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1 ATU gene at the homologous locus in the new macronucleus.
2 n, which produces a transcriptionally active macronucleus.
3 only wild-type genes in the polycopy somatic macronucleus.
4 nucleus and during anlagen formation for the macronucleus.
5 omial feeding apparatus and a large C-shaped macronucleus.
6 ot completely, eliminated from the polyploid macronucleus.
7 sion of the gene during development of a new macronucleus.
8 on of polytene chromosomes in the developing macronucleus.
9 s into a germline micronucleus and a somatic macronucleus.
10 s to eliminate DNA not wanted in the somatic macronucleus.
11 ion of the germline micronucleus and somatic macronucleus.
12 ninterrupted coding sequences in its somatic macronucleus.
13 age in the mitotic micronucleus and amitotic macronucleus.
14 clei: a germ line micronucleus and a somatic macronucleus.
15 and division of the Tetrahymena thermophila macronucleus.
16 mitotic micronucleus and polyploid amitotic macronucleus.
17 s of the 1.8 kb H1 Indel are retained in the macronucleus.
18 the creation of the transcriptionally active macronucleus.
19 ated subunit, p69, from the cytoplasm to the macronucleus.
20 and is located exclusively in the developing macronucleus.
21 ated cells and is absent from the vegetative macronucleus.
22 e efficiently eliminated from the developing macronucleus.
23 ngement during the formation of a functional macronucleus.
24 he formation of the transcriptionally active macronucleus.
25 cesses occur concomitantly in the developing macronucleus.
26 e represented at an average of 45 copies per macronucleus.
27 electron-dense structures in the developing macronucleus.
28 on chromosome 1L that are also found in the macronucleus.
29 those of the Tec elements in the developing macronucleus.
30 cell: a germline micronucleus and a somatic macronucleus.
31 ar genome into the somatic genome of the new macronucleus.
32 ring formation of a transcriptionally active macronucleus.
33 e found in markedly different numbers in the macronucleus.
34 d cells, with pronounced localization in the macronucleus.
35 During development of a micronucleus into a macronucleus after cell mating the IESs are excised from
37 sion of a micronucleus to a somatic nucleus (macronucleus) after cell mating, all IESs are excised fr
40 fter, pair separation, resorption of the old macronucleus, and elimination of one of the new micronuc
42 Results of a parallel mapping effort in the macronucleus, and the correspondence between the two gen
43 ed from the genome of the developing somatic macronucleus, and the old parental macronucleus is degra
45 uences (MDSs), that give rise to the somatic macronucleus are interrupted by internal eliminated sequ
49 pears from the centromeres in the developing macronucleus, consistent with centromeric sequences bein
50 nuclei: a somatic, transcriptionally active macronucleus containing hyperacetylated chromatin and a
51 e of the progeny; in contrast, the expressed macronucleus contains many copies of hundreds of small c
52 nthesis when expressed in the P. tetraurelia macronucleus, despite 24% primary sequence divergence of
53 IESs are AT-rich DNA segments that separate macronucleus-destined segments (MDSs) in micronuclear ge
54 have examined the chromatin structure of the macronucleus-destined sequences and Tec transposons, whi
56 he parental macronucleus is degraded and new macronucleus develops from a mitotic product of the zygo
59 amecium IES, the presence of this IES in the macronucleus does not completely inhibit excision of its
60 t a partially functional Cbs retained in the macronucleus does not induce chromosome breakage during
61 n that accompanies breakdown of the parental macronucleus during conjugation, correcting the previous
66 CnjBp colocalize with Twi1p in the parental macronucleus early in conjugation and in the new develop
67 ion and segregation, the same markers in the macronucleus fall into coassortment groups (CAGs) under
70 he development of a transcriptionally active macronucleus from a transcriptionally inert micronucleus
71 ation accompanies development of the somatic macronucleus from the germ-line micronucleus during the
76 genome shotgun sequencing of the Tetrahymena macronucleus has recently been completed at The Institut
77 th the mitotic micronucleus and the amitotic macronucleus in response to DSBs induced by chemical age
78 onuclear genome into the genome of a somatic macronucleus in Tetrahymena thermophila requires several
80 IES elements) eliminated from the developing macronucleus in the ciliate Tetrahymena thermophila are
81 us into the transcriptionally active somatic macronucleus in the ciliated protozoan Tetrahymena therm
82 y regulated excision during formation of the macronucleus in the ciliated protozoan TETRAHYMENA: Anal
83 s in the polyploid, transcriptionally active macronucleus, indicating that neither of the two genes i
86 ual reproduction (conjugation), the parental macronucleus is degraded and new macronucleus develops f
88 m distribution of alleles in the Tetrahymena macronucleus is due to the random distribution of the MA
91 nuclei: the transcriptionally active somatic macronucleus (MAC) and the transcriptionally silent germ
93 ves as the genetic blueprint for the somatic macronucleus (MAC), which is responsible for all transcr
97 A copy number is unaffected in the polyploid macronucleus, mechanisms that prevent reinitiation appea
100 trait: deletion elements present in the old macronucleus of one partner of a mating pair were suffic
101 fficult to clone since the 800-ploid somatic macronucleus of P. tetraurelia is a formidable obstacle
102 micronucleus and retention of others in the macronucleus of related species suggest an evolutionary
103 of DNA segments from the developing somatic macronucleus of Tetrahymena, yet how specific internal e
106 er of 30%, occurs in the developing amitotic macronucleus of the ciliate Tetrahymena thermophila.
107 50 copies of each chromosome in the somatic macronucleus of the ciliated protozoan TETRAHYMENA: Appr
109 by identical sequences are expressed in the macronucleus, only the former undergoes mitochondrial im
110 nscriptional activation and retention in the macronucleus or heterochromatization and elimination.
112 icronucleus and the transcriptionally active macronucleus - provides a powerful means for controlling
115 ive transcription products in the developing macronucleus; some even contain free-standing genes.
116 ly transcriptionally inactive, and a somatic macronucleus that contains a reduced, fragmented and rea
119 ssive divisions of an initially heterozygous macronucleus, the random distribution of alleles of loci
121 omic library through microinjection into the macronucleus, we have isolated a DNA fragment that compl
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