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1 mosome are nonrecombining, while the rest is pseudoautosomal.
2                Especially the border between pseudoautosomal and male-specific regions of the Y has n
3 ne might be in a state of transition between pseudoautosomal and X-unique locations.
4            We pinpointed the location of the pseudoautosomal boundaries (PAB) and determined the size
5 orangutan non-coding divergence at the Xp/Yp pseudoautosomal boundary (K=3.5%) and in the SYBL1 gene
6  gene Fxy (also known as MID1 [7]) spans the pseudoautosomal boundary (PAB) in the laboratory mouse (
7                         The evolution of the pseudoautosomal boundary (PAB) is well documented in hap
8           In particular, data from the mouse pseudoautosomal boundary (PAB) suggested that locally in
9 clease recognition site just proximal to the pseudoautosomal boundary by homologous recombination.
10                                          The pseudoautosomal boundary has shifted at least six times
11 ously described a gene, Fxy , that spans the pseudoautosomal boundary in mice such that the first thr
12 nd Y chromosomes followed by movement of the pseudoautosomal boundary to create X-unique regions.
13 chromosome, which we have used to define the pseudoautosomal boundary, that is, the point of divergen
14 roximately 0.2-cM interval that includes the pseudoautosomal boundary.
15 located in Xp22.3 in humans, proximal to the pseudoautosomal boundary.
16       This constitutes the first report of a pseudoautosomal DNA marker for plant sex chromosomes.
17 utosomal genes, three X-linked genes, and 10 pseudoautosomal genes associated with LOY.
18 ide non-coding divergence (K) to that in the pseudoautosomal genes which were reported to recombine m
19                               Defects of the pseudoautosomal homeobox gene SHOX were previously shown
20             We have named the gene PHOG, for pseudoautosomal homeobox-containing osteogenic gene.
21 linked genes are increased relative to their pseudoautosomal homologs, both at synonymous and amino a
22                                            A pseudoautosomal location for a dosage-sensitive locus in
23 leles occur on both the X and Y chromosomes (pseudoautosomal loci).
24             Recombination rates between this pseudoautosomal marker and the differentiating portion o
25  completed using 292 autosomal and three X-Y pseudoautosomal markers.
26                        BAC57, containing the pseudoautosomal microsatellite INRA3O, mapped to the dis
27                            Clones containing pseudoautosomal or sex-linked microsatellites were isola
28                                              Pseudoautosomal PacI restriction fragments, up to 2 Mb i
29 complex (MHC) and one in the sex chromosomal pseudoautosomal pairing region PAR1.
30 g male meiosis is restricted to the terminal pseudoautosomal pairing regions.
31 t 170-fold higher for synonymous sites) when pseudoautosomal (present on both the X and Y chromosomes
32 e SpdyA was frequently lost from the X-Y non-pseudoautosomal region (non-PAR) telomeres.
33 nes located in the human and orangutan Xp/Yp pseudoautosomal region (p-PAR), where recombination is o
34                             The S. latifolia pseudoautosomal region (PAR) includes several genes extr
35                                          The pseudoautosomal region (PAR) is a segment of shared homo
36  distal one-third of the long arm, where the pseudoautosomal region (PAR) is located terminally.
37 5% of chr5, an autosome, translocated to the pseudoautosomal region (PAR) of an ancestral sex chromos
38                                          The pseudoautosomal region (PAR) of mammalian sex chromosome
39                                          The pseudoautosomal region (PAR) of mammalian sex chromosome
40 le for LWD, SHOX, localizes to the short-arm pseudoautosomal region (PAR) of the X and Y chromosomes.
41 that this molecular marker is located in the pseudoautosomal region (PAR) of the X and Y chromosomes.
42 id sulfatase (Sts) as this is located in the pseudoautosomal region (PAR) of the X-chromosome and con
43  but incomplete loci in the mouse genome-the pseudoautosomal region (PAR) on the sex chromosomes and
44                                          The pseudoautosomal region (PAR) was strongly associated wit
45                               Six of 783 non-pseudoautosomal region (PAR) X-chromosome genes (ATRX, C
46 s share only a small homologous segment, the pseudoautosomal region (PAR), in which the formation of
47 cloned and mapped to Xp22.3, proximal to the pseudoautosomal region (PAR).
