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1                                              Sex-limited Cholesky structural equation models were use
2 a provide evidence for the importance of the sex-limited chromosome in a female heterogametic species
3 ation, gene expression levels decline on the sex-limited chromosome, and this can lead to selection f
4 erogametic sex - Y and W - that are known as sex-limited chromosomes (SLCs).
5 t sex-specific selection can act to preserve sex-limited chromosomes from degrading forces.
6             We map the genetic basis of this sex-limited colour dimorphism to a region containing the
7 scertainment bias in unstratified data for a sex-limited disease.
8  neurodevelopmental disorders, and suggest a sex-limited effect on the penetrance of the pathological
9 nalyses suggested that these QTLs might have sex-limited effects.
10 h male lethality is probably responsible for sex-limited expression of these disorders, as affected w
11 ily size or transmission through males given sex-limited expression.
12 to be identified in Chlamydomonas that shows sex-limited expression.
13 ance, which include sex-linked transmission, sex-limited fertility reduction, and X-autosome epistasi
14        The evolution of sexual dimorphism by sex-limited gene expression alleviates this problem.
15 ffects in the other sex, due to incompletely sex-limited gene expression.
16 rehensive genomic sampling of biparental and sex-limited genetic variation to identify and control fo
17  collection of D. pulex clones suggests that sex-limited meiosis suppression in D. pulex has spread w
18 st striking examples of sexual dimorphism is sex-limited mimicry in butterflies, a phenomenon in whic
19                                              Sex-limited mimicry is phylogenetically widespread in th
20       Testicular germ cell tumors (TGCT) are sex limited, occurring only in males with a Y chromosome
21                                              Sex-limited polymorphisms are an intriguing form of sexu
22 0-base pair enhancer, derived from the mouse sex-limited protein (Slp) gene, is activated solely by t
23 the androgen-dependent enhancer of the mouse sex-limited protein (Slp) gene.
24  the androgen-specific enhancer of the mouse sex-limited protein (Slp) gene.
25 erwise male-specific liver proteins, such as sex-limited protein (Slp), major urinary proteins (MUPs)
26 gene expression, most dramatically for mouse sex-limited protein (Slp), which provides an in vivo rep
27 zed the mouse protein Slp, coded by the gene sex-limited protein (Slp).
28 ns requires the N/C interaction, whereas the sex-limited protein gene and mouse mammary tumor virus l
29 ce, females inappropriately express the male Sex-limited protein, Slp.
30                                            A sex-limited role for the roX RNAs in autosomal gene expr
31 a large number of families and is frequently sex limited: Sex linkage has not yet been demonstrated,
32 wever, because the majority of genes are not sex-limited, the potential for substantial conflict may
33 design because the spermatozoal phenotype is sex-limited (to males) while the genotype is sex-linked
34 h reference to sex-linkage of this important sex-limited trait.
35                                              Sex-limited trivariate Cholesky structural equation mode

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