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1                                              A chromosome 11 variant (rs59232451, HBE1-HBB locus, P =
2                                              A chromosome 14 inversion was found in a patient who dev
3                                              A chromosome 1q21.3 region that is frequently amplified
4                                              A chromosome 1q25 variant (rs10911021) has been associat
5                                              A chromosome 2-specific PAC library was also produced fr
6                                              A chromosome 22q13 locus strongly associates with increa
7                                              A chromosome 6 locus (7,370,061-7,606,946) was sequenced
8                                              A chromosome 7 locus was identified to be linked to lymp
9                                              A chromosome cap distinguishes the chromosome end from a
10                                              A chromosome conformation capture (3C) assay shows that
11                                              A chromosome conformation capture assay coupled with chr
12                                              A chromosome conformation capture assay performed in hum
13                                              A chromosome dimer is lethal unless resolved.
14                                              A chromosome duplication implicated FtsA overproduction
15                                              A chromosome end, including a telomere and adjacent sequ
16                                              A chromosome fragmentation assay was used to measure the
17                                              A chromosome in an individual of recently admixed ancest
18                                              A chromosome inversion was observed in the euchromatic r
19                                              A chromosome is represented as beads-on-a-string and sto
20                                              A chromosome number of four was confirmed by cytological
21                                              A chromosome Pv03 dirigent-like gene, involved in lignin
22                                              A chromosome region maintenance 1 (CRM1)-dependent nucle
23                                              A chromosome structure consistent of many stacked layers
24                                              A chromosome transmission fidelity (ctf) mutant, s138, o
25                                              A chromosome with mutations in both GSL1 and GSL5 render
26                                              A chromosome with one entirely vertebrate-sequence telom
27                                              A chromosome-by-chromosome account is given to direct fu
28                                              A chromosome-encoded three-component nitroarene dioxygen
29                                              A chromosome-level genome assembly and annotation were e
30                                              A chromosome-located locus (BMQ_1820, renamed gerWB) is
31 our inserts have been localized among all 10 A chromosome pairs by FISH using the yeast DNA probe tog
32  translocation, which collectively define 35 A chromosome breakpoints.
33 leward spindle microtubule flux and anaphase A chromosome movement occur at similar rates ( approxima
34 ence photoactivation analysis, both anaphase A chromosome movement and poleward spindle microtubule f
35 wed the transition to anaphase, but anaphase A chromosome movements were slowed, anaphase B spindle e
36 , a diet-induced obesity study, including B6.A chromosome substitution-strain (consomic) mice, showed
37 rary B chromosome and an arm of an essential A chromosome.
38 tain segments of two nonhomologous essential A chromosomes in tandem arrangement attached to a segmen
39 an unusually high frequency of trisomies for A chromosomes was observed.
40  the generation of minichromosomes of normal A chromosomes by selection of spontaneous polyploid even
41 etectable homology between any of the normal A chromosomes and the B chromosome.
42  can cause in trans down- or upregulation of A chromosome-encoded genic fragments.
43 sent in addition to the normal complement of A chromosomes.
44 w is that they are derived from fragments of A chromosomes and/or generated in response to interspeci
45 ing us to trace their origin to fragments of A chromosomes, with the largest parts corresponding to r
46 ed for euchromatic (non-C-banded) regions of A chromosomes.
47 s are optional additions to the basic set of A chromosomes, and occur in all eukaryotic groups.
48 es, and exerts tissue-specific influences on A chromosome gene expression.
49 ome accumulation affects R-loop formation on A chromosomes, and exerts tissue-specific influences on
50 uding its origin by recombination of several A chromosomes followed by capturing of additional A-deri
51   In addition to the normal set of standard (A) chromosomes, some eukaryote species harbor supernumer
52  capable of impacting gene expression of the A chromosomes.
53 uch smaller bands than those observed on the A chromosomes.
54 revealed the presence of diploids with their A chromosomes derived solely from the tetraploid parent
55 on in the region of shared homology of these A chromosome segments creates a B-A-A translocation.
56 ow differential condensation with respect to A chromosomes and display dark C-bands of heterochromati
57 d plants containing an extra copy of the two A chromosome segments.
58 erally derived from a pair of classical type-A chromosomes, and relatively few alternative models hav
59                                Compared with A chromosomes, B chromosomes were also found to accumula