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1 es involved in prezygotic isolation are also sex linked.
2 enes from both addition events are now fully sex-linked.
3 s causing multiple genes to become partially sex-linked.
4  that genes involved in speciation are often sex-linked.
5       We report spontaneous emergence of non-sex-linked agammaglobulinemia with B-cell deficiency and
6 in intestinal iron transport by study of the sex-linked anaemia (sla) mouse, which has a block in int
7 basolateral multi-copper ferroxidase) in the sex-linked anaemic mouse (sla) and ferroportin1 (basolat
8 nalysis of the relative rate of evolution of sex-linked and autosomal genes in primates.
9  Age-related changes in additive, dominance, sex-linked and maternal variance and covariance between
10 supports previous findings that the trait is sex-linked and polygenic.
11 e process that regulates sleep propensity is sex-linked, and that sleep amount and sleep propensity a
12                                    Mice with sex-linked anemia (sla) have a mutant form of Hephaestin
13                                     However, sex-linked anemia (sla) mice harboring a 194-amino acid
14 ingly, the truncated hephaestin expressed in sex-linked anemia (sla) mice still has measurable, but d
15                     Children showed the same sex-linked behavior found with infant monkeys: young boy
16 ale behavioral response to pheromone is also sex-linked, but maps 20-30 cM away.
17         Whether sexually selected traits are sex linked can have profound effects on their evolution.
18  facultative parthenogenesis in snakes and a sex-linked color mutation in the ball python (Python reg
19 sets are diurnal New World monkeys that show sex-linked cone photopigment polymorphism, whereby all m
20  Y, or the genome regions that are not fully sex-linked, consistent with a domestication bottleneck.
21 zones of admixture involving haplodiploid or sex-linked cytonuclear data.
22 for any of these characteristics, ruling out sex-linked, cytoplasmic, and endosymbiotic factors.
23 to this pattern, including meiotic drive and sex-linked deleterious mutations, but further work is ne
24   At 6 of the polymorphic loci variation was sex-linked, despite the fact that these microsatellites
25                               In marmosets a sex-linked dichotomy results in dichromatic and trichrom
26  testosterone may have a role in determining sex-linked differences in cerebrovascular disease as wel
27              Fabry's disease (FD) is a rare, sex-linked disorder resulting from alpha-galactosidase d
28 elated to JIA pathogenesis seem to display a sex-linked disparity.
29 te this genetically, we isolated a number of sex-linked DNA markers.
30                    Tests for the presence of sex-linked effects have been plagued by the need to make
31  of CRC carcinogenesis, particularly whether sex-linked factors play any role.
32 rated that the phenotype of the mouse mutant sex-linked fidget ( slf ) is caused by developmental mal
33 is, and molecular evolutionary analysis of a sex-linked gene from S. latifolia, DD44 (Differential Di
34 e respective X- and Y-linked copy of another sex-linked gene pair, SlCypX/SlCypY.
35 rt, this result is based on analyses of five sex-linked gene sequences, and the maximum divergence (a
36 scordant, and only one molecular marker, the sex-linked gene Tpi, has evidence for pheromone strain e
37 DNA sequence diversity in a newly identified sex-linked gene, SlX9/SlY9, in Silene latifolia (Caryoph
38       We present a pipeline for detection of sex linked genes based on nucleotide polymorphism analys
39 ons results in massive mis-expression of neo-sex linked genes, and little correspondence between func
40 tion of the total variance (in IQ) is due to sex linked genes, it is of more importance that a boy sh
41              We mapped 29 S. latifolia fully sex-linked genes (including 21 newly discovered from tra
42 ccumulates at transcriptional start sites of sex-linked genes activated in an RNF8-dependent manner,
43 anding the extent and specificity with which sex-linked genes and hormones define brain structure and
44 inked housekeeping genes, germ-cell-specific sex-linked genes are subject to meiotic sex-chromosome i
45         In female heterogamous (ZW) species, sex-linked genes coding for maternal products that are p
46                                              Sex-linked genes could also contribute to human gender d
47           The average genetic environment of sex-linked genes differs from that of autosomal genes, s
48 in males than females, a pathogenic role for sex-linked genes has been suggested.
49 ith other mammalian species, and the role of sex-linked genes in fertility.
50 es arising from the different complements of sex-linked genes in male and female cells has received l
51 ur comparative mapping shows that most fully sex-linked genes in S. latifolia are located on a single
52 her with comparative mapping of S. latifolia sex-linked genes in S. vulgaris (a related hermaphrodite
53 gene expression has evolved in autosomal and sex-linked genes in the dioecious species.
54 number of sex chromosomes, the expression of sex-linked genes is equalized by a process known as dosa
55 matocytes and that postmeiotic expression of sex-linked genes is variable.
56 omosomes, made possible by the sequencing of sex-linked genes on both the X and Y chromosomes, which
57  expression are generally sex-biased for all sex-linked genes relative to autosomes, including those
58                           Thus, 13 of the 14 sex-linked genes we examined showed some degree of postm
59                             Although all the sex-linked genes we investigated underwent MSCI, 14 of t
60 es in the mutagenesis and study of essential sex-linked genes, and indicate that OGT participation in
61 [5-8], it remains very difficult to discover sex-linked genes, and it is unclear whether Y-linked gen
62  Our approach identifies several hundred new sex-linked genes, and we show that this young Y chromoso
63                                  To identify sex-linked genes, regardless of their expression, we seq
64 file with candidate transcriptionally active sex-linked genes, sorted by their relevance.
