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1 n sex-determining gene DMRT1 and ends at the pseudoautosomal region.
2 f a non-recombining region and a recombining pseudoautosomal region.
3 nce increases with genetic distance from the pseudoautosomal region.
4 ice because of a 4-Megabase expansion of the pseudoautosomal region.
5 lso offer insights into recombination in the pseudoautosomal region.
6 ric recombination suppression (PRS) into the pseudoautosomal region.
7 followed by autosomal genes and genes in the pseudoautosomal region.
8 mosome lengths, flanked at either end by two pseudoautosomal regions.
9 x linked, not including those in recombining pseudoautosomal regions.
10 -recombining sex-determining region into the pseudoautosomal regions.
11 G gene, which spans the boundary between the pseudoautosomal region 1 (PAR1) and the X-specific regio
12 emales of SHOX, a height-related gene in the pseudoautosomal region 1 (PAR1) on the X and Y sex chrom
13 tartling suggestion that the boundary of the pseudoautosomal region 1 (PAR1), where the human X and Y
14 x whole genome sequence (WGS), including the pseudoautosomal region 1 (PAR1).
15 st that the boundary between the recombining pseudoautosomal region 1 and the non-recombining portion
16 avy chain gene IGH@ on 14q32 to CRLF2 in the pseudoautosomal region 1 of Xp22.3/Yp11.3, whereas 10 (3
17 SFR alpha chain, encoded in the X-chromosome pseudoautosomal region 1.
18                             The 320-kb human pseudoautosomal region 2 (PAR2) at the tips of the long
19 pseudoautosomal region in distal Xq28 (PAR2; pseudoautosomal region 2), gave a combined maximum LOD s
20 , which is X-linked, human SPRY3 maps to the pseudoautosomal region 2; however, the human Y-linked al
21                     We have also refined the pseudoautosomal region and boundary in the cat and show
22         The OA1 gene is located close to the pseudoautosomal region and predicts a novel protein whos
23 ersity among species in their composition of pseudoautosomal regions and degree of Z/W differentiatio
24 ence, including new sequences from the human pseudoautosomal regions and from cancer-testis ampliconi
25 nake Z Chromosome, including the recombining pseudoautosomal region, and find evidence for partial do
26 lation: SYBL1, a housekeeping gene in the Xq pseudoautosomal region, and GPC3, a tissue-specific gene
27 elative to autosomes, including those in the pseudoautosomal region, and the male-bias increases afte
28 V system) recovering the sex determining and pseudoautosomal regions, and then to the mating-type chr
29 ease/decrease in sharing when markers in the pseudoautosomal region are analyzed.
30 st that all CpG islands on Xq, including the pseudoautosomal region, are subject to X inactivation-in
31 variable boundary at the sex-determining and pseudoautosomal regions as well as genes that exhibit ma
32                Sequence exchange outside the pseudoautosomal regions could play a role in protecting
33 on the mammalian Y chromosome outside of the pseudoautosomal region do not recombine with those on th
34 human X-linked genes outside the X-Y pairing pseudoautosomal regions escape X-inactivation.
35                  We examined the long arm XY pseudoautosomal region for linkage to asthma, serum IgE,
36                           We find eighteen X-pseudoautosomal region genes have conserved testes expre
37                                              Pseudoautosomal regions have been described in a broad t
38 polymorphisms at the distal tip of the Xp/Yp pseudoautosomal region in 47,XYY males, their parents an
39  Marker DXYS154, which is located within the pseudoautosomal region in distal Xq28 (PAR2; pseudoautos
40 ssion events moved the PAB and shortened the pseudoautosomal region in haplorrhines.
41 however, this gene spans the boundary of the pseudoautosomal region in mouse but not in humans.
42 the distal end of the bivalent acts as a neo-pseudoautosomal region in these males.
43  mice, there is synapsis between the X and Y pseudoautosomal regions; in XSxr(a)O mice, with a single
44  that the combined haploinsufficiency of the pseudoautosomal region likely plays a key role in these
45 e or more X/Y homolog genes, possibly in the pseudoautosomal region, may underlie pathophysiology and
46 e SpdyA was frequently lost from the X-Y non-pseudoautosomal region (non-PAR) telomeres.