48 ion (SDR) and proportionally elevated in the pseudoautosomal region (PAR).
49 over in a very small region of homology, the pseudoautosomal region (PAR).
50 mosomes, consistent with localization to the pseudoautosomal region (PAR).
51 lished linkage to the marker DXYS6814 in the pseudoautosomal region (PAR1) of the X and Y chromosomes
52                             The 2.7-Mb major pseudoautosomal region (PAR1) on the short arms of the h
53 s hypothesis by studying the human short-arm pseudoautosomal region (PAR1), which recombines between
54 icated a critical region of <2 Mb within the pseudoautosomal region (PAR1).
55 L1 gene (K=2.7%), located in the human Xq/Yq pseudoautosomal region (q-PAR), where recombination is k
56 G gene, which spans the boundary between the pseudoautosomal region 1 (PAR1) and the X-specific regio
57 emales of SHOX, a height-related gene in the pseudoautosomal region 1 (PAR1) on the X and Y sex chrom
58 tartling suggestion that the boundary of the pseudoautosomal region 1 (PAR1), where the human X and Y
59 x whole genome sequence (WGS), including the pseudoautosomal region 1 (PAR1).
60 st that the boundary between the recombining pseudoautosomal region 1 and the non-recombining portion
61 avy chain gene IGH@ on 14q32 to CRLF2 in the pseudoautosomal region 1 of Xp22.3/Yp11.3, whereas 10 (3
62 SFR alpha chain, encoded in the X-chromosome pseudoautosomal region 1.
63                             The 320-kb human pseudoautosomal region 2 (PAR2) at the tips of the long
64 pseudoautosomal region in distal Xq28 (PAR2; pseudoautosomal region 2), gave a combined maximum LOD s
65 , which is X-linked, human SPRY3 maps to the pseudoautosomal region 2; however, the human Y-linked al
66                     We have also refined the pseudoautosomal region and boundary in the cat and show
67         The OA1 gene is located close to the pseudoautosomal region and predicts a novel protein whos
68 ease/decrease in sharing when markers in the pseudoautosomal region are analyzed.
69 on the mammalian Y chromosome outside of the pseudoautosomal region do not recombine with those on th
70                  We examined the long arm XY pseudoautosomal region for linkage to asthma, serum IgE,
71                           We find eighteen X-pseudoautosomal region genes have conserved testes expre
72 polymorphisms at the distal tip of the Xp/Yp pseudoautosomal region in 47,XYY males, their parents an
73  Marker DXYS154, which is located within the pseudoautosomal region in distal Xq28 (PAR2; pseudoautos
74 ssion events moved the PAB and shortened the pseudoautosomal region in haplorrhines.
75 however, this gene spans the boundary of the pseudoautosomal region in mouse but not in humans.
76 the distal end of the bivalent acts as a neo-pseudoautosomal region in these males.
77  that the combined haploinsufficiency of the pseudoautosomal region likely plays a key role in these
78             We find that, while PolII in the pseudoautosomal region occupies both chromosomes at simi
79 obligatory exchange occurs in PAR1, an Xp/Yp pseudoautosomal region of 2.6 Mb, which creates a male-s
80                It has been proposed that the pseudoautosomal region of mammals has evolved by sequent
81             One was a 1.6-Mb deletion in the pseudoautosomal region of one maternal X chromosome enco
82 e pairs were preferentially clustered in the pseudoautosomal region of the sex chromosomes and locate
83 ature homeobox-containing gene (SHOX) in the pseudoautosomal region of the sex chromosomes may cause
84 ce for close linkage to three markers in the pseudoautosomal region of the sex chromosomes.
85 ntigens of the XG blood group located in the pseudoautosomal region of the sex chromosomes.
86 nd no genetic risk factors for AD on the non-pseudoautosomal region of the X-chromosome, but it ident
87  PCR assays potentially originating from the pseudoautosomal region or other areas of X-Y or autosome
88                          GYG2 is outside the pseudoautosomal region PAR1 but still in a region of X-Y
89 t Moa1 is located much farther away from the pseudoautosomal region than its human homolog.
