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1 es on the recent origin and a candidate male sex determining gene.
2 tal proof that Sry was the elusive mammalian sex-determining gene.
3 wn to be a duplicate of another Hymenopteran sex-determining gene.
4 ement in the fem-3 3'UTR and repressing this sex-determining gene.
5 ) gene on the Y chromosome as candidate male sex-determining gene.
6 ve linkage of sexually antagonistic genes to sex-determining genes.
7 genetic programme that involves most of the sex-determining genes.
8 n animals and fungi is regulated by specific sex-determining genes.
9 been produced of a plant chromosome carrying sex-determining genes.
10 or are therefore likely under the control of sex-determining genes.
11 f the AFLP markers and to locate the mutated sex-determining genes.
12 he group with the highest diversity of known sex-determining genes.
13 ution of new regulatory interactions between sex-determining genes and genes that control spatial pat
14 ombine with the X chromosome and carries the sex-determining genes and genes with other male function
15 n for the observed preponderance of dominant sex determining genes, and hint that drift-induced selec
17 ene may be the ancestral precursor of Sry, a sex-determining gene, and Sox3 has been proposed to play
18 tis and are thought to express Sry, the male sex-determining gene, and to play a crucial role in dire
19 on from hermaphroditism to monoecy, multiple sex determining genes are involved, including male-steri
23 ic selection can promote the spread of novel sex-determining genes as well as maintain ancestral sex-
24 animal lineages are inevitably controlled by sex-determining genes, but the genetic basis of sexually
25 orphic sex chromosomes and rapid turnover of sex-determining genes can complicate establishing the se
28 nificant up-regulation of a circRNA from the sex-determining gene dmrt1 (circular RNA dmrt1) and a ln
29 ome, which initiates from the putative avian sex-determining gene DMRT1 and ends at the pseudoautosom
32 e aggressive behavior independent of another sex determining gene, doublesex (dsx), although dsx is i
33 ere, we found that one of the two Drosophila sex-determining genes, doublesex (dsx), specifies a male
34 tterns of expression of maternal and zygotic sex determining genes expected to result from conflict o
35 st intron of Fem1c, a gene homologous to the sex-determining gene fem-1 of Caenorhabditis elegans.
36 abditis elegans hermaphrodite germ line, the sex-determining gene fem-3 is repressed posttranscriptio
38 nal class specified by one of the Drosophila sex determining genes, fruitless (fru), belongs to the n
39 is has also happened in honeybees, where the sex-determining gene has now been shown to be a duplicat
40 sperm families, the actual identification of sex-determining genes has been elusive, and their regula
41 edaka, a duplicate of dmrt1-acting as master sex-determining gene-has a tightly timely and spatially
42 tagonistic loci that are tightly linked to a sex-determining gene have a vastly stronger influence on
43 uences of alleles of the honey bee's primary sex-determining gene have extremely high diversity, with
45 the maximum possible time during which their sex-determining genes have existed must be much shorter
47 C-2 associates with the promoter of the male sex-determining gene her-1 to repress its transcription.
48 ing a transgene activation system, the human sex-determining gene hSRY is activated in the single-cel
49 in both species that are believed to contain sex-determining genes, i.e. the male-specific Y (MSY) re
50 ether the expression of SOX9, a central male sex-determining gene in mammals, or three other conserve
51 strate that Dmrt1 is a candidate master male sex-determining gene in this TSD species, consistent wit
52 ggests the possible continued involvement of sex-determining genes in maintaining ovarian function th
54 discovery of many of the now-known mammalian sex-determining genes, including SRY, RSPO1, SOX9, NR5A1
55 indifferent until the transient action of a sex-determining gene initiates gonadal differentiation.
58 female heterogamety (ZZ/ZW), but the master sex-determining gene is unknown, as it is for all reptil
59 alancing selection acting on mating types or sex-determining genes is expected to lead to the accumul
61 ermine whether interactions between multiple sex-determining genes might be partly responsible for th
63 onal genomic analysis of sex chromosomes and sex-determining genes of other blow flies will allow a r
65 x phenotype mutants, we identified candidate sex-determining genes on the Y in locations consistent w
67 ual differentiation processes, is an ancient sex-determining gene present in all studied species.(2)(
69 mbination, which surrounds the male-specific sex-determining gene, remains very small, despite ancien
72 he initial expression of the female-specific sex-determining gene Sex-lethal in the blastoderm embryo
76 embryo in response to the expression of the sex determining gene, Sry, in Sertoli cell precursors.
77 n morphological event downstream of the male sex determining gene, Sry, is the induction of prolifera
78 stis development just downstream of the male sex-determining gene, Sry: (1) for the proliferation of
81 ning loci, the transposition of an ancestral sex-determining gene to an autosome, and the maintenance
82 se results significantly narrow the putative sex-determining gene to the very terminal region of the
86 inized by a loss-of-function mutation in the sex-determining gene tra-3 results in masculinization of
89 oogenesis relies on regulation of the fem-3 sex-determining gene via a regulatory element in the fem
91 ermining genes as well as maintain ancestral sex-determining genes when the invasion of the novel sex
92 recombination in the SDR and share candidate sex-determining genes, whereas in Tetrastigma, the regio
93 ased delivery system applied in the study of sex-determining gene, which indicates an attractive pros
94 rmining genes when the invasion of the novel sex-determining gene would involve transitions from male