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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                                        Using human Y chromosome antigen DBY, we showed that mutation
20                                      Because human Y chromosomes are clonally inherited, it has been
21 tromeres without bound CENP-B, including the human Y chromosome, are shown to mis-segregate in cells
22 at least three nonoverlapping regions of the human Y chromosome-AZFa, AZFb, and AZFc ("azoospermia fa
23                                          The human Y chromosome began to evolve from an autosome hund
24 nalyzed by polymerase chain reaction for the human Y chromosome (birth, monthly to 6 months; blood, m
25 he gorilla Y Chromosome to be similar to the human Y Chromosome, but not to the chimpanzee Y Chromoso
26                                          The human Y chromosome carries a number of genes specificall
27  region (AZoospermia Factor-a) region of the human Y chromosome cause irreversible spermatogenic fail
28 ns of the AZFa region on the long arm of the human Y chromosome cause male infertility.
29 arkers on the non-recombining portion of the human Y chromosome continue to have applications in many
30  probe to identify homologous sequences in a human Y chromosome cosmid library.
31 ogenetic relationships of archaic and modern human Y chromosomes differ from the population relations
32 trate the method on two different data sets: human Y chromosome DNA data and fungus DNA data.
33 e RBM (RNA-binding motif) gene family on the human Y chromosome encodes proteins with an RNA-binding
34 suggestions that the most recent ancestor of human Y chromosomes existed around 50,000 years ago and
35  complete 62,460,029-base-pair sequence of a human Y chromosome from the HG002 genome (T2T-Y) that co
36     The estimation of the age of the MRCA of human Y chromosomes from a sample of no variation is dis
37 gh-coverage complete sequences of 36 diverse human Y chromosomes from Africa, Europe, South Asia, Eas
38                    Little is known about how human Y-Chromosome gene expression directly contributes
39 te the inevitable detailed reconstruction of human Y chromosome genealogy based on several tens to ev
40                                              Human Y chromosome haplogroup J1-M267 is a common male l
41                   Massive palindromes in the human Y chromosome harbor mirror-image gene pairs essent
42 olution of the Y chromosome because only the human Y chromosome has been fully sequenced.
43                                          The human Y chromosome has been notoriously difficult to seq
44 ce of highly repetitive sequences within the human Y chromosome has prevented its complete assembly t
45            The nonrecombining portion of the human Y chromosome has proven to be a valuable tool for
46  loci from the nonrecombining portion of the human Y chromosome in 15 diverse human populations to ev
47 ert 1 Mb of DNA around the centromere of the human Y chromosome in chicken DT40 hybrid somatic cells.
48  increasing appreciation for the role of the human Y chromosome in phenotypic differences between the
49 man lipoprotein lipase (LPL) gene locus, the human Y-chromosome in several populations and a multi-lo
50 rators present an intriguing new face to the human Y chromosome, including eight massive palindromic
51 ng differences between Neandertal and modern human Y chromosomes, including potentially damaging chan
52  Neandertal lineage as an outgroup to modern human Y chromosomes-including A00, the highly divergent
53          The DAZ gene on the long arm of the human Y chromosome is a strong candidate for the 'azoosp
54                                          The human Y chromosome is intriguing not only because it har
55 on ancestor (TMRCA) of Neandertal and modern human Y chromosomes is approximately 588 thousand years
56 han the TMRCA of A00 and other extant modern human Y-chromosome lineages.
57             Deletion interval 6 (DI6) of the human Y chromosome, located at the distal end of the lon
58 BAC clones derived from the DAZ locus of the human Y chromosome long arm, a locus in which the entire
59  extensive genetic decay has resulted in the human Y chromosome losing 97% of its ancestral genes whi
60  abundant in the male-specific region of the human Y chromosome (MSY) and provide targets for intrach
61  sequence of the male-specific region of the human Y chromosome (MSY) has been determined recently; h
62                        The properties of the human Y chromosome - namely, male specificity, haploidy
63 c search of the nonrecombining region of the human Y chromosome (NRY) identified 12 novel genes or fa
64            The non-recombining region of the human Y chromosome (NRY), which comprises 95% of the chr
65             We report the sequences of 1,244 human Y chromosomes randomly ascertained from 26 worldwi
66  ongoing decay and looming extinction of the human Y chromosome, remarkably little is known about how
67      Deletion of any of three regions of the human Y chromosome results in spermatogenic failure and
68 f the Azoospermia Factor (AZF) region of the human Y chromosome results in spermatogenic failure.
69 didate fertility factors that lie within the human Y chromosome's AZFc region, whose deletion is a co
70 s are at odds with prominent accounts of the human Y chromosome's imminent demise.
71 escribe the first haploid minisatellite, the human Y chromosome-specific locus, MSY1.
72 h of its length; for example, only 5% of the human Y chromosome still shows X-Y recombination.
73  Earlier, we showed that introduction of the human Y chromosome suppresses the in vivo tumorigenicity
74 have made it clear that there is more to the human Y chromosome than a heap of evolutionary debris, h
75 (RBM) gene family has been identified on the human Y chromosome that maps to the same deletion interv
76                    We propose that, like the human Y chromosome, the chicken W chromosome is essentia
77 matic DNA of the male-specific region of the human Y chromosome, the MSY.
78 riation on the nonrecombining portion of the human Y chromosome to investigate human evolution during
79 ition contributed to the gene content of the human Y chromosome, together with two other molecular ev
80                                          The human Y chromosome, transmitted clonally through males,
81          Recently, the gr/gr deletion on the human Y chromosome was associated with increased risk of
82  polymorphic C-->T transition located on the human Y chromosome was found by the systematic comparati
83                 1.33 Mb of sequence from the human Y chromosome was searched for tri- to hexanucleoti
84            DNA in situ hybridization for the human Y chromosome was then performed on the same sample
85 terochromatic and euchromatic regions of the human Y chromosome were hybridized onto slot blots of ap
86 ctural variation of the P8 palindrome on the human Y chromosome, which contains two copies of the VCY
87  a lineage shared by Neanderthals and modern human Y chromosomes, which diverged from each other arou
88 der was remarkably conserved between cat and human Y chromosomes, with only one marker (SMCY) positio