47             We find that, while PolII in the pseudoautosomal region occupies both chromosomes at simi
48 obligatory exchange occurs in PAR1, an Xp/Yp pseudoautosomal region of 2.6 Mb, which creates a male-s
49                It has been proposed that the pseudoautosomal region of mammals has evolved by sequent
50             One was a 1.6-Mb deletion in the pseudoautosomal region of one maternal X chromosome enco
51 e pairs were preferentially clustered in the pseudoautosomal region of the sex chromosomes and locate
52 ature homeobox-containing gene (SHOX) in the pseudoautosomal region of the sex chromosomes may cause
53 ce for close linkage to three markers in the pseudoautosomal region of the sex chromosomes.
54 ntigens of the XG blood group located in the pseudoautosomal region of the sex chromosomes.
55 nd no genetic risk factors for AD on the non-pseudoautosomal region of the X-chromosome, but it ident
56 red regions, analogous to the nonpairing and pseudoautosomal regions of animal sex chromosomes.
57   However, with this approach, data from the pseudoautosomal regions on the X chromosome pose special
58                                  Outside the pseudoautosomal regions on the X chromosome, we similarl
59  PCR assays potentially originating from the pseudoautosomal region or other areas of X-Y or autosome
60 nes located in the human and orangutan Xp/Yp pseudoautosomal region (p-PAR), where recombination is o
61                             The S. latifolia pseudoautosomal region (PAR) includes several genes extr
62                                          The pseudoautosomal region (PAR) is a segment of shared homo
63  distal one-third of the long arm, where the pseudoautosomal region (PAR) is located terminally.
64 5% of chr5, an autosome, translocated to the pseudoautosomal region (PAR) of an ancestral sex chromos
65                                          The pseudoautosomal region (PAR) of mammalian sex chromosome
66                                          The pseudoautosomal region (PAR) of mammalian sex chromosome
67 le for LWD, SHOX, localizes to the short-arm pseudoautosomal region (PAR) of the X and Y chromosomes.
68 that this molecular marker is located in the pseudoautosomal region (PAR) of the X and Y chromosomes.
69 id sulfatase (Sts) as this is located in the pseudoautosomal region (PAR) of the X-chromosome and con
70  but incomplete loci in the mouse genome-the pseudoautosomal region (PAR) on the sex chromosomes and
71                                          The pseudoautosomal region (PAR) was strongly associated wit
72                               Six of 783 non-pseudoautosomal region (PAR) X-chromosome genes (ATRX, C
73 s share only a small homologous segment, the pseudoautosomal region (PAR), in which the formation of
74 ion (SDR) and proportionally elevated in the pseudoautosomal region (PAR).
75 over in a very small region of homology, the pseudoautosomal region (PAR).
76 mosomes, consistent with localization to the pseudoautosomal region (PAR).
77 cloned and mapped to Xp22.3, proximal to the pseudoautosomal region (PAR).
78 se characteristics are those residing in the pseudoautosomal regions (PAR) of the sex chromosomes.
79                          GYG2 is outside the pseudoautosomal region PAR1 but still in a region of X-Y
80 lished linkage to the marker DXYS6814 in the pseudoautosomal region (PAR1) of the X and Y chromosomes
81                             The 2.7-Mb major pseudoautosomal region (PAR1) on the short arms of the h
82 s hypothesis by studying the human short-arm pseudoautosomal region (PAR1), which recombines between
83 icated a critical region of <2 Mb within the pseudoautosomal region (PAR1).
84 DSB locations and fail to target DSBs to the pseudoautosomal regions (PARs) of sex chromosomes.
85 arly important role in targeting DSBs to the pseudoautosomal regions (PARs) of sex chromosomes.
86  of recombination that normally characterize pseudoautosomal regions (PARs) of X and Y chromosomes.
87 s pairing and exchange occurs within the two pseudoautosomal regions (PARs) together comprising <5% o
88 e of the horse (1.8 Mb) and donkey (1.88 Mb) pseudoautosomal regions (PARs).
89 at it is still ongoing in the recombining or pseudoautosomal, regions (PARs) of these chromosomes.
90 L1 gene (K=2.7%), located in the human Xq/Yq pseudoautosomal region (q-PAR), where recombination is k
91 t Moa1 is located much farther away from the pseudoautosomal region than its human homolog.
92 ls on the Y chromosome short arm outside the pseudoautosomal region that are homologous to Xq2l.3.
93                                  Outside the pseudoautosomal regions, the mammalian sex chromosomes a
94 ic map was 118.7 cM (female only) and of the pseudoautosomal region was 13.0 cM (male only).
95 stages from the mating-type locus toward the pseudoautosomal regions was not found, but evidence of s
96            In addition to the genes from the pseudoautosomal region, which have long been anticipated