戻る
「早戻しボタン」を押すと検索画面に戻ります。

今後説明を表示しない

[OK]

コーパス検索結果 (1語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します
1 loped DCM or the other phenotypes, including sex bias.
2 minantly affect females, indicating a strong sex bias.
3 resent muscle damage in soleus with a strong sex bias.
4 rom >4,100 cancers across 21 tumor types for sex bias.
5 Z chromosome, and shows other differences in sex bias.
6 genes, dosage compensation, and evolution of sex bias.
7 T does not seem to be affected by ethnic and sex bias.
8 r complex disorders that exhibit significant sex biases.
9  of mortality is the propensity for it to be sex-biased.
10 mber of genes that were female-biased or non-sex-biased.
11 owed functional clustering only if they were sex-biased.
12  are enriched for nearby and correspondingly sex-biased accessible chromatin regions, as well as sex-
13 sex bias, we demonstrate a rapid turnover of sex bias across this clade driven by sexual selection an
14 rtially migratory and that migration was not sex-biased across surveyed areas.
15 cultural populations, we find no evidence of sex-biased admixture during the migration that spread fa
16     We demonstrate increased power to detect sex-biased admixture in African-American individuals fro
17 duced arthritis (CIA) in mice is the lack of sex bias and autoantibodies in the animal model.
18 pproaches as well as the correlation between sex bias and expression breadth.
19 ntradictory, with some studies indicating no sex bias and others indicating either female or male bia
20 ss the island reveals that the admixture was sex biased and happened heterogeneously across Madagasca
21 lps; a freely adjustable sex ratio magnifies sex biases and promotes helping; and sib-mating, promisc
22 w that complex dispersal dynamics, including sex biases and strong density dependence, emerge natural
23 cross pregnancy for gene candidates that are sex-biased and stress-responsive in mice and translate t
24 significant differences in selection between sex-biased and unbiased genes, which relate primarily to
25 ptome shows switches between nonsex bias and sex bias, and just 0.9% of the transcriptome shows rever
26     However, mechanisms responsible for this sex bias are not clear.
27 n in men, but the mechanisms underlying this sex bias are unknown.
28                                              Sex biases are eliminated if both sexes evaluate mate av
29 that X chromosome dosage contributed to this sex bias as female pDCs have an enhanced TLR7-mediated I
30 utoreactive B cells and begin to explain the sex bias associated with the condition.
31 systems are implicated in diverse domains of sex-biased behavior and pathology, but we lack a basic u
32 sed accessible chromatin regions, as well as sex-biased binding sites for growth hormone-regulated tr
33 d developmental abnormalities leading to 1:2 sex biases, caused by lethality of half of the male or f
34 matin states are thus a major determinant of sex-biased chromatin accessibility and gene expression,
35 ined by miRNA-specific regulation, including sex-biased chromatin accessibility at promoters, rather
36 ng sex-biased genes by binding to sites in a sex-biased chromatin state.
37 females, with translational implications for sex biases commonly found in midbrain DA-associated diso
38 oof of principle that when CRF is in excess, sex-biased CRF1 coupling translates into divergent cell
39 es in male and female brains, as a result of sex-biased CRF1 signaling.
40 nervous system, locomotor abnormalities, and sex-biased defects in adult craniofacial morphology.
41  in the absence of these, also by historical sex-biased demographic events or other processes.
42 (iv) Sex-biased STAT5 binding is enriched at sex-biased DHS marked as active enhancers and preferenti
43                                          (i) Sex-biased DHS, but not sex-biased genes, are frequently
44 tic conflict caused by ancient admixture and sex-biased differences in genomic transmission.
45 f genes, respectively, exhibited strain- and sex-bias differential gene or exon expression.
46                            We report greater sex-biased differential expression in the pituitary as c
47 tion model to explore interactive effects of sex-biased dispersal and demographic stochasticity.
48                                              Sex-biased dispersal and extra-pair mating may also have
49 erent host plants, potentially influenced by sex-biased dispersal and female philopatry.
