ライフサイエンスコーパス: human X chromosome

1 on for both the chicken Z chromosome and the human X chromosome.

2 omplexes and their components encoded on the human X chromosome.

3 of more than 1000 informative loci along the human X chromosome.

4 e test this concept experimentally using 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 approximately 28 kb in the q28 region of the human X chromosome.

12 nd stronger purifying selection than for 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 mples of genomic duplications present on the human X chromosome and autosomes.

16 PGK1 gene derived from an active or inactive human X chromosome and having differential methylation p

17 sion of a GCC repeat in proximal Xq28 of the human X chromosome and is associated with a mild form of

18 ite FRAXE is located in proximal Xq28 of the human X chromosome and lies approximately 600 kb distal

19 o infer genealogies across the length of the human X chromosome and to examine time to most recent co

20 ted regions, to define the centromere of the human X chromosome and to explore the evolution of seque

21 This gene is located on the human X chromosome, and it is homologous to a family of

22 We report that the human X chromosome appears to have one-third the density

23 m type I), two genes that are located on the human X chromosome at band p22.3 and in close proximity

24 cription factor TFIID, is expressed from the human X chromosome, at least in somatic cells.

25 transferase (GST) family termed GST-5 on the human X chromosome (band Xp11).

26 We used a novel human X chromosome cDNA microarray (XCA) to survey the e

27 peat region of the alpha-satellite region on human X chromosome centromeres that is consistent with i

28 chromosome with the finished sequence of the human X chromosome demonstrates that each evolved indepe

29 (RDT) expanded content library to enrich the human X chromosome exome (2.5 Mb) from 26 male samples f

30 ltiplex primer library covered 98.05% of the human X chromosome exome in a single tube with 11,845 di

31 ich and enable the routine sequencing of the human X chromosome exome suggests a wide variety of pote

32 The DNA methylation status of human X chromosomes from male and female neutrophils was

33 e mouse homologue of DAX1 (DSS-AHC Region on Human X Chromosome, Gene1) which is the gene responsible

34 The human X chromosome has a unique biology that was shaped

35 the Xq24-q26 cytogenetic band region of the human X chromosome has been assembled.

36 ion, genes from several other regions of the human X chromosome have now been shown to escape inactiv

37 ressed from both the active and the inactive human X chromosomes helping to explain the recessive nat

38 ertebrate Genome Annotation database) on the human X chromosome in 250 families with X-linked mental

39 lize in reactivants or in naturally inactive human X chromosomes in mouse/ human hybrid cells.

40 The comparable region of the human X chromosome includes the disease locus for RP3, a

41 l of somatic cell hybrids retaining inactive human X chromosomes, including two independent hybrids t

42 expression of the FRAXE fragile site on the human X chromosome is associated with the expansion of a

43 ting that the LINE-1 (L1) composition of the human X chromosome is fundamentally distinct from that o

44 The human X chromosome is known to contain several disease g

45 Here we show that human X-chromosome-linked IAP directly inhibits at least

46 Comparison of the horse and human X chromosome maps shows remarkable conservation of

47 nged syntenic segments between mouse and cat/human X chromosome marker order.

48 ial cells derived from CD34+ cells contained human X chromosome only.

49 A human X chromosome, present in a DT40-human microcell hy

50 First, we improved the accuracy of the human X-chromosome reference sequence through single-hap

51 5 kb of genomic sequence from the homologous human X chromosome region.

52 comprehensive X-inactivation profile of the human X chromosome, representing an estimated 95% of ass

53 brids with either the active or the inactive human X chromosome reveal that TCEAL7 is subjected to X

54 The human X chromosome sequence was used as a template to se

55 Despite this independence, the chicken Z and human X chromosomes share features that distinguish them

56 studies of the pericentromeric region of the human X chromosome short arm (Xp) revealed an age gradie

57 an approximately 5.5-megabase region on the human X chromosome spanning Xp11.21-p11.22.

58 the most evolutionary recent segments of the human X chromosome that are depleted of LINE1 and enrich

59 E.PTN-homologous sequences were found in the human X chromosome, the human hereditary haemochromatosi

60 For example, two recent studies compared human X chromosome to autosomal variation to make infere

61 ork map over 20-25 Mb of the long arm of the human X chromosome using yeast artificial chromosome (YA

62 c mice that carry a single copy of a minimal human X chromosome visual pigment gene array in which th

63 f DNA replication in the Xq27 portion of the human X chromosome was studied in cells derived from nor

64 To identify the essential sequences on human X chromosomes, we transfected male mouse ES cells

65 several protein-coding genes present on the human X Chromosome were absent from the pig, and 38 pig-

66 d Page previously observed that genes on the human X chromosome were physically arranged along the ch

67 The ABP280 gene is located on the human X chromosome, whereas the newly identified Fh1 gen

68 marker order was observed between feline and human X chromosomes, whereas the same markers identified

69 When examining samples from the human X chromosome, which represent a mixture of haploid

70 /hamster hybrid cells containing an inactive human X chromosome with the DNA demethylating agent 5-az

71 Contrasting the genetic diversity of the human X chromosome (X) and autosomes has facilitated und