ライフサイエンスコーパス: human Y chromosome

1 tion rate, that of base substitutions on the human Y chromosome.

2 e rate of base substitution mutations on the human Y chromosome.

3 icroarray containing 178 BAC clones from the human Y chromosome.

4 y) for high-throughput SNP genotyping of the human Y chromosome.

5 LY1, in the centromeric alphoid array of the human Y chromosome.

6 s revealed four full-length DAZ genes on the human Y chromosome.

7 markers that are currently available for the human Y chromosome.

8 s are illustrated using recent data from the human Y chromosome.

9 been mapped to two different regions of the human Y chromosome.

10 gerprinting approach to build contigs on the human Y chromosome.

11 iven extensive structural polymorphism among human Y chromosomes.

12 ese data to study the ancestral genealogy of human Y chromosomes.

13 CY, DBY, and DFFRY) in a worldwide sample of human Y chromosomes.

14 luster/four-gene arrangement found on modern human Y chromosomes.

15 population growth in the effective number of human Y chromosomes.

16 cosmid library constructed from flow-sorted human Y chromosomes.

17 or reconstructing the worldwide genealogy of human Y chromosomes and for illuminating patrilineal rel

18 The CDY genes have been localized to the human Y chromosome, and we report here that they are der

19 Because human Y chromosomes are clonally inherited, it has been

20 tromeres without bound CENP-B, including the human Y chromosome, are shown to mis-segregate in cells

21 at least three nonoverlapping regions of the human Y chromosome-AZFa, AZFb, and AZFc ("azoospermia fa

22 The human Y chromosome began to evolve from an autosome hund

23 nalyzed by polymerase chain reaction for the human Y chromosome (birth, monthly to 6 months; blood, m

24 he gorilla Y Chromosome to be similar to the human Y Chromosome, but not to the chimpanzee Y Chromoso

25 The human Y chromosome carries a number of genes specificall

26 region (AZoospermia Factor-a) region of the human Y chromosome cause irreversible spermatogenic fail

27 ns of the AZFa region on the long arm of the human Y chromosome cause male infertility.

28 arkers on the non-recombining portion of the human Y chromosome continue to have applications in many

29 probe to identify homologous sequences in a human Y chromosome cosmid library.

30 trate the method on two different data sets: human Y chromosome DNA data and fungus DNA data.

31 e RBM (RNA-binding motif) gene family on the human Y chromosome encodes proteins with an RNA-binding

32 suggestions that the most recent ancestor of human Y chromosomes existed around 50,000 years ago and

33 The estimation of the age of the MRCA of human Y chromosomes from a sample of no variation is dis

34 gh-coverage complete sequences of 36 diverse human Y chromosomes from Africa, Europe, South Asia, Eas

35 te the inevitable detailed reconstruction of human Y chromosome genealogy based on several tens to ev

36 Massive palindromes in the human Y chromosome harbor mirror-image gene pairs essent

37 olution of the Y chromosome because only the human Y chromosome has been fully sequenced.

38 The nonrecombining portion of the human Y chromosome has proven to be a valuable tool for

39 loci from the nonrecombining portion of the human Y chromosome in 15 diverse human populations to ev

40 ert 1 Mb of DNA around the centromere of the human Y chromosome in chicken DT40 hybrid somatic cells.

41 increasing appreciation for the role of the human Y chromosome in phenotypic differences between the

42 man lipoprotein lipase (LPL) gene locus, the human Y-chromosome in several populations and a multi-lo

43 rators present an intriguing new face to the human Y chromosome, including eight massive palindromic

44 ng differences between Neandertal and modern human Y chromosomes, including potentially damaging chan

45 Neandertal lineage as an outgroup to modern human Y chromosomes-including A00, the highly divergent

46 The DAZ gene on the long arm of the human Y chromosome is a strong candidate for the 'azoosp

47 The human Y chromosome is intriguing not only because it har

48 on ancestor (TMRCA) of Neandertal and modern human Y chromosomes is approximately 588 thousand years

49 han the TMRCA of A00 and other extant modern human Y-chromosome lineages.

50 Deletion interval 6 (DI6) of the human Y chromosome, located at the distal end of the lon

51 BAC clones derived from the DAZ locus of the human Y chromosome long arm, a locus in which the entire

52 abundant in the male-specific region of the human Y chromosome (MSY) and provide targets for intrach

53 sequence of the male-specific region of the human Y chromosome (MSY) has been determined recently; h

54 The properties of the human Y chromosome - namely, male specificity, haploidy

55 c search of the nonrecombining region of the human Y chromosome (NRY) identified 12 novel genes or fa

56 The non-recombining region of the human Y chromosome (NRY), which comprises 95% of the chr

57 We report the sequences of 1,244 human Y chromosomes randomly ascertained from 26 worldwi

58 ongoing decay and looming extinction of the human Y chromosome, remarkably little is known about how

59 Deletion of any of three regions of the human Y chromosome results in spermatogenic failure and

60 f the Azoospermia Factor (AZF) region of the human Y chromosome results in spermatogenic failure.

61 didate fertility factors that lie within the human Y chromosome's AZFc region, whose deletion is a co

62 s are at odds with prominent accounts of the human Y chromosome's imminent demise.

63 escribe the first haploid minisatellite, the human Y chromosome-specific locus, MSY1.

64 h of its length; for example, only 5% of the human Y chromosome still shows X-Y recombination.

65 Earlier, we showed that introduction of the human Y chromosome suppresses the in vivo tumorigenicity

66 have made it clear that there is more to the human Y chromosome than a heap of evolutionary debris, h

67 (RBM) gene family has been identified on the human Y chromosome that maps to the same deletion interv

68 We propose that, like the human Y chromosome, the chicken W chromosome is essentia

69 matic DNA of the male-specific region of the human Y chromosome, the MSY.

70 riation on the nonrecombining portion of the human Y chromosome to investigate human evolution during

71 ition contributed to the gene content of the human Y chromosome, together with two other molecular ev

72 The human Y chromosome, transmitted clonally through males,

73 Recently, the gr/gr deletion on the human Y chromosome was associated with increased risk of

74 polymorphic C-->T transition located on the human Y chromosome was found by the systematic comparati

75 1.33 Mb of sequence from the human Y chromosome was searched for tri- to hexanucleoti

76 DNA in situ hybridization for the human Y chromosome was then performed on the same sample

77 terochromatic and euchromatic regions of the human Y chromosome were hybridized onto slot blots of ap

78 der was remarkably conserved between cat and human Y chromosomes, with only one marker (SMCY) positio