50 between mammals and birds, mating system and sex-biased dispersal are far from perfectly associated w
51              The hypothesis that patterns of sex-biased dispersal are related to social mating system
52  behavioral differences in mating system and sex-biased dispersal between mammals and birds, mating s
53                                              Sex-biased dispersal created spatial clines in the sex r
54 e fine-scale spatial genetic structuring and sex-biased dispersal have important implications for the
55                      Additionally, tests for sex-biased dispersal imply that dispersal frequency is s
56 elationship between social mating system and sex-biased dispersal in birds when the effects of phylog
57 f the relationship between mating system and sex-biased dispersal in mammals and birds.
58 mes and the influence of sex chromosomes and sex-biased dispersal in post-speciation gene flow.
59 ulation structure and looked for evidence of sex-biased dispersal in smooth snakes (Coronella austria
60 ) the relationship between mating system and sex-biased dispersal in these vertebrate groups has not
61 t the relationship between mating system and sex-biased dispersal is more complex than a simple contr
62 st experimental evidence for an influence of sex-biased dispersal on invasion velocity, highlighting
63  laboratory mesocosms to test the effects of sex-biased dispersal on range expansion, and a simulatio
64 thers maintain that any kind of lineality or sex-biased dispersal only emerged much later.
65 , theoretical studies on mate finding and on sex-biased dispersal produce opposing predictions: in th
66 life history or behaviour (skewed sex ratio, sex-biased dispersal, and sex-specific mating behaviours
67                                         With sex-biased dispersal, the effective number of gametes is
68 nce in male reproductive success and limited sex-biased dispersal, which enables us to control to som
69 f male and female snakes showed evidence for sex-biased dispersal, with three of four analyses findin
70 eading-edge sex ratios, perhaps overwhelming sex-biased dispersal.
71 aphic stochasticity would weaken a signal of sex-biased dispersal.
72 l to diurnal activity patterns, but not with sex-biased dispersal.
73 trapolate dispersal frequencies and test for sex-biased dispersal.
74 mune-mediated disease of the CNS and shows a sex-biased distribution in which 60-75% of all cases are
75 ent STAT5 binding correlated positively with sex-biased DNase hypersensitivity and H3-K4me1 and H3-K4
76        We demonstrate how the close age- and sex-biased dyadic relationships are correlated with the
77        We tested the burden and the possible sex-biased effect of CNVs at 16p13.11 in a sample of 10,
78 with controls (OR = 2.59; p = 0.0005), and a sex-biased effect, with a significant enrichment of CNVs
79 ex ratio, one male per litter, revealing its sex-biased effect.
80 of human Dab2 as a tumor suppressor, and the sex-biased embryonic lethality suggests a genetic intera
81 al network and by the dynamics of changes in sex-biased epigenetic states.
82 se populations, quantifying the postcolonial sex-biased European gene flow across multiple regions.
83                                      Despite sex-biased eve expression, the gene networks downstream
84  transcription factor, giant (gt), we traced sex-biased eve patterning to gt dose, indicating that ea
85  specialties in which the greatest and least sex biases exist.
86                  Objectives: To determine if sex bias exists in human surgical clinical research, to
87                   Conclusions and Relevance: Sex bias exists in human surgical clinical research.
88  in preclinical studies, we explored whether sex bias exists in skin research.
89                                         That sex-biased exposure might translate to sex-specific adve
90 human brain, and we identified genes showing sex biased expression at major developmental stages (pre
91  in multiple outcrossing species with strong sex-biased expression are even more likely to be missing
92  Numerous studies have shown that genes with sex-biased expression are under- or over-represented on
93                         Moreover, genes with sex-biased expression as revealed by comparing amounts i
94 s showing the same growth hormone-regulated, sex-biased expression as their mouse counterparts.
95                        We show that averaged sex-biased expression changes accumulate monotonically o
96                                              Sex-biased expression characterized 247 liver lincRNAs,
97 identified several OR transcripts displaying sex-biased expression in adults, as well as larval-enric
98        About 80% of the expressed genes show sex-biased expression in each species.
99                We report tissue-specific and sex-biased expression in genes commonly investigated whe
100  rattlesnake to establish baseline levels of sex-biased expression in homomorphic sex chromosomes, an
101         To address this problem, we measured sex-biased expression in multiple Drosophila species and
102 lacking germline tissue to define genes with sex-biased expression in terminally differentiated somat
103 s been identified in a screen for genes with sex-biased expression in the head.
