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1 omes associate pre-meiotically in meiocytes (germ-line cells).
2 ct on spontaneous mutagenesis in somatic and germ line cells.
3 enescence, and do not segregate somatic from germ line cells.
4  response to this signal in both somatic and germ line cells.
5 es, and are specifically expressed in female germ-line cells.
6                            During mitosis in germ line cells and embryos, IMA-2 surrounded the conden
7 e MAGE gene family that is expressed in male germ line cells and placenta under normal physiological
8  through reciprocal interactions between the germ line cells and the somatic follicle cells that surr
9 s, topo I is detected in the nuclei of early germ-line cells and follicle cells.
10  7.3-kb AaVgR mRNA is present only in female germ-line cells and is abundant in previtellogenic oocyt
11                      The Ca channels of male germ-line cells are partially characterized, but the mol
12 cer/Testis (CT) genes, normally expressed in germ line cells but also activated in a wide range of ca
13 ) genes are predominantly expressed in human germ line cells, but not somatic tissues, and frequently
14 tors of germ-line expression because only in germ-line cells can retrotransposition result in inherit
15                                 Defining the germ-line cell compartments where the trinucleotide repe
16                      S. typhimurium-mediated germ-line cell death is not observed in C. elegans ced-3
17                          While the number of germ-line cell divisions might contribute to differences
18                                Men have more germ-line cell divisions than women.
19 erentiation of follicle cells and for proper germ line cell encapsulation during Drosophila oogenesis
20 es cytoplasmic proteins that are required in germ-line cells for cyst formation, nurse cell chromosom
21           IMA-2 was expressed exclusively in germ line cells from the early embryonic through adult s
22 ubunit, which is preferentially expressed in germ-line cells, has the greatest sequence divergence am
23 oprotein whose activity has been detected in germ line cells, immortal cells, and most cancer cells.
24                       There are extranumeral germ-line cells in individual egg chambers, while the fo
25 ntrosomal antigen previously detected in non-germ line cells is likely hCenexin1.
26 er in the absence of Bam (bag-of-marbles) in germ-line cells or the overexpression of Dpp (decapentap
27  Furthermore, bacterial load is increased in germ-line cells passing through infected niches, support
28                                           In germ line cells, recombination is required for gene reas
29                                 By contrast, germ-line cells showed no difference in mtDNA copy numbe
30 riations is higher for cancer cells than for germ-line cells, suggesting weaker purifying selection a
31                During the differentiation of germ-line cells, telomeres undergo significant reorganiz
32      StARD6, which is expressed only in male germ-line cells, thus exhibits biological and biophysica
33 ERVs) on several occasions, integrating into germ line cells to become part of the host genome, and s
34  of mus209(B1) is partly due to a failure of germ-line cells to proliferate.
35 fter exposure to ionising irradiation, or in germ line cells undergoing meiotic recombination.

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