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1 nd stronger purifying selection than for the human X chromosome.
2 on for both the chicken Z chromosome and the human X chromosome.
3 omplexes and their components encoded on the human X chromosome.
4 of more than 1000 informative loci along the human X chromosome.
5 eviously unknown sequence differences on the human X chromosome.
6 on-related genes are over-represented on the human X chromosome.
7 d mouse X chromosomes and 23.7% contain only human X chromosome.
8 e data from eight loci spanning >1 Mb on the human X chromosome.
9 c recombination across the centromere of the human X chromosome.
10 ely 15-17 Mb of the proximal long arm of the human X chromosome.
11 e test this concept experimentally using the human X chromosome.
12 approximately 28 kb in the q28 region of the human X chromosome.
13 lated from a cosmid library specific for the human X chromosome.
14 eterogeneity, with five reported loci on the human X-chromosome.
15 a common spacer deletion that affects 13% of human X Chromosomes.
16 from 0.14% to 0.06% in the recently finished human X chromosome (154.3 Mbp), and from 3.6% to 0% with
17                  Focusing our efforts on the human X chromosome(3), we reconstructed the centromeric
18 mples of genomic duplications present on the human X chromosome and autosomes.
19 PGK1 gene derived from an active or inactive human X chromosome and having differential methylation p
20 sion of a GCC repeat in proximal Xq28 of the human X chromosome and is associated with a mild form of
21 ite FRAXE is located in proximal Xq28 of the human X chromosome and lies approximately 600 kb distal
22 o infer genealogies across the length of the human X chromosome and to examine time to most recent co
23 ted regions, to define the centromere of the human X chromosome and to explore the evolution of seque
24 nome Aggregation Database, gnomAD) of 13,860 human X chromosomes and autosomes.
25                  This gene is located on the human X chromosome, and it is homologous to a family of
26                           We report that the human X chromosome appears to have one-third the density
27 m type I), two genes that are located on the human X chromosome at band p22.3 and in close proximity
28                         SLC9A7 is located on human X chromosome at Xp11.3 and has not yet been associ
29 cription factor TFIID, is expressed from the human X chromosome, at least in somatic cells.
30 transferase (GST) family termed GST-5 on the human X chromosome (band Xp11).
31                              We used a novel human X chromosome cDNA microarray (XCA) to survey the e
32 peat region of the alpha-satellite region on human X chromosome centromeres that is consistent with i
33          We identified 26 palindromes on the human X Chromosome, constituting more than 2% of its seq
34 chromosome with the finished sequence of the human X chromosome demonstrates that each evolved indepe
35 (RDT) expanded content library to enrich the human X chromosome exome (2.5 Mb) from 26 male samples f
36 ltiplex primer library covered 98.05% of the human X chromosome exome in a single tube with 11,845 di
37 ich and enable the routine sequencing of the human X chromosome exome suggests a wide variety of pote
38                The DNA methylation status of human X chromosomes from male and female neutrophils was
39 e mouse homologue of DAX1 (DSS-AHC Region on Human X Chromosome, Gene1) which is the gene responsible
40                                          The human X-chromosome harbors only 4% of our genome but car
41                                          The human X chromosome has a unique biology that was shaped
42  the Xq24-q26 cytogenetic band region of the human X chromosome has been assembled.
43 ion, genes from several other regions of the human X chromosome have now been shown to escape inactiv
44 ressed from both the active and the inactive human X chromosomes helping to explain the recessive nat
45 ertebrate Genome Annotation database) on the human X chromosome in 250 families with X-linked mental
46 lize in reactivants or in naturally inactive human X chromosomes in mouse/ human hybrid cells.
47                 The comparable region of the human X chromosome includes the disease locus for RP3, a
48 l of somatic cell hybrids retaining inactive human X chromosomes, including two independent hybrids t
49  expression of the FRAXE fragile site on the human X chromosome is associated with the expansion of a
50 ting that the LINE-1 (L1) composition of the human X chromosome is fundamentally distinct from that o
51                                          The human X chromosome is known to contain several disease g
52  of the human X centromere, demonstrate that human X chromosome is partitioned into repeat subfamilie
53                            Here we show that human X-chromosome-linked IAP directly inhibits at least
54                  Comparison of the horse and human X chromosome maps shows remarkable conservation of
55 nged syntenic segments between mouse and cat/human X chromosome marker order.
56 ial cells derived from CD34+ cells contained human X chromosome only.
57                                            A human X chromosome, present in a DT40-human microcell hy
58 d gRNA deletions along the PIGA locus on the human X chromosome ranging from 17 kb to 2 Mb.
59       First, we improved the accuracy of the human X-chromosome reference sequence through single-hap
60 5 kb of genomic sequence from the homologous human X chromosome region.
61  comprehensive X-inactivation profile of the human X chromosome, representing an estimated 95% of ass
62 brids with either the active or the inactive human X chromosome reveal that TCEAL7 is subjected to X
63                                          The human X chromosome sequence was used as a template to se
64 Despite this independence, the chicken Z and human X chromosomes share features that distinguish them
65 studies of the pericentromeric region of the human X chromosome short arm (Xp) revealed an age gradie
66  an approximately 5.5-megabase region on the human X chromosome spanning Xp11.21-p11.22.
67 the most evolutionary recent segments of the human X chromosome that are depleted of LINE1 and enrich
68 E.PTN-homologous sequences were found in the human X chromosome, the human hereditary haemochromatosi
69     For example, two recent studies compared human X chromosome to autosomal variation to make infere
70 ork map over 20-25 Mb of the long arm of the human X chromosome using yeast artificial chromosome (YA
71 c mice that carry a single copy of a minimal human X chromosome visual pigment gene array in which th
72 f DNA replication in the Xq27 portion of the human X chromosome was studied in cells derived from nor
73       To identify the essential sequences on human X chromosomes, we transfected male mouse ES cells
74  several protein-coding genes present on the human X Chromosome were absent from the pig, and 38 pig-
75 d Page previously observed that genes on the human X chromosome were physically arranged along the ch
76            The ABP280 gene is located on the human X chromosome, whereas the newly identified Fh1 gen
77 marker order was observed between feline and human X chromosomes, whereas the same markers identified
78              When examining samples from the human X chromosome, which represent a mixture of haploid
79 /hamster hybrid cells containing an inactive human X chromosome with the DNA demethylating agent 5-az
80     Contrasting the genetic diversity of the human X chromosome (X) and autosomes has facilitated und
81     Combined with sequence variation between human X chromosomes, XCI gives rise to intra-individual