104              We give examples of genes where sex-biased expression is both disease-relevant and likel
105  sexual antagonism, and that the majority of sex-biased expression is due to adaptive changes in male
106                                              Sex-biased expression is explained by miRNA-specific reg
107 ormone (GH) secretory patterns determine the sex-biased expression of >1,000 genes in mouse and rat l
108 cific chromatin states appear not to explain sex-biased expression of genes.
109 osage compensation raises the possibility of sex-biased expression of key developmental genes, such a
110 ces between males and females arise from the sex-biased expression of nearly identical genomes can re
111 gned species-specific microarrays to examine sex-biased expression of orthologues and species-restric
112                   We find that Dsx regulates sex-biased expression predominantly in males, that Dsx's
113           One model predicts that genes with sex-biased expression should be enriched on the X chromo
114                      Comparative analysis of sex-biased expression should deepen our understanding of
115 bustness of the pattern to Gene Ontology and sex-biased expression suggest that partly recessive bene
116                     Additionally, genes with sex-biased expression tend to be narrowly expressed in a
117  alleles to one sex, whereas ratites evolved sex-biased expression to confine the product of a sexual
118 ary, Nasonia accomplish a striking degree of sex-biased expression without sex chromosomes or epigene
119 ome is the result of selection on genes with sex-biased expression, narrowly expressed genes, or some
120 % of expressed genes displayed significantly sex-biased expression.
121 viding for direct and indirect regulation of sex-biased expression.
122 e-sensitive aneuploid effects also influence sex-biased expression.
123 0.9% of the transcriptome shows reversals of sex-biased expression.
124 in, loss, increase, decrease, or reversal of sex-biased expression.
125 ors that should be considered when analyzing sex-biased expression.
126 and evaluated ASD risk genes for evidence of sex-biased expression.
127 in the Drosophila genome may be spliced in a sex-biased fashion, raising the possibility that alterna
128  or protection from autoimmunity, creating a sex bias for autoimmune diseases.
129 nique opportunity to investigate a potential sex bias for different types of mutations.
130                               Furthermore, a sex bias for severe sequelae from coxsackievirus infecti
131  strains, C and C57BL/6J (B), demonstrated a sex bias for susceptibility.
132 ver, levels of gene expression are generally sex-biased for all sex-linked genes relative to autosome
133  the X chromosome has acquired a paradoxical sex-biased function by redistributing gene contents [5,
134 o distinct co-expression networks, and shows sex-biased gene expression and exon usage.
135 m manipulation disproportionately influences sex-biased gene expression but show that the direction o
136  modifications accompanied these cGH-induced sex-biased gene expression changes.
137  test the links between sexual selection and sex-biased gene expression evolution in a comparative fr
138      Our results support a scenario in which sex-biased gene expression evolved during the evolution
139                                We found that sex-biased gene expression has evolved in autosomal and
140                           Separate sexes and sex-biased gene expression have repeatedly evolved in an
141     Here, we review our current knowledge of sex-biased gene expression in both model and nonmodel or
142 rate that previously unexplained patterns of sex-biased gene expression in Drosophila melanogaster mi
143 pidly evolved new gene networks and impacted sex-biased gene expression in Drosophila.
144 iver and WAT indicates that RSL1 accentuates sex-biased gene expression in liver but greatly diminish
145 sex-differential chromatin accessibility and sex-biased gene expression in mouse liver.
146              Such studies have revealed that sex-biased gene expression is abundant in many species,
147 Xenopus to provide an additional test of how sex-biased gene expression may contribute to differences
148 hanges cannot explain the extensive level of sex-biased gene expression observed.
149 ycle of the chicken to assess the pattern of sex-biased gene expression on the Z chromosome.
150 males and females are likely rooted from the sex-biased gene expression regulation during brain devel
151                 Sexual dimorphism depends on sex-biased gene expression, but the contributions of mic
152 on, whereas other sex-specific signals cause sex-biased gene expression.
