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1 t they are the only cells that progress into diplotene.
2 ed to mouse meiotic chromosomes at pachytene/diplotene.
3 at the E18.5, when most oocytes are entering diplotene.
4  overlaps with the sex body chromatin during diplotene.
5 ytes, while staining intensity diminished in diplotene and meiotically dividing spermatocytes, the ce
6 ower percentages at later stages (pachytene, diplotene and metaphase I) providing evidence that delet
7 teracting protein, PCH2, joins the BB in mid-diplotene, and by late-diplotene, it lies in the middle
8 9-1 basidia enter the diffuse stage of early diplotene, and then 50% of these cells enter metaphase I
9 ain SYP-1,2 along the full lengths of coiled diplotene axes.
10 scripts are stripped away, the oval shape of diplotene bivalents between chiasmata, and the rigidity
11 mpanied by increased cell death in pachytene/diplotene cells with markedly elevated levels of phospho
12 s from the chromosome arms in late-pachytene-diplotene cells.
13 ath during early prophase; oocytes reach the diplotene/dictyate stage in nearly normal numbers, but m
14 , which we now identify as occurring at late diplotene, immediately before diakinesis.
15 NH3-Ser50 phosphorylation begins in prophase/diplotene, increases to a maximum at prometaphase-metaph
16 terochromatin, which normally occurs in late diplotene, is reduced in spermatocytes from heterozygous
17 , joins the BB in mid-diplotene, and by late-diplotene, it lies in the middle of the HOP1 filament.
18 pachytene SCs, as compared to more condensed diplotene-metaphase I bivalents, makes mapping crossover
19  the number and distribution of chiasmata on diplotene-metaphase I chromosomes.
20          However, the release of SYN1 during diplotene occurred normally, indicating that this proces
21 lin A1 in the pericentromeric region in late diplotene of meiosis, perhaps in assembly or function of
22                        Therefore, in stage 1 diplotene oocytes there is a unique mechanism causing a
23                   However, by early stage 1 (diplotene oocytes, 50-200 microm), all three of the RNAs
24 ually reproducing animals, oocytes arrest at diplotene or diakinesis and resume meiosis (meiotic matu
25                                    A diffuse diplotene phase coincides with dissolution of the synapt
26                        We show that in early diplotene pre-stage 1 oocytes (25-50 microm in diameter)
27 th spermatogenic arrest predominately at the diplotene premeiotic stage and almost no sperm detected
28                                           As diplotene progresses, the BB increases in width and acqu
29 the germ line, specifically to pachytene and diplotene spermatocytes and early spermatids.
30 mal complexes failed to desynapse and normal diplotene spermatocytes were not observed.
31 granules are prominent in late pachytene and diplotene spermatocytes, and in elongating spermatids.
32 combination nodule, was delayed in Cul4a -/- diplotene spermatocytes, which potentially led to subseq
33 re localized to the XY body in pachytene and diplotene spermatocytes, while only SUMO2/3 and UBE2I we
34 suggested a role for SPO11alpha in pachytene/diplotene spermatocytes.
35  down-regulated, failed to transition to the diplotene stage, and then quickly died.
36 achytene stage but failed to progress to the diplotene stage.
37 -/-) undergoes critical meiocyte loss at the diplotene stage.
38 nesis was arrested around the late pachytene-diplotene stages of prophase I; surprisingly, without an
39 s detected in spermatocytes at pachytene and diplotene stages.
40                                           At diplotene, the numbers of HEI10 foci, a marker for Class
41 ore protein, DSN1, from within the BB at mid-diplotene to the edge of the homologs facing the poles b