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1 on in fully synapsed chromosomes at the late pachytene stage.
2 ls were defective in progressing through the pachytene stage.
3 d Rad51 foci and absence of Mlh1 foci in the pachytene stage.
4  contained oocytes that were arrested at the pachytene stage.
5  increasing accumulation of mRNA through the pachytene stage.
6 or germ cell maturation during the early-mid pachytene stage.
7  house mice via spermatogenic failure at the pachytene stage.
8 end-to-end synapsis of homologues during the pachytene stage(5,6).
9 THDC2-deficient germ cells to advance to the pachytene stage and properly express many meiotic marker
10       Cleavage of genic targets began at the pachytene stage and resulted in progressive repression t
11 ologous chromosomes are fully aligned at the pachytene stage, and germ cells survive to complete meio
12 s to the sex chromosomes at the onset of the pachytene stage, and the subsequent formation of an isol
13 ntered meiotic prophase and were arrested at pachytene stage, and there was a significant increase in
14 d meiotic progression of germ cells into the pachytene stage, as spermatogonial and Sertoli cells wer
15 otic and differentiation of cells beyond the pachytene stage began to falter.
16 the mutant mice synapsed and advanced to the pachytene stage but failed to progress to the diplotene
17            GLD-1 levels are high through the pachytene stage but fall to background as germ cells exi
18              However, cells that survive the pachytene stage display chromosome nondisjunction at the
19 nlarging oocytes, originating primarily from pachytene-stage germ cells.
20 etic landscape of meiotic chromosomes at the pachytene stage in mouse oocytes.
21 nts showing that him-14 functions during the pachytene stage, indicate that him-14 is not needed to e
22 e findings reveal a process in which, at the pachytene stage, individual telomere/nuclear envelope (N
23 thout significant delay, in Atmsh5-1 but the pachytene stage is extended by several hours, indicative
24 imited to a very transient period during the pachytene stage of first meiotic prophase.
25 ocalized to P granules beginning at the late pachytene stage of male gametogenesis.
26 nd actively mobilizing TEs commencing at the pachytene stage of meiosis during germ cell development;
27 with abnormal spermatocytes appearing at the pachytene stage of meiosis I and subsequent accumulation
28 hat the crossovers were induced at the early pachytene stage of meiosis I.
29 auses arrest of spermatogenesis prior to the pachytene stage of meiosis prophase I.
30              In budding yeast, exit from the pachytene stage of meiosis requires the mid-meiosis tran
31  in somatic root tip metaphase cells, in the pachytene stage of meiosis, and in interphase nuclei.
32  cell proliferation, progression through the pachytene stage of meiosis, and the formation of bivalen
33 eflects the compaction of chromosomes at the pachytene stage of meiosis.
34 their histone modifications beginning at the pachytene stage of meiosis.
35 expression corresponds with the onset of the pachytene stage of meiosis.
36 ay a role in the exit of germ cells from the pachytene stage of meiotic prophase and/or gamete differ
37 t spermatogenesis is arrested at mid to late pachytene stage of meiotic prophase with defective synap
38               The hop2 mutant arrests at the pachytene stage of meiotic prophase with the RecA-like p
39                   Both mutants arrest at the pachytene stage of meiotic prophase, sae1-1 temporarily
40 e bivalents is acquired by the middle of the pachytene stage of meiotic prophase, several days after
41 ue to checkpoint-induced arrest/delay at the pachytene stage of meiotic prophase.
42 heckpoint that causes cells to arrest at the pachytene stage of meiotic prophase.
43 is undergo checkpoint-mediated arrest at the pachytene stage of meiotic prophase.
44 gression through gametogenesis occurs at the pachytene stage of meiotic prophase.
45          Meiosis is arrested at the zygotene/pachytene stage of prophase I as a result of abnormal ch
46 turbation could be traced as far back as the pachytene stage of spermatogenesis.
47 molog axes at sites of crossovers during the pachytene stage of the meiotic prophase.
48 spermatogenesis is disrupted at mid- or late pachytene stages of meiosis or early spermiogenesis.
49  meiotic chromosomes during the zygotene and pachytene stages of meiosis.
50 sed in spermatocytes in the preleptotene and pachytene stages of meiosis.
51 ed solely in germ cells during the leptotene-pachytene stages of spermatogenesis.
52 s to permit meiotic progression from the mid-pachytene stage onward.
53  male germ cells, as it was found in meiotic pachytene stage oocytes as well.
54                       Here, we used an Ewsr1 pachytene stage-specific knockout mouse model to study t
55 ditory nerve) maintained normal function but pachytene stage spermatocytes underwent apoptosis.
56 tly normal late recombination nodules at the pachytene stage, suggesting that the mutant's defects in
57                                       At the pachytene stage, telomeres rearranged again by dispersin
58 ely in germ cells of the testis from the mid-pachytene stage until the elongating spermatid stage.
59 mature termination of spermatogenesis at the pachytene stage was accompanied by increased apoptosis b
60 ages, but not genes that are markers for the pachytene stage, was observed.
61  concert with a requirement for c-Abl at the pachytene stage, we show that, in contrast to wild-type
62                                       At the pachytene stage, when other co-translational RNA surveil
63 es without PIWI proteins are arrested at the pachytene stage, when the sex chromosomes undergo transc
64 asynapsed autosomes undergo apoptosis at the pachytene stage, while those with only asynapsed sex chr
65 ns in early meiotic Prophase I, prior to the pachytene stage, with increasing accumulation of mRNA th