153 and transcriptional dimorphism, often termed sex-biased gene expression.
154 ferences in gene expression is the result of sex-biased gene expression.
155 ying the transcription factors that regulate sex-biased gene expression.
156 ences gene expression, including patterns in sex-biased gene expression.
157 h as dosage compensation, also may influence sex-biased gene expression.
158              In addition, various degrees of sex-biased gene flow exhibiting disproportionately highe
159                           Results indicate a sex-biased gene flow from Europeans, the male contributi
160 ng that sex biases in expression may reflect sex-biased gene regulatory structures.
161                          Thus, the temporal, sex-biased gene responses to persistent GH stimulation a
162 , these analyses reveal an important role of sex biased genes in brain development and neurodevelopme
163 fectors expressed in the head, and report 46 sex-biased genes (>4-fold/P < 0.01).
164         However, there are little overlap of sex-biased genes among the major developmental stages, a
165  opening and STAT5, but not BCL6, regulating sex-biased genes by binding to sites in a sex-biased chr
166 h contributes to a nonrandom distribution of sex-biased genes compared to the remainder of the genome
167                                 We find that sex-biased genes do change in expression but, contrary t
168 rgence in the alternate sex, suggesting that sex-biased genes endure stronger selection when expresse
169 tion of dynamic expression regulation of the sex-biased genes in the brain during development.
170 on divergence than non-sex-biased genes, and sex-biased genes show higher levels of expression diverg
171 l expression can be achieved for hundreds of sex-biased genes simply based on the GH input signal pat
172                                              Sex-biased genes were clustered by chromatin environment
173  active enhancers and preferentially targets sex-biased genes with sex-differences in local chromatin
174 her levels of expression divergence than non-sex-biased genes, and sex-biased genes show higher level
175                  (i) Sex-biased DHS, but not sex-biased genes, are frequently characterized by sex-di
176                                              Sex-biased genes, especially those with male-biased expr
177 e chromosomal locations and the evolution of sex-biased genes.
178 e the genomic and evolutionary properties of sex-biased genes.
179 utionary forces that govern the evolution of sex-biased genes.
180                 We confirm recent reports of sex-biased genetic effects in 17q by showing highly sign
181 ctivating) marks, correlated negatively with sex-biased H3-K27me3 (repressive) marks, and was associa
182 l common variants largely do not explain the sex bias in ADHD prevalence.
183 variation, we find evidence of a significant sex bias in admixture proportions consistent with dispro
184 is relatively favoured when there is a small sex bias in adult dispersal in favour of the sex with th
185              Our findings identify a natural sex bias in appendage regenerative capacity and indicate
186                                          The sex bias in AS is not explained by X-chromosome-encoded
187                       There is a significant sex bias in AS, and there are differences in recurrence
188 mit moth dispersal and whether there was any sex bias in attraction to light.
189 -estradiol is crucial in the pathogenesis of sex bias in cancer and autoimmunity.
190 ase-hypersensitive sites (DHS) classified by sex bias in chromatin accessibility and enhancer modific
191  in these strains, revealing or abrogating a sex bias in disease expression depending on the genotype
192 esented within a social group (when there is sex bias in dispersal and/or variance in reproductive su
193 ate-finding difficulties can select for less sex bias in dispersal when mate finding occurs after dis
194  and IL-6 may act synergistically to promote sex bias in experimental DILI by reducing Tregs.
195                               An established sex bias in HIV pathogenesis is linked to immune respons
196 ulating the spatial pattern of dysbiosis and sex bias in IBD.
197               Numerous studies have reported sex bias in infectious diseases, with bias direction dep
198                                       Strong sex bias in laying order and growth patterns enabled mit
199        The disease model best explaining the sex bias in occurrence and transmission of AS is a polyg
200 ever, a possible molecular mechanism for the sex bias in physiological adaptation to oxidative stress
201 ot differ by sex, as evidenced by absence of sex bias in programmed death receptor-1 and responses to
202 rstand the role of DR4 in susceptibility and sex bias in RA.