90 ls on the Y chromosome short arm outside the pseudoautosomal region that are homologous to Xq2l.3.
91 ic map was 118.7 cM (female only) and of the pseudoautosomal region was 13.0 cM (male only).
92 nake Z Chromosome, including the recombining pseudoautosomal region, and find evidence for partial do
93 lation: SYBL1, a housekeeping gene in the Xq pseudoautosomal region, and GPC3, a tissue-specific gene
94 elative to autosomes, including those in the pseudoautosomal region, and the male-bias increases afte
95 st that all CpG islands on Xq, including the pseudoautosomal region, are subject to X inactivation-in
96 e or more X/Y homolog genes, possibly in the pseudoautosomal region, may underlie pathophysiology and
97            In addition to the genes from the pseudoautosomal region, which have long been anticipated
98 ric recombination suppression (PRS) into the pseudoautosomal region.
99 followed by autosomal genes and genes in the pseudoautosomal region.
100 n sex-determining gene DMRT1 and ends at the pseudoautosomal region.
101 nce increases with genetic distance from the pseudoautosomal region.
102 f a non-recombining region and a recombining pseudoautosomal region.
103 ice because of a 4-Megabase expansion of the pseudoautosomal region.
104 lso offer insights into recombination in the pseudoautosomal region.
105 se characteristics are those residing in the pseudoautosomal regions (PAR) of the sex chromosomes.
106 arly important role in targeting DSBs to the pseudoautosomal regions (PARs) of sex chromosomes.
107 DSB locations and fail to target DSBs to the pseudoautosomal regions (PARs) of sex chromosomes.
108  of recombination that normally characterize pseudoautosomal regions (PARs) of X and Y chromosomes.
109 s pairing and exchange occurs within the two pseudoautosomal regions (PARs) together comprising <5% o
110 e of the horse (1.8 Mb) and donkey (1.88 Mb) pseudoautosomal regions (PARs).
111 ersity among species in their composition of pseudoautosomal regions and degree of Z/W differentiatio
112 ence, including new sequences from the human pseudoautosomal regions and from cancer-testis ampliconi
113 variable boundary at the sex-determining and pseudoautosomal regions as well as genes that exhibit ma
114                Sequence exchange outside the pseudoautosomal regions could play a role in protecting
115 human X-linked genes outside the X-Y pairing pseudoautosomal regions escape X-inactivation.
116                                              Pseudoautosomal regions have been described in a broad t
117 red regions, analogous to the nonpairing and pseudoautosomal regions of animal sex chromosomes.
118   However, with this approach, data from the pseudoautosomal regions on the X chromosome pose special
119                                  Outside the pseudoautosomal regions on the X chromosome, we similarl
120 stages from the mating-type locus toward the pseudoautosomal regions was not found, but evidence of s
121 V system) recovering the sex determining and pseudoautosomal regions, and then to the mating-type chr
122                                  Outside the pseudoautosomal regions, the mammalian sex chromosomes a
123 -recombining sex-determining region into the pseudoautosomal regions.
124 mosome lengths, flanked at either end by two pseudoautosomal regions.
125 x linked, not including those in recombining pseudoautosomal regions.
126  mice, there is synapsis between the X and Y pseudoautosomal regions; in XSxr(a)O mice, with a single
127 at it is still ongoing in the recombining or pseudoautosomal, regions (PARs) of these chromosomes.
128 om a chromosomal rearrangement that includes pseudoautosomal sequences and affects XY pairing.
129  association analyses of X chromosome and XY pseudoautosomal single nucleotide polymorphisms (SNPs) a
130                            Only Smcx and the pseudoautosomal Sts gene on the mouse X chromosome have
131               Satisfying the requirement for pseudoautosomal synapsis by providing a pairing partner
132  adjacent like repeats, as seen at the Xp/Yp pseudoautosomal telomere.
133 nscripts tested here, 34 (three of which are pseudoautosomal) were expressed in as many as nine Xi hy
134 mcx gene is the first known example of a non-pseudoautosomal X-linked gene in mouse that normally esc

 
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