted that measuring AGD i
14 astrocytes are also critical contributors to masculinization and illustrate the importance of nonneur
15 yperandrogenism and is an important cause of masculinization and infertility in women.
16 signaling prevents PGE(2)-induced behavioral masculinization and whether activation of glutamate rece
17  function, such as Menidia, feminization and masculinization are equally detrimental.
18 ebra finch, steroids that impact song system masculinization are most likely not synthesized from the
19 nalysis of the quantitative genetic basis of masculinization, as indicated by the anogenital distance
20                                          The masculinization, but not the suppression of XO lethality
21 xposed to endocrine disrupters, specifically masculinization by exposure to androgens and feminizatio
22                       Measures of behavioral masculinization correlate with a twofold increase in spi
23 ren born with congenital genitourinary tract masculinization disorders by array-comparative genomic h
24 tive urogenital traits observed in boys with masculinization disorders such as cryptorchidism, urethr
25 es to dibutyl phthalate (DBP), which induces masculinization disorders, dose-dependently prevented th
26  strongly androgenic, thereby explaining the masculinization effects.
27 re is family-specific and typically leads to masculinization (female-to-male sex reversal), resulting
28 each male and female is a mosaic of relative masculinization, feminization, and sameness, which theor
29 othesis that either prenatal feminization or masculinization hormone influences in utero or later soc
30 , such as sel-10(n1074), cause a more severe masculinization, including a reversal of the life versus
31 tional prostaglandin synthesis prevents this masculinization, indicating a positive feedforward proce
32                                         This masculinization is associated with transmission of the S
33                                Additionally, masculinization is generally more detrimental to populat
34                                     Although masculinization is well studied, no unifying concept exp
35 ed FSD emerged only recently and that female masculinization may be the ancestral lemur condition, an
36                             We conclude that masculinization might constitute an alternative mechanis
37     Prostaglandin E(2) (PGE(2)) mediates the masculinization of adult sex behavior in rats in respons
38  anti-androgens or androgens and showed that masculinization of all reproductive tract tissues was pr
39                    Ht31 does not prevent the masculinization of behavior by ACPD plus kainate cotreat
40 mined that PKA signaling is required for the masculinization of behavior by PGE(2).
41 PGE(2), EP(2) and EP(4) are required for the masculinization of behavior by PGE(2).
42 54 myosin heavy chain promoter caused strong masculinization of both C. briggsae and C. elegans herma
43 s, including suppression of XO lethality and masculinization of both XX and XO animals.
44 ne during early development is necessary for masculinization of brain structures in rodents.
45                                          The masculinization of DE in OS female twins is unlikely to
46  differences in microglia, estradiol-induced masculinization of dendritic spine density, and adult co
47 r with the finding of rapid androgen-induced masculinization of female vocalizations, provides an inv
48                              Androgen-driven masculinization of females was also confined to the same
49 to oogenesis at 25 degrees C, resulting in a masculinization of germline (Mog) phenotype.
50             Loss of sel-10 results in a mild masculinization of hermaphrodites, whereas dominant alle
51 event downstream of Sry that is critical for masculinization of mammalian embryos.
52                                        Thus, masculinization of MePD astrocytes is a result of both A
53 al androgen receptors (ARs) are required for masculinization of MePD astrocytes, as these measures ar
54                        Moreover, the genetic masculinization of neurons in an otherwise wild-type her
55 in the sex-determining gene tra-3 results in masculinization of somatic tissues, consistent with QKI-
56 e two signaling pathways interact to control masculinization of the brain and behavior remains to be
57              Biological factors, such as the masculinization of the central nervous system by prenata
58 ell differentiation, testis morphogenesis or masculinization of the embryos.
59 androgen receptor (AR) gene cause incomplete masculinization of the external genitalia by disrupting
60         We show here that mag-1(RNAi) causes masculinization of the germ line (Mog phenotype) in RNA-
61 S exposure is likely to pose minimal risk to masculinization of the human fetus.
62  differences primarily arose due to hormonal masculinization of the male brain (and to a lesser exten
63 rogen receptors (ERs) alone mediate prenatal masculinization of the mouse brain to organize reproduct
64 or activation has been shown to be vital for masculinization of the rodent brain, our results indicat
65                   These results suggest that masculinization of the song system is not determined sol
66 ogen receptor (AR) mRNA were measured, since masculinization of the song system is, in part, accompli
67   Adult androgen exposure can induce partial masculinization of the syrinx, but other factors must be
68  46XX females can result in vaginal atresia, masculinization of the urethra, a single urogenital sinu
69                   Lack of Wnt4 gives rise to masculinization of the XX gonad and we showed previously
70  led to feminization of the X chromosome and masculinization of the Y chromosome.
71                                          The masculinization of these cells is independent of AR but
72 xists for both AR and SNX2 to be involved in masculinization of these two brain regions.
73                                    Selective masculinization of third-order neurons transforms their
74 tions at the perineum play a crucial role in masculinization of this neural system.
75 ice, a targeted deletion of Wnt-4 causes the masculinization of XX pups.
76 his sex steroid receptor is associated with "masculinization" of adolescent cortical maturation.
77 gross changes in general behaviour, and (4) 'masculinization' of FruM-expressing neurons in females i
78 nt stages of X differentiation, resulting in masculinization or demasculinization of the X-chromosoma
79  it unlikely that in utero femininization or masculinization or socialization effects of growing up w
80 sent genetic evidence that the sel-10(n1074) masculinization phenotype is dependent upon skr-1 and cu
81 ound resulted in a highly penetrant germline-masculinization phenotype.
82 versing treatment itself interfered with the masculinization process, or that a male genome is requir
83 ar to androgen production/action during the 'masculinization programming window' (MPW; e15.5-e18.5).
84 t androgen production/action during a fetal 'masculinization programming window'.
85 to propose that the natural process of brain masculinization puts males at risk by moving them closer
86                           Disorders of fetal masculinization, resulting in hypospadias or cryptorchid
87 neural development generally and song system masculinization specifically.
88 ch activates two processes in male neonates; masculinization, the development of male-type behaviors,
89  the innate immune system in directing brain masculinization, the evidence for which we review here.
90 n is maintained by the active suppression of masculinization via DNA methylation.
91 s that implicates (as a putative mechanism) 'masculinization' via androgen exposure; however, relativ
92 of dying out but with less extreme pressure, masculinization will not be detectable since the proport
93 of both phenotypic and genetic components in masculinization with effects being greater in females.

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