203 izophrenia and autism, which often exhibit a sex bias in rates of presentation, age of onset, and sym
204                       Although a significant sex bias in seropositivity was detected in adult deer mi
205  detected in adult deer mice, no significant sex bias in seropositivity was detected in juvenile anim
206 ex bias observed in human disease.IMPORTANCE Sex bias in severe sequelae from enteric viral infection
207 odevelopmental disorders, which often have a sex bias in severity and prevalence.
208  providing support for the role of Ifi202 in sex bias in SLE.
209                                              Sex bias in susceptibility to autoimmune diseases is evi
210 IFNgamma/IL-26 gene region may contribute to sex bias in susceptibility to RA, by distorting the prop
211 skin and soft tissue infections (SSTIs), yet sex bias in susceptibility to S. aureus SSTI has not bee
212                             The existence of sex bias in the delivery of cardiac care is controversia
213                     Here, we have revealed a sex bias in the efficiency of clinically relevant LT bio
214 ty of HSV-1 0DeltaNLS and uncover a probable sex bias in the induction of IFN-alpha/beta in the corne
215 nvestigated the genetic aspects of the large sex bias in the prevalence of autism spectrum disorder b
216        Most neuropsychiatric diseases have a sex bias in their presentation, age of onset, or treatme
217                                          The sex bias in urine testing is not clinically supported an
218                                              Sex biases in autoimmunity and infection suggest that st
219 uences, and provide evidence suggesting that sex biases in expression may reflect sex-biased gene reg
220  demonstrate that escape from XCI results in sex biases in gene expression, establishing incomplete X
221  identifying several traits with significant sex biases in genetic susceptibilities.
222 gnificant mechanistic implications regarding sex biases in NDDs.
223  host and pathogen genetic data can identify sex biases in pathogen spatial spread, which may be a wi
224 pmental disorders (NDDs), many of which show sex biases in prevalence, onset and/or severity.
225 mbined with cellular aging processes promote sex biases in stress dysregulation.
226  and highlight new avenues for research into sex biases in stress-related disorders.
227 s and found evidence for different levels of sex-bias in these areas: the strongest male-bias was obs
228                  We test the hypothesis that sex-biases in infection are related to variation in mult
229  chronic oxidative stress show a significant sex bias, including neurodegenerative diseases, cancer,
230       In mouse, but not opossum and chicken, sex bias is coordinated across tissues such that autosom
231                         The etiology of this sex bias is far from known, but pivotal for understandin
232 ess, and is relatively disfavoured when this sex bias is large or in the opposite direction.
233 men, although the mechanistic basis for this sex bias is not well understood.
234                     A combination of heavily sex-biased laying order and sex differences in growth pa
235                           The basis for this sex bias lies in the X chromosome, which contains many i
236                                          The sex-biased lincRNA genes are enriched for nearby and cor
237 tors implicated in growth hormone-regulated, sex-biased liver gene expression, leading to the followi
238 s assigned a physiological role, accentuates sex-biased liver gene expression, most dramatically for
239 esity, and increased leptin sensitivity in a sex-biased manner.
240  and many inflammatory diseases present in a sex-biased manner.
241 ng the molecular mechanisms controlling this sex bias may reveal novel targets to promote host innate
242  change over adolescence--with relevance for sex-biased mental disorders emerging in youth.
243 rough both severe population bottlenecks and sex-biased migration.
244 analyses uncovered numerous cases of somatic sex-biased miRNA expression, with the largest proportion
245                                              Sex-biased miRNAs also targeted genes related to Wnt and
246 l. applied a pan-cancer analysis to identify sex-biased molecular signatures and revealed two sex-eff
247  whereas the other shows much more extensive sex-biased molecular signatures.
248 f this more vulnerable sex in expectation of sex-biased mortality.
249 o Y chromosomal translocation has revealed a sex bias much lower than previous estimates.
250 hromosome population datasets emphasizes the sex-biased nature of recent demographic transitions in E
251                          Studies have linked sex-biased neurodevelopmental disorders, including autis
252 ss during pregnancy predisposes offspring to sex-biased neurodevelopmental disorders, including schiz
253 et and penetrance of disease, abrogating the sex bias normally seen in the NOD model.
254 ine and should be considered in light of the sex bias observed in human disease.IMPORTANCE Sex bias i
255 iation in length of aganglionic segment, and sex bias observed in human HSCR patients.
256 response, specifically in the context of the sex bias observed in susceptibility to infectious and au
257                                              Sex bias occurrence of HCC associated with EGFR was conf
258                                              Sex bias occurrence was conserved in our model, with mal
259 dy provides evidence for the role of EGFR in sex bias occurrences of liver cancer and as the driver m
260 tterfly Hypolimnas bolina the suppression of sex biases occurs extremely fast, with a switch from a 1
261  the chicken and zebra finch, with regard to sex bias of autosomal versus Z chromosome genes, dosage
262  not affect the time of onset, incidence, or sex bias of type 1 diabetes in NOD/ShiLtJ mice.
263        Although several of these domains are sex biased, our fundamental understanding of cerebellar
264  maternal stress exposure that may relate to sex-biased outcomes in neurodevelopment.
265  study a species with an unusual, apparently sex-biased pattern of distribution, and test the hypothe
266 evels of African ancestry, consistent with a sex-biased pattern of gene flow with an excess of Europe
267 ly controlled at least in part by genes with sex-biased patterns of expression.
268 ch varied in density, genetic diversity, and sex-biased philopatry.
269                           We conclude that a sex-biased process that reduced the female effective pop
270  evolutionary history, a coherent picture of sex-biased processes has yet to emerge.
271 rently contradictory evidence on the role of sex-biased processes in human evolutionary history and s
272 ther than piggybacking of intronic miRNAs on sex-biased protein-coding genes.
273 ons, and further specifying their timing and sex-biases, provides potent new research targets for bas
274 male and female affected persons without any sex bias, replicating recent findings, though the author
275 n of histone H3 at K27 (H3K27me3) is a major sex-biased repressive mark at highly female-biased but n
276                        Of the 20 QTL, 8 were sex biased, sex specific, or sex antagonistic.
277  putative genetic mechanisms underlying this sex bias: sex-specific heterogeneity and higher burden o
278 1 to Gs-independent signaling pathways, this sex-biased signaling is proposed to result in distinct c
279 of clinically actionable genes (60/114) show sex-biased signatures.
280 nge of biological functions showed that most sex-biased splicing occurs in the gonads.
281       To investigate potential mechanisms of sex-biased splicing, we used real-time PCR to examine th
282                    Most of these loci showed sex-biased splicing, whereas genotype-specific splicing
283                                         (iv) Sex-biased STAT5 binding is enriched at sex-biased DHS m
284 males and persistent in females-regulate the sex-biased, STAT5-dependent expression of hundreds of ge
285 minant gene, resistance to HSV-1 is strongly sex biased such that female mice are significantly more
286 tion between sex-dependent STAT5 binding and sex-biased target gene expression.
287 iod of multiple generations, with a level of sex bias that excludes a pulse migration during a single
288 development of SLE is known to have a strong sex bias, the molecular mechanisms remain unknown.
289  suggested that 17beta-estradiol may enhance sex bias through IL-6 induction, which subsequently disc
290                                The degree of sex bias to SARS-CoV infection increased with advancing
291 remain viable, though flightless, and show a sex bias towards maleness.
292 n, for example when using mixed controls for sex-biased traits.
293                 Here, we present analyses of sex-biased transcriptome divergence in sexually mature a
294                        Five newly identified sex-biased transcripts in Drosophila are full of surpris
295               X (or Z) chromosomes also show sex-biased transmission (i.e., X chromosomes show female
296                                          The sex-biased transmission of the Z and its hemizygosity in
297       Recently we reported a vaccine-induced sex bias: vaccinated female but not male rhesus macaques
298                            Importantly, this sex bias was mediated by a sex-specific response to the
299          Through ancestral reconstruction of sex bias, we demonstrate a rapid turnover of sex bias ac
300 ously found that the CRF1 receptor (CRF1) is sex biased whereby coupling to its GTP-binding protein,

WebLSDに未収録の専門用語(用法)は "新規対訳" から投稿できます。
 
Page Top