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1 es involved in prezygotic isolation are also sex linked.
2  that genes involved in speciation are often sex-linked.
3 al in T. castaneum, and whether the trait is sex-linked.
4 s causing multiple genes to become partially sex-linked.
5 enes from both addition events are now fully sex-linked.
6 heritance evolves to ensure the integrity of sex-linked adaptations.
7       We report spontaneous emergence of non-sex-linked agammaglobulinemia with B-cell deficiency and
8 phenotypes were stable, inheritable, and not sex linked, although there was a trend for greater respo
9                                          The sex-linked ampliconic transcriptional regulators Slx and
10 in intestinal iron transport by study of the sex-linked anaemia (sla) mouse, which has a block in int
11 basolateral multi-copper ferroxidase) in the sex-linked anaemic mouse (sla) and ferroportin1 (basolat
12 nalysis of the relative rate of evolution of sex-linked and autosomal genes in primates.
13 cousin pedigree design to estimate additive, sex-linked and dominance (co)variances for 12 traits in
14  Age-related changes in additive, dominance, sex-linked and maternal variance and covariance between
15                            133 Mb completely sex-linked and partially degenerated region, possibly re
16 supports previous findings that the trait is sex-linked and polygenic.
17 e process that regulates sleep propensity is sex-linked, and that sleep amount and sleep propensity a
18                                    Mice with sex-linked anemia (sla) have a mutant form of Hephaestin
19                                     However, sex-linked anemia (sla) mice harboring a 194-amino acid
20 ingly, the truncated hephaestin expressed in sex-linked anemia (sla) mice still has measurable, but d
21                     Children showed the same sex-linked behavior found with infant monkeys: young boy
22 ale behavioral response to pheromone is also sex-linked, but maps 20-30 cM away.
23 hanges when genome regions become completely sex-linked, by analyses of multiple species of flatworms
24         Whether sexually selected traits are sex linked can have profound effects on their evolution.
25 l tools and demonstrate the utility of using sex-linked Cas9 strains for genetic control of animals.
26  facultative parthenogenesis in snakes and a sex-linked color mutation in the ball python (Python reg
27 c architecture and evolutionary history of a sex-linked colour polymorphism in the Gouldian finch Ery
28 sets are diurnal New World monkeys that show sex-linked cone photopigment polymorphism, whereby all m
29  Y, or the genome regions that are not fully sex-linked, consistent with a domestication bottleneck.
30 zones of admixture involving haplodiploid or sex-linked cytonuclear data.
31 for any of these characteristics, ruling out sex-linked, cytoplasmic, and endosymbiotic factors.
32 should be parsed into neutral, adaptive, and sex-linked datasets to generate the most accurate infere
33 to this pattern, including meiotic drive and sex-linked deleterious mutations, but further work is ne
34   At 6 of the polymorphic loci variation was sex-linked, despite the fact that these microsatellites
35                               In marmosets a sex-linked dichotomy results in dichromatic and trichrom
36  testosterone may have a role in determining sex-linked differences in cerebrovascular disease as wel
37 s of pPTSD was linked to remarkable age- and sex-linked differences in the microstructure of major wh
38  to evaluate if LOXL2-induced functional and sex-linked differences, both male and female four-month-
39 r causative factor for fragile X syndrome, a sex-linked disorder associated with cognitive impairment
40              Fabry's disease (FD) is a rare, sex-linked disorder resulting from alpha-galactosidase d
41 elated to JIA pathogenesis seem to display a sex-linked disparity.
42 te this genetically, we isolated a number of sex-linked DNA markers.
43                    Tests for the presence of sex-linked effects have been plagued by the need to make
44 e small, repeat-rich Merian elements and the sex-linked element.
45  of CRC carcinogenesis, particularly whether sex-linked factors play any role.
46 rated that the phenotype of the mouse mutant sex-linked fidget ( slf ) is caused by developmental mal
47  generates a fundamental dosage imbalance in sex-linked gene expression, with one sex having one copy
48 is, and molecular evolutionary analysis of a sex-linked gene from S. latifolia, DD44 (Differential Di
49 e respective X- and Y-linked copy of another sex-linked gene pair, SlCypX/SlCypY.