65 de of these effects being greatest for older sex-linked genes.
66 tween males and females in the expression of sex-linked genes.
67 ion and long-term compensatory adaptation by sex-linked genes.
68 the heterogametic sex is hemizygous for most sex-linked genes.
69 ated the time of divergence in four pairs of sex-linked genes.
70 hat genetic effects on residual variance are sex linked; heritable, sex-specific residuals might have
71              Our data demonstrate that, like sex-linked housekeeping genes, germ-cell-specific sex-li
72 males had suggested that the PEPB-1 locus is sex-linked in chinook salmon (Oncorhynchus tshawytscha).
73                    Studies on pairs of genes sex-linked in mammals suggests rapid divergence of DNA s
74  region and several genes that are partially sex-linked in Silene latifolia, using Silene dioica, a c
75 the fact that these microsatellites were not sex-linked in the other passerine birds where they were
76                    Here, we show that per is sex-linked in the silkmoth, Antheraea per-nyi.
77 ver before as a single sex-linked locus, but sex-linked inheritance is thought to facilitate the rapi
78 ication of plant secondary metabolites under sex-linked inheritance.
79 stimated in F(1) hybrids reveal evidence for sex-linked loci contributing to the evolution of recombi
80 linked gene and the first pair of homologous sex-linked loci to be found in plants.
81 ype frequencies from population samples at a sex-linked locus in which functional alleles occur on bo
82 le-gene changes and never before as a single sex-linked locus, but sex-linked inheritance is thought
83 colour is genetically determined by a single sex-linked locus, Red.
84 llele frequency differences at only a single sex-linked locus, Tpi.
85 sing mutation is due to a change in a single sex-linked locus.
86 he female pheromone is governed by a single, sex-linked locus.
87                                              Sex-linked male deafness and dystonia (Mohr-Tranebjaerg
88    Here, we use crosses and genotyping for a sex-linked marker to reject this model: sex in diploid d
89                                 No perfectly sex-linked marker was found in the dioecious species, bu
90               Analysis of the segregation of sex-linked markers revealed that N. furzeri has a geneti
91                                  To identify sex-linked markers, to understand mechanisms of sex dete
92 ation and read depth identified 52 candidate sex-linked markers.
93  (94% females), suggesting that there may be sex-linked meiotic drive or a cytoplasmic sex-ratio fact
94 t the mutation segregates as a single-locus, sex-linked Mendelian trait on both islands.
95         Clones containing pseudoautosomal or sex-linked microsatellites were isolated from a bovine b
96                           Although levels of sex-linked mRNAs were mildly elevated, meiotic sex chrom
97 oalpha mutant (WHAM) chicken has a recessive sex-linked mutation in the ABCA1 transporter gene that r
98           Approximately 35% of the loci were sex linked, not including those in recombining pseudoaut
99                Here we show, using the first sex-linked nuclear sequences from an extinct species, th
100  by a two-gene inheritance model involving a sex-linked oncogene, Xmrk, and an autosomal tumor suppre
101 be annotated as either coding or non-coding, sex-linked or autosomal, selected or neutral, and have a
102  the sexually dimorphic expression of either sex-linked or IFN-responsive genes.
103 h-swordtail hybrids, which carry a different sex-linked pigment pattern locus, Sp.
104 y to be involved in the persistence of these sex-linked polymorphisms and consider the impact of Xd o
105                           These included two sex-linked QTL on chromosome I affecting knockdown and r
106 we detect QTL that are unique, a QTL that is sex linked, QTL that overlap with QTL for stage of diapa
107 ested that HNRNPGT functionally replaces the sex-linked RBMX and RBMY genes during male meiosis.
108 egative); 7 ocular (2 autosomal recessive, 5 sex-linked recessive).
109 hromosomes differs strikingly, with a larger sex-linked region in the dioecious population compared w
110 s has revealed that sex-determining loci and sex-linked regions evolved independently in many plant l
111 ese data indicate that DMRT1 is an essential sex-linked regulator of gonadal differentiation in avian
112 which may be a candidate gene for mouse sla (sex linked sideroblastic anemia), near the X inactivatio
113 ong statistical evidence for a large effect, sex-linked, site-specific modifier of recombination rate
114 se sex chromosomes that multiple families of sex-linked spermatid-expressed genes are highly amplifie
115 sex-limited (to males) while the genotype is sex-linked (to females).
116 est that sperm length in G. bimaculatus is a sex-linked trait that is influenced by genes which are a
117 ray platelet syndrome (GPS) segregating as a sex-linked trait.
118    A survey of mitochondrial, imprinted, and sex-linked traits revealed modest associations with X-li
119 at the details of inheritance, which include sex-linked transmission, sex-limited fertility reduction
120 chromosomes are produced as a consequence of sex-linked transmission.
121 ker/100 kb distributed across the genome for sex-linked variation.
122                Because this phenotype is not sex linked, we evaluated the role of sex steroids.
123  cat as Orange, and in the Syrian hamster as Sex-linked yellow (Sly), but are curiously absent from o

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