50 rt, this result is based on analyses of five sex-linked gene sequences, and the maximum divergence (a
51 scordant, and only one molecular marker, the sex-linked gene Tpi, has evidence for pheromone strain e
52 ll non-recombining regions (down to a single sex-linked gene).
53 DNA sequence diversity in a newly identified sex-linked gene, SlX9/SlY9, in Silene latifolia (Caryoph
54       We present a pipeline for detection of sex linked genes based on nucleotide polymorphism analys
55 ons results in massive mis-expression of neo-sex linked genes, and little correspondence between func
56 tion of the total variance (in IQ) is due to sex linked genes, it is of more importance that a boy sh
57              We mapped 29 S. latifolia fully sex-linked genes (including 21 newly discovered from tra
58  result in an imbalance of gene products for sex-linked genes [5].
59 ccumulates at transcriptional start sites of sex-linked genes activated in an RNF8-dependent manner,
60 anding the extent and specificity with which sex-linked genes and hormones define brain structure and
61  F1 mapping population were used to identify sex-linked genes and the nonrecombining region.
62 inked housekeeping genes, germ-cell-specific sex-linked genes are subject to meiotic sex-chromosome i
63                                      Because sex-linked genes are transmitted less frequently, they a
64 and that profound degeneration may evolve if sex-linked genes become duplicated to autosomes, a proce
65         In female heterogamous (ZW) species, sex-linked genes coding for maternal products that are p
66                                              Sex-linked genes could also contribute to human gender d
67           The average genetic environment of sex-linked genes differs from that of autosomal genes, s
68 cross-regulation of DDX3X and DDX3Y as these sex-linked genes evolved from ordinary alleles of their
69 in males than females, a pathogenic role for sex-linked genes has been suggested.
70 ith other mammalian species, and the role of sex-linked genes in fertility.
71 es arising from the different complements of sex-linked genes in male and female cells has received l
72 s of sex-linked genes to autosomal genes and sex-linked genes in males relative to females, our resul
73 ur comparative mapping shows that most fully sex-linked genes in S. latifolia are located on a single
74 her with comparative mapping of S. latifolia sex-linked genes in S. vulgaris (a related hermaphrodite
75 copy number lead to global overexpression of sex-linked genes in spermatids and either a distorted se
76 gene expression has evolved in autosomal and sex-linked genes in the dioecious species.
77 number of sex chromosomes, the expression of sex-linked genes is equalized by a process known as dosa
78 le-specific genes, while divergence of other sex-linked genes is similar to autosomal genes.
79 matocytes and that postmeiotic expression of sex-linked genes is variable.
80 omosomes, made possible by the sequencing of sex-linked genes on both the X and Y chromosomes, which
81 apayas to assess gene expression patterns of sex-linked genes on the papaya sex chromosomes.
82  expression are generally sex-biased for all sex-linked genes relative to autosomes, including those
83             Our analysis identifies specific sex-linked genes that are expressed from two copies in e
84                   Our analyses also identify sex-linked genes that could assist future research aimed
85            By analyzing expression ratios of sex-linked genes to autosomal genes and sex-linked genes
86                           Thus, 13 of the 14 sex-linked genes we examined showed some degree of postm
87                             Although all the sex-linked genes we investigated underwent MSCI, 14 of t
88 es in the mutagenesis and study of essential sex-linked genes, and indicate that OGT participation in
89 [5-8], it remains very difficult to discover sex-linked genes, and it is unclear whether Y-linked gen
90  Our approach identifies several hundred new sex-linked genes, and we show that this young Y chromoso
91  arrested in pachynema and failed to repress sex-linked genes, indicating a defective MSCI.
92                                  To identify sex-linked genes, regardless of their expression, we seq
93 file with candidate transcriptionally active sex-linked genes, sorted by their relevance.
94 ard orthologues compared with those of other sex-linked genes.
95 ion and long-term compensatory adaptation by sex-linked genes.
96 de of these effects being greatest for older sex-linked genes.
97 tween males and females in the expression of sex-linked genes.
98 the heterogametic sex is hemizygous for most sex-linked genes.
99 ated the time of divergence in four pairs of sex-linked genes.
100 he difficulty in estimating non-additive and sex-linked genetic variances using traditional quantitat
101 duals (termed 'gonochorism' in animals) have sex-linked genome regions.
102 ution analyses by CUT&RUN revealed shifts in sex-linked H3.3 associations from discrete intergenic si
103 hat genetic effects on residual variance are sex linked; heritable, sex-specific residuals might have
104              Our data demonstrate that, like sex-linked housekeeping genes, germ-cell-specific sex-li
105 males had suggested that the PEPB-1 locus is sex-linked in chinook salmon (Oncorhynchus tshawytscha).
106                    Studies on pairs of genes sex-linked in mammals suggests rapid divergence of DNA s
107  region and several genes that are partially sex-linked in Silene latifolia, using Silene dioica, a c
108 the fact that these microsatellites were not sex-linked in the other passerine birds where they were
109                    Here, we show that per is sex-linked in the silkmoth, Antheraea per-nyi.
110 ver before as a single sex-linked locus, but sex-linked inheritance is thought to facilitate the rapi
111 ication of plant secondary metabolites under sex-linked inheritance.
112 l number of genetic factors, one of which is sex linked (Ku2 locus).(3-5) However, the genetic underp
113 stimated in F(1) hybrids reveal evidence for sex-linked loci contributing to the evolution of recombi
114 linked gene and the first pair of homologous sex-linked loci to be found in plants.
115 ns with arbitrary dominance coefficients, to sex-linked loci with sex-specific selection coefficients
116 ype frequencies from population samples at a sex-linked locus in which functional alleles occur on bo
117 le-gene changes and never before as a single sex-linked locus, but sex-linked inheritance is thought
118 colour is genetically determined by a single sex-linked locus, Red.
119 llele frequency differences at only a single sex-linked locus, Tpi.
120 he female pheromone is governed by a single, sex-linked locus.
121 sing mutation is due to a change in a single sex-linked locus.
122                                              Sex-linked male deafness and dystonia (Mohr-Tranebjaerg
123 ator, reduction alters neurodevelopment in a sex-linked manner.
124  in shaping brain regions and behaviors in a sex-linked manner.
125    Here, we use crosses and genotyping for a sex-linked marker to reject this model: sex in diploid d
126                                 No perfectly sex-linked marker was found in the dioecious species, bu
127               Analysis of the segregation of sex-linked markers revealed that N. furzeri has a geneti
128                                  To identify sex-linked markers, to understand mechanisms of sex dete
129 ation and read depth identified 52 candidate sex-linked markers.
130  (94% females), suggesting that there may be sex-linked meiotic drive or a cytoplasmic sex-ratio fact
131 t the mutation segregates as a single-locus, sex-linked Mendelian trait on both islands.
132         Clones containing pseudoautosomal or sex-linked microsatellites were isolated from a bovine b
133                           Although levels of sex-linked mRNAs were mildly elevated, meiotic sex chrom
134 s (> 25X coverage) do not appear to have any sex-linked Muller F elements (typical for many Diptera)
135 oalpha mutant (WHAM) chicken has a recessive sex-linked mutation in the ABCA1 transporter gene that r
136  human preterm infant cerebellum also showed sex-linked myelination marker alteration, suggesting sim
137           Approximately 35% of the loci were sex linked, not including those in recombining pseudoaut
138                Here we show, using the first sex-linked nuclear sequences from an extinct species, th
139  by a two-gene inheritance model involving a sex-linked oncogene, Xmrk, and an autosomal tumor suppre
140 be annotated as either coding or non-coding, sex-linked or autosomal, selected or neutral, and have a
141  the sexually dimorphic expression of either sex-linked or IFN-responsive genes.
142 olor genes, there is no apparent homolog for Sex-linked orange in other mammals.
143                                 We show that Sex-linked orange is caused by a 5-kb deletion that lead
144 of the PKA catalytic subunit (PKA(C)); thus, Sex-linked orange is genetically and biochemically downs
145                                          The Sex-linked orange mutation in domestic cats causes varie
146                    Our work documents that a sex-linked organelle quality control mechanism drives th
147 h-swordtail hybrids, which carry a different sex-linked pigment pattern locus, Sp.
148 s in specific domains, implicating dose- and sex-linked plasticity mechanisms.
149 y to be involved in the persistence of these sex-linked polymorphisms and consider the impact of Xd o
150  k-mer based methods successfully identified sex-linked polymorphisms without the need for a referenc
151                                              Sex-linked preferences can drive the evolution of traits
152                           These included two sex-linked QTL on chromosome I affecting knockdown and r
153 we detect QTL that are unique, a QTL that is sex linked, QTL that overlap with QTL for stage of diapa
154 ested that HNRNPGT functionally replaces the sex-linked RBMX and RBMY genes during male meiosis.
155 ized both naturally occurring and engineered sex-linked recessive lethal alleles (RLAs) to create sex
156 egative); 7 ocular (2 autosomal recessive, 5 sex-linked recessive).
157  inversion generally assumed for suppressing sex-linked recombination.
158 a sequence capture array to identify a novel sex-linked region (SLR) in Salix nigra, a basal species
159 ed on a gene-by-gene level rather than whole sex-linked region in papaya.
160 hromosomes differs strikingly, with a larger sex-linked region in the dioecious population compared w
161 reference male and female genomes, a 1.15 Mb sex-linked region on Chr15W was confirmed to be absent i
162 uals show phenotype-genotype mismatch in the sex-linked region, and along with observation of leakine
163 ns, to study the evolutionary history of the sex-linked regions (SLRs).
164 t of all processes leading to gene loss from sex-linked regions and that profound degeneration may ev
165                                              Sex-linked regions are predicted to become enriched in g
166                          Consequently, their sex-linked regions could either have evolved soon after
167 s has revealed that sex-determining loci and sex-linked regions evolved independently in many plant l
168 ifferences help to understand why completely sex-linked regions may evolve.
169 e; and the extent to which the properties of sex-linked regions of genomes reflect responses to new s
170 ke predictions about genome evolution in the sex-linked regions of haploids that can now be tested by
171 ed response regulator gene is present in the sex-linked regions of P. davidiana and P. tremula.
172 e analyses and genetic mapping show that the sex-linked regions of these two species are the same, bu
173                             Recently evolved sex-linked regions offer an opportunity to understand th
174                     Some plants have massive sex-linked regions.
175 maphrodite haplotype structures and identify sex-linked regions.
176 ney, a limited set of genes showed conserved sex-linked regulation, whereas analysis of the mouse liv
177 ese data indicate that DMRT1 is an essential sex-linked regulator of gonadal differentiation in avian
178    The present findings demonstrate a major, sex-linked, role for the CRF(1) receptor in sociability
179                                              Sex-linked scaffolds show increased rates of female-spec
180 and annotation, aid in the identification of sex-linked sequences, and quantify patterns of sequence
181 which may be a candidate gene for mouse sla (sex linked sideroblastic anemia), near the X inactivatio
182 as developed and used to detect and position sex-linked single nucleotide polymorphism (SNP) markers
183 ong statistical evidence for a large effect, sex-linked, site-specific modifier of recombination rate
184                                      Several sex-linked sites displayed ectopic H3.3 occupancy that d
185                                          The sex-linked SNP markers identified will be useful for pot
186 se sex chromosomes that multiple families of sex-linked spermatid-expressed genes are highly amplifie
187 hydration associated genes two of which were sex-linked, suggesting that dehydration tolerance may be
188 ll-type-specific binding sites and potential sex-linked TF regulators, furthering our understanding o
189 ession analyses controlling for genotype and sex linked these networks to specific behavioral domains
190 sex-limited (to males) while the genotype is sex-linked (to females).
191 est that sperm length in G. bimaculatus is a sex-linked trait that is influenced by genes which are a
192 ray platelet syndrome (GPS) segregating as a sex-linked trait.
193 adigmatic model for studying the genetics of sex-linked traits and Y Chromosome-driven evolution for
194    A survey of mitochondrial, imprinted, and sex-linked traits revealed modest associations with X-li
195 e is controlled by cis-acting variation in a sex-linked transcription factor expressed in the develop
196 at the details of inheritance, which include sex-linked transmission, sex-limited fertility reduction
197 chromosomes are produced as a consequence of sex-linked transmission.
198 etic correlations, (2) higher proportions of sex-linked variance, or (3) differences between sexes in
199 ker/100 kb distributed across the genome for sex-linked variation.
200                Because this phenotype is not sex linked, we evaluated the role of sex steroids.
201 s reduced structural conservation across the sex-linked X chromosome.
202  cat as Orange, and in the Syrian hamster as Sex-linked yellow (Sly), but are curiously absent